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Identification of Holliday junction resolvases from humans and yeast.
Ip, Stephen C Y; Rass, Ulrich; Blanco, Miguel G; Flynn, Helen R; Skehel, J Mark; West, Stephen C.
Afiliación
  • Ip SC; Genetic Recombination Laboratory, Cancer Research UK, London Research Institute, Clare Hall Laboratories, South Mimms, Herts EN6 3LD, UK.
Nature ; 456(7220): 357-61, 2008 Nov 20.
Article en En | MEDLINE | ID: mdl-19020614
ABSTRACT
Four-way DNA intermediates, also known as Holliday junctions, are formed during homologous recombination and DNA repair, and their resolution is necessary for proper chromosome segregation. Here we identify nucleases from Saccharomyces cerevisiae and human cells that promote Holliday junction resolution, in a manner analogous to that shown by the Escherichia coli Holliday junction resolvase RuvC. The human Holliday junction resolvase, GEN1, and its yeast orthologue, Yen1, were independently identified using two distinct experimental approaches GEN1 was identified by mass spectrometry following extensive fractionation of HeLa cell-free extracts, whereas Yen1 was detected by screening a yeast gene fusion library for nucleases capable of Holliday junction resolution. The eukaryotic Holliday junction resolvases represent a new subclass of the Rad2/XPG family of nucleases. Recombinant GEN1 and Yen1 resolve Holliday junctions by the introduction of symmetrically related cuts across the junction point, to produce nicked duplex products in which the nicks can be readily ligated.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Saccharomyces cerevisiae / Proteínas de Saccharomyces cerevisiae / Resolvasas de Unión Holliday Tipo de estudio: Diagnostic_studies Límite: Humans Idioma: En Revista: Nature Año: 2008 Tipo del documento: Article País de afiliación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Saccharomyces cerevisiae / Proteínas de Saccharomyces cerevisiae / Resolvasas de Unión Holliday Tipo de estudio: Diagnostic_studies Límite: Humans Idioma: En Revista: Nature Año: 2008 Tipo del documento: Article País de afiliación: Reino Unido