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MFS transportome of the human pathogenic yeast Candida albicans
BACKGROUND: The major facilitator superfamily (MFS) is one of the two largest superfamilies of membrane transporters present ubiquitously in bacteria, archaea, and eukarya and includes members that function as uniporters, symporters or antiporters. We report here the complete transportome of MFS pro...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2636803/ https://www.ncbi.nlm.nih.gov/pubmed/19055746 http://dx.doi.org/10.1186/1471-2164-9-579 |
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author | Gaur, Manisha Puri, Nidhi Manoharlal, Raman Rai, Versha Mukhopadhayay, Gauranga Choudhury, Devapriya Prasad, Rajendra |
author_facet | Gaur, Manisha Puri, Nidhi Manoharlal, Raman Rai, Versha Mukhopadhayay, Gauranga Choudhury, Devapriya Prasad, Rajendra |
author_sort | Gaur, Manisha |
collection | PubMed |
description | BACKGROUND: The major facilitator superfamily (MFS) is one of the two largest superfamilies of membrane transporters present ubiquitously in bacteria, archaea, and eukarya and includes members that function as uniporters, symporters or antiporters. We report here the complete transportome of MFS proteins of a human pathogenic yeast Candida albicans. RESULTS: Computational analysis of C. albicans genome enabled us to identify 95 potential MFS proteins which clustered into 17 families using Saier's Transport Commission (TC) system. Among these SP, DHA1, DHA2 and ACS represented major families consisting of 22, 22, 9 and 16 members, respectively. Family designations in C. albicans were validated by subjecting Saccharomyces cerevisiae genome to TC system. Based on the published available genomics/proteomics data, 87 of the putative MFS genes of C. albicans were found to express either at mRNA or protein levels. We checked the expression of the remaining 8 genes by using RT-PCR and observed that they are not expressed under basal growth conditions implying that either these 8 genes are expressed under specific growth conditions or they may be candidates for pseudogenes. CONCLUSION: The in silico characterisation of MFS transporters in Candida albicans genome revealed a large complement of MFS transporters with most of them showing expression. Considering the clinical relevance of C. albicans and role of MFS members in antifungal resistance and nutrient transport, this analysis would pave way for identifying their physiological relevance. |
format | Text |
id | pubmed-2636803 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-26368032009-02-06 MFS transportome of the human pathogenic yeast Candida albicans Gaur, Manisha Puri, Nidhi Manoharlal, Raman Rai, Versha Mukhopadhayay, Gauranga Choudhury, Devapriya Prasad, Rajendra BMC Genomics Research Article BACKGROUND: The major facilitator superfamily (MFS) is one of the two largest superfamilies of membrane transporters present ubiquitously in bacteria, archaea, and eukarya and includes members that function as uniporters, symporters or antiporters. We report here the complete transportome of MFS proteins of a human pathogenic yeast Candida albicans. RESULTS: Computational analysis of C. albicans genome enabled us to identify 95 potential MFS proteins which clustered into 17 families using Saier's Transport Commission (TC) system. Among these SP, DHA1, DHA2 and ACS represented major families consisting of 22, 22, 9 and 16 members, respectively. Family designations in C. albicans were validated by subjecting Saccharomyces cerevisiae genome to TC system. Based on the published available genomics/proteomics data, 87 of the putative MFS genes of C. albicans were found to express either at mRNA or protein levels. We checked the expression of the remaining 8 genes by using RT-PCR and observed that they are not expressed under basal growth conditions implying that either these 8 genes are expressed under specific growth conditions or they may be candidates for pseudogenes. CONCLUSION: The in silico characterisation of MFS transporters in Candida albicans genome revealed a large complement of MFS transporters with most of them showing expression. Considering the clinical relevance of C. albicans and role of MFS members in antifungal resistance and nutrient transport, this analysis would pave way for identifying their physiological relevance. BioMed Central 2008-12-03 /pmc/articles/PMC2636803/ /pubmed/19055746 http://dx.doi.org/10.1186/1471-2164-9-579 Text en Copyright © 2008 Gaur et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Gaur, Manisha Puri, Nidhi Manoharlal, Raman Rai, Versha Mukhopadhayay, Gauranga Choudhury, Devapriya Prasad, Rajendra MFS transportome of the human pathogenic yeast Candida albicans |
title | MFS transportome of the human pathogenic yeast Candida albicans |
title_full | MFS transportome of the human pathogenic yeast Candida albicans |
title_fullStr | MFS transportome of the human pathogenic yeast Candida albicans |
title_full_unstemmed | MFS transportome of the human pathogenic yeast Candida albicans |
title_short | MFS transportome of the human pathogenic yeast Candida albicans |
title_sort | mfs transportome of the human pathogenic yeast candida albicans |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2636803/ https://www.ncbi.nlm.nih.gov/pubmed/19055746 http://dx.doi.org/10.1186/1471-2164-9-579 |
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