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Regulation of the Fanconi anemia pathway by monoubiquitination.
Gregory, Richard C; Taniguchi, Toshiyasu; D'Andrea, Alan D.
Affiliation
  • Gregory RC; Department of Pediatric Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Mayer 640, 44 Binney Street, Boston, MA 02115, USA.
Semin Cancer Biol ; 13(1): 77-82, 2003 Feb.
Article in En | MEDLINE | ID: mdl-12507559
Fanconi anemia (FA) is an autosomal recessive cancer susceptibility syndrome characterized by multiple congenital anomalies, bone marrow failure, and cellular sensitivity to mitomycin C (MMC). To date, six FA genes have been cloned, and the encoded proteins function in a novel pathway. The FA pathway is required for the normal cellular response to DNA damage. Following DNA damage, the pathway is activated, leading to monoubiquitination of the FA protein, FANCD2, and its targeting to subnuclear foci. Disruption of the FA pathway results in the absence of FANCD2 nuclear foci, leading to the cellular and clinical abnormalities of FA. Here, we review the recent studies describing the regulated monoubiquitination of the FANCD2 protein and discuss the interaction of the FA pathway with other DNA damage response pathways.
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Collection: 01-internacional Database: MEDLINE Main subject: Nuclear Proteins / Ubiquitins / Signal Transduction / DNA Repair / Fanconi Anemia Limits: Humans Language: En Journal: Semin Cancer Biol Journal subject: NEOPLASIAS Year: 2003 Document type: Article Affiliation country: United States Country of publication: United kingdom
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Collection: 01-internacional Database: MEDLINE Main subject: Nuclear Proteins / Ubiquitins / Signal Transduction / DNA Repair / Fanconi Anemia Limits: Humans Language: En Journal: Semin Cancer Biol Journal subject: NEOPLASIAS Year: 2003 Document type: Article Affiliation country: United States Country of publication: United kingdom