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Transcript
RISE Talks Series
Who?
Brittany Barreto, Drew ’13, Baylor College of
Medicine
What?
Role of small RNA, gcvB, in Stress-Induced
Mutagenesis
When?
12:00-1:00 on Wednesday, April 15
Where?
Hall of Sciences, Room 326
Organisms evolve under stressful conditions by increasing mutation rate
through stress-induced mutagenesis (SIM). A prominent mechanism of
SIM in Escherichia coli is mutagenic DNA break repair, in which repair
of DNA double-strand breaks by homologous recombination becomes
error-prone. Mutagenic break repair requires activation of four different
stress responses, and so creates mutations when the organism is
maladapted to the environment. SIM mechanisms occur in bacterial,
yeast and human cells, and produce genetic diversity. A network of 93
proteins promotes SIM, but the screen that identified these genes was
biased against small genes including small RNAs (sRNA). In this
project, we investigate the possible roles of sRNAs in mutagenic break
repair in E. coli. We found 3 sRNAs that are required for SIM including
gcvB, micF, and rybB. Furthermore we discovered gcvB promotes SIM
by regulating the sigma factor, rpoS. RpoS is required to activate the
general stress response which is necessary for mutagenic break repair.
Thus in this study we found new players in SIM and the mechanism
behind the small RNA, gcvB. Researching the roles of sRNAs in SIM
will further our understanding of evolution and illness. Mechanisms of
SIM are likely to provide important models for mutagenesis that
underlies drug resistance, aging, and cancer progression.