Literature DB >> 33811916

Transcription Regulation Through Nascent RNA Folding.

Leonard Schärfen1, Karla M Neugebauer2.   

Abstract

Folding of RNA into secondary structures through intramolecular base pairing determines an RNA's three-dimensional architecture and associated function. Simple RNA structures like stem loops can provide specialized functions independent of coding capacity, such as protein binding, regulation of RNA processing and stability, stimulation or inhibition of translation. RNA catalysis is dependent on tertiary structures found in the ribosome, tRNAs and group I and II introns. While the extent to which non-coding RNAs contribute to cellular maintenance is generally appreciated, the fact that both non-coding and coding RNA can assume relevant structural states has only recently gained attention. In particular, the co-transcriptional folding of nascent RNA of all classes has the potential to regulate co-transcriptional processing, RNP (ribonucleoprotein particle) formation, and transcription itself. Riboswitches are established examples of co-transcriptionally folded coding RNAs that directly regulate transcription, mainly in prokaryotes. Here we discuss recent studies in both prokaryotes and eukaryotes showing that structure formation may carry a more widespread regulatory logic during RNA synthesis. Local structures forming close to the catalytic center of RNA polymerases have the potential to regulate transcription by reducing backtracking. In addition, stem loops or more complex structures may alter co-transcriptional RNA processing or its efficiency. Several examples of functional structures have been identified to date, and this review provides an overview of physiologically distinct processes where co-transcriptionally folded RNA plays a role. Experimental approaches such as single-molecule FRET and in vivo structural probing to further advance our insight into the significance of co-transcriptional structure formation are discussed.
Copyright © 2021 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  RNA folding; RNA polymerase; RNA splicing; nascent RNA; transcription

Mesh:

Substances:

Year:  2021        PMID: 33811916      PMCID: PMC8184640          DOI: 10.1016/j.jmb.2021.166975

Source DB:  PubMed          Journal:  J Mol Biol        ISSN: 0022-2836            Impact factor:   6.151


  107 in total

Review 1.  How RNA folds.

Authors:  I Tinoco; C Bustamante
Journal:  J Mol Biol       Date:  1999-10-22       Impact factor: 5.469

2.  RNA polymerase II transcription complexes may become arrested if the nascent RNA is shortened to less than 50 nucleotides.

Authors:  Andrea Ujvári; Mahadeb Pal; Donal S Luse
Journal:  J Biol Chem       Date:  2002-06-26       Impact factor: 5.157

3.  Global analysis of nascent RNA reveals transcriptional pausing in terminal exons.

Authors:  Fernando Carrillo Oesterreich; Stephan Preibisch; Karla M Neugebauer
Journal:  Mol Cell       Date:  2010-11-24       Impact factor: 17.970

Review 4.  RNA polymerase I and III: similar yet unique.

Authors:  Heena Khatter; Matthias K Vorländer; Christoph W Müller
Journal:  Curr Opin Struct Biol       Date:  2017-07-22       Impact factor: 6.809

5.  First exon length controls active chromatin signatures and transcription.

Authors:  Nicole I Bieberstein; Fernando Carrillo Oesterreich; Korinna Straube; Karla M Neugebauer
Journal:  Cell Rep       Date:  2012-07-20       Impact factor: 9.423

6.  Folding of a large ribozyme during transcription and the effect of the elongation factor NusA.

Authors:  T Pan; I Artsimovitch; X W Fang; R Landick; T R Sosnick
Journal:  Proc Natl Acad Sci U S A       Date:  1999-08-17       Impact factor: 11.205

7.  Genome-wide measurement of RNA folding energies.

Authors:  Yue Wan; Kun Qu; Zhengqing Ouyang; Michael Kertesz; Jun Li; Robert Tibshirani; Debora L Makino; Robert C Nutter; Eran Segal; Howard Y Chang
Journal:  Mol Cell       Date:  2012-09-13       Impact factor: 17.970

8.  A periodic pattern of mRNA secondary structure created by the genetic code.

Authors:  Svetlana A Shabalina; Aleksey Y Ogurtsov; Nikolay A Spiridonov
Journal:  Nucleic Acids Res       Date:  2006-05-08       Impact factor: 16.971

9.  Pre-mRNA Splicing in the Nuclear Landscape.

Authors:  Tucker J Carrocci; Karla M Neugebauer
Journal:  Cold Spring Harb Symp Quant Biol       Date:  2020-06-03

10.  Structural disruption of exonic stem-loops immediately upstream of the intron regulates mammalian splicing.

Authors:  Kaushik Saha; Whitney England; Mike Minh Fernandez; Tapan Biswas; Robert C Spitale; Gourisankar Ghosh
Journal:  Nucleic Acids Res       Date:  2020-06-19       Impact factor: 16.971

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  5 in total

Review 1.  Regulation of Gene Expression Through Effector-dependent Conformational Switching by Cobalamin Riboswitches.

Authors:  Shelby R Lennon; Robert T Batey
Journal:  J Mol Biol       Date:  2022-04-12       Impact factor: 6.151

Review 2.  Secondary structures in RNA synthesis, splicing and translation.

Authors:  Ilias Georgakopoulos-Soares; Guillermo E Parada; Martin Hemberg
Journal:  Comput Struct Biotechnol J       Date:  2022-05-27       Impact factor: 6.155

Review 3.  Merging Established Mechanisms with New Insights: Condensates, Hubs, and the Regulation of RNA Polymerase II Transcription.

Authors:  Megan Palacio; Dylan J Taatjes
Journal:  J Mol Biol       Date:  2021-08-30       Impact factor: 5.469

4.  R-loops at microRNA encoding loci promote co-transcriptional processing of pri-miRNAs in plants.

Authors:  Lucia Gonzalo; Ileana Tossolini; Tomasz Gulanicz; Damian A Cambiagno; Anna Kasprowicz-Maluski; Dariusz Jan Smolinski; María Florencia Mammarella; Federico D Ariel; Sebastian Marquardt; Zofia Szweykowska-Kulinska; Artur Jarmolowski; Pablo A Manavella
Journal:  Nat Plants       Date:  2022-04-21       Impact factor: 17.352

5.  Transcription complexes as RNA chaperones.

Authors:  Nelly Said; Markus C Wahl
Journal:  Transcription       Date:  2021-11-01
  5 in total

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