This proposal continues our study of the mechanisms of homologous recombination in the model system, the budding yeast Saccharomyces cerevisiae. The mating-type (MAT) locus is induced to switch to the opposite mating-type through the repair of a double-strand break (DSB). Inducible expression of the HO endonuclease gene can be used to analyze MAT switching and other DSB repair events by physical monitoring of DNA undergoing recombination. The relationship between gene conversion and break-induced replication will be studied, including analysis of protein and cell cycle requirements. Density-transfer experiments will be used to determine the extent and location of newly synthesized DNA during recombination. Chromatin immunoprecipitation will be used to analyze the roles of specific recombination proteins. Genetic and molecular biological approaches will also be used to analyze the histone modification of chromatin during recombination and the reassembly of chromatin when recombination is complete. Mutations affecting control of crossing-over will be analyzed to understand how most gene conversions in mitotic cells occur without exchange, avoiding loss of heterozygosity and chromosome rearrangements. Break-induced replication will be further characterized to understand its role in maintaining telomeres in the absence of telomerase and in generating nonreciprocal translocations. The MAT switching system will also be used to learn about the regulation of accessibility of chromosome regions for recombination events. The choice of one of two distant donor sequences, HML or HMR, for recombination with MAT is controlled by a locus control region, the recombination enhancer (RE). Emphasis is placed on determining how the entire left arm of chromosome III is sequestered in MATa cells and how RE and its associated forkhead Fhkl protein makes the arm """"""""hot"""""""" for recombination. Each of these subjects has high relevance for our understanding of the ways broken chromosomes are repaired in humans and how mutations in a number of genes that facilitate recombination lead to an increased predisposition to cancer.
Gallagher, Danielle N; Haber, James E (2018) Repair of a Site-Specific DNA Cleavage: Old-School Lessons for Cas9-Mediated Gene Editing. ACS Chem Biol 13:397-405 |
Lemos, Brenda R; Kaplan, Adam C; Bae, Ji Eun et al. (2018) CRISPR/Cas9 cleavages in budding yeast reveal templated insertions and strand-specific insertion/deletion profiles. Proc Natl Acad Sci U S A 115:E2040-E2047 |
Haber, James E (2018) DNA Repair: The Search for Homology. Bioessays 40:e1700229 |
Eapen, Vinay V; Waterman, David P; Bernard, Amélie et al. (2017) A pathway of targeted autophagy is induced by DNA damage in budding yeast. Proc Natl Acad Sci U S A 114:E1158-E1167 |
Mehta, Anuja; Beach, Annette; Haber, James E (2017) Homology Requirements and Competition between Gene Conversion and Break-Induced Replication during Double-Strand Break Repair. Mol Cell 65:515-526.e3 |
Tsabar, Michael; Haase, Julian; Harrison, Benjamin et al. (2016) A Cohesin-Based Partitioning Mechanism Revealed upon Transcriptional Inactivation of Centromere. PLoS Genet 12:e1006021 |
Tsabar, Michael; Hicks, Wade M; Tsaponina, Olga et al. (2016) Re-establishment of nucleosome occupancy during double-strand break repair in budding yeast. DNA Repair (Amst) 47:21-29 |
Lee, Cheng-Sheng; Wang, Ruoxi W; Chang, Hsiao-Han et al. (2016) Chromosome position determines the success of double-strand break repair. Proc Natl Acad Sci U S A 113:E146-54 |
Av?aro?lu, Bar??; Bronk, Gabriel; Li, Kevin et al. (2016) Chromosome-refolding model of mating-type switching in yeast. Proc Natl Acad Sci U S A 113:E6929-E6938 |
Tsabar, Michael; Waterman, David P; Aguilar, Fiona et al. (2016) Asf1 facilitates dephosphorylation of Rad53 after DNA double-strand break repair. Genes Dev 30:1211-24 |
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