GERGELITS, Vaclav, Emil PARVANOV, Petr SIMECEK and Jiri FOREJT. Chromosome-wide characterization of meiotic noncrossovers (gene conversions) in mouse hybrids. Genetics. BETHESDA (USA): GENETICS SOCIETY AMERICA, 2021, vol. 217, No 1, 14 pp. ISSN 0016-6731. Available from: https://dx.doi.org/10.1093/genetics/iyaa013.
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Basic information
Original name Chromosome-wide characterization of meiotic noncrossovers (gene conversions) in mouse hybrids
Authors GERGELITS, Vaclav, Emil PARVANOV, Petr SIMECEK and Jiri FOREJT.
Edition Genetics, BETHESDA (USA), GENETICS SOCIETY AMERICA, 2021, 0016-6731.
Other information
Original language English
Type of outcome Article in a journal
Field of Study 10603 Genetics and heredity
Country of publisher United States of America
Confidentiality degree is not subject to a state or trade secret
WWW URL
Impact factor Impact factor: 4.402
Doi http://dx.doi.org/10.1093/genetics/iyaa013
UT WoS 000637217400010
Keywords in English homologous recombination; gene conversion; PRDM9 motif erosion; hybrid sterility; noncrossover-associated GC bias
Tags CF BIOIT
Tags International impact, Reviewed
Changed by Changed by: Mgr. Eva Dubská, učo 77638. Changed: 11/6/2024 11:18.
Abstract
During meiosis, the recombination-initiating DNA double-strand breaks (DSBs) are repaired by crossovers or noncrossovers (gene conversions). While crossovers are easily detectable, noncrossover identification is hampered by the small size of their converted tracts and the necessity of sequence polymorphism. We report identification and characterization of a mouse chromosome-wide set of noncrossovers by next-generation sequencing of 10 mouse intersubspecific chromosome substitution strains. Based on 94 identified noncrossovers, we determined the mean length of a conversion tract to be 32 bp. The spatial chromosome-wide distribution of noncrossovers and crossovers significantly differed, although both sets overlapped the known hotspots of PRDM9-directed histone methylation and DNA DSBs, thus supporting their origin in the standard DSB repair pathway. A significant deficit of noncrossovers descending from asymmetric DSBs proved their proposed adverse effect on meiotic recombination and pointed to sister chromatids as an alternative template for their repair. The finding has implications for the molecular mechanism of hybrid sterility in mice from crosses between closely related Mus musculus musculus and Mus musculus domesticus subspecies.
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