Massachusetts Institute of Technology
Regulation of Mu transposition via communication between the transposase and Mu-encoded accessory protein
Abstract
dc:description.abstractTransposable elements comprise a significant portion of both prokaryotic and eukaryotic genomes. These mobile segments of DNA have helped to shape the course of evolution by generating genetic mutations and contributing to genomic rearrangements. Transposable elements often target transposition to non-random DNA sites. Ideal target sites must be common, so as to ensure efficient propagation of the transposable element, and yet non-essential, so as to protect the host cell on which the element depends. Transposable elements have devised a plethora of strategies for targeting transposition to desirable DNA. This thesis investigates the molecular mechanisms involved in Mu transposition. We explore the interactions between the Mu transposase, MuA, and a Mu-encoded accessory protein, MuB. Together, these two proteins regulate Mu transposition and targeting. We demonstrate that MuB interacts with multiple subunits of the MuA transposase complex to stimulate transposition. These results corroborate previous theories that MuB acts as an allosteric regulator of MuA. We also investigate the mechanism by which Mu transposes into selected DNA. We find that MuB "delivers" favorable target DNA to the Mu transposase by tethering the DNA to MuA. This interaction is independent of ATP hydrolysis by MuB. The work described herein has contributed to our understanding of the protein-protein interactions involved in Mu transposition.
Degree
thesis:*- Department dc:contributor.department
- Massachusetts Institute of Technology. Dept. of Biology.
- Grantor dc:publisher
- Massachusetts Institute of Technology
- Year dc:date.issued
- 2007
Author and committee
dc:creator, dc:contributor.*- Author dc:creator
-
- Schweidenback, Caterina Taiani Hill
- Advisor dc:contributor.advisor
-
- Tania A. Baker.
Subjects
dc:subject × 1Rights
dc:rights- Statement dc:rights
-
- M.I.T. theses are protected by copyright. They may be viewed from this source for any purpose, but reproduction or distribution in any format is prohibited without written permission. See provided URL for inquiries about permission.
- Licence dc:rights.uri
- Language dc:language.iso
- eng
Identifiers
dc:identifier.*- Handle dc:identifier.uri
- http://hdl.handle.net/1721.1/40962
- OAI identifier oai:identifier
- oai:dspace.mit.edu:1721.1/40962