Per citar aquest document: http://ddd.uab.cat/record/113421
Gene amplification in human cells knocked down for RAD54
Ruiz-Herrera Moreno, Aurora (Universitat Autònoma de Barcelona. Departament de Biologia Cel·lular, de Fisiologia i d'Immunologia)
Smirnova, Alexandra (Università di Pavia. Dipartimento di Genetica e Microbiologia "Adriano Buzzati-Traverso")
Khouriauli, Lela (Università di Pavia. Dipartimento di Genetica e Microbiologia "Adriano Buzzati-Traverso")
Nergadze, Solomon G. (Università di Pavia. Dipartimento di Genetica e Microbiologia "Adriano Buzzati-Traverso")
Mondello, Chiara (Istituto di Genetica Molecolare (Pàvia, Itàlia))
Giulotto, Elena (Università di Pavia. Dipartimento di Genetica e Microbiologia "Adriano Buzzati-Traverso")

Data: 2011
Resum: Background: In mammalian cells gene amplification is a common manifestation of genome instability promoted by DNA double-strand breaks (DSBs). The repair of DSBs mainly occurs through two mechanisms: non-homologous end-joining (NHEJ) and homologous recombination (HR). We previously showed that defects in the repair of DSBs via NHEJ could increase the frequency of gene amplification. In this paper we explored whether a single or a combined defect in DSBs repair pathways can affect gene amplification. Results: We constructed human cell lines in which the expression of RAD54 and/or DNA-PKcs was constitutively knocked-down by RNA interference. We analyzed their radiosensitivity and their capacity to generate amplified DNA. Our results showed that both RAD54 and DNA-PKcs deficient cells are hypersensitive to γ-irradiation and generate methotrexate resistant colonies at a higher frequency compared to the proficient cell lines. In addition, the analysis of the cytogenetic organization of the amplicons revealed that isochromosome formation is a prevalent mechanism responsible for copy number increase in RAD54 defective cells. Conclusions: Defects in the DSBs repair mechanisms can influence the organization of amplified DNA. The high frequency of isochromosome formation in cells deficient for RAD54 suggests that homologous recombination proteins might play a role in preventing rearrangements at the centromeres.
Drets: Aquest document està subjecte a una llicència d'ús Creative Commons. Es permet la reproducció total o parcial, la distribució, la comunicació pública de l'obra i la creació d'obres derivades, fins i tot amb finalitats comercials, sempre i quan es reconegui l'autoria de l'obra original. Creative Commons
Llengua: Anglès
Document: article ; publishedVersion
Publicat a: Genome integrity, Vol. 2, N. 5 (March 2011) , p. 1-10, ISSN 2041-9414



10 p, 2.1 MB

Additional file 1
2 p, 9.5 KB

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