MRNA degradation in Mycobacterium tuberculosis with DosR ectopically induced

ABSTRACT: After induction of DosR from a tet regulated promoter (uninduced controls were treated with an equivalent ammount of the solvent, DMSO), transcription was arrested using 50 ug/ul of rifampin leaving RNA degradation as the sole vector responsible for mRNA abundance. mRNA half-lives were calculated from the decay of signal intensity from T0.

ORGANISM(S): Mycobacterium tuberculosis H37Rv

PROVIDER: GSE36344 | GEO | 2012/03/08

SECONDARY ACCESSION(S): PRJNA155563

REPOSITORIES: GEO