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Genome-Wide Transcriptome Profiling of Mycobacterium smegmatis MC(2) 155 Cultivated in Minimal Media Supplemented with Cholesterol, Androstenedione or Glycerol
Mycobacterium smegmatis strain MC(2) 155 is an attractive model organism for the study of M. tuberculosis and other mycobacterial pathogens, as it can grow well using cholesterol as a carbon resource. However, its global transcriptomic response remains largely unrevealed. In this study, M. smegmatis...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4881515/ https://www.ncbi.nlm.nih.gov/pubmed/27164097 http://dx.doi.org/10.3390/ijms17050689 |
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author | Li, Qun Ge, Fanglan Tan, Yunya Zhang, Guangxiang Li, Wei |
author_facet | Li, Qun Ge, Fanglan Tan, Yunya Zhang, Guangxiang Li, Wei |
author_sort | Li, Qun |
collection | PubMed |
description | Mycobacterium smegmatis strain MC(2) 155 is an attractive model organism for the study of M. tuberculosis and other mycobacterial pathogens, as it can grow well using cholesterol as a carbon resource. However, its global transcriptomic response remains largely unrevealed. In this study, M. smegmatis MC(2) 155 cultivated in androstenedione, cholesterol and glycerol supplemented media were collected separately for a RNA-Sequencing study. The results showed that 6004, 6681 and 6348 genes were expressed in androstenedione, cholesterol and glycerol supplemented media, and 5891 genes were expressed in all three conditions, with 237 specially expressed in cholesterol added medium. A total of 1852 and 454 genes were significantly up-regulated by cholesterol compared with the other two supplements. Only occasional changes were observed in basic carbon and nitrogen metabolism, while almost all of the genes involved in cholesterol catabolism and mammalian cell entry (MCE) were up-regulated by cholesterol, but not by androstenedione. Eleven and 16 gene clusters were induced by cholesterol when compared with glycerol or androstenedione, respectively. This study provides a comprehensive analysis of the cholesterol responsive transcriptome of M. smegmatis. Our results indicated that cholesterol induced many more genes and increased the expression of the majority of genes involved in cholesterol degradation and MCE in M. smegmatis, while androstenedione did not have the same effect. |
format | Online Article Text |
id | pubmed-4881515 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-48815152016-05-27 Genome-Wide Transcriptome Profiling of Mycobacterium smegmatis MC(2) 155 Cultivated in Minimal Media Supplemented with Cholesterol, Androstenedione or Glycerol Li, Qun Ge, Fanglan Tan, Yunya Zhang, Guangxiang Li, Wei Int J Mol Sci Article Mycobacterium smegmatis strain MC(2) 155 is an attractive model organism for the study of M. tuberculosis and other mycobacterial pathogens, as it can grow well using cholesterol as a carbon resource. However, its global transcriptomic response remains largely unrevealed. In this study, M. smegmatis MC(2) 155 cultivated in androstenedione, cholesterol and glycerol supplemented media were collected separately for a RNA-Sequencing study. The results showed that 6004, 6681 and 6348 genes were expressed in androstenedione, cholesterol and glycerol supplemented media, and 5891 genes were expressed in all three conditions, with 237 specially expressed in cholesterol added medium. A total of 1852 and 454 genes were significantly up-regulated by cholesterol compared with the other two supplements. Only occasional changes were observed in basic carbon and nitrogen metabolism, while almost all of the genes involved in cholesterol catabolism and mammalian cell entry (MCE) were up-regulated by cholesterol, but not by androstenedione. Eleven and 16 gene clusters were induced by cholesterol when compared with glycerol or androstenedione, respectively. This study provides a comprehensive analysis of the cholesterol responsive transcriptome of M. smegmatis. Our results indicated that cholesterol induced many more genes and increased the expression of the majority of genes involved in cholesterol degradation and MCE in M. smegmatis, while androstenedione did not have the same effect. MDPI 2016-05-07 /pmc/articles/PMC4881515/ /pubmed/27164097 http://dx.doi.org/10.3390/ijms17050689 Text en © 2016 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC-BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Li, Qun Ge, Fanglan Tan, Yunya Zhang, Guangxiang Li, Wei Genome-Wide Transcriptome Profiling of Mycobacterium smegmatis MC(2) 155 Cultivated in Minimal Media Supplemented with Cholesterol, Androstenedione or Glycerol |
title | Genome-Wide Transcriptome Profiling of Mycobacterium
smegmatis MC(2) 155 Cultivated in Minimal Media Supplemented with Cholesterol, Androstenedione or Glycerol |
title_full | Genome-Wide Transcriptome Profiling of Mycobacterium
smegmatis MC(2) 155 Cultivated in Minimal Media Supplemented with Cholesterol, Androstenedione or Glycerol |
title_fullStr | Genome-Wide Transcriptome Profiling of Mycobacterium
smegmatis MC(2) 155 Cultivated in Minimal Media Supplemented with Cholesterol, Androstenedione or Glycerol |
title_full_unstemmed | Genome-Wide Transcriptome Profiling of Mycobacterium
smegmatis MC(2) 155 Cultivated in Minimal Media Supplemented with Cholesterol, Androstenedione or Glycerol |
title_short | Genome-Wide Transcriptome Profiling of Mycobacterium
smegmatis MC(2) 155 Cultivated in Minimal Media Supplemented with Cholesterol, Androstenedione or Glycerol |
title_sort | genome-wide transcriptome profiling of mycobacterium
smegmatis mc(2) 155 cultivated in minimal media supplemented with cholesterol, androstenedione or glycerol |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4881515/ https://www.ncbi.nlm.nih.gov/pubmed/27164097 http://dx.doi.org/10.3390/ijms17050689 |
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