The SNF5 protein (also called INI1) is a subunit common to two closely related mammalian SWI/SNF complexes that function as chromatin-remodeling machines. The human gene, hSNF5, is mutated in early childhood malignant rhabdoid tumors (MRT). In the December EMBO Reports, Klochendler-Yeivin et al. describe a mouse model for SNF5 deficiency (EMBO Reports 2000, 1:500-506). Knockout mice embryos lacking a functional SNF5 gene die shortly after implantation. Experiments with blastocytes in culture show that the lack of SNF5 affects outgrowth of the inner cell mass and results in widespread apoptosis. Careful analysis of viable heterozygous SNF5+/- mice revealed cancer susceptibility. A third of these animals developed tumors that shared features of the human MRT disease. The mice provide an interesting model to study the link between chromatin and tumorigenesis.

Interested in reading more?

Become a Member of

Receive full access to more than 35 years of archives, as well as TS Digest, digital editions of The Scientist, feature stories, and much more!
Already a member?