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Natural variation in non-coding regions underlying phenotypic diversity in budding yeast
Linkage mapping studies in model organisms have typically focused their efforts in polymorphisms within coding regions, ignoring those within regulatory regions that may contribute to gene expression variation. In this context, differences in transcript abundance are frequently proposed as a source...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4761897/ https://www.ncbi.nlm.nih.gov/pubmed/26898953 http://dx.doi.org/10.1038/srep21849 |
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author | Salinas, Francisco de Boer, Carl G. Abarca, Valentina García, Verónica Cuevas, Mara Araos, Sebastian Larrondo, Luis F. Martínez, Claudio Cubillos, Francisco A. |
author_facet | Salinas, Francisco de Boer, Carl G. Abarca, Valentina García, Verónica Cuevas, Mara Araos, Sebastian Larrondo, Luis F. Martínez, Claudio Cubillos, Francisco A. |
author_sort | Salinas, Francisco |
collection | PubMed |
description | Linkage mapping studies in model organisms have typically focused their efforts in polymorphisms within coding regions, ignoring those within regulatory regions that may contribute to gene expression variation. In this context, differences in transcript abundance are frequently proposed as a source of phenotypic diversity between individuals, however, until now, little molecular evidence has been provided. Here, we examined Allele Specific Expression (ASE) in six F1 hybrids from Saccharomyces cerevisiae derived from crosses between representative strains of the four main lineages described in yeast. ASE varied between crosses with levels ranging between 28% and 60%. Part of the variation in expression levels could be explained by differences in transcription factors binding to polymorphic cis-regulations and to differences in trans-activation depending on the allelic form of the TF. Analysis on highly expressed alleles on each background suggested ASN1 as a candidate transcript underlying nitrogen consumption differences between two strains. Further promoter allele swap analysis under fermentation conditions confirmed that coding and non-coding regions explained aspartic and glutamic acid consumption differences, likely due to a polymorphism affecting Uga3 binding. Together, we provide a new catalogue of variants to bridge the gap between genotype and phenotype. |
format | Online Article Text |
id | pubmed-4761897 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-47618972016-02-29 Natural variation in non-coding regions underlying phenotypic diversity in budding yeast Salinas, Francisco de Boer, Carl G. Abarca, Valentina García, Verónica Cuevas, Mara Araos, Sebastian Larrondo, Luis F. Martínez, Claudio Cubillos, Francisco A. Sci Rep Article Linkage mapping studies in model organisms have typically focused their efforts in polymorphisms within coding regions, ignoring those within regulatory regions that may contribute to gene expression variation. In this context, differences in transcript abundance are frequently proposed as a source of phenotypic diversity between individuals, however, until now, little molecular evidence has been provided. Here, we examined Allele Specific Expression (ASE) in six F1 hybrids from Saccharomyces cerevisiae derived from crosses between representative strains of the four main lineages described in yeast. ASE varied between crosses with levels ranging between 28% and 60%. Part of the variation in expression levels could be explained by differences in transcription factors binding to polymorphic cis-regulations and to differences in trans-activation depending on the allelic form of the TF. Analysis on highly expressed alleles on each background suggested ASN1 as a candidate transcript underlying nitrogen consumption differences between two strains. Further promoter allele swap analysis under fermentation conditions confirmed that coding and non-coding regions explained aspartic and glutamic acid consumption differences, likely due to a polymorphism affecting Uga3 binding. Together, we provide a new catalogue of variants to bridge the gap between genotype and phenotype. Nature Publishing Group 2016-02-22 /pmc/articles/PMC4761897/ /pubmed/26898953 http://dx.doi.org/10.1038/srep21849 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Salinas, Francisco de Boer, Carl G. Abarca, Valentina García, Verónica Cuevas, Mara Araos, Sebastian Larrondo, Luis F. Martínez, Claudio Cubillos, Francisco A. Natural variation in non-coding regions underlying phenotypic diversity in budding yeast |
title | Natural variation in non-coding regions underlying phenotypic diversity in budding yeast |
title_full | Natural variation in non-coding regions underlying phenotypic diversity in budding yeast |
title_fullStr | Natural variation in non-coding regions underlying phenotypic diversity in budding yeast |
title_full_unstemmed | Natural variation in non-coding regions underlying phenotypic diversity in budding yeast |
title_short | Natural variation in non-coding regions underlying phenotypic diversity in budding yeast |
title_sort | natural variation in non-coding regions underlying phenotypic diversity in budding yeast |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4761897/ https://www.ncbi.nlm.nih.gov/pubmed/26898953 http://dx.doi.org/10.1038/srep21849 |
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