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Merck

Mutations in the SMAD4/DPC4 gene in juvenile polyposis.

Science (New York, N.Y.) (1998-06-06)
J R Howe, S Roth, J C Ringold, R W Summers, H J Järvinen, P Sistonen, I P Tomlinson, R S Houlston, S Bevan, F A Mitros, E M Stone, L A Aaltonen
摘要

Familial juvenile polyposis is an autosomal dominant disease characterized by a predisposition to hamartomatous polyps and gastrointestinal cancer. Here it is shown that a subset of juvenile polyposis families carry germ line mutations in the gene SMAD4 (also known as DPC4), located on chromosome 18q21.1, that encodes a critical cytoplasmic mediator in the transforming growth factor-beta signaling pathway. The mutant SMAD4 proteins are predicted to be truncated at the carboxyl-terminus and lack sequences required for normal function. These results confirm an important role for SMAD4 in the development of gastrointestinal tumors.