Cargando…

An Evolutionary Mechanism for the Generation of Competing RNA Structures Associated with Mutually Exclusive Exons

Alternative splicing is a commonly-used mechanism of diversifying gene products. Mutually exclusive exons (MXE) represent a particular type of alternative splicing, in which one and only one exon from an array is included in the mature RNA. A number of genes with MXE do so by using a mechanism that...

Descripción completa

Detalles Bibliográficos
Autores principales: Ivanov, Timofei M., Pervouchine, Dmitri D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6071210/
https://www.ncbi.nlm.nih.gov/pubmed/30018239
http://dx.doi.org/10.3390/genes9070356
_version_ 1783343831807164416
author Ivanov, Timofei M.
Pervouchine, Dmitri D.
author_facet Ivanov, Timofei M.
Pervouchine, Dmitri D.
author_sort Ivanov, Timofei M.
collection PubMed
description Alternative splicing is a commonly-used mechanism of diversifying gene products. Mutually exclusive exons (MXE) represent a particular type of alternative splicing, in which one and only one exon from an array is included in the mature RNA. A number of genes with MXE do so by using a mechanism that depends on RNA structure. Transcripts of these genes contain multiple sites called selector sequences that are all complementary to a regulatory element called the docking site; only one of the competing base pairings can form at a time, which exposes one exon from the cluster to the spliceosome. MXE tend to have similar lengths and sequence content and are believed to originate through tandem genomic duplications. Here, we report that pre-mRNAs of this class of exons have an increased capacity to fold into competing secondary structures. We propose an evolutionary mechanism for the generation of such structures via duplications that affect not only exons, but also their adjacent introns with stem-loop structures. If one of the two arms of a stem-loop is duplicated, it will generate two selector sequences that compete for the same docking site, a pattern that is associated with MXE splicing. A similar partial duplication of two independent stem-loops produces a pattern that is consistent with the so-called bidirectional pairing model. These models explain why tandem exon duplications frequently result in mutually exclusive splicing.
format Online
Article
Text
id pubmed-6071210
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-60712102018-08-09 An Evolutionary Mechanism for the Generation of Competing RNA Structures Associated with Mutually Exclusive Exons Ivanov, Timofei M. Pervouchine, Dmitri D. Genes (Basel) Article Alternative splicing is a commonly-used mechanism of diversifying gene products. Mutually exclusive exons (MXE) represent a particular type of alternative splicing, in which one and only one exon from an array is included in the mature RNA. A number of genes with MXE do so by using a mechanism that depends on RNA structure. Transcripts of these genes contain multiple sites called selector sequences that are all complementary to a regulatory element called the docking site; only one of the competing base pairings can form at a time, which exposes one exon from the cluster to the spliceosome. MXE tend to have similar lengths and sequence content and are believed to originate through tandem genomic duplications. Here, we report that pre-mRNAs of this class of exons have an increased capacity to fold into competing secondary structures. We propose an evolutionary mechanism for the generation of such structures via duplications that affect not only exons, but also their adjacent introns with stem-loop structures. If one of the two arms of a stem-loop is duplicated, it will generate two selector sequences that compete for the same docking site, a pattern that is associated with MXE splicing. A similar partial duplication of two independent stem-loops produces a pattern that is consistent with the so-called bidirectional pairing model. These models explain why tandem exon duplications frequently result in mutually exclusive splicing. MDPI 2018-07-17 /pmc/articles/PMC6071210/ /pubmed/30018239 http://dx.doi.org/10.3390/genes9070356 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Ivanov, Timofei M.
Pervouchine, Dmitri D.
An Evolutionary Mechanism for the Generation of Competing RNA Structures Associated with Mutually Exclusive Exons
title An Evolutionary Mechanism for the Generation of Competing RNA Structures Associated with Mutually Exclusive Exons
title_full An Evolutionary Mechanism for the Generation of Competing RNA Structures Associated with Mutually Exclusive Exons
title_fullStr An Evolutionary Mechanism for the Generation of Competing RNA Structures Associated with Mutually Exclusive Exons
title_full_unstemmed An Evolutionary Mechanism for the Generation of Competing RNA Structures Associated with Mutually Exclusive Exons
title_short An Evolutionary Mechanism for the Generation of Competing RNA Structures Associated with Mutually Exclusive Exons
title_sort evolutionary mechanism for the generation of competing rna structures associated with mutually exclusive exons
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6071210/
https://www.ncbi.nlm.nih.gov/pubmed/30018239
http://dx.doi.org/10.3390/genes9070356
work_keys_str_mv AT ivanovtimofeim anevolutionarymechanismforthegenerationofcompetingrnastructuresassociatedwithmutuallyexclusiveexons
AT pervouchinedmitrid anevolutionarymechanismforthegenerationofcompetingrnastructuresassociatedwithmutuallyexclusiveexons
AT ivanovtimofeim evolutionarymechanismforthegenerationofcompetingrnastructuresassociatedwithmutuallyexclusiveexons
AT pervouchinedmitrid evolutionarymechanismforthegenerationofcompetingrnastructuresassociatedwithmutuallyexclusiveexons