We would like to thank past and present members of the Samuelson laboratory for their assistance in the refinement of this method and/or discussion that aided the development of this manuscript. Research reported in this publication was supported by the National Institute on Aging of the National Institutes of Health under Award Numbers RF1AG062593 and R21AG064519. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

1. Preparation of reagents
<ol>
	<li>Select genes of interest to be inactivated via feeding-based RNAi. Purchase stocks of HT115 E. coli containing the RNAi clone of interest20. Alternatively, subclone the cDNA of the gene of interest into the multicloning site of the L4440 plasmid. 
	NOTE: To prevent degradation of dsRNA within the bacteria, use the HT115 strain. This is an RNase III-deficient E. coli strain with IPTG-inducible T7 polymerase activity. For proteostasis studies that do not use feeding-based RNAi, either HT115 or OP50 E. coli on standard NGM plates can be used.</li>
	<li>Prepare 5 x 6 cm plates per test condition. For experiments using RNAi, induce dsRNA production in transformed HT115 E. coli. For studies without RNAi, OP50 E. coli on standard NGM plates can be used (See Supplemental File 1 for standard NGM and RNAi plate recipes). 
	NOTE: RNAi plates can be stored at 4 &#176;C for several months before seeding with bacteria.</li>
	<li>Grow cultures of E. coli overnight (16-20 h) at 37 &#176;C in a shaking incubator at 220 rpm. Grow HT115 E. coli in Luria Broth (LB) with ampicillin (50 &#956;g/mL). 
	NOTE: Standard OP50 E. coli is not antibiotic resistant, but streptomycin resistant variants are also available.
	<ol>
		<li>Concentrate bacteria by centrifugation at 2,400 x g for 15-20 min in a benchtop centrifuge, aspirate the supernatant, and re-suspend the pellet in 1/10th the starting volume (i.e., 10x concentration) of LB with ampicillin for HT115, or LB without ampicillin for standard OP50.</li>
		<li>Aliquot 200 &#181;L of concentrated 10x bacteria to each plate (3-4 replicates per test condition, with 2 extra backup plates, to be used in the event of contamination).</li>
		<li>Allow open plates to dry in a clean environment such as a laminar flow bench until all liquid has been absorbed or allow covered plates to dry on a lab bench overnight.</li>
	</ol>
	</li>
	<li>For seeded RNAi plates dried in a hood, store dried plates within a worm box overnight (up to 24 hours) at room temperature. After 1 day at RT, plates can be stored at 4 &#176;C for up to 2 weeks in a sealed bag (to prevent plates from drying out). Before use, allow plates stored at 4 &#176;C to return to room temperature within the zip-lock bag to prevent condensation from introducing airborne fungal contaminates.
	<ol>
		<li>When using feeding-based RNAi, leave seeded HT115 bacteria on RNAi plates at room temperature for at least 12 hours prior to adding C. elegans. RNAi plates contain IPTG, which induces dsRNA production. Alternatively, IPTG can be added to the liquid cultures at the end of step 1.3.1, 2 hours prior to seeding.</li>
		<li>Avoid long-term storage of seeded HT115 plates at room temperature (greater than a few days) to avoid cracking of the agar that will cause C. elegans to burrow into agar.</li>
	</ol>
	</li>
</ol>
2. Synchronization of C. elegans
NOTE:&#160;Choose whether to synchronize C. elegans by either alkaline hypochlorite treatment of gravid adults or egg lay.
<ol>
	<li>Synchronize animals by hypochlorite treatment of gravid adult animals to promote the release of embryos22.
	<ol>
		<li>For hypochlorite treatment, wash gravid hermaphrodites 2 times with M9 buffer, then resuspend in 5 mL hypochlorite solution (3.25 mL of hypochlorite solution, 1 mL of M9 buffer and 0.75 mL of 5 M NaOH) for 5 min, shaking resuspended animals every minute. After 5 min, spin down animals and wash 3 times with M9 buffer. 
		NOTE: Hypochlorite treatment has been posited to affect proteostasis21.</li>
		<li>After hypochlorite treatment, allow embryos to hatch overnight in 3 mL of M9 solution with rotation at 20 &#176;C.</li>
		<li>Calculate the density of L1 animals (or alternatively, embryos) per &#181;L by dropping 10 &#181;L of L1 solution 3x onto a 6 cm plate and counting the number of L1 animals to calculate the average number of L1 animals per &#181;L. L1 animals will settle over time. Therefore, periodically mix L1 solutions to avoid settling.</li>
		<li>Seed 50 L1 animals per plate, count and record the number seeded, and move plates to a 20 &#176;C incubator. It is important to know the actual number of animals on each plate at the start of the assay. 
		NOTE: Synchronizing L1 animals by overnight hatching in M9 is routinely used as it minimizes developmental heterogeneity after placing animals onto food. However, synchronization occurs through developmental arrest in response to starvation cues, which for some studies should be avoided (see23 for additional discussion). As an alternative, roughly synchronized animals can be obtained through an egg-lay, see 2.2.</li>
		<li>Freeze and store leftover L1 animals in liquid nitrogen or a -80 &#176;C freezer. In this way, a sample of each strain at the time of the experimental setup is preserved, creating a valuable resource for future studies and improving reproducibility. 
		NOTE: See&#160;Supplemental File 1&#160;for hypochlorite and M9 solution recipes.</li>
	</ol>
	</li>
	<li>To synchronize animals via egg lay, place 20&#160;young gravid adult animals (day 1 of adulthood) onto each plate for 4-6 hours, and allow them to lay eggs until there are approximately 50 eggs per plate.&#160;Remove all gravid adults and move plates with eggs to a 20 &#176;C incubator. 
	NOTE: The gravid adult animals should be synchronized at the first day of adulthood. Older animals may lay eggs that have been retained in the uterus, causing the release of eggs that are in a more advanced developmental stage.</li>
</ol>
3. Progeny production
NOTE: Steps must be taken to either prevent progeny production or to separate the synchronized starting population from their progeny. Preventing progeny production can be achieved chemically with addition of 5-Fluoro-2&#39;-deoxyuridine (FUdR) to plates, which is described here. Some studies have reported that FUdR can alter proteostasis24,25. Alternative approaches to prevent progeny production are discussed below.
<ol>
	<li>Make a 1000x stock solution of FUdR by dissolving 1 g of FUdR into 10 mL of ultrapure H2O. Filter sterilize stock FUdR with a 0.2 &#956;m filter and a 10 mL syringe. Aliquot 1 mL of stock into a sterile 1.5 mL tube. Freeze and store at -20 &#176;C.</li>
	<li>Grow animals at 20 &#176;C until the L4 stage. N2 animals raised from synchronized L1s from hypochlorite treatment require approximately 40 hours of growth at 20 &#176;C to reach L4. Growth rates for other strains should be empirically tested prior to experimentation. For details on how to accurately stage C. elegans see26.
	<ol>
		<li>To each 6 cm plate with L4 animals, add 100 &#181;L of 80x FUdR. It is critical to add FUdR at the L4 stage.</li>
	</ol>
	</li>
	<li>Return plates to a worm box and put the box in a zip-lock bag. Return to appropriate incubator.</li>
</ol>
4. Measuring the decline in proteostasis in muscle tissue by using polyglutamine-expressing animals
NOTE: Two methods can be used to identify proteostasis decline in muscle cells: imaging the formation of protein aggregates during aging (4.1) and measuring the proteotoxicity these aggregates cause with age through the onset of paralysis (4.2).
<ol>
	<li>Imaging polyglutamine aggregate formation in the muscle during aging 
	NOTE: The age-dependent progression of protein aggregation in the muscle cells is imaged using polyglutamine (polyQ) repeats fused to a yellow fluorescent protein (YFP). This protocol outlines use of strain AM140 rmIs132[unc-54p::Q35::YFP], but other polyglutamine variant strains can also be used. The polyQ::YFP transgene is expressed in the muscle using the unc-54 muscle-specific promoter. Synchronized unc-54p::polyQ::YFP expressing animals are visualized at Day 1, 2, 3 and 4 of adulthood. To visualize unc-54p::polyQ::YFP aggregates, use a compound microscope equipped for fluorescence or a fluorescent dissecting microscope. AM140 is available from the Caenorhabditis Genetics Center (CGC) at: https://cgc.umn.edu/strain/AM140.
	<ol>
		<li>On imaging days (Day 1, 2, 3 and 4 of adulthood), pick 20 animals and mount on a microscope slide setup with a 3% agarose pad and a 5 &#956;L drop of 10 mM sodium azide (diluted in M9 buffer).</li>
		<li>After all animals&#160;are immobilized by sodium azide (~ 5 minutes), image the whole bodies of the animals using a 10x magnification lens (Figure 1A). For imaging, use a FITC filter and the same exposure for every animal. Discard slides after imaging. 
		NOTE: Alternatively, YFP foci can also be quantified directly on plates, but movement must be inhibited by applying a stream of carbon dioxide onto the plate while scoring. This alternative method is most appropriate when screening a large number of conditions (see discussion for more details).</li>
		<li>After acquisition of images, count the number of foci in the body wall muscles of the whole animal. Foci are brighter punctuated signals that can be differentiated from the dimmer soluble signal in the background.</li>
		<li>Plot the progression of YFP foci accumulation from days 1, 2, 3 and 4. Plot an XY graph where X represents days of adulthood and Y represents number of unc-54p::polyQ::YFP foci (Figure 1B). The number of foci in the experimental condition (e.g., gene downregulation or overexpression) is compared to control animals. Perform statistical analysis between the groups at each time point observed for each trial.
		<ol>
			<li>When comparing foci counts for only two conditions, perform an independent sample t-test at each time point.</li>
			<li>When comparing foci counts for more than two conditions, perform an omnibus one-way ANOVA analysis for each time point, including the data for all the conditions at that time point. If the omnibus ANOVA yields a significant p-value (i.e., p &#60; 0.005), perform a post-hoc analysis with pairwise independent sample t-tests to determine the specific conditions between which a significant difference in foci was detected (e.g., for groups A, B, and C compare A &#38; B, A &#38; C, and B &#38; C).</li>
		</ol>
		</li>
	</ol>
	</li>
	<li>Measuring animal paralysis rates as a surrogate for polyglutamine toxicity in muscle cells 
	NOTE: The age-dependent increase of polyQ aggregates in muscle causes the decline of muscular function that drives locomotion. This defect in locomotion can be determined by measuring the progressive rate of paralysis in polyQ-expressing animals. For the paralysis assay, synchronized unc-54p::polyQ::YFP expressing animals are scored at Day 3, 5, 7 and 9 of adulthood. Add additional time points, as needed to extend the scoring range, such that you can assess the effect of genetic perturbation.
	<ol>
		<li>On scoring days (Day 3, 5, 7 and 9 of adulthood), look at the 6 cm plates containing 50 animals and record the number of paralyzed animals. Remove paralyzed animals from the plate. If animals have crawled off the plate, or have died, they should be censored; record the event so it can be accounted for in the analysis. 
		NOTE: An animal is considered to be paralyzed when no movement is observed after exposing them to light or gentle touch stimuli. Pharyngeal pumping activity is used to determine whether nonmoving animals are alive or dead.</li>
		<li>At the completion of the experiment, calculate the paralysis rate for each condition. Do this at each time point by dividing the fraction of paralyzed animals by the total number of animals observed for that condition at that time. If observing multiple plates per condition per time point (i.e., replicate plates), calculate the ratio separately for each replicate.</li>
		<li>Plot the progression of paralysis rate in an XY graph (scatterplot). X represents days of adulthood and Y represents paralysis rates. The paralysis rate of unc-54p::polyQ::YFP animals is compared to control animals (Figure 1C). Perform statistical analysis between the groups; for multiple trials, treat trials independently. Use the Cox Proportional-Hazards Regression and the Wald test. Most data analysis tools that support survival analysis also support Cox modeling.
		<ol>
			<li>Transform the data: each condition should have two columns, one for time, and another for &#8220;event&#8221;. At each time point observed, add a row with &#8220;0&#8221; for each paralyzed animal, and a &#8220;1&#8221; for each censored animal. The total number of rows should be equal to the number of starting animals on the plate for that condition.</li>
			<li>Perform Cox Proportional-Hazards modeling, followed by the Wald test, according to instructions for your statistical software. A univariate model will be appropriate for typical experiment designs. For more than two conditions, if a test with all conditions included indicates a significant result (i.e., p &#60; 0.005), pairwise tests between conditions can be performed to determine the specific significant pair(s) of conditions. 
			NOTE: The Cox model relies on an assumption that the test condition(s) modulate the probability of an event proportionally over time. This means, for example, that the Cox model would not be appropriate for comparing a condition under which most animals are paralyzed at day 1 to a condition under which most animals are paralyzed at day 9. Extensions of the Cox model, and other approaches for comparing proportions paralyzed at each time point, are available for cases where the proportional hazards assumption does not hold, see27,28,29,30.</li>
		</ol>
		</li>
	</ol>
	</li>
</ol>
5. Measuring the decline in proteostasis in neuronal tissue by using polyglutamine expressing animals.
NOTE: Two complementary methods are used to assay proteostasis decline in neurons (1) by quantifying the formation of protein aggregates (fluorescent foci) during aging and (2) by measuring age-associated decline in the neuronal proteome via a movement-based assay.
<ol>
	<li>Imaging polyglutamine aggregate formation in the neurons during aging 
	NOTE: Similar to the assay already discussed in muscle tissue, the age-dependent progression of protein aggregation in the neurons is imaged by expressing a polyQ::YFP fusion protein driven by the pan-neuronal tissue-specific promoter of rgef-1. Specifically we use AM101: rmIs110 [rgef-1p::Q40::YFP], a forty glutamine fusion to YFP16. To visualize rgef-1p::polyQ::YFP, use a compound microscope equipped for fluorescence with a 40x magnification lens. AM101 is available from the CGC at: https://cgc.umn.edu/strain/AM101.
	<ol>
		<li>On imaging days (Day 4, 6, 8 and 10 of adulthood), pick 20 animals and mount on a microscope slide containing a 3% agarose pad with a 5 &#956;L drop of 10 mM sodium azide (diluted in M9 buffer).</li>
		<li>After all animals are immobilized by sodium azide (~ 5 minutes), take z-stack images of the head of the animals using a 40x magnification lens (Figure 2A). Discard slides after imaging.</li>
		<li>After acquisition of images, process&#160;z-stacks to obtain the maximum projection and use to quantify the number of foci in neurons located on the nerve ring area. Foci are brighter punctuated signals that can be differentiated from the dimmer soluble signal in the background. 
		NOTE: We specifically selected the nerve ring area to quantify rgef-1p::polyQ::YFP aggregates since this is the region where most neurons converge to make synaptic connections. However, in order to measure levels of aggregate formation in motor neurons, rgef-1p::polyQ::YFP aggregates located on the dorsal or ventral nerve cord can be quantified.</li>
		<li>Plot the progression of YFP foci accumulation from D4, D6, D8 and D10. Do this on an XY graph where X represents days of adulthood and Y represents number of rgef-1p::polyQ::YFP foci (Figure 2B). The number of foci in the experimental condition (e.g., gene downregulation or overexpression) is compared to control animals. Statistical analysis of foci counts for neurons is done in the same manner as for muscle polyQ foci; see steps 4.1.4&#160;and the associated notes.</li>
	</ol>
	</li>
	<li>Measuring body bends as a surrogate measure of polyglutamine proteotoxicity in neurons. 
	NOTE: The proteotoxic stress induced from the progressive aggregate accumulation of neuronal polyQ is determined by looking at motor neuron defects through a thrashing assay. Quantify the number of body bends in a period of 30 seconds while suspended in M9 physiological buffer (Supplemental File 1).
	<ol>
		<li>On Day 2 of adulthood, pick 10 synchronized animals from the plate and place on a 10 &#956;L drop of M9 buffer on a microscope slide. Repeat this step at least four times to get a sample of 40 or more animals.</li>
		<li>Video record the movement of the 10 animals placed on the microscope slide with 10 &#956;L of M9 buffer for a period of 30 s on a stereomicroscope with a video-capable camera. Repeat this step 4 times for a total sample number of 40. Zoom and position should be adjusted such that all the animals are visible in the frame for the full 30 seconds.</li>
		<li>Once all the videos with the animals to be analyzed are recorded, play the video and score the body bends of each animal. One body bend is defined as when the vulva of the animal goes from one side to the opposite and all the way back to the starting position. 
		NOTE: We find wild type animals typically have 49 &#177; 0.79 body bends in 30 seconds.</li>
		<li>Plot the number of body bends for each animal in a column graph where each dot represents the number of body bends in 30 s (Y axis) with the different conditions tested on the X axis. The number of body bends of unc-54p::polyQ::YFP animals is compared to control animals (Figure 2C). Perform statistical analysis between the groups independently for each trial; if the assay is repeated at multiple time points, analyze the data independently for each time point.
		<ol>
			<li>When considering only two conditions, perform an independent-sample t-test.</li>
			<li>When considering more than two conditions at once, first perform an omnibus one-way ANOVA analysis, including the data for all the conditions at that time trial/time point. If the omnibus ANOVA yields a significant p-value (i.e., p &#60; 0.005), perform a post-hoc analysis with pairwise independent sample t-tests to determine the specific conditions between which a significant difference in body bend count was detected.</li>
		</ol>
		</li>
	</ol>
	</li>
</ol>

The authors declare that they have no competing financial interests.

Aging is characterized by a gradual decline in proteostasis. Proteostasis is maintained by a complex system, the proteostatic network, for the coordinated, dynamic, stress-responsive control of protein folding, degradation, and translation. Why proteostasis fails in the course of aging is poorly understood, but a decaying epigenome, declining inducibility of stress responses, and loss of compensatory crosstalk all coincide with this breakdown. In C. elegans, the transcriptional inducibility of multiple forms of ...

Protein homeostasis (proteostasis) is defined as the cellular ability to maintain proper function and folding of the proteome. The inherent challenge to proteostasis is ensuring all proteins are properly folded and maintained in a native conformation, which is further amplified by the varied nature of protein size, amino acid composition, structural conformation, stability, turnover, expression, sub-cellular compartmentalization, and modifications1. Proteostasis is maintained through the coordinated action of a large proteostatic network, consisting of approximately 2000 unique proteins, which regulate proper synthesis, folding, trafficking, and degradation within the proteome2,3. The workhorse components of the proteostatic network are nine major families of molecular chaperones4. Every tissue and cell type preferentially utilizes specific subsets of molecular chaperones, presumably in alignment with the differing demands of distinct proteomes5.
One hallmark of normal organismal aging is the progressive decline and collapse of cellular proteostasis, which is thought to be an underlying basis for the onset and progression of a growing number of age-associated diseases. For instance, Alzheimer&#8217;s disease, Parkinson&#8217;s disease, Huntington&#8217;s disease, and Amyotrophic Lateral Sclerosis (ALS) share a common characteristic: in each case manifestation of neurodegeneration is driven by genetic alterations that predisposes a mutant protein to aggregation (amyloid-&#946;/Tau, &#945;-synuclein, HTT, FUS/TBD-43/SOD-1, respectively)6,7,8,9,10. During aging, the integrity and inducibility of the proteostatic network declines, which results in the accumulation of proteotoxic aggregates that result in cellular dysfunction and neurodegeneration. Of note, protein conformational diseases are not unique to neurons, and occur across multiple tissues, as highlighted by type II diabetes, multiple myeloma, and cystic fibrosis11,12,13,14. Therefore, elucidating mechanisms capable of preserving proteostasis will facilitate the development of targeted interventions for the treatment of disease and to promote healthy aging.
The small soil nematode Caenorhabditis elegans (C. elegans) has been instrumental in discovering genes and elucidating pathways that alter proteostasis. Many components of the proteostatic network and the signal transduction pathways that regulate proteostasis are evolutionarily conserved. Furthermore, C. elegans has reduced complexity and redundancy relative to vertebrate systems, making it more amenable to genetic analysis and gene discovery. Additional advantages of C. elegans that have led to it being widely used as a model system to study proteostasis include: powerful genetic and functional genomics, a short life cycle (3 days) and lifespan (3 weeks), a compact and well-annotated genome, the availability of a wide assortment of genetic mutants, and the ease of visualizing tissue-specific changes in cell biology using fluorescent reporters.
The progressive decay of proteostasis during aging can be easily quantified in C. elegans. The Morimoto laboratory first demonstrated that a polyglutamine expansion fused to yellow fluorescent protein (polyQ::YFP) could be used to quantify proteostatic decline in C. elegans during aging15,16,17,18. YFP fusions to 35 glutamine repeats or more result in an age-associated formation of fluorescent foci along with signs of cellular pathology. Of note, this range of glutamine expansion mirrors the length of the polyglutamine tract of the Huntingtin protein at which Huntington&#8217;s Disease pathology begins to be observed in humans (typically &#62;35 CAG repeats)19. Strains with expression of polyQ::YFP within muscle, intestinal, or neuronal cells have been utilized to confirm that the age-associated decline of proteostasis occurs across different cell and tissue types. Muscle-specific polyQ::YFP expression (i.e., unc-54p::Q35::YFP) has been the most widely used tissue-specific reporter, as accumulating fluorescent foci are easy to quantify over the first few days of adulthood using a simple fluorescent dissecting microscope (Figure 1A-1B). Additionally, animals become paralyzed during mid-life, as the proteome within the muscle collapses due to the proteotoxic effect of the reporter (Figure 1C). Similarly, the age-associated decline in neuronal proteostasis can be followed (rgef-1p::Q40::YFP) by directly quantifying foci/aggregate formation and age-associated declines in coordinated body-bends after placing animals into liquid (Figure 2).
Here, we present a detailed protocol on how to measure the age-dependent progression of protein aggregate accumulation and the associated proteotoxicity induced by the expression of polyglutamine repeats within neuronal and muscle tissue in C. elegans. We provide examples of typical results generated using these strains and methods. Further, we show how we have utilized these methods to study transcriptional regulation of the proteostatic network. We discuss additional ways these reporters can be easily integrated with other existing reagents or adapted for larger screens.

<table>
	<tbody>
		<tr>
			<td>24 Well Culture Plates</td>
			<td>Greiner Bio-One</td>
			<td>#662102</td>
			<td></td>
		</tr>
		<tr>
			<td>2 mL 96-well plates</td>
			<td>Greiner Bio-One</td>
			<td>#780286</td>
			<td></td>
		</tr>
		<tr>
			<td>600 &#181;L 96-well plates</td>
			<td>Greiner Bio-One</td>
			<td>#786261</td>
			<td></td>
		</tr>
		<tr>
			<td>96-pin plate replicator</td>
			<td>Nunc</td>
			<td>250520</td>
			<td></td>
		</tr>
		<tr>
			<td>Air-permeable plate seal</td>
			<td>VWR</td>
			<td>60941-086</td>
			<td></td>
		</tr>
		<tr>
			<td>bacteriological agar</td>
			<td>Affymetrix/USB</td>
			<td>10906</td>
			<td></td>
		</tr>
		<tr>
			<td>bacto-peptone</td>
			<td>VWR</td>
			<td>90000-368</td>
			<td></td>
		</tr>
		<tr>
			<td>C. elegans RNAi clone library in HT115 bacteria- Ahringer</td>
			<td>Source Bioscience</td>
			<td>C. elegans RNAi Collection (Ahringer)</td>
			<td>See also Kamath et. al, Nature 2003.</td>
		</tr>
		<tr>
			<td>C. elegans RNAi clone library in HT115 bacteria- Vidal</td>
			<td>Source Bioscience</td>
			<td>C. elegans ORF-RNAi Resource (Vidal)</td>
			<td>See also Rual et. al, Genome Research 2004. This library is also available from Dharmacon.</td>
		</tr>
		<tr>
			<td>FuDR (5-Fluoro-2&#39;-deoxyuridine)</td>
			<td>Alfa Aesar</td>
			<td>L16497</td>
			<td></td>
		</tr>
		<tr>
			<td>Glass microscope cover slips</td>
			<td>VWR</td>
			<td>48404-455</td>
			<td></td>
		</tr>
		<tr>
			<td>Glass microscope slides</td>
			<td>VWR</td>
			<td>160004-422</td>
			<td></td>
		</tr>
		<tr>
			<td>IPTG (isopropyl beta-D-1-thigalactopyranoside)</td>
			<td>Gold Bio</td>
			<td>12481C100</td>
			<td></td>
		</tr>
		<tr>
			<td>Retangular non-treated single-well plate, 128x86mm</td>
			<td>Thermo-Fisher</td>
			<td>242811</td>
			<td></td>
		</tr>
		<tr>
			<td>Sodium Azide, CAS #26628-22-8</td>
			<td>Sigma-Aldrich</td>
			<td>S2002</td>
			<td></td>
		</tr>
		<tr>
			<td>Zeiss Axio Imager M2m microscope with AxioVision v4.8.2.0 software</td>
			<td>Zeiss</td>
			<td>unknown</td>
			<td></td>
		</tr>
		<tr>
			<td>Zeiss StemiSV11 M2 Bio Quad microscope</td>
			<td>Zeiss</td>
			<td>unknown</td>
			<td></td>
		</tr>
	</tbody>
</table>

quantifying tissue-specific proteostatic decline in caenorhabditis elegans

The ability to maintain proper function and folding of the proteome (protein homeostasis) declines during normal aging, facilitating the onset of a growing number of age-associated diseases. For instance, proteins with polyglutamine expansions are prone to aggregation, as exemplified with the huntingtin protein and concomitant onset of Huntington&#8217;s disease. The age-associated deterioration of the proteome has been widely studied through the use of transgenic Caenorhabditis elegans expressing polyQ repeats fused to a yellow fluorescent protein (YFP). This polyQ::YFP transgenic animal model facilitates the direct quantification of the age-associated decline of the proteome through imaging the progressive formation of fluorescent foci (i.e., protein aggregates) and subsequent onset of locomotion defects that develop as a result of the collapse of the proteome. Further, the expression of the polyQ::YFP transgene can be driven by tissue-specific promoters, allowing the assessment of proteostasis across tissues in the context of an intact multicellular organism. This model is highly amenable to genetic analysis, thus providing an approach to quantify aging that is complementary to lifespan assays. We describe how to accurately measure polyQ::YFP foci formation within either neurons or body wall muscle during aging, and the subsequent onset of behavioral defects. Next, we highlight how these approaches can be adapted for higher throughput, and potential future applications using other emerging strategies for C. elegans genetic analysis.

In C. elegans, the polyglutamine repeat model has been instrumental for the identification of genes that regulate the proteostatic network. For instance, we previously showed that the homeodomain interacting protein kinase (hpk-1), a transcriptional cofactor, influences proteostasis during aging by regulating expression of autophagy and molecular chaperones31. We found that loss of hpk-1, either by RNAi silencing or in hpk-1(pk1393) null mutant animals, increase...

Watch this Scientific Journal Video about Quantifying Tissue-Specific Proteostatic Decline in Caenorhabditis elegans at JoVE.com

Quantifying Tissue-Specific Proteostatic Decline in Caenorhabditis elegans

Proteostatic decline is a hallmark of aging, facilitating the onset of neurodegenerative diseases. We outline a protocol to quantifiably measure proteostasis in two different Caenorhabditis elegans tissues through heterologous expression of polyglutamine repeats fused to a fluorescent reporter. This model allows rapid in vivo genetic analysis of proteostasis.

Quantifying Tissue-Specific Proteostatic Decline in Caenorhabditis elegans

The ability to maintain proper function and folding of the proteome (protein homeostasis) declines during normal aging, facilitating the onset of a ...

quantifying-tissue-specific-proteostatic-decline-caenorhabditis

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2.8K Views.  University of Rochester Medical Center. Proteostatic decline is a hallmark of aging, facilitating the onset of neurodegenerative diseases. We outline a protocol to quantifiably measure proteostasis in two different Caenorhabditis elegans tissues through heterologous expression of polyglutamine repeats fused to a fluorescent reporter. This model allows rapid in vivo genetic analysis of proteostasis.

Video: Quantifying Tissue-Specific Proteostatic Decline in Caenorhabditis elegans

Isolation and In vitro Activation of Caenorhabditis elegans Sperm

Males and hermaphrodites are the two naturally found sexual forms in the nematode C. elegans. The amoeboid sperm are produced by both males and hermaphrodites. In the earlier phase of gametogenesis, the germ cells of hermaphrodites differentiate into limited number of sperm - around 300 - and are stored in a small 'bag' called the spermatheca. Later on, hermaphrodites continually produce oocytes1. In contrast, males produce exclusively sperm throughout their adulthood. The males produce so much sperm that it accounts for &gt;50% of the total cells in a typical adult worm2. Therefore, isolating sperm from males is easier than from that of hermaphrodites.
Only a small proportion of males are naturally generated due to spontaneous non-disjunction of X chromosome3. Crossing hermaphrodites with males or more conveniently, the introduction of mutations to give rise to Him (High Incidence of Males) phenotype are some of strategies through which one can enrich the male population3.
Males can be easily distinguished from hermaphrodites by observing the tail morphology4. Hermaphrodite's tail is pointed, whereas male tail is rounded with mating structures.
Cutting the tail releases vast number of spermatids stored inside the male reproductive tract. Dissection is performed under a stereo microscope using 27 gauge needles. Since spermatids are not physically connected with any other cells, hydraulic pressure expels internal contents of male body, including spermatids2.
Males are directly dissected on a small drop of 'Sperm Medium'. Spermatids are sensitive to alteration in the pH. Hence, HEPES, a compound with good buffering capacity is used in sperm media. Glucose and other salts present in sperm media help maintain osmotic pressure to maintain the integrity of sperm.
Post-meiotic differentiation of spermatids into spermatozoa is termed spermiogenesis or sperm activation. Shakes5, and Nelson6 previously showed that round spermatids can be induced to differentiate into spermatozoa by adding various activating compounds including Pronase E. Here we demonstrate in vitro spermiogenesis of C. elegans spermatids using Pronase E.
Successful spermiogenesis is pre-requisite for fertility and hence the mutants defective in spermiogenesis are sterile. Hitherto several mutants have been shown to be defective specifically in spermiogenesis process7. Abnormality found during in vitro activation of novel Spe (Spermatogenesis defective) mutants would help us discover additional players participating in this event.

Isolation and In vitro Activation of Caenorhabditis elegans Sperm

A protocol for isolating and activating spermatids from male C. elegans is described here. Cutting the posterior end of male releases spermatids. The spermatids can be activated by addition of protease.

Males and hermaphrodites are the two naturally found sexual forms in the nematode C. elegans. The amoeboid sperm are produced by both males and ...

Solid Plate-based Dietary Restriction in Caenorhabditis elegans

Reduction of food intake without malnutrition or starvation is known to increase lifespan and delay the onset of various age-related diseases in a wide range of species, including mammals. It also causes a decrease in body weight and fertility, as well as lower levels of plasma glucose, insulin, and IGF-1 in these animals. This treatment is often referred to as dietary restriction (DR) or caloric restriction (CR). The nematode Caenorhabditis elegans has emerged as an important model organism for studying the biology of aging. Both environmental and genetic manipulations have been used to model DR and have shown to extend lifespan in C. elegans. However, many of the reported DR studies in C. elegans were done by propagating animals in liquid media, while most of the genetic studies in the aging field were done on the standard solid agar in petri plates. Here we present a DR protocol using standard solid NGM agar-based plate with killed bacteria.

Solid Plate-based Dietary Restriction in Caenorhabditis elegans

Here we present a protocol for performing solid plate-based dietary restriction in C. elegans with killed bacteria.

Reduction of food intake without malnutrition or starvation is known to increase lifespan and delay the onset of various age-related diseases in a wide ...

Time-lapse Microscopy of Early Embryogenesis in Caenorhabditis elegans

Caenorhabditis elegans has often been used as a model system in studies of early developmental processes. The transparency of the 
embryos, the genetic resources, and the relative ease of transformation are qualities that make C. elegans an excellent model for early embryogenesis. Laser-based 
confocal microscopy and fluorescently labeled tags allow researchers to follow specific cellular structures and proteins in the developing embryo. For example, 
one can follow specific organelles, such as lysosomes or mitochondria, using fluorescently labeled dyes. These dyes can be delivered to the early embryo by means 
of microinjection into the adult gonad. Also, the localization of specific proteins can be followed using fluorescent protein tags. Examples are presented here 
demonstrating the use of a fluorescent lysosomal dye as well as fluorescently tagged histone and ubiquitin proteins. The labeled histone is used to visualize 
the DNA and thus identify the stage of the cell cycle. GFP-tagged ubiquitin reveals the dynamics of ubiquitinated vesicles in the early embryo. Observations 
of labeled lysosomes and GFP:: ubiquitin can be used to determine if there is colocalization between ubiquitinated vesicles and lysosomes. A technique for 
the microinjection of the lysosomal dye is presented. Techniques for generating transgenenic strains are presented elsewhere (1, 2). For imaging, embryos 
are cut out of adult hermaphrodite nematodes and mounted onto 2% agarose pads followed by time-lapse microscopy on a standard laser scanning confocal 
microscope or a spinning disk confocal microscope. This methodology provides for the high resolution visualization of early embryogenesis.

Time-lapse Microscopy of Early Embryogenesis in Caenorhabditis elegans

This article describes a technique for the visualization of the early events of embryogenesis in the nematode Caenorhabditis elegans.

Caenorhabditis elegans has often been used as a model system in studies of early developmental processes.  The transparency of the 
embryos, the genetic ...

Basic Caenorhabditis elegans Methods: Synchronization and Observation

Research into the molecular and developmental biology of the nematode Caenorhabditis elegans was begun in the early seventies by Sydney Brenner and it has since been used extensively as a model organism 1. C. elegans possesses key attributes such as simplicity, transparency and short life cycle that have made it a suitable experimental system for fundamental biological studies for many years 2. Discoveries in this nematode have broad implications because many cellular and molecular processes that control animal development are evolutionary conserved 3.
C. elegans life cycle goes through an embryonic stage and four larval stages before animals reach adulthood. Development can take 2 to 4 days depending on the temperature. In each of the stages several characteristic traits can be observed. The knowledge of its complete cell lineage 4,5 together with the deep annotation of its genome turn this nematode into a great model in fields as diverse as the neurobiology 6, aging 7,8, stem cell biology 9 and germ line biology 10. 
An additional feature that makes C. elegans an attractive model to work with is the possibility of obtaining populations of worms synchronized at a specific stage through a relatively easy protocol. The ease of maintaining and propagating this nematode added to the possibility of synchronization provide a powerful tool to obtain large amounts of worms, which can be used for a wide variety of small or high-throughput experiments such as RNAi screens, microarrays, massive sequencing, immunoblot or in situ hybridization, among others. 
Because of its transparency, C. elegans structures can be distinguished under the microscope using Differential Interference Contrast microscopy, also known as Nomarski microscopy. The use of a fluorescent DNA binder, DAPI (4',6-diamidino-2-phenylindole), for instance, can lead to the specific identification and localization of individual cells, as well as subcellular structures/defects associated to them.

Basic Caenorhabditis elegans Methods: Synchronization and Observation

The easiness of maintaining and propagating the nematode C. elegans make it a nice model organism to work with. The possibility of synchronizing worms allows the work with a significant amount of subjects at the same developmental stage, what facilitates the study of one particular process in many animals.

Research into the molecular and developmental biology of the nematode Caenorhabditis elegans was begun in the early seventies by Sydney Brenner and it has ...

Prostaglandin Extraction and Analysis in Caenorhabditis elegans

Caenorhabditis elegans is emerging as a powerful animal model to study the biology of lipids1-9. Prostaglandins are an important class of eicosanoids, which are lipid signals derived from polyunsaturated fatty acids (PUFAs)10-14. These signalling molecules are difficult to study because of their low abundance and reactive nature. The characteristic feature of prostaglandins is a cyclopentane ring structure located within the fatty acid backbone. In mammals, prostaglandins can be formed through cyclooxygenase enzyme-dependent and -independent pathways10,15. C. elegans synthesizes a wide array of prostaglandins independent of cyclooxygenases6,16,17. A large class of F-series prostaglandins has been identified, but the study of eicosanoids is at an early stage with ample room for new discoveries. Here we describe a procedure for extracting and analyzing prostaglandins and other eicosanoids. Charged lipids are extracted from mass worm cultures using a liquid-liquid extraction technique and analyzed by liquid chromatography coupled to electrospray ionization tandem mass spectrometry (LC-ESI-MS/MS). The inclusion of deuterated analogs of prostaglandins, such as PGF2 &alpha;-d4 as an internal standard is recommended for quantitative analysis. Multiple reaction monitoring or MRM can be used to quantify and compare specific prostaglandin types between wild-type and mutant animals. Collision-induced decomposition or MS/MS can be used to obtain information on important structural features. Liquid chromatography mass spectrometry (LC-MS) survey scans of a selected mass range, such as m/z 315-360 can be used to evaluate global changes in prostaglandin levels. We provide examples of all three analyses. These methods will provide researchers with a toolset for discovering novel eicosanoids and delineating their metabolic pathways.

Prostaglandin Extraction and Analysis in Caenorhabditis elegans

In this paper, we describe an optimized procedure for extracting and analyzing prostaglandins and other eicosanoids from C. elegans using LC-MS/MS.

Caenorhabditis elegans is emerging as a powerful animal model to study the biology of lipids1-9. Prostaglandins are an important class of eicosanoids, ...

Cultivation of Caenorhabditis elegans in Three Dimensions in the Laboratory

The use of genetic model organisms such as Caenorhabditis elegans has led to seminal discoveries in biology over the last five decades. Most of what we know about C. elegans is limited to laboratory cultivation of the nematodes that may not necessarily reflect the environments they normally inhabit in nature. Cultivation of C. elegans in a 3D habitat that is more similar to the 3D matrix that worms encounter in rotten fruits and vegetative compost in nature could reveal novel phenotypes and behaviors not observed in 2D. In addition, experiments in 3D can address how phenotypes we observe in 2D are relevant for the worm in nature. Here, a new method in which C. elegans grows and reproduces normally in three dimensions is presented. Cultivation of C. elegans in Nematode Growth Tube-3D (NGT-3D) can allow us to measure the reproductive fitness of C. elegans strains or different conditions in a 3D environment. We also present a novel method, termed Nematode Growth Bottle-3D (NGB-3D), to cultivate C. elegans in 3D for microscopic analysis. These methods allow scientists to study C. elegans biology in conditions that are more reflective of the environments they encounter in nature. These can help us to understand the overlying evolutionary relevance of the physiology and behavior of C. elegans we observe in the laboratory.

Cultivation of Caenorhabditis elegans in Three Dimensions in the Laboratory

We present a simple method to construct 3D nematode cultivation systems called NGT-3D and NGB-3D. These can be used to study nematode fitness and behaviors in habitats that are more similar to natural Caenorhabditis elegans habitats than the standard 2D laboratory C. elegans culture plates.

The use of genetic model organisms such as Caenorhabditis elegans has led to seminal discoveries in biology over the last five decades. Most of what we ...

Combined Nucleotide and Protein Extractions in Caenorhabditis elegans

A single biological sample holds a plethora of information, and it is now common practice to simultaneously investigate several macromolecules to capture a full picture of the multiple levels of molecular processing and changes between different conditions. This protocol presents the method of isolating DNA, RNA, and protein from the same sample of the nematode Caenorhabditis elegans to remove the variation introduced when these biomolecules are isolated from replicates of similarly treated but ultimately different samples. Nucleic acids and protein are extracted from the nematode using the acid guanidinium thiocyanate-phenol-chloroform extraction method, with subsequent precipitation, washing, and solubilization of each. We show the successful isolation of RNA, DNA, and protein from a single sample from three strains of nematode and HeLa cells, with better protein isolation results in adult animals. Additionally, guanidinium thiocyanate-phenol-chloroform-extracted protein from nematodes improves the resolution of larger proteins, with enhanced detectable levels as observed by immunoblotting, compared to the traditional RIPA extraction of protein.
The method presented here is useful when investigating samples using a multiomic approach, specifically for the exploration of the proteome and transcriptome. Techniques that simultaneously assess multiomics are appealing because molecular signaling underlying complex biological phenomena is thought to occur at complementary levels; however, it has become increasingly common to see that changes in mRNA levels do not always reflect the same change in protein levels and that the time of collection is relevant in the context of circadian regulations. This method removes any intersample variation when assaying different contents within the same sample (intrasample.)

Combined Nucleotide and Protein Extractions in Caenorhabditis elegans

Here, we present a protocol for the isolation of RNA, DNA, and protein from the same sample, in an effort to reduce variation, improve reproducibility, and facilitate interpretations.

A single biological sample holds a plethora of information, and it is now common practice to simultaneously investigate several macromolecules to capture ...

Measurement of Oxygen Consumption Rates in Intact Caenorhabditis elegans

Optimal mitochondrial function is critical for healthy cellular activity, particularly in cells that have high energy demands like those in the nervous system and muscle. Consistent with this, mitochondrial dysfunction has been associated with a myriad of neurodegenerative diseases and aging in general. Caenorhabditis elegans have been a powerful model system for elucidating the many intricacies of mitochondrial function. Mitochondrial respiration is a strong indicator of mitochondrial function and recently developed respirometers offer a state-of-the-art platform to measure respiration in cells. In this protocol, we provide a technique to analyze live, intact C. elegans. This protocol spans a period of ~7 days and includes steps for (1) growing and synchronization of C. elegans, (2) preparation&#160;of compounds to be injected and hydration of probes, (3) drug loading and cartridge equilibration, (4) preparation of worm assay plate and assay run, and (5) post-experiment data analysis.

Measurement of Oxygen Consumption Rates in Intact Caenorhabditis elegans

Mitochondrial respiration is critical for organismal survival; therefore, oxygen consumption rate is an excellent indicator of mitochondrial health. In this protocol, we describe the use of a commercially available respirometer to measure basal and maximal oxygen consumption rates in live, intact, and freely-motile Caenorhabditis elegans.

Optimal mitochondrial function is critical for healthy cellular activity, particularly in cells that have high energy demands like those in the nervous ...

Using Caenorhabditis elegans to Screen for Tissue-Specific Chaperone Interactions

Correct folding and assembly of proteins and protein complexes are essential for cellular function. Cells employ quality control pathways that correct, sequester or eliminate damaged proteins to maintain a healthy proteome, thus ensuring cellular proteostasis and preventing further protein damage. Because of redundant functions within the proteostasis network, screening for detectable phenotypes using knockdown or mutations in chaperone-encoding genes in the multicellular organism Caenorhabditis elegans results in the detection of minor or no phenotypes in most cases. We have developed a targeted screening strategy to identify chaperones required for a specific function and thus bridge the gap between phenotype and function. Specifically, we monitor novel chaperone interactions using RNAi synthetic interaction screens, knocking-down chaperone expression, one chaperone at a time, in animals carrying a mutation in a chaperone-encoding gene or over-expressing a chaperone of interest. By disrupting two chaperones that individually present no gross phenotype, we can identify chaperones that aggravate or expose a specific phenotype when both perturbed. We demonstrate that this approach can identify specific sets of chaperones that function together to modulate the folding of a protein or protein complexes associated with a given phenotype.

Using Caenorhabditis elegans to Screen for Tissue-Specific Chaperone Interactions

To study chaperone-chaperone and chaperone-substrate interactions, we perform synthetic interaction screens in Caenorhabditis elegans using RNA interference in combination with mild mutations or over-expression of chaperones and monitor tissue-specific protein dysfunction at the organismal level.

Correct folding and assembly of proteins and protein complexes are essential for cellular function. Cells employ quality control pathways that correct, ...

Modeling Age-Associated Neurodegenerative Diseases in Caenorhabditis elegans

Battling human neurodegenerative pathologies and managing their pervasive socioeconomic impact is becoming a global priority. Notwithstanding their detrimental effects on the human life quality and the healthcare system, the majority of human neurodegenerative disorders still remain incurable and non-preventable. Therefore, the development of novel therapeutic interventions against such maladies is becoming a pressing urgency. Age-associated deterioration of neuronal circuits and function is evolutionarily conserved in organisms as diverse as the lowly worm Caenorhabditis elegans and humans, signifying similarities in the underlying cellular and molecular mechanisms. C. elegans is a highly malleable genetic model, which offers a well-characterized nervous system, body transparency and a diverse repertoire of genetic and imaging techniques to assess neuronal activity and quality control during ageing. Here, we introduce and describe methodologies utilizing some versatile nematode models, including hyperactivated ion channel-induced necrosis (e.g., deg-3(d) and mec-4(d)) and protein aggregate (e.g., &#945;-syunclein and poly-glutamate)-induced neurotoxicity, to monitor and dissect the cellular and molecular underpinnings of age-related neuronal breakdown. A combination of these animal neurodegeneration models, together with genetic and pharmacological screens for cell death modulators will lead to an unprecedented understanding of age-related breakdown of neuronal function and will provide critical insights with broad relevance to human health and quality of life.

Modeling Age-Associated Neurodegenerative Diseases in Caenorhabditis elegans

Here, we introduce and describe widely accessible methodologies utilizing some versatile nematode models, including hyperactivated ion channel-induced necrosis and protein aggregate-induced neurotoxicity, to monitor and dissect the cellular and molecular underpinnings of age-associated neurodegenerative diseases.

Battling human neurodegenerative pathologies and managing their pervasive socioeconomic impact is becoming a global priority. Notwithstanding their ...