Inherited mutations in the human BRCA2 gene cause about half of the ca
ses of early-onset breast cancer. The embryonic expression pattern of
the mouse Brca2 gene is now defined and an interaction identified of t
he Brca2 protein with the DNA-repair protein Rad51. Developmental arre
st in Brca2-deficient embryos, their radiation sensitivity, and the as
sociation of Brca2 with Rad51 indicate that Brca2 may be an essential
cofactor in the Rad51-dependent DNA repair of double-strand breaks, th
ereby explaining the tumour-suppressor function of Brca2.