Literature DB >> 15936160

Regional organization of gene expression in Streptomyces coelicolor.

Nitsara Karoonuthaisiri1, David Weaver, Jianqiang Huang, Stanley N Cohen, Camilla M Kao.   

Abstract

Based on the chromosomal locations of genes inferred from sequence analysis to be essential for the viability of Streptomyces coelicolor, Bentley et al. [Bentley, S.D., et al. 2002. Complete genome sequence of the model actinomycete Streptomyces coelicolor A3(2), Nature 417, 141-147.] have suggested that a 4.9 Mb central region of the linear S. coelicolor chromosome encodes 'core' functions expressed during vegetative growth of this species, while 1.5 Mb and 2.3 Mb chromosomal DNA segments lateral to this core encode auxiliary functions proposed to be required under other growth conditions. To examine this hypothesis and experimentally identify genes expressed during vegetative growth of S. coelicolor cultures, we used DNA microarrays to measure globally the abundance of S. coelicolor transcripts in cells growing in liquid medium. We found that, overall, genes corresponding to the 4.9 Mb core region of the S. coelicolor M145 chromosome were more highly expressed under non-limiting growth conditions than genes in the 1.5 Mb left and 2.3 Mb right chromosome arms, supporting the notion of the core versus auxiliary organization of genes on the chromosome. To examine how this chromosomal distribution of transcripts changes under other growth conditions, we also measured gene expression changes during stationary phase and several stress conditions. During stationary phase, the composition of S. coelicolor transcripts appears to shift from large quantities of growth-related transcripts encoded in the core region to those of less characterized genes, which may be essential for differentiation and other physiological responses, encoded throughout the chromosome. After temperature and osmotic upshifts, we found that S. coelicolor transiently induces a set of several hundred genes located throughout the chromosome, which may function in response mechanisms common to the two stress conditions.

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Year:  2005        PMID: 15936160     DOI: 10.1016/j.gene.2005.03.042

Source DB:  PubMed          Journal:  Gene        ISSN: 0378-1119            Impact factor:   3.688


  18 in total

1.  Characterization of a large, stable, high-copy-number Streptomyces plasmid that requires stability and transfer functions for heterologous polyketide overproduction.

Authors:  Ryan Fong; Jonathan A Vroom; Zhihao Hu; C Richard Hutchinson; Jianqiang Huang; Stanley N Cohen; Stanley Cohen; Camilla M Kao; Camilla Kao
Journal:  Appl Environ Microbiol       Date:  2006-12-01       Impact factor: 4.792

2.  Reciprocal regulation between SigK and differentiation programs in Streptomyces coelicolor.

Authors:  Xu-Ming Mao; Zhan Zhou; Xiao-Ping Hou; Wen-Jun Guan; Yong-Quan Li
Journal:  J Bacteriol       Date:  2009-09-04       Impact factor: 3.490

3.  RNA-Seq and RNA immunoprecipitation analyses of the transcriptome of Streptomyces coelicolor identify substrates for RNase III.

Authors:  Marcha L Gatewood; Patricia Bralley; M Ryan Weil; George H Jones
Journal:  J Bacteriol       Date:  2012-03-02       Impact factor: 3.490

Review 4.  Omics-based natural product discovery and the lexicon of genome mining.

Authors:  Henrique Machado; Robert N Tuttle; Paul R Jensen
Journal:  Curr Opin Microbiol       Date:  2017-11-23       Impact factor: 7.934

5.  The anti-anti-sigma factor BldG is involved in activation of the stress response sigma factor σ(H) in Streptomyces coelicolor A3(2).

Authors:  Beatrica Sevcikova; Bronislava Rezuchova; Dagmar Homerova; Jan Kormanec
Journal:  J Bacteriol       Date:  2010-09-03       Impact factor: 3.490

6.  Population Genomics Insights into Adaptive Evolution and Ecological Differentiation in Streptomycetes.

Authors:  Yisong Li; Adrián A Pinto-Tomás; Xiaoying Rong; Kun Cheng; Minghao Liu; Ying Huang
Journal:  Appl Environ Microbiol       Date:  2019-03-22       Impact factor: 4.792

Review 7.  Genetics of Streptomyces rimosus, the oxytetracycline producer.

Authors:  Hrvoje Petković; John Cullum; Daslav Hranueli; Iain S Hunter; Natasa Perić-Concha; Jasenka Pigac; Arinthip Thamchaipenet; Dusica Vujaklija; Paul F Long
Journal:  Microbiol Mol Biol Rev       Date:  2006-09       Impact factor: 11.056

8.  Streptomyces coelicolor genes ftsL and divIC play a role in cell division but are dispensable for colony formation.

Authors:  Jennifer A Bennett; Rachel M Aimino; Joseph R McCormick
Journal:  J Bacteriol       Date:  2007-10-19       Impact factor: 3.490

9.  DNA mapping and kinetic modeling of the HrdB regulon in Streptomyces coelicolor.

Authors:  Klára Šmídová; Alice Ziková; Jirí Pospíšil; Marek Schwarz; Jan Bobek; Jiri Vohradsky
Journal:  Nucleic Acids Res       Date:  2019-01-25       Impact factor: 16.971

10.  Acidic pH shock induces the expressions of a wide range of stress-response genes.

Authors:  Yoon Jung Kim; Myung Hee Moon; Jae Yang Song; Colin P Smith; Soon-Kwang Hong; Yong Keun Chang
Journal:  BMC Genomics       Date:  2008-12-16       Impact factor: 3.969

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