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CSU52, a novel regulator functions as a repressor of L-sorbose utilization in Candida albicans
BACKGROUND AND OBJECTIVES: Monosomy of chromosome 5 associated with utilization of non-canonical sugar L-sorbose is one of the well-studied aneuploidies in Candida albicans. Stress-induced ploidy changes are crucial determinants for pathogenicity and genetic diversity in C. albicans. The five scatte...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Tehran University of Medical Sciences
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8421577/ https://www.ncbi.nlm.nih.gov/pubmed/34557282 http://dx.doi.org/10.18502/ijm.v13i4.6978 |
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author | Pullepu, Dileep Uddin, Wasim Narayanan, Aswathy Kabir, M. Anaul |
author_facet | Pullepu, Dileep Uddin, Wasim Narayanan, Aswathy Kabir, M. Anaul |
author_sort | Pullepu, Dileep |
collection | PubMed |
description | BACKGROUND AND OBJECTIVES: Monosomy of chromosome 5 associated with utilization of non-canonical sugar L-sorbose is one of the well-studied aneuploidies in Candida albicans. Stress-induced ploidy changes are crucial determinants for pathogenicity and genetic diversity in C. albicans. The five scattered regulatory regions (A, B, C, 135, and 139) comprising of two functionally redundant pathways (SUR1 and SUR2) were found to be responsible for the growth on L-sorbose. So far, three genes such as CSU51, CSU53 and CSU57 have been identified in region A, region 135 and region C, respectively. In this study we have verified the role of region B in this regulatory pathway. MATERIALS AND METHODS: We employed a combinatorial gene deletion approach to verify the role of region B followed by co-over expression studies and qRT-PCR to identify the regulatory role of this region. RESULTS: We confirmed the role of region B in the regulation of SOU1 gene expression. The qRT-PCR results showed that regulation occurs at transcriptional level along with other two regions in SUR1 pathway. A previously uncharacterized open reading frame in region B has been implicated in this regulation and designated as CSU52. Integrating multiple copies of CSU52 in the genome at tandem, suppresses the growth of recipient strain on L-sorbose, establishing it as a repressor of SOU1 gene. CONCLUSION: This finding completes the identification of regulators in SUR1 pathway. This result paves the way to study the underlying molecular mechanisms of SOU1 gene regulation that in-turn helps to understand stress induced aneuploidy. |
format | Online Article Text |
id | pubmed-8421577 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Tehran University of Medical Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-84215772021-09-22 CSU52, a novel regulator functions as a repressor of L-sorbose utilization in Candida albicans Pullepu, Dileep Uddin, Wasim Narayanan, Aswathy Kabir, M. Anaul Iran J Microbiol Original Article BACKGROUND AND OBJECTIVES: Monosomy of chromosome 5 associated with utilization of non-canonical sugar L-sorbose is one of the well-studied aneuploidies in Candida albicans. Stress-induced ploidy changes are crucial determinants for pathogenicity and genetic diversity in C. albicans. The five scattered regulatory regions (A, B, C, 135, and 139) comprising of two functionally redundant pathways (SUR1 and SUR2) were found to be responsible for the growth on L-sorbose. So far, three genes such as CSU51, CSU53 and CSU57 have been identified in region A, region 135 and region C, respectively. In this study we have verified the role of region B in this regulatory pathway. MATERIALS AND METHODS: We employed a combinatorial gene deletion approach to verify the role of region B followed by co-over expression studies and qRT-PCR to identify the regulatory role of this region. RESULTS: We confirmed the role of region B in the regulation of SOU1 gene expression. The qRT-PCR results showed that regulation occurs at transcriptional level along with other two regions in SUR1 pathway. A previously uncharacterized open reading frame in region B has been implicated in this regulation and designated as CSU52. Integrating multiple copies of CSU52 in the genome at tandem, suppresses the growth of recipient strain on L-sorbose, establishing it as a repressor of SOU1 gene. CONCLUSION: This finding completes the identification of regulators in SUR1 pathway. This result paves the way to study the underlying molecular mechanisms of SOU1 gene regulation that in-turn helps to understand stress induced aneuploidy. Tehran University of Medical Sciences 2021-08 /pmc/articles/PMC8421577/ /pubmed/34557282 http://dx.doi.org/10.18502/ijm.v13i4.6978 Text en Copyright © 2021 The Authors. Published by Tehran University of Medical Sciences https://creativecommons.org/licenses/by-nc/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International license (https://creativecommons.org/licenses/by-nc/4.0/). Non-commercial uses of the work are permitted, provided the original work is properly cited. |
spellingShingle | Original Article Pullepu, Dileep Uddin, Wasim Narayanan, Aswathy Kabir, M. Anaul CSU52, a novel regulator functions as a repressor of L-sorbose utilization in Candida albicans |
title | CSU52, a novel regulator functions as a repressor of L-sorbose utilization in Candida albicans |
title_full | CSU52, a novel regulator functions as a repressor of L-sorbose utilization in Candida albicans |
title_fullStr | CSU52, a novel regulator functions as a repressor of L-sorbose utilization in Candida albicans |
title_full_unstemmed | CSU52, a novel regulator functions as a repressor of L-sorbose utilization in Candida albicans |
title_short | CSU52, a novel regulator functions as a repressor of L-sorbose utilization in Candida albicans |
title_sort | csu52, a novel regulator functions as a repressor of l-sorbose utilization in candida albicans |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8421577/ https://www.ncbi.nlm.nih.gov/pubmed/34557282 http://dx.doi.org/10.18502/ijm.v13i4.6978 |
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