<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Dewey EB</submitter><funding>National Cancer Institute</funding><funding>NCI NIH HHS</funding><funding>National Institute of General Medical Sciences</funding><funding>NIGMS NIH HHS</funding><pagination>iyac164</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9836020</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>223(1)</volume><pubmed_abstract>Proper repair of DNA double-strand breaks is essential to the maintenance of genomic stability and avoidance of genetic disease. Organisms have many ways of repairing double-strand breaks, including the use of homologous sequences through homology-directed repair. While homology-directed repair is often error free, in single-strand annealing homologous repeats flanking a double-strand break are annealed to one another, leading to the deletion of one repeat and the intervening sequences. Studies in yeast have shown a relationship between the length of the repeat and single-strand annealing efficacy. We sought to determine the effects of homology length on single-strand annealing in Drosophila, as Drosophila uses a different annealing enzyme (Marcal1) than yeast. Using an in vivo single-stra</pubmed_abstract><journal>Genetics</journal><pubmed_title>The effect of repeat length on Marcal1-dependent single-strand annealing in Drosophila.</pubmed_title><pmcid>PMC9836020</pmcid><funding_grant_id>R35 GM118127</funding_grant_id><funding_grant_id>1R35GM118127</funding_grant_id><funding_grant_id>T32 CA217824</funding_grant_id><pubmed_authors>Saghaey K</pubmed_authors><pubmed_authors>Wittmer ME</pubmed_authors><pubmed_authors>Korda Holsclaw J</pubmed_authors><pubmed_authors>Dewey EB</pubmed_authors><pubmed_authors>Sekelsky J</pubmed_authors></additional><is_claimable>false</is_claimable><name>The effect of repeat length on Marcal1-dependent single-strand annealing in Drosophila.</name><description>Proper repair of DNA double-strand breaks is essential to the maintenance of genomic stability and avoidance of genetic disease. Organisms have many ways of repairing double-strand breaks, including the use of homologous sequences through homology-directed repair. While homology-directed repair is often error free, in single-strand annealing homologous repeats flanking a double-strand break are annealed to one another, leading to the deletion of one repeat and the intervening sequences. Studies in yeast have shown a relationship between the length of the repeat and single-strand annealing efficacy. We sought to determine the effects of homology length on single-strand annealing in Drosophila, as Drosophila uses a different annealing enzyme (Marcal1) than yeast. Using an in vivo single-stra</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Jan</publication><modification>2026-03-27T15:46:12.937Z</modification><creation>2025-04-06T13:10:04.284Z</creation></dates><accession>S-EPMC9836020</accession><cross_references><pubmed>36303322</pubmed><doi>10.1093/genetics/iyac164</doi></cross_references></HashMap>