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In This Article

  • Summary
  • Abstract
  • Introduction
  • Protocol
  • Representative Results
  • Discussion
  • Acknowledgements
  • Materials
  • References
  • Reprints and Permissions

Summary

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.

Abstract

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.

Introduction

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,....

Protocol

1. Rearing and selecting Drosophila larvae

  1. Maintain/culture the fly strain (w1118, wildtype) on standard fly food medium at 25 ˚C in a humidified incubator.
  2. Select 10 wandering 3rd instar larvae 72 h after egg laying.
  3. Place the larvae in a 35 mm empty Petri dish and gently wash them by transferring the larvae to the new dish containing tap water using forceps. Do this 2x to remove any remaining .......

Representative Results

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 .......

Discussion

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.......

Acknowledgements

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.

....

Materials

NameCompanyCatalog NumberComments
3-(N-morpholino) propanesulfonic acid (MOPS)Research Product Internation (RPI)M92020
Agilent High Sensitivity DNA KitAgilent Technologies 5067-4626
Agilent software 2100 expert free download demoAgilent Technologieshttps://www.agilent.com/en/product/automated-electrophoresis/bioanalyzer-systems/bioanalyzer-software/2100-expert-software-228259
Apex 100 bp-Low DNA LadderGenesee Scientific19-109
BioanalyzerAgilent 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 lineDrosophila Genomics Resource Center stock #181
Drosophila Schneider’s MediumThermo Fisher Scientific21720024
Ehidium bromideGenesee scientific 20-276
Fetal bovine serum (FBS)Sigma-AldrichF4135
Forceps Dumont 5  Fine Science tools 11254-20
Nuclease free waterThermo Fisher Scientific AM9932
PBS 10xResearch Product Internation (RPI) P32200
Poly(A) Tail-Length Assay KitThermo Fisher Scientific 764551KT
RiboRuler Low Range RNA LadderThermo Fisher Scientific SM1833
RNA Gel Loading Dye (2x)Thermo Fisher Scientific R0641
RNA microprep kitZymoresearch R1050 
RNA miniprep kitZymoresearch R1055
Scissors-Vannas Spring Scissors - 2.5 mm Cutting EdgeFine Science tools 15000-08
TopVision Agarose TabletsThermo Fisher ScientificR2802
Tris-Acetate-EDTA (TAE)Thermo Fisher ScientificB49

References

  1. Stewart, M. Polyadenylation and nuclear export of mRNAs. Journal of Biological Chemistry. 294 (9), 2977-2987 (2019).
  2. Machida, K., et al. Dynamic interaction of poly(A)-binding protein with the ribosome. Scient....

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