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Identification of essential genes in Caenorhabditis elegans through whole-genome sequencing of legacy mutant collections
It has been estimated that 15%–30% of the ∼20,000 genes in C. elegans are essential, yet many of these genes remain to be identified or characterized. With the goal of identifying unknown essential genes, we performed whole-genome sequencing on complementation pairs from legacy collections of matern...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8664450/ https://www.ncbi.nlm.nih.gov/pubmed/34550348 http://dx.doi.org/10.1093/g3journal/jkab328 |
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author | Li-Leger, Erica Feichtinger, Richard Flibotte, Stephane Holzkamp, Heinke Schnabel, Ralf Moerman, Donald G |
author_facet | Li-Leger, Erica Feichtinger, Richard Flibotte, Stephane Holzkamp, Heinke Schnabel, Ralf Moerman, Donald G |
author_sort | Li-Leger, Erica |
collection | PubMed |
description | It has been estimated that 15%–30% of the ∼20,000 genes in C. elegans are essential, yet many of these genes remain to be identified or characterized. With the goal of identifying unknown essential genes, we performed whole-genome sequencing on complementation pairs from legacy collections of maternal-effect lethal and sterile mutants. This approach uncovered maternal genes required for embryonic development and genes with apparent sperm-specific functions. In total, 58 putative essential genes were identified on chromosomes III–V, of which 52 genes are represented by novel alleles in this collection. Of these 52 genes, 19 (40 alleles) were selected for further functional characterization. The terminal phenotypes of embryos were examined, revealing defects in cell division, morphogenesis, and osmotic integrity of the eggshell. Mating assays with wild-type males revealed previously unknown male-expressed genes required for fertilization and embryonic development. The result of this study is a catalog of mutant alleles in essential genes that will serve as a resource to guide further study toward a more complete understanding of this important model organism. As many genes and developmental pathways in C. elegans are conserved and essential genes are often linked to human disease, uncovering the function of these genes may also provide insight to further our understanding of human biology. |
format | Online Article Text |
id | pubmed-8664450 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-86644502021-12-13 Identification of essential genes in Caenorhabditis elegans through whole-genome sequencing of legacy mutant collections Li-Leger, Erica Feichtinger, Richard Flibotte, Stephane Holzkamp, Heinke Schnabel, Ralf Moerman, Donald G G3 (Bethesda) Investigation It has been estimated that 15%–30% of the ∼20,000 genes in C. elegans are essential, yet many of these genes remain to be identified or characterized. With the goal of identifying unknown essential genes, we performed whole-genome sequencing on complementation pairs from legacy collections of maternal-effect lethal and sterile mutants. This approach uncovered maternal genes required for embryonic development and genes with apparent sperm-specific functions. In total, 58 putative essential genes were identified on chromosomes III–V, of which 52 genes are represented by novel alleles in this collection. Of these 52 genes, 19 (40 alleles) were selected for further functional characterization. The terminal phenotypes of embryos were examined, revealing defects in cell division, morphogenesis, and osmotic integrity of the eggshell. Mating assays with wild-type males revealed previously unknown male-expressed genes required for fertilization and embryonic development. The result of this study is a catalog of mutant alleles in essential genes that will serve as a resource to guide further study toward a more complete understanding of this important model organism. As many genes and developmental pathways in C. elegans are conserved and essential genes are often linked to human disease, uncovering the function of these genes may also provide insight to further our understanding of human biology. Oxford University Press 2021-09-22 /pmc/articles/PMC8664450/ /pubmed/34550348 http://dx.doi.org/10.1093/g3journal/jkab328 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of Genetics Society of America. 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 reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Investigation Li-Leger, Erica Feichtinger, Richard Flibotte, Stephane Holzkamp, Heinke Schnabel, Ralf Moerman, Donald G Identification of essential genes in Caenorhabditis elegans through whole-genome sequencing of legacy mutant collections |
title | Identification of essential genes in Caenorhabditis elegans through whole-genome sequencing of legacy mutant collections |
title_full | Identification of essential genes in Caenorhabditis elegans through whole-genome sequencing of legacy mutant collections |
title_fullStr | Identification of essential genes in Caenorhabditis elegans through whole-genome sequencing of legacy mutant collections |
title_full_unstemmed | Identification of essential genes in Caenorhabditis elegans through whole-genome sequencing of legacy mutant collections |
title_short | Identification of essential genes in Caenorhabditis elegans through whole-genome sequencing of legacy mutant collections |
title_sort | identification of essential genes in caenorhabditis elegans through whole-genome sequencing of legacy mutant collections |
topic | Investigation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8664450/ https://www.ncbi.nlm.nih.gov/pubmed/34550348 http://dx.doi.org/10.1093/g3journal/jkab328 |
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