An alanine expanded PABPN1 causes increased utilization of intronic polyadenylation sites

Muscle degeneration: RNA structures as modulator of muscle function Transcriptional and post-transcriptional regulation of gene expression has a fundamental role in shaping the protein landscape. In skeletal muscles, the RNA landscape plays an important role in muscle function in both health and dis...

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Autores principales: Tooba Abbassi-Daloii, Soheil Yousefi, Eleonora de Klerk, Laurens Grossouw, Muhammad Riaz, Peter A. C. ’t Hoen, Vered Raz
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Publicado: Nature Portfolio 2017
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Acceso en línea:https://doaj.org/article/f81d49d188ae4f5e9ff99d5513a56155
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spelling oai:doaj.org-article:f81d49d188ae4f5e9ff99d5513a561552021-12-02T16:05:43ZAn alanine expanded PABPN1 causes increased utilization of intronic polyadenylation sites10.1038/s41514-017-0007-x2056-3973https://doaj.org/article/f81d49d188ae4f5e9ff99d5513a561552017-04-01T00:00:00Zhttps://doi.org/10.1038/s41514-017-0007-xhttps://doaj.org/toc/2056-3973Muscle degeneration: RNA structures as modulator of muscle function Transcriptional and post-transcriptional regulation of gene expression has a fundamental role in shaping the protein landscape. In skeletal muscles, the RNA landscape plays an important role in muscle function in both health and disease conditions. PABPN1 is a key regulator of mRNA processing in a late-onset muscular dystrophy and in aging. Here, the authors demonstrate that a decrease in PABPN1 function results in genome-wide alterations in mRNA structures. Reduced PABPN1 function alters both mRNA levels and RNA structures leading to altered protein sequences. Importantly, among the affected genes are muscle function regulators. Together, this study calls for a better understanding of alterations in RNA structures in disease and aging.Tooba Abbassi-DaloiiSoheil YousefiEleonora de KlerkLaurens GrossouwMuhammad RiazPeter A. C. ’t HoenVered RazNature PortfolioarticleGeriatricsRC952-954.6ENnpj Aging and Mechanisms of Disease, Vol 3, Iss 1, Pp 1-8 (2017)
institution DOAJ
collection DOAJ
language EN
topic Geriatrics
RC952-954.6
spellingShingle Geriatrics
RC952-954.6
Tooba Abbassi-Daloii
Soheil Yousefi
Eleonora de Klerk
Laurens Grossouw
Muhammad Riaz
Peter A. C. ’t Hoen
Vered Raz
An alanine expanded PABPN1 causes increased utilization of intronic polyadenylation sites
description Muscle degeneration: RNA structures as modulator of muscle function Transcriptional and post-transcriptional regulation of gene expression has a fundamental role in shaping the protein landscape. In skeletal muscles, the RNA landscape plays an important role in muscle function in both health and disease conditions. PABPN1 is a key regulator of mRNA processing in a late-onset muscular dystrophy and in aging. Here, the authors demonstrate that a decrease in PABPN1 function results in genome-wide alterations in mRNA structures. Reduced PABPN1 function alters both mRNA levels and RNA structures leading to altered protein sequences. Importantly, among the affected genes are muscle function regulators. Together, this study calls for a better understanding of alterations in RNA structures in disease and aging.
format article
author Tooba Abbassi-Daloii
Soheil Yousefi
Eleonora de Klerk
Laurens Grossouw
Muhammad Riaz
Peter A. C. ’t Hoen
Vered Raz
author_facet Tooba Abbassi-Daloii
Soheil Yousefi
Eleonora de Klerk
Laurens Grossouw
Muhammad Riaz
Peter A. C. ’t Hoen
Vered Raz
author_sort Tooba Abbassi-Daloii
title An alanine expanded PABPN1 causes increased utilization of intronic polyadenylation sites
title_short An alanine expanded PABPN1 causes increased utilization of intronic polyadenylation sites
title_full An alanine expanded PABPN1 causes increased utilization of intronic polyadenylation sites
title_fullStr An alanine expanded PABPN1 causes increased utilization of intronic polyadenylation sites
title_full_unstemmed An alanine expanded PABPN1 causes increased utilization of intronic polyadenylation sites
title_sort alanine expanded pabpn1 causes increased utilization of intronic polyadenylation sites
publisher Nature Portfolio
publishDate 2017
url https://doaj.org/article/f81d49d188ae4f5e9ff99d5513a56155
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