Cargando…

The Modular Adaptive Ribosome

The ribosome is an ancient machine, performing the same function across organisms. Although functionally unitary, recent experiments suggest specialized roles for some ribosomal proteins. Our central thesis is that ribosomal proteins function in a modular fashion to decode genetic information in a c...

Descripción completa

Detalles Bibliográficos
Autores principales: Yadav, Anupama, Radhakrishnan, Aparna, Panda, Anshuman, Singh, Amartya, Sinha, Himanshu, Bhanot, Gyan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5094737/
https://www.ncbi.nlm.nih.gov/pubmed/27812193
http://dx.doi.org/10.1371/journal.pone.0166021
_version_ 1782465163235950592
author Yadav, Anupama
Radhakrishnan, Aparna
Panda, Anshuman
Singh, Amartya
Sinha, Himanshu
Bhanot, Gyan
author_facet Yadav, Anupama
Radhakrishnan, Aparna
Panda, Anshuman
Singh, Amartya
Sinha, Himanshu
Bhanot, Gyan
author_sort Yadav, Anupama
collection PubMed
description The ribosome is an ancient machine, performing the same function across organisms. Although functionally unitary, recent experiments suggest specialized roles for some ribosomal proteins. Our central thesis is that ribosomal proteins function in a modular fashion to decode genetic information in a context dependent manner. We show through large data analyses that although many ribosomal proteins are essential with consistent effect on growth in different conditions in yeast and similar expression across cell and tissue types in mice and humans, some ribosomal proteins are used in an environment specific manner. The latter set of variable ribosomal proteins further function in a coordinated manner forming modules, which are adapted to different environmental cues in different organisms. We show that these environment specific modules of ribosomal proteins in yeast have differential genetic interactions with other pathways and their 5’UTRs show differential signatures of selection in yeast strains, presumably to facilitate adaptation. Similarly, we show that in higher metazoans such as mice and humans, different modules of ribosomal proteins are expressed in different cell types and tissues. A clear example is nervous tissue that uses a ribosomal protein module distinct from the rest of the tissues in both mice and humans. Our results suggest a novel stratification of ribosomal proteins that could have played a role in adaptation, presumably to optimize translation for adaptation to diverse ecological niches and tissue microenvironments.
format Online
Article
Text
id pubmed-5094737
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-50947372016-11-18 The Modular Adaptive Ribosome Yadav, Anupama Radhakrishnan, Aparna Panda, Anshuman Singh, Amartya Sinha, Himanshu Bhanot, Gyan PLoS One Research Article The ribosome is an ancient machine, performing the same function across organisms. Although functionally unitary, recent experiments suggest specialized roles for some ribosomal proteins. Our central thesis is that ribosomal proteins function in a modular fashion to decode genetic information in a context dependent manner. We show through large data analyses that although many ribosomal proteins are essential with consistent effect on growth in different conditions in yeast and similar expression across cell and tissue types in mice and humans, some ribosomal proteins are used in an environment specific manner. The latter set of variable ribosomal proteins further function in a coordinated manner forming modules, which are adapted to different environmental cues in different organisms. We show that these environment specific modules of ribosomal proteins in yeast have differential genetic interactions with other pathways and their 5’UTRs show differential signatures of selection in yeast strains, presumably to facilitate adaptation. Similarly, we show that in higher metazoans such as mice and humans, different modules of ribosomal proteins are expressed in different cell types and tissues. A clear example is nervous tissue that uses a ribosomal protein module distinct from the rest of the tissues in both mice and humans. Our results suggest a novel stratification of ribosomal proteins that could have played a role in adaptation, presumably to optimize translation for adaptation to diverse ecological niches and tissue microenvironments. Public Library of Science 2016-11-03 /pmc/articles/PMC5094737/ /pubmed/27812193 http://dx.doi.org/10.1371/journal.pone.0166021 Text en © 2016 Yadav et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Yadav, Anupama
Radhakrishnan, Aparna
Panda, Anshuman
Singh, Amartya
Sinha, Himanshu
Bhanot, Gyan
The Modular Adaptive Ribosome
title The Modular Adaptive Ribosome
title_full The Modular Adaptive Ribosome
title_fullStr The Modular Adaptive Ribosome
title_full_unstemmed The Modular Adaptive Ribosome
title_short The Modular Adaptive Ribosome
title_sort modular adaptive ribosome
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5094737/
https://www.ncbi.nlm.nih.gov/pubmed/27812193
http://dx.doi.org/10.1371/journal.pone.0166021
work_keys_str_mv AT yadavanupama themodularadaptiveribosome
AT radhakrishnanaparna themodularadaptiveribosome
AT pandaanshuman themodularadaptiveribosome
AT singhamartya themodularadaptiveribosome
AT sinhahimanshu themodularadaptiveribosome
AT bhanotgyan themodularadaptiveribosome
AT yadavanupama modularadaptiveribosome
AT radhakrishnanaparna modularadaptiveribosome
AT pandaanshuman modularadaptiveribosome
AT singhamartya modularadaptiveribosome
AT sinhahimanshu modularadaptiveribosome
AT bhanotgyan modularadaptiveribosome