| Literature DB >> 24910428 |
Yaling Huang1, Justin W C Leung1, Megan Lowery2, Nobuko Matsushita3, Yucai Wang1, Xi Shen1, Do Huong1, Minoru Takata4, Junjie Chen1, Lei Li5.
Abstract
The Fanconi anemia (FA) core complex provides the essential E3 ligase function for spatially defined FANCD2 ubiquitination and FA pathway activation. Of the seven FA gene products forming the core complex, FANCL possesses a RING domain with demonstrated E3 ligase activity. The other six components do not have clearly defined roles. Through epistasis analyses, we identify three functional modules in the FA core complex: a catalytic module consisting of FANCL, FANCB, and FAAP100 is absolutely required for the E3 ligase function, and the FANCA-FANCG-FAAP20 and the FANCC-FANCE-FANCF modules provide nonredundant and ancillary functions that help the catalytic module bind chromatin or sites of DNA damage. Disruption of the catalytic module causes complete loss of the core complex function, whereas loss of any ancillary module component does not. Our work reveals the roles of several FA gene products with previously undefined functions and a modularized assembly of the FA core complex.Entities:
Mesh:
Substances:
Year: 2014 PMID: 24910428 PMCID: PMC4157997 DOI: 10.1016/j.celrep.2014.04.029
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423