Cargando…

Functional and structural basis of extreme conservation in vertebrate 5’ untranslated regions

The lack of knowledge about extreme conservation in genomes remains a major gap in our understanding of the evolution of gene regulation. Here, we reveal an unexpected role of extremely conserved 5’UTRs in non-canonical translational regulation that is linked to the emergence of essential developmen...

Descripción completa

Detalles Bibliográficos
Autores principales: Byeon, Gun Woo, Cenik, Elif Sarinay, Jiang, Lihua, Tang, Hua, Das, Rhiju, Barna, Maria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8825242/
https://www.ncbi.nlm.nih.gov/pubmed/33821006
http://dx.doi.org/10.1038/s41588-021-00830-1
_version_ 1784647170845048832
author Byeon, Gun Woo
Cenik, Elif Sarinay
Jiang, Lihua
Tang, Hua
Das, Rhiju
Barna, Maria
author_facet Byeon, Gun Woo
Cenik, Elif Sarinay
Jiang, Lihua
Tang, Hua
Das, Rhiju
Barna, Maria
author_sort Byeon, Gun Woo
collection PubMed
description The lack of knowledge about extreme conservation in genomes remains a major gap in our understanding of the evolution of gene regulation. Here, we reveal an unexpected role of extremely conserved 5’UTRs in non-canonical translational regulation that is linked to the emergence of essential developmental features in vertebrate species. Endogenous deletion of conserved elements within these 5’UTRs decreased gene expression, and extremely conserved 5’UTRs possess cis-regulatory elements that promote cell-type specific regulation of translation. We further developed in-cell mutate-and-map (icM(2)), a novel methodology that maps RNA structure inside cells. Using icM(2), we determined that an extremely conserved 5’UTR encodes multiple alternative structures and that each single nucleotide within the conserved element maintains the balance of alternative structures important to control the dynamic range of protein expression. These results explain how extreme sequence conservation can lead to RNA-level biological functions encoded in the untranslated regions of vertebrate genomes.
format Online
Article
Text
id pubmed-8825242
institution National Center for Biotechnology Information
language English
publishDate 2021
record_format MEDLINE/PubMed
spelling pubmed-88252422022-02-09 Functional and structural basis of extreme conservation in vertebrate 5’ untranslated regions Byeon, Gun Woo Cenik, Elif Sarinay Jiang, Lihua Tang, Hua Das, Rhiju Barna, Maria Nat Genet Article The lack of knowledge about extreme conservation in genomes remains a major gap in our understanding of the evolution of gene regulation. Here, we reveal an unexpected role of extremely conserved 5’UTRs in non-canonical translational regulation that is linked to the emergence of essential developmental features in vertebrate species. Endogenous deletion of conserved elements within these 5’UTRs decreased gene expression, and extremely conserved 5’UTRs possess cis-regulatory elements that promote cell-type specific regulation of translation. We further developed in-cell mutate-and-map (icM(2)), a novel methodology that maps RNA structure inside cells. Using icM(2), we determined that an extremely conserved 5’UTR encodes multiple alternative structures and that each single nucleotide within the conserved element maintains the balance of alternative structures important to control the dynamic range of protein expression. These results explain how extreme sequence conservation can lead to RNA-level biological functions encoded in the untranslated regions of vertebrate genomes. 2021-05 2021-04-05 /pmc/articles/PMC8825242/ /pubmed/33821006 http://dx.doi.org/10.1038/s41588-021-00830-1 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Byeon, Gun Woo
Cenik, Elif Sarinay
Jiang, Lihua
Tang, Hua
Das, Rhiju
Barna, Maria
Functional and structural basis of extreme conservation in vertebrate 5’ untranslated regions
title Functional and structural basis of extreme conservation in vertebrate 5’ untranslated regions
title_full Functional and structural basis of extreme conservation in vertebrate 5’ untranslated regions
title_fullStr Functional and structural basis of extreme conservation in vertebrate 5’ untranslated regions
title_full_unstemmed Functional and structural basis of extreme conservation in vertebrate 5’ untranslated regions
title_short Functional and structural basis of extreme conservation in vertebrate 5’ untranslated regions
title_sort functional and structural basis of extreme conservation in vertebrate 5’ untranslated regions
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8825242/
https://www.ncbi.nlm.nih.gov/pubmed/33821006
http://dx.doi.org/10.1038/s41588-021-00830-1
work_keys_str_mv AT byeongunwoo functionalandstructuralbasisofextremeconservationinvertebrate5untranslatedregions
AT cenikelifsarinay functionalandstructuralbasisofextremeconservationinvertebrate5untranslatedregions
AT jianglihua functionalandstructuralbasisofextremeconservationinvertebrate5untranslatedregions
AT tanghua functionalandstructuralbasisofextremeconservationinvertebrate5untranslatedregions
AT dasrhiju functionalandstructuralbasisofextremeconservationinvertebrate5untranslatedregions
AT barnamaria functionalandstructuralbasisofextremeconservationinvertebrate5untranslatedregions