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Comparative Analyses of Homocitrate Synthase Genes of Ascomycetous Yeasts

Most ascomycetous yeasts have 2 homocitrate synthases (HCSs). Among the fungal lysine biosynthesis-related genes, only the HCS gene was duplicated in the course of evolution. It was recently reported that HCS of Saccharomyces cerevisiae has an additional function in nuclear activities involving chro...

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Autor principal: Nishida, Hiromi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3317173/
https://www.ncbi.nlm.nih.gov/pubmed/22518332
http://dx.doi.org/10.1155/2012/254941
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author Nishida, Hiromi
author_facet Nishida, Hiromi
author_sort Nishida, Hiromi
collection PubMed
description Most ascomycetous yeasts have 2 homocitrate synthases (HCSs). Among the fungal lysine biosynthesis-related genes, only the HCS gene was duplicated in the course of evolution. It was recently reported that HCS of Saccharomyces cerevisiae has an additional function in nuclear activities involving chromatin regulation related to DNA damage repair, which is not related to lysine biosynthesis. Thus, it is possible that the bifunctionality is associated with HCS gene duplication. Phylogenetic analysis showed that duplication has occurred multiple times during evolution of the ascomycetous yeasts. It is likely that the HCS gene duplication in S. cerevisiae occurred in the course of Saccharomyces evolution. Although the nucleosome position profiles of the two S. cerevisiae HCS genes were similar in the coding regions, they were different in the promoter regions, suggesting that they are subject to different regulatory controls. S. cerevisiae has maintained HCS activity for lysine biosynthesis and has obtained bifunctionality.
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spelling pubmed-33171732012-04-19 Comparative Analyses of Homocitrate Synthase Genes of Ascomycetous Yeasts Nishida, Hiromi Int J Evol Biol Research Article Most ascomycetous yeasts have 2 homocitrate synthases (HCSs). Among the fungal lysine biosynthesis-related genes, only the HCS gene was duplicated in the course of evolution. It was recently reported that HCS of Saccharomyces cerevisiae has an additional function in nuclear activities involving chromatin regulation related to DNA damage repair, which is not related to lysine biosynthesis. Thus, it is possible that the bifunctionality is associated with HCS gene duplication. Phylogenetic analysis showed that duplication has occurred multiple times during evolution of the ascomycetous yeasts. It is likely that the HCS gene duplication in S. cerevisiae occurred in the course of Saccharomyces evolution. Although the nucleosome position profiles of the two S. cerevisiae HCS genes were similar in the coding regions, they were different in the promoter regions, suggesting that they are subject to different regulatory controls. S. cerevisiae has maintained HCS activity for lysine biosynthesis and has obtained bifunctionality. Hindawi Publishing Corporation 2012 2012-03-18 /pmc/articles/PMC3317173/ /pubmed/22518332 http://dx.doi.org/10.1155/2012/254941 Text en Copyright © 2012 Hiromi Nishida. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Nishida, Hiromi
Comparative Analyses of Homocitrate Synthase Genes of Ascomycetous Yeasts
title Comparative Analyses of Homocitrate Synthase Genes of Ascomycetous Yeasts
title_full Comparative Analyses of Homocitrate Synthase Genes of Ascomycetous Yeasts
title_fullStr Comparative Analyses of Homocitrate Synthase Genes of Ascomycetous Yeasts
title_full_unstemmed Comparative Analyses of Homocitrate Synthase Genes of Ascomycetous Yeasts
title_short Comparative Analyses of Homocitrate Synthase Genes of Ascomycetous Yeasts
title_sort comparative analyses of homocitrate synthase genes of ascomycetous yeasts
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3317173/
https://www.ncbi.nlm.nih.gov/pubmed/22518332
http://dx.doi.org/10.1155/2012/254941
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