TY - JOUR
T1 - Super DksAs
T2 - Substitutions in DksA enhancing its effects on transcription initiation
AU - Blankschien, Matthew D.
AU - Lee, Jeong Hyun
AU - Grace, Elicia D.
AU - Lennon, Christopher W.
AU - Halliday, Jennifer A.
AU - Ross, Wilma
AU - Gourse, Richard L.
AU - Herman, Christophe
PY - 2009/6/17
Y1 - 2009/6/17
N2 - At specific times during bacterial growth, the transcription factor DksA and the unusual nucleotide regulator ppGpp work synergistically to inhibit some Escherichia coli promoters (e.g. rRNA promoters) and to stimulate others (e.g. promoters for amino-acid synthesis and transport). However, the mechanism of DksA action remains uncertain, in part because DksA does not function like conventional transcription factors. To gain insights into DksA function, we identified mutations in dksA that bypassed the requirement for ppGpp by selecting for growth of cells lacking ppGpp on minimal medium without amino acids. We show here that two substitutions in DksA, L15F and N88I, result in higher DksA activity both in vivo and in vitro, primarily by increasing the apparent affinity of DksA for RNA polymerase (RNAP). The mutant DksA proteins suggest potential roles for ppGpp in DksA function, identify potential surfaces on DksA crucial for RNAP binding, and provide tools for future studies to elucidate the mechanism of DksA action.
AB - At specific times during bacterial growth, the transcription factor DksA and the unusual nucleotide regulator ppGpp work synergistically to inhibit some Escherichia coli promoters (e.g. rRNA promoters) and to stimulate others (e.g. promoters for amino-acid synthesis and transport). However, the mechanism of DksA action remains uncertain, in part because DksA does not function like conventional transcription factors. To gain insights into DksA function, we identified mutations in dksA that bypassed the requirement for ppGpp by selecting for growth of cells lacking ppGpp on minimal medium without amino acids. We show here that two substitutions in DksA, L15F and N88I, result in higher DksA activity both in vivo and in vitro, primarily by increasing the apparent affinity of DksA for RNA polymerase (RNAP). The mutant DksA proteins suggest potential roles for ppGpp in DksA function, identify potential surfaces on DksA crucial for RNAP binding, and provide tools for future studies to elucidate the mechanism of DksA action.
KW - DksA
KW - PpGpp
KW - RNA polymerase secondary channel
KW - Stringent response
KW - Transcription factor
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UR - http://www.scopus.com/inward/citedby.url?scp=67649552968&partnerID=8YFLogxK
U2 - 10.1038/emboj.2009.126
DO - 10.1038/emboj.2009.126
M3 - Article
C2 - 19424178
AN - SCOPUS:67649552968
SN - 0261-4189
VL - 28
SP - 1720
EP - 1731
JO - EMBO Journal
JF - EMBO Journal
IS - 12
ER -