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Susan Gottesman, Ph.D.

Portait Photo of Susan Gottesman
Laboratory of Molecular Biology
Head, Biochemical Genetics Section
Laboratory Co-Chief
Center for Cancer Research
National Cancer Institute
Building 37, Room 5132
Bethesda, MD 20892
Phone:  
301-496-3524
Fax:  
Fax Number not listed
E-Mail:  
Gottesms@helix.nih.gov

Biography

Dr. Gottesman received her Ph.D. from the Department of Microbiology at Harvard University and became a postdoctoral fellow at the NIH. She then went to the Massachusetts Institute of Technology (MIT) as a research associate and returned to the NIH in 1976 as a senior investigator in the Laboratory of Molecular Biology, where she has remained. She was elected to the National Academy of Sciences in 1998 and the American Academy of Arts and Sciences in 1999. She received the Abbott-ASM Lifetime Achievement Award in 2011.

Research

Small Regulatory RNAs and Energy-Dependent Proteolysis: Novel Modes for the Regulation of Gene Expression

Our laboratory has been interested in novel mechanisms for gene regulation and how these mechanisms contribute to global control circuits in Escherichia coli. For many years, the focus of the laboratory was energy-dependent proteolysis. In the past decade, much of the lab has shifted to studying small regulatory RNAs, although we continue to investigate the mechanisms for regulating energy-dependent proteolysis. We first encountered small RNAs when studying the regulation of synthesis of a substrate for the energy-dependent proteases, and we continue to see significant overlap between mRNAs regulated by small RNAs and the products of these mRNAs that are regulated by proteolysis.

This is exemplified in the regulation of RpoS, a stress sigma factor of E. coli. RpoS is rapidly degraded during exponential growth by the ClpXP protease but not when the cell is starved, stressed, or enters stationary phase. This degradation requires the response regulator protein RssB. RssB, an adaptor protein for RpoS degradation, affects degradation only of RpoS, and not of other ClpXP substrates, in vivo and in vitro. The primary question has been how environmental signals regulate RpoS degradation. Using a genetic screen, we identified multiple small anti-adaptor proteins that are made in response to specific stress signals and interfere with the ability of RssB to deliver RpoS to the protease. In collaboration with Dr. Sue Wickner, in vivo and in vitro studies are providing insight into how many anti-adaptors there are, how the anti-adaptors work, and how RssB functions.

In addition to this complex regulation of RpoS degradation, the translation of RpoS is positively regulated by multiple small RNAs. One of these, DsrA. is synthesized preferentially at low temperatures and is necessary for the low-temperature expression of RpoS. DsrA modulates RpoS synthesis by positively affecting translation of this protein by pairing with parts of the RpoS untranslated leader. A second small RNA regulator of RpoS, RprA, was also identified. RprA acts by a mechanism similar to that of DsrA in stimulating RpoS synthesis, but is regulated not by low temperature but by a two-component regulatory system responsive to cell surface status. We identified a third small RNA regulator of RpoS, ArcZ, that also positively regulates RpoS but is controlled by regulators that sense aerobic vs. anaerobic growth. Each of these small RNAs also negatively regulate other mRNAs, providing complex combinatorial regulation. The small RNAs link RpoS regulation to multiple environmental and metabolic inputs.

In collaboration with G. Storz (NICHD) and others, we carried out a number of genome-wide searches for other small regulatory RNAs. Initially, highly conserved stretches within intergenic regions were found to be reliable hallmarks of small RNAs. In another genome-wide collaborative study, we defined small RNAs that bind the RNA chaperone Hfq, used by fully 1/3 of the small RNAs in the cell. This led to identification of yet other, less conserved small RNAs. This work combined with studies by others have defined more than 80 small RNAs in E. coli, and studies of these demonstrate that small RNAs are important and previously underappreciated components of many regulatory circuits.

A large number of the small RNAs that bind Hfq have now been studied. Small RNAs that bind Hfq act by pairing to target mRNAs to change mRNA stability and translation. In addition to defining targets, we need to define their upstream regulators so we can understand when they act. One of these, RyhB, is synthesized only when iron is limiting (it is repressed by the Fur repressor). RyhB redirects cellular metabolism to respond to the iron limitation by down-regulating synthesis of non-essential proteins that use Fe. A number of small RNAs were found to regulate major cell surface proteins, including proteins implicated in attachment of bacteria to surfaces. Another, controlled by a two-component system important for virulence, regulates modification of LPS. These small RNA effects on the cell surface may modulate interactions with hosts, affecting the immune response and/or pathogenesis. The lab has now developed rapid and flexible methods to scan all Hfq-binding small RNAs for their ability to regulate genes of interest.

While the bacterial small RNAs parallel microRNAs in their ability to affect the stability and translation of target mRNAs, the pathway for their function is rather different. We are studying how Hfq, a member of the Sm/Lsm family of proteins, acts to bring RNAs together, and what other functions are necessary for small RNA function.

Collaborators on this research include Gisela Storz, Sue Wickner, Michael Maurizi and Xinhua Ji, at NIH and Sarah Woodson, Johns Hopkins University

This page was last updated on 11/26/2013.