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Fluorescence resonance energy transfer (FRET) is an imaging technique for detecting protein interactions in living cells. Here, a FRET protocol is presented to study the association of histone-modifying enzymes with transcription factors that recruit them to the target promoters for epigenetic regulation of gene expression in plant tissues.
Epigenetic regulation of gene expression is commonly affected by histone modifying enzymes (HMEs) that generate heterochromatic or euchromatic histone marks for transcriptional repression or activation, respectively. HMEs are recruited to their target chromatin by transcription factors (TFs). Thus, detecting and characterizing direct interactions between HMEs and TFs are critical for understanding their function and specificity better. These studies would be more biologically relevant if performed in vivo within living tissues. Here, a protocol is described for visualizing interactions in plant leaves between a plant histone deubiquitinase and a plant transcription factor using fluorescence resonance energy transfer (FRET), which allows the detection of complexes between protein molecules that are within <10 nm from each other. Two variations of the FRET technique are presented: SE-FRET (sensitized emission) and AB-FRET (acceptor bleaching), in which the energy is transferred non-radiatively from the donor to the acceptor or emitted radiatively by the donor upon photobleaching of the acceptor. Both SE-FRET and AB-FRET approaches can be adapted easily to discover other interactions between other proteins in planta.
Plant histone deubiquitinases play an important role in controlling gene expression by post-translational modification of histones, specifically by erasing their monoubiquitylation marks1. So far, OTLD1 is one of the only few plant histone deubiquitinases characterized at the molecular level in Arabidopsis2,3. OTLD1 removes monoubiquitin groups from the H2B histone molecules, thereby promoting the removal or addition of euchromatic acetylation and methylation modifications of H3 histones in the target gene chromatin4,5. Moreover....
Nicotiana benthamiana, Agrobacterium tumefaciens strain EHA105, or GV3101 were used for the present study.
1. FRET vector construction
Figure 2 illustrates the typical results of a SE-FRET experiment, in which the cell nuclei were simultaneously recorded in three channels (i.e., donor GFP, acceptor mRFP, and SE-FRET). These data were used to generate images of SE-FRET efficiency coded in a pseudo-color scale. On this scale, the transition from blue to red corresponds to an increase in FRET efficiency, a measure of protein-protein proximity from 0% to 100%. In this representative experiment, the SE-FRET signal was recorded i.......
This FRET protocol is simple and easy to reproduce; it also requires minimal supply investment and utilizes standard equipment for many modern laboratories. Specifically, five main technical features distinguish the versatility of this procedure. First, the FRET constructs are generated using site-specific recombination, a cloning approach that is easy to use, produces accurate results, and saves time compared to traditional restriction enzyme-based cloning. Second, N. benthamiana plants are simple to grow, prod.......
No conflicts of interest were declared.
The work in V.C.'s laboratory is supported by grants from NIH (R35GM144059 and R01GM50224), NSF (MCB1913165 and IOS1758046), and BARD (IS-5276-20) to V.C.
....Name | Company | Catalog Number | Comments |
Acetosyringone (3′,5′-Dimethoxy-4′-hydroxyacetophenone) | Sigma-Aldrich | #D134406-1G | |
Bacto Agar | BD Biosciences | #214010 | |
Bacto trypton | BD Biosciences | #211705 | |
Bacto yeast extract | BD Biosciences | #212750 | |
Confocal laser scanning microscope (CLSM) | Zeiss | LSM900 | Any CLSM with similar capabilities is suitable |
EHA105 | VWR | 104013-310 | We use the stock in the Citovsky bacterial lab stock collection |
Gateway BP Clonase II | Invitrogen | #11789100 | |
Gateway LR Clonase II | Invitrogen | #11791020 | |
GV3101 | VWR | 104013-296 | We use the stock in the Citovsky bacterial lab stock collection |
ImageJ | https://imagej.nih.gov/ij/download.html | ||
MES | Sigma-Aldrich | #69889-10G | |
MgCl2 | Sigma-Aldrich | #63068-250G | |
NaCl | Sigma-Aldrich | #S5886-500G | |
Nicotiana benthamiana seeds | Herbalistics Pty | RA4 or LAB | We use the stock in the Citovsky seed lab stock collection |
pDONR207 | Invitrogen | #12213013 | |
pPZP-RCS2A-DEST-EGFP-N1 | N/A | Refs. 15, 28 | |
pPZP-RCS2A-DEST-mRFP-C1 | N/A | Generated based on the pPZP-RCS2A-DEST-EGFP-C1 construct (see refs. 15, 28) | |
pPZP-RCS2A-DEST-mRFP-N1 | N/A | Generated based on the pPZP-RCS2A-DEST-EGFP-N1 construct | |
Rifampicin | Sigma-Aldrich | #R7382-5G | |
Spectinomycin | Sigma-Aldrich | #S4014-5G | |
Syringes without needles | BD | 309659 | |
Zen software for CLSM imaging | Zeiss | ZEN 3.0 version | The software should be compatible with the CLSM used |
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