Cargando…

Genome-wide quantification of contributions to sexual fitness identifies genes required for spore viability and health in fission yeast

Numerous genes required for sexual reproduction remain to be identified even in simple model species like Schizosaccharomyces pombe. To address this, we developed an assay in S. pombe that couples transposon mutagenesis with high-throughput sequencing (TN-seq) to quantitatively measure the fitness c...

Descripción completa

Detalles Bibliográficos
Autores principales: Billmyre, R. Blake, Eickbush, Michael T., Craig, Caroline J., Lange, Jeffrey J., Wood, Christopher, Helston, Rachel M., Zanders, Sarah E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9668190/
https://www.ncbi.nlm.nih.gov/pubmed/36301993
http://dx.doi.org/10.1371/journal.pgen.1010462
_version_ 1784831862320922624
author Billmyre, R. Blake
Eickbush, Michael T.
Craig, Caroline J.
Lange, Jeffrey J.
Wood, Christopher
Helston, Rachel M.
Zanders, Sarah E.
author_facet Billmyre, R. Blake
Eickbush, Michael T.
Craig, Caroline J.
Lange, Jeffrey J.
Wood, Christopher
Helston, Rachel M.
Zanders, Sarah E.
author_sort Billmyre, R. Blake
collection PubMed
description Numerous genes required for sexual reproduction remain to be identified even in simple model species like Schizosaccharomyces pombe. To address this, we developed an assay in S. pombe that couples transposon mutagenesis with high-throughput sequencing (TN-seq) to quantitatively measure the fitness contribution of nonessential genes across the genome to sexual reproduction. This approach identified 532 genes that contribute to sex, including more than 200 that were not previously annotated to be involved in the process, of which more than 150 have orthologs in vertebrates. Among our verified hits was an uncharacterized gene, ifs1 (important for sex), that is required for spore viability. In two other hits, plb1 and alg9, we observed a novel mutant phenotype of poor spore health wherein viable spores are produced, but the spores exhibit low fitness and are rapidly outcompeted by wild type. Finally, we fortuitously discovered that a gene previously thought to be essential, sdg1 (social distancing gene), is instead required for growth at low cell densities and can be rescued by conditioned medium. Our assay will be valuable in further studies of sexual reproduction in S. pombe and identifies multiple candidate genes that could contribute to sexual reproduction in other eukaryotes, including humans.
format Online
Article
Text
id pubmed-9668190
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-96681902022-11-17 Genome-wide quantification of contributions to sexual fitness identifies genes required for spore viability and health in fission yeast Billmyre, R. Blake Eickbush, Michael T. Craig, Caroline J. Lange, Jeffrey J. Wood, Christopher Helston, Rachel M. Zanders, Sarah E. PLoS Genet Research Article Numerous genes required for sexual reproduction remain to be identified even in simple model species like Schizosaccharomyces pombe. To address this, we developed an assay in S. pombe that couples transposon mutagenesis with high-throughput sequencing (TN-seq) to quantitatively measure the fitness contribution of nonessential genes across the genome to sexual reproduction. This approach identified 532 genes that contribute to sex, including more than 200 that were not previously annotated to be involved in the process, of which more than 150 have orthologs in vertebrates. Among our verified hits was an uncharacterized gene, ifs1 (important for sex), that is required for spore viability. In two other hits, plb1 and alg9, we observed a novel mutant phenotype of poor spore health wherein viable spores are produced, but the spores exhibit low fitness and are rapidly outcompeted by wild type. Finally, we fortuitously discovered that a gene previously thought to be essential, sdg1 (social distancing gene), is instead required for growth at low cell densities and can be rescued by conditioned medium. Our assay will be valuable in further studies of sexual reproduction in S. pombe and identifies multiple candidate genes that could contribute to sexual reproduction in other eukaryotes, including humans. Public Library of Science 2022-10-27 /pmc/articles/PMC9668190/ /pubmed/36301993 http://dx.doi.org/10.1371/journal.pgen.1010462 Text en © 2022 Billmyre et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://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
Billmyre, R. Blake
Eickbush, Michael T.
Craig, Caroline J.
Lange, Jeffrey J.
Wood, Christopher
Helston, Rachel M.
Zanders, Sarah E.
Genome-wide quantification of contributions to sexual fitness identifies genes required for spore viability and health in fission yeast
title Genome-wide quantification of contributions to sexual fitness identifies genes required for spore viability and health in fission yeast
title_full Genome-wide quantification of contributions to sexual fitness identifies genes required for spore viability and health in fission yeast
title_fullStr Genome-wide quantification of contributions to sexual fitness identifies genes required for spore viability and health in fission yeast
title_full_unstemmed Genome-wide quantification of contributions to sexual fitness identifies genes required for spore viability and health in fission yeast
title_short Genome-wide quantification of contributions to sexual fitness identifies genes required for spore viability and health in fission yeast
title_sort genome-wide quantification of contributions to sexual fitness identifies genes required for spore viability and health in fission yeast
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9668190/
https://www.ncbi.nlm.nih.gov/pubmed/36301993
http://dx.doi.org/10.1371/journal.pgen.1010462
work_keys_str_mv AT billmyrerblake genomewidequantificationofcontributionstosexualfitnessidentifiesgenesrequiredforsporeviabilityandhealthinfissionyeast
AT eickbushmichaelt genomewidequantificationofcontributionstosexualfitnessidentifiesgenesrequiredforsporeviabilityandhealthinfissionyeast
AT craigcarolinej genomewidequantificationofcontributionstosexualfitnessidentifiesgenesrequiredforsporeviabilityandhealthinfissionyeast
AT langejeffreyj genomewidequantificationofcontributionstosexualfitnessidentifiesgenesrequiredforsporeviabilityandhealthinfissionyeast
AT woodchristopher genomewidequantificationofcontributionstosexualfitnessidentifiesgenesrequiredforsporeviabilityandhealthinfissionyeast
AT helstonrachelm genomewidequantificationofcontributionstosexualfitnessidentifiesgenesrequiredforsporeviabilityandhealthinfissionyeast
AT zanderssarahe genomewidequantificationofcontributionstosexualfitnessidentifiesgenesrequiredforsporeviabilityandhealthinfissionyeast