Fortini, Barbara Karmen Kraatz (2011) Biochemical and genetic studies of genomic stability. Dissertation (Ph.D.), California Institute of Technology. http://resolver.caltech.edu/CaltechTHESIS:05172011-123048725
Genomes face a constant barrage of threats from endogenous and exogenous sources. The need to maintain fidelity while replicating the entire genome during each cell division necessitates a dynamic cadre of proteins and protein complexes that participate in the DNA replication process. Furthermore, DNA can be damaged during all phases of the cell’s life and that damage must be recognized and repaired in a way that preserves genetic information. These studies focus on one enzyme at the nexus of DNA replication and DNA repair, the helicase/nuclease Dna2. We show that Dna2 possesses a novel ATP/Mn2+ dependent flap endo/exonuclease activity and a DNA end-independent endonuclease activity that is inhibited by Replication Protein A. The regulation of Dna2 activity in the context of the global DNA damage response is of great interest. To that end, we explored the relationship of Dna2 and the DNA damage sensor kinase Mec1. We find that Dna2 is phosphorylated by Mec1 following DNA damage in its N-terminal domain. We then extended these studies from yeast to higher eukaryotes utilizing the Xenopus cell free extract system. Using simulated double strand breaks (DSBs), we constructed a timeline of protein processing steps required for homologous recombination mediated repair. This strategy using Xenopus extracts also place Dna2 on chromatin during DNA replication, physically interacting with other proteins involved in lagging strand replication. Taken together, these biochemical and genetic studies elucidate the multiple roles the Dna2 enzyme plays in order to ensure genomic stability.
|Item Type:||Thesis (Dissertation (Ph.D.))|
|Subject Keywords:||DNA replication, DNA repair, genomic stability, DNA2|
|Degree Grantor:||California Institute of Technology|
|Thesis Availability:||Restricted to Caltech community only|
|Defense Date:||26 May 2011|
|Default Usage Policy:||No commercial reproduction, distribution, display or performance rights in this work are provided.|
|Deposited By:||Barbara Fortini|
|Deposited On:||31 May 2011 18:24|
|Last Modified:||18 Jan 2013 00:41|
- Final Version
Restricted to Caltech community only until 1 June 2013.
See Usage Policy.
Repository Staff Only: item control page