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DNA end resection during homologous recombination.
Gnügge, Robert; Symington, Lorraine S.
Afiliación
  • Gnügge R; Department of Microbiology & Immunology, Columbia University Irving Medical Center, New York, NY 10032, USA.
  • Symington LS; Department of Microbiology & Immunology, Columbia University Irving Medical Center, New York, NY 10032, USA; Department of Genetics & Development, Columbia University Irving Medical Center, New York, NY 10032, USA. Electronic address: lss5@cumc.columbia.edu.
Curr Opin Genet Dev ; 71: 99-105, 2021 12.
Article en En | MEDLINE | ID: mdl-34329854
ABSTRACT
Exposure to environmental mutagens but also cell-endogenous processes can create DNA double-strand breaks (DSBs) in a cell's genome. DSBs need to be repaired accurately and timely to ensure genomic integrity and cell survival. One major DSB repair mechanism, called homologous recombination, relies on the nucleolytic degradation of the 5'-terminated strands in a process termed end resection. Here, we review new insights into end resection with a focus on the mechanistic interplay of the nucleases, helicases, and accessory factors involved.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Roturas del ADN de Doble Cadena / Recombinación Homóloga Idioma: En Revista: Curr Opin Genet Dev Asunto de la revista: GENETICA Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Roturas del ADN de Doble Cadena / Recombinación Homóloga Idioma: En Revista: Curr Opin Genet Dev Asunto de la revista: GENETICA Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos