Abstract
The poly-adenosine, or poly(A) tail, plays key roles in controlling the stability and translation of messenger RNAs in all eukaryotes, and, as such, facile assays that can measure poly(A) length are needed. This chapter describes an approach that couples RNase H-mediated cleavage of an RNA of interest with high-resolution denaturing gel electrophoresis and northern blot-based detection. Major advantages of this method include the ability to directly measure the abundance of any RNA and the length of its poly(A) tail without amplification steps. The assay provides high specificity, sensitivity, and reproducibility for accurate quantitation using standard molecular biology equipment and reagents. Overall, the high-resolution northern blotting approach offers a cost-effective means of poly(A) RNA analysis that is especially useful for small numbers of transcripts and comparisons between experimental conditions or time points.
Original language | English (US) |
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Title of host publication | Methods in Molecular Biology |
Publisher | Humana Press Inc. |
Pages | 93-111 |
Number of pages | 19 |
DOIs | |
State | Published - 2024 |
Publication series
Name | Methods in Molecular Biology |
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Volume | 2723 |
ISSN (Print) | 1064-3745 |
ISSN (Electronic) | 1940-6029 |
Bibliographical note
Publisher Copyright:© This is a U.S. government work and not under copyright protection in the U.S.; foreign copyright protection may apply 2024.
Keywords
- Northern blot
- Poly(A)
- Poly-adenosine tail
- RNase H
- RNA/genetics
- Blotting, Northern
- Reproducibility of Results
- Poly A/genetics
- Ribonuclease H
- RNA, Messenger/genetics
PubMed: MeSH publication types
- Journal Article
- Research Support, N.I.H., Extramural
- Research Support, U.S. Gov't, Non-P.H.S.