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The Ancestral Caenorhabditis elegans Cuticle Suppresses rol-1

Genetic background commonly modifies the effects of mutations. We discovered that worms mutant for the canonical rol-1 gene, identified by Brenner in 1974, do not roll in the genetic background of the wild strain CB4856. Using linkage mapping, association analysis and gene editing, we determined tha...

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Autores principales: Noble, Luke M., Miah, Asif, Kaur, Taniya, Rockman, Matthew V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Genetics Society of America 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7341120/
https://www.ncbi.nlm.nih.gov/pubmed/32423919
http://dx.doi.org/10.1534/g3.120.401336
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author Noble, Luke M.
Miah, Asif
Kaur, Taniya
Rockman, Matthew V.
author_facet Noble, Luke M.
Miah, Asif
Kaur, Taniya
Rockman, Matthew V.
author_sort Noble, Luke M.
collection PubMed
description Genetic background commonly modifies the effects of mutations. We discovered that worms mutant for the canonical rol-1 gene, identified by Brenner in 1974, do not roll in the genetic background of the wild strain CB4856. Using linkage mapping, association analysis and gene editing, we determined that N2 carries an insertion in the collagen gene col-182 that acts as a recessive enhancer of rol-1 rolling. From population and comparative genomics, we infer the insertion is derived in N2 and related laboratory lines, likely arising during the domestication of Caenorhabditis elegans, and breaking a conserved protein. The ancestral version of col-182 also modifies the phenotypes of four other classical cuticle mutant alleles, and the effects of natural genetic variation on worm shape and locomotion. These results underscore the importance of genetic background and the serendipity of Brenner’s choice of strain.
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spelling pubmed-73411202020-07-21 The Ancestral Caenorhabditis elegans Cuticle Suppresses rol-1 Noble, Luke M. Miah, Asif Kaur, Taniya Rockman, Matthew V. G3 (Bethesda) Investigations Genetic background commonly modifies the effects of mutations. We discovered that worms mutant for the canonical rol-1 gene, identified by Brenner in 1974, do not roll in the genetic background of the wild strain CB4856. Using linkage mapping, association analysis and gene editing, we determined that N2 carries an insertion in the collagen gene col-182 that acts as a recessive enhancer of rol-1 rolling. From population and comparative genomics, we infer the insertion is derived in N2 and related laboratory lines, likely arising during the domestication of Caenorhabditis elegans, and breaking a conserved protein. The ancestral version of col-182 also modifies the phenotypes of four other classical cuticle mutant alleles, and the effects of natural genetic variation on worm shape and locomotion. These results underscore the importance of genetic background and the serendipity of Brenner’s choice of strain. Genetics Society of America 2020-05-18 /pmc/articles/PMC7341120/ /pubmed/32423919 http://dx.doi.org/10.1534/g3.120.401336 Text en Copyright © 2020 Noble et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Investigations
Noble, Luke M.
Miah, Asif
Kaur, Taniya
Rockman, Matthew V.
The Ancestral Caenorhabditis elegans Cuticle Suppresses rol-1
title The Ancestral Caenorhabditis elegans Cuticle Suppresses rol-1
title_full The Ancestral Caenorhabditis elegans Cuticle Suppresses rol-1
title_fullStr The Ancestral Caenorhabditis elegans Cuticle Suppresses rol-1
title_full_unstemmed The Ancestral Caenorhabditis elegans Cuticle Suppresses rol-1
title_short The Ancestral Caenorhabditis elegans Cuticle Suppresses rol-1
title_sort ancestral caenorhabditis elegans cuticle suppresses rol-1
topic Investigations
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7341120/
https://www.ncbi.nlm.nih.gov/pubmed/32423919
http://dx.doi.org/10.1534/g3.120.401336
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