Abstract

B2 RNA is a mouse non-coding RNA that binds directly to RNA polymerase II (Pol II) and represses transcription by disrupting critical interactions between the polymerase and promoter DNA. How the structural regions within B2 RNA work together to mediate transcriptional repression is not well understood. To address this question, we systematically deleted structural regions from B2 RNA and determined the effects on transcriptional repression using a highly purified Pol II in vitro transcription system. Deletions that compromised the ability of B2 RNA to function as a transcriptional repressor were also tested for their ability to bind directly to Pol II, which enabled us to distinguish regions uniquely important for repression from those important for binding. We found that transcriptional repression requires a pattern of RNA structural motifs consisting of an extended single-stranded region bordered by two stem‑loops. Hence, there is modularity in the function of the stem-loops in B2 RNA—when one stem‑loop is deleted, another can take its place to enable transcriptional repression.

Highlights

  • Non-coding RNAs are understood to be active participants in regulating the process of transcription [1,2]

  • Non-Coding RNA 2015, 1 of ~180 nucleotide RNAs that are transcribed by RNA polymerase III (Pol III) from SINEs that are abundant in the mouse genome [3]

  • We found that B2 RNA acts as a repressor of mRNA transcription by Pol II after heat shock, thereby revealing a mechanism by which mRNA genes can be repressed during a cellular stress as well as identifying a function for SINE RNAs [4]

Read more

Summary

Introduction

Non-coding RNAs (ncRNAs) are understood to be active participants in regulating the process of transcription [1,2]. One such ncRNA transcriptional regulator is mouse B2 RNA. When B2 RNA is bound, Pol II is able to interact with general transcription factors and assemble into complexes on promoter DNA [5]. In these complexes, the majority of polymerase/promoter contacts are disrupted [8]. It is likely that a network of protein-protein and protein-DNA interactions hold complexes containing Pol II and B2 RNA on the promoter even when

Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call