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S. pombe wtf drivers use dual transcriptional regulation and selective protein exclusion from spores to cause meiotic drive
Meiotic drivers bias gametogenesis to ensure their transmission into more than half the offspring of a heterozygote. In Schizosaccharomyces pombe, wtf meiotic drivers destroy the meiotic products (spores) that do not inherit the driver from a heterozygote, thereby reducing fertility. wtf drivers enc...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9762604/ https://www.ncbi.nlm.nih.gov/pubmed/36477651 http://dx.doi.org/10.1371/journal.pgen.1009847 |
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author | Nuckolls, Nicole L. Nidamangala Srinivasa, Ananya Mok, Anthony C. Helston, Rachel M. Bravo Núñez, María Angélica Lange, Jeffrey J. Gallagher, Todd J. Seidel, Chris W. Zanders, Sarah E. |
author_facet | Nuckolls, Nicole L. Nidamangala Srinivasa, Ananya Mok, Anthony C. Helston, Rachel M. Bravo Núñez, María Angélica Lange, Jeffrey J. Gallagher, Todd J. Seidel, Chris W. Zanders, Sarah E. |
author_sort | Nuckolls, Nicole L. |
collection | PubMed |
description | Meiotic drivers bias gametogenesis to ensure their transmission into more than half the offspring of a heterozygote. In Schizosaccharomyces pombe, wtf meiotic drivers destroy the meiotic products (spores) that do not inherit the driver from a heterozygote, thereby reducing fertility. wtf drivers encode both a Wtf(poison) protein and a Wtf(antidote) protein using alternative transcriptional start sites. Here, we analyze how the expression and localization of the Wtf proteins are regulated to achieve drive. We show that transcriptional timing and selective protein exclusion from developing spores ensure that all spores are exposed to Wtf4(poison), but only the spores that inherit wtf4 receive a dose of Wtf4(antidote) sufficient for survival. In addition, we show that the Mei4 transcription factor, a master regulator of meiosis, controls the expression of the wtf4(poison) transcript. This transcriptional regulation, which includes the use of a critical meiotic transcription factor, likely complicates the universal suppression of wtf genes without concomitantly disrupting spore viability. We propose that these features contribute to the evolutionary success of the wtf drivers. |
format | Online Article Text |
id | pubmed-9762604 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-97626042022-12-20 S. pombe wtf drivers use dual transcriptional regulation and selective protein exclusion from spores to cause meiotic drive Nuckolls, Nicole L. Nidamangala Srinivasa, Ananya Mok, Anthony C. Helston, Rachel M. Bravo Núñez, María Angélica Lange, Jeffrey J. Gallagher, Todd J. Seidel, Chris W. Zanders, Sarah E. PLoS Genet Research Article Meiotic drivers bias gametogenesis to ensure their transmission into more than half the offspring of a heterozygote. In Schizosaccharomyces pombe, wtf meiotic drivers destroy the meiotic products (spores) that do not inherit the driver from a heterozygote, thereby reducing fertility. wtf drivers encode both a Wtf(poison) protein and a Wtf(antidote) protein using alternative transcriptional start sites. Here, we analyze how the expression and localization of the Wtf proteins are regulated to achieve drive. We show that transcriptional timing and selective protein exclusion from developing spores ensure that all spores are exposed to Wtf4(poison), but only the spores that inherit wtf4 receive a dose of Wtf4(antidote) sufficient for survival. In addition, we show that the Mei4 transcription factor, a master regulator of meiosis, controls the expression of the wtf4(poison) transcript. This transcriptional regulation, which includes the use of a critical meiotic transcription factor, likely complicates the universal suppression of wtf genes without concomitantly disrupting spore viability. We propose that these features contribute to the evolutionary success of the wtf drivers. Public Library of Science 2022-12-07 /pmc/articles/PMC9762604/ /pubmed/36477651 http://dx.doi.org/10.1371/journal.pgen.1009847 Text en © 2022 Nuckolls 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 Nuckolls, Nicole L. Nidamangala Srinivasa, Ananya Mok, Anthony C. Helston, Rachel M. Bravo Núñez, María Angélica Lange, Jeffrey J. Gallagher, Todd J. Seidel, Chris W. Zanders, Sarah E. S. pombe wtf drivers use dual transcriptional regulation and selective protein exclusion from spores to cause meiotic drive |
title | S. pombe wtf drivers use dual transcriptional regulation and selective protein exclusion from spores to cause meiotic drive |
title_full | S. pombe wtf drivers use dual transcriptional regulation and selective protein exclusion from spores to cause meiotic drive |
title_fullStr | S. pombe wtf drivers use dual transcriptional regulation and selective protein exclusion from spores to cause meiotic drive |
title_full_unstemmed | S. pombe wtf drivers use dual transcriptional regulation and selective protein exclusion from spores to cause meiotic drive |
title_short | S. pombe wtf drivers use dual transcriptional regulation and selective protein exclusion from spores to cause meiotic drive |
title_sort | s. pombe wtf drivers use dual transcriptional regulation and selective protein exclusion from spores to cause meiotic drive |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9762604/ https://www.ncbi.nlm.nih.gov/pubmed/36477651 http://dx.doi.org/10.1371/journal.pgen.1009847 |
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