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Polygenic Molecular Architecture Underlying Non-Sexual Cell Aggregation in Budding Yeast
Cell aggregation in unicellular organisms, induced by either cell non-sexual adhesion to yield flocs and biofilm, or pheromone-driving sexual conjugation is of great significance in cellular stress response, medicine, and brewing industries. Most current literatures have focused on one form of cell...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3576658/ https://www.ncbi.nlm.nih.gov/pubmed/23284084 http://dx.doi.org/10.1093/dnares/dss033 |
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author | Li, Jiarui Wang, Lin Wu, Xiaoping Fang, Ou Wang, Luwen Lu, Chenqi Yang, Shengjie Hu, Xiaohua Luo, Zewei |
author_facet | Li, Jiarui Wang, Lin Wu, Xiaoping Fang, Ou Wang, Luwen Lu, Chenqi Yang, Shengjie Hu, Xiaohua Luo, Zewei |
author_sort | Li, Jiarui |
collection | PubMed |
description | Cell aggregation in unicellular organisms, induced by either cell non-sexual adhesion to yield flocs and biofilm, or pheromone-driving sexual conjugation is of great significance in cellular stress response, medicine, and brewing industries. Most current literatures have focused on one form of cell aggregation termed flocculation and its major molecular determinants, the flocculation (FLO) family genes. Here, we implemented a map-based approach for dissecting the molecular basis of non-sexual cell aggregation in Saccharomyces cerevisiae. Genome-wide mapping has identified four major quantitative trait loci (QTL) underlying nature variation in the cell aggregation phenotype. High-resolution mapping following up with knockout and allele replacement experiments resolved the QTL into the underlying genes (AMN1, RGA1, FLO1, and FLO8) or even into the causative nucleotide. Genetic variation in the QTL genes can explain up to 46% of phenotypic variation of this trait. Of these genes, AMN1 plays the leading role, differing from the FLO family members, in regulating expression of cell clumping phenotype through inducing cell segregation defect. These findings provide novel insights into the molecular mechanism of how cell aggregation is regulated in budding yeast, and the data will be directly implicated to understand the molecular basis and evolutionary implications of cell aggregation in other fungus species. |
format | Online Article Text |
id | pubmed-3576658 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-35766582013-02-20 Polygenic Molecular Architecture Underlying Non-Sexual Cell Aggregation in Budding Yeast Li, Jiarui Wang, Lin Wu, Xiaoping Fang, Ou Wang, Luwen Lu, Chenqi Yang, Shengjie Hu, Xiaohua Luo, Zewei DNA Res Full Papers Cell aggregation in unicellular organisms, induced by either cell non-sexual adhesion to yield flocs and biofilm, or pheromone-driving sexual conjugation is of great significance in cellular stress response, medicine, and brewing industries. Most current literatures have focused on one form of cell aggregation termed flocculation and its major molecular determinants, the flocculation (FLO) family genes. Here, we implemented a map-based approach for dissecting the molecular basis of non-sexual cell aggregation in Saccharomyces cerevisiae. Genome-wide mapping has identified four major quantitative trait loci (QTL) underlying nature variation in the cell aggregation phenotype. High-resolution mapping following up with knockout and allele replacement experiments resolved the QTL into the underlying genes (AMN1, RGA1, FLO1, and FLO8) or even into the causative nucleotide. Genetic variation in the QTL genes can explain up to 46% of phenotypic variation of this trait. Of these genes, AMN1 plays the leading role, differing from the FLO family members, in regulating expression of cell clumping phenotype through inducing cell segregation defect. These findings provide novel insights into the molecular mechanism of how cell aggregation is regulated in budding yeast, and the data will be directly implicated to understand the molecular basis and evolutionary implications of cell aggregation in other fungus species. Oxford University Press 2013-02 2013-01-02 /pmc/articles/PMC3576658/ /pubmed/23284084 http://dx.doi.org/10.1093/dnares/dss033 Text en © The Author 2013. Published by Oxford University Press on behalf of Kazusa DNA Research Institute. http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Full Papers Li, Jiarui Wang, Lin Wu, Xiaoping Fang, Ou Wang, Luwen Lu, Chenqi Yang, Shengjie Hu, Xiaohua Luo, Zewei Polygenic Molecular Architecture Underlying Non-Sexual Cell Aggregation in Budding Yeast |
title | Polygenic Molecular Architecture Underlying Non-Sexual Cell Aggregation in Budding Yeast |
title_full | Polygenic Molecular Architecture Underlying Non-Sexual Cell Aggregation in Budding Yeast |
title_fullStr | Polygenic Molecular Architecture Underlying Non-Sexual Cell Aggregation in Budding Yeast |
title_full_unstemmed | Polygenic Molecular Architecture Underlying Non-Sexual Cell Aggregation in Budding Yeast |
title_short | Polygenic Molecular Architecture Underlying Non-Sexual Cell Aggregation in Budding Yeast |
title_sort | polygenic molecular architecture underlying non-sexual cell aggregation in budding yeast |
topic | Full Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3576658/ https://www.ncbi.nlm.nih.gov/pubmed/23284084 http://dx.doi.org/10.1093/dnares/dss033 |
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