The BRCA1-interacting helicase BRIP1 is deficient in Fanconi anemia

O Levran, C Attwooll, RT Henry, KL Milton, K Neveling… - Nature …, 2005 - nature.com
O Levran, C Attwooll, RT Henry, KL Milton, K Neveling, P Rio, SD Batish, R Kalb, E Velleuer…
Nature genetics, 2005nature.com
Seven Fanconi anemia–associated proteins (FANCA, FANCB, FANCC, FANCE, FANCF,
FANCG and FANCL) form a nuclear Fanconi anemia core complex that activates the
monoubiquitination of FANCD2, targeting FANCD2 to BRCA1-containing nuclear foci. Cells
from individuals with Fanconi anemia of complementation groups D1 and J (FA-D1 and FA-
J) have normal FANCD2 ubiquitination. Using genetic mapping, mutation identification and
western-blot data, we identify the defective protein in FA-J cells as BRIP1 (also called …
Abstract
Seven Fanconi anemia–associated proteins (FANCA, FANCB, FANCC, FANCE, FANCF, FANCG and FANCL) form a nuclear Fanconi anemia core complex that activates the monoubiquitination of FANCD2, targeting FANCD2 to BRCA1-containing nuclear foci. Cells from individuals with Fanconi anemia of complementation groups D1 and J (FA-D1 and FA-J) have normal FANCD2 ubiquitination. Using genetic mapping, mutation identification and western-blot data, we identify the defective protein in FA-J cells as BRIP1 (also called BACH1), a DNA helicase that is a binding partner of the breast cancer tumor suppressor BRCA1.
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