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The protocol describes an efficient and reliable method for quantifying the poly(A) length of the gene of interest from the Drosophila nervous system, which can be easily adapted to tissues or cell types from other species.
Polyadenylation is a crucial posttranscriptional modification that adds poly(A) tails to the 3' end of mRNA molecules. The length of the poly(A) tail is tightly regulated by cellular processes. Dysregulation of mRNA polyadenylation has been associated with abnormal gene expression and various diseases, including cancer, neurological disorders, and developmental abnormalities. Therefore, comprehending the dynamics of polyadenylation is vital for unraveling the complexities of mRNA processing and posttranscriptional gene regulation.
This paper presents a method for measuring poly(A) tail lengths in RNA samples isolated from Drosophila larval brains and Drosophila Schneider S2 cells. We employed the guanosine/inosine (G/I) tailing approach, which involves the enzymatic addition of G/I residues at the 3' end of mRNA using yeast poly(A) polymerase. This modification protects the RNA's 3' end from enzymatic degradation. The protected full-length poly(A) tails are then reverse-transcribed using a universal antisense primer. Subsequently, PCR amplification is performed using a gene-specific oligo that targets the gene of interest, along with a universal sequence oligo used for reverse transcription.
This generates PCR products encompassing the poly(A) tails of the gene of interest. Since polyadenylation is not a uniform modification and results in tails of varying lengths, the PCR products display a range of sizes, leading to a smear pattern on agarose gel. Finally, the PCR products are subjected to high-resolution capillary gel electrophoresis, followed by quantification using the sizes of the poly(A) PCR products and the gene-specific PCR product. This technique offers a straightforward and reliable tool for analyzing poly(A) tail lengths, enabling us to gain deeper insights into the intricate mechanisms governing mRNA regulation.
Most eukaryotic mRNAs are posttranscriptionally polyadenylated at their 3′ terminus in the nucleus by the addition of non-templated adenosines by canonical poly(A) polymerases. An intact poly(A) tail is pivotal throughout the lifecycle of mRNA, as it is essential for mRNA nuclear export1, facilitates interaction with poly(A)-binding proteins to enhance translational efficiency2, and imparts resistance against degradation3. In certain cases, the poly(A) tail can also undergo extension in the cytoplasm, facilitated by noncanonical poly(A) polymerases4. In the cytoplasm,....
1. Rearing and selecting Drosophila larvae
Here, we analyzed the poly(A) tail length of Dscam1 and GAPDH from Drosophila larval brains (Figure 4). Isolated RNAs were visualized on an agarose gel for quality control. A single RNA band at around 600 nucleotide size indicates intact RNA preparation (Figure 2A). RNAs were subjected to the G/I tailing and high-resolution capillary electrophoresis using an Agilent 2100 bioanalyzer. The gel images were exported using the Agilent 2100 .......
In this protocol, we describe the technique to dissect the Drosophila larval brain from wandering 3rd instar stage as well as the sample preparation from Drosophila S2 cells. Due to the labile nature of mRNAs, sample collection requires extra caution. For larval brain dissection, brains should not be damaged during isolation and should not be kept in solution for a prolonged duration. Keeping dissection time to 8-10 min for a round of dissection is essential. It may also be beneficial to supp.......
This study was supported by the National Institute of Neurological Disorders and Stroke Grant R01NS116463 to J.K., and the Cellular and Molecular Imaging Core facility at the University of Nevada, Reno, which was supported by National Institutes of Health Grant P20GM103650 and used for research reported in this study.
....Name | Company | Catalog Number | Comments |
3-(N-morpholino) propanesulfonic acid (MOPS) | Research Product Internation (RPI) | M92020 | |
Agilent High Sensitivity DNA Kit | Agilent Technologies | 5067-4626 | |
Agilent software 2100 expert free download demo | Agilent Technologies | https://www.agilent.com/en/product/automated-electrophoresis/bioanalyzer-systems/bioanalyzer-software/2100-expert-software-228259 | |
Apex 100 bp-Low DNA Ladder | Genesee Scientific | 19-109 | |
Bioanalyzer | Agilent 2100 Bioanalyzer G2938C | ||
Diethyl pyrocarbonate (DEPC) | Research Product Internation (RPI) | D43060 | |
DNA dye (Gel Loading Dye, Purple (6x) | New England biolabs | B7024S | |
Drosophila S2 cell line | Drosophila Genomics Resource Center stock #181 | ||
Drosophila Schneider’s Medium | Thermo Fisher Scientific | 21720024 | |
Ehidium bromide | Genesee scientific | 20-276 | |
Fetal bovine serum (FBS) | Sigma-Aldrich | F4135 | |
Forceps Dumont 5 | Fine Science tools | 11254-20 | |
Nuclease free water | Thermo Fisher Scientific | AM9932 | |
PBS 10x | Research Product Internation (RPI) | P32200 | |
Poly(A) Tail-Length Assay Kit | Thermo Fisher Scientific | 764551KT | |
RiboRuler Low Range RNA Ladder | Thermo Fisher Scientific | SM1833 | |
RNA Gel Loading Dye (2x) | Thermo Fisher Scientific | R0641 | |
RNA microprep kit | Zymoresearch | R1050 | |
RNA miniprep kit | Zymoresearch | R1055 | |
Scissors-Vannas Spring Scissors - 2.5 mm Cutting Edge | Fine Science tools | 15000-08 | |
TopVision Agarose Tablets | Thermo Fisher Scientific | R2802 | |
Tris-Acetate-EDTA (TAE) | Thermo Fisher Scientific | B49 |
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