Ribosomal proteins: mutant phenotypes by the numbers and associated gene expression changes

Ribosomal proteins are highly conserved, many universally so among organisms. All ribosomal proteins are structural parts of the same molecular machine, the ribosome. However, when ribosomal proteins are mutated individually, they often lead to distinct and intriguing phenotypes, including specific...

Full description

Bibliographic Details
Main Author: Michael Polymenis
Format: Article
Language:English
Published: The Royal Society 2020-08-01
Series:Open Biology
Subjects:
Online Access:https://royalsocietypublishing.org/doi/pdf/10.1098/rsob.200114
id doaj-72620f223b1e40ffabd8e92f81cb233c
record_format Article
spelling doaj-72620f223b1e40ffabd8e92f81cb233c2020-11-25T02:48:10ZengThe Royal SocietyOpen Biology2046-24412020-08-0110810.1098/rsob.200114200114Ribosomal proteins: mutant phenotypes by the numbers and associated gene expression changesMichael PolymenisRibosomal proteins are highly conserved, many universally so among organisms. All ribosomal proteins are structural parts of the same molecular machine, the ribosome. However, when ribosomal proteins are mutated individually, they often lead to distinct and intriguing phenotypes, including specific human pathologies. This review is an attempt to collect and analyse all the reported phenotypes of each ribosomal protein mutant in several eukaryotes (Saccharomyces cerevisiae, Caenorhabditis elegans, Drosophila melanogaster, Danio rerio, Mus musculus, Homo sapiens). These phenotypes were processed with unbiased computational approaches to reveal associations between different phenotypes and the contributions of individual ribosomal protein genes. An overview of gene expression changes in ribosomal protein mutants, with emphasis on ribosome profiling studies, is also presented. The available data point to patterns that may account for most of the observed phenotypes. The information presented here may also inform future studies about the molecular basis of the phenotypes that arise from mutations in ribosomal proteins.https://royalsocietypublishing.org/doi/pdf/10.1098/rsob.200114yeastwormsflieszebrafishmousehuman
collection DOAJ
language English
format Article
sources DOAJ
author Michael Polymenis
spellingShingle Michael Polymenis
Ribosomal proteins: mutant phenotypes by the numbers and associated gene expression changes
Open Biology
yeast
worms
flies
zebrafish
mouse
human
author_facet Michael Polymenis
author_sort Michael Polymenis
title Ribosomal proteins: mutant phenotypes by the numbers and associated gene expression changes
title_short Ribosomal proteins: mutant phenotypes by the numbers and associated gene expression changes
title_full Ribosomal proteins: mutant phenotypes by the numbers and associated gene expression changes
title_fullStr Ribosomal proteins: mutant phenotypes by the numbers and associated gene expression changes
title_full_unstemmed Ribosomal proteins: mutant phenotypes by the numbers and associated gene expression changes
title_sort ribosomal proteins: mutant phenotypes by the numbers and associated gene expression changes
publisher The Royal Society
series Open Biology
issn 2046-2441
publishDate 2020-08-01
description Ribosomal proteins are highly conserved, many universally so among organisms. All ribosomal proteins are structural parts of the same molecular machine, the ribosome. However, when ribosomal proteins are mutated individually, they often lead to distinct and intriguing phenotypes, including specific human pathologies. This review is an attempt to collect and analyse all the reported phenotypes of each ribosomal protein mutant in several eukaryotes (Saccharomyces cerevisiae, Caenorhabditis elegans, Drosophila melanogaster, Danio rerio, Mus musculus, Homo sapiens). These phenotypes were processed with unbiased computational approaches to reveal associations between different phenotypes and the contributions of individual ribosomal protein genes. An overview of gene expression changes in ribosomal protein mutants, with emphasis on ribosome profiling studies, is also presented. The available data point to patterns that may account for most of the observed phenotypes. The information presented here may also inform future studies about the molecular basis of the phenotypes that arise from mutations in ribosomal proteins.
topic yeast
worms
flies
zebrafish
mouse
human
url https://royalsocietypublishing.org/doi/pdf/10.1098/rsob.200114
work_keys_str_mv AT michaelpolymenis ribosomalproteinsmutantphenotypesbythenumbersandassociatedgeneexpressionchanges
_version_ 1724749417706160128