The vast numbers of transposable elements littering our genomes are thought to have contributed to genome evolution on the 1 hand and genome instability on the other. The long term goal of this research is to understand the mechanisms underlying the genetic success of these elements. Phage Mu has a served as a paradigm for transposition for a quarter of a century. While much has been learned about the chemistry of phosphoryl transfer, much remains to be learned about the mechanism and regulation of transposition including transpososome assembly, control of directionality, and target DNA selection. Almost nothing is known about the integration mechanism of the linear Mu virion DNA into the host chromosome, a process with many similarities to linear HIV DNA integration. We plan to build on the major advances in our last grant proposal, as well as our preliminary new results, to propose the following 3 specific aims: (1) Dissect the detailed architecture of the 5-noded 3-site Mu synaptic complex, and understand the role of the enhancer in its assembly. (2) Design experiments to understand the opposing activities of target site selection and target immunity. (3) Lay the groundwork for analyzing how flanking host sequences are processed upon integration of infecting Mu DNA in vivo, which occurs by a variation of the established cointegrate mechanism. These studies will provide important new perspectives on several fundamental aspects of the movement of transposable elements, and will contribute not only to understanding their insistent presence throughout the biological world, but also to how they affect human health. Mobile genetic elements impact our daily lives in significant ways. On the 1 hand, DNA transposition is responsible for the transmission of drug resistance in bacteria, integration of retroviral genomes into host chromosomes, and genome instabilities leading to cancer. On the other hand, transposition mechanisms have been widely exploited as tools for genetic engineering and in strategies for gene therapy. Our studies are expected to impact both areas of research. ? ? ?

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
2R01GM033247-22
Application #
7144530
Study Section
Prokaryotic Cell and Molecular Biology Study Section (PCMB)
Program Officer
Dearolf, Charles R
Project Start
1990-01-01
Project End
2010-06-30
Budget Start
2006-07-01
Budget End
2007-06-30
Support Year
22
Fiscal Year
2006
Total Cost
$313,900
Indirect Cost
Name
University of Texas Austin
Department
Biology
Type
Schools of Arts and Sciences
DUNS #
170230239
City
Austin
State
TX
Country
United States
Zip Code
78712
Jang, Sooin; Harshey, Rasika M (2015) Repair of transposable phage Mu DNA insertions begins only when the E.?coli replisome collides with the transpososome. Mol Microbiol 97:746-58
Harshey, Rasika M (2014) Transposable Phage Mu. Microbiol Spectr 2:
Choi, Wonyoung; Saha, Rudra P; Jang, Sooin et al. (2014) Controlling DNA degradation from a distance: a new role for the Mu transposition enhancer. Mol Microbiol 94:595-608
Choi, Wonyoung; Jang, Sooin; Harshey, Rasika M (2014) Mu transpososome and RecBCD nuclease collaborate in the repair of simple Mu insertions. Proc Natl Acad Sci U S A 111:14112-7
Saha, Rudra P; Lou, Zheng; Meng, Luke et al. (2013) Transposable prophage Mu is organized as a stable chromosomal domain of E. coli. PLoS Genet 9:e1003902
Lee, Jaemin; Harshey, Rasika M (2012) Loss of FlhE in the flagellar Type III secretion system allows proton influx into Salmonella and Escherichia coli. Mol Microbiol 84:550-65
Harshey, Rasika M (2012) The Mu story: how a maverick phage moved the field forward. Mob DNA 3:21
Lazova, Milena D; Butler, Mitchell T; Shimizu, Thomas S et al. (2012) Salmonella chemoreceptors McpB and McpC mediate a repellent response to L-cystine: a potential mechanism to avoid oxidative conditions. Mol Microbiol 84:697-711
Jang, Sooin; Sandler, Steven J; Harshey, Rasika M (2012) Mu insertions are repaired by the double-strand break repair pathway of Escherichia coli. PLoS Genet 8:e1002642
Ge, Jun; Lou, Zheng; Cui, Hong et al. (2011) Analysis of phage Mu DNA transposition by whole-genome Escherichia coli tiling arrays reveals a complex relationship to distribution of target selection protein B, transcription and chromosome architectural elements. J Biosci 36:587-601

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