Genomic mapping of cAMP receptor protein (CRPMt) in Mycobacterium tuberculosis: relation to transcriptional start sites and the role of CRPMt as a transcription factor
Data(s) |
2014
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Resumo |
Chromatin immunoprecipitation identified 191 binding sites of Mycobacterium tuberculosis cAMP receptor protein (CRPMt) at endogenous expression levels using a specific alpha-CRPMt antibody. Under these native conditions an equal distribution between intragenic and intergenic locations was observed. CRPMt binding overlapped a palindromic consensus sequence. Analysis by RNA sequencing revealed widespread changes in transcriptional profile in a mutant strain lacking CRPMt during exponential growth, and in response to nutrient starvation. Differential expression of genes with a CRPMt-binding site represented only a minor portion of this transcriptional reprogramming with similar to 19% of those representing transcriptional regulators potentially controlled by CRPMt. The subset of genes that are differentially expressed in the deletion mutant under both culture conditions conformed to a pattern resembling canonical CRP regulation in Escherichia coli, with binding close to the transcriptional start site associated with repression and upstream binding with activation. CRPMt can function as a classical transcription factor in M. tuberculosis, though this occurs at only a subset of CRPMt-binding sites. |
Formato |
application/pdf |
Identificador |
http://eprints.iisc.ernet.in/50046/1/nuc_aci_res_42-13_8320_2014.pdf Kahramanoglou, Christina and Cortes, Teresa and Matange, Nishad and Hunt, Debbie M and Visweswariah, Sandhya S and Young, Douglas B and Buxton, Roger S (2014) Genomic mapping of cAMP receptor protein (CRPMt) in Mycobacterium tuberculosis: relation to transcriptional start sites and the role of CRPMt as a transcription factor. In: NUCLEIC ACIDS RESEARCH, 42 (13). 8320-U108. |
Relação |
http://dx.doi.org/ 10.1093/nar/gku548 http://eprints.iisc.ernet.in/50046/ |
Palavras-Chave | #Molecular Reproduction, Development & Genetics (formed by the merger of DBGL and CRBME) |
Tipo |
Journal Article PeerReviewed |