Identification of FAP Locus Genes from Chromosome 5q21

Kenneth W. Kinzler(Johns Hopkins University), Mef Nilbert(Johns Hopkins University), Li-Kuo Su(Johns Hopkins University), Bert Vogelstein(Johns Hopkins University), Tracy M. Bryan(Johns Hopkins University), Daniel B. Levy(Johns Hopkins University), K Smith(Johns Hopkins University), Antonette C. Preisinger(Johns Hopkins University), Philip Hedge(AkzoNobel (Canada)), Douglas GJ McKechnie(AkzoNobel (Canada)), R.S. Finniear(AkzoNobel (Canada)), Alex Markham(AkzoNobel (Canada)), John Groffen(University of Southern California), Mark S. Boguski(National Center for Biotechnology Information), Stephen F. Altschul(National Center for Biotechnology Information), Akira Horii(The Cancer Institute Hospital), Hiroshi Ando(The Cancer Institute Hospital), Yasuo Miyoshi(The Cancer Institute Hospital), Yoshio Miki(The Cancer Institute Hospital), Isamu Nishisho(The Cancer Institute Hospital), Yusuke Nakamura(The Cancer Institute Hospital)
Science
August 9, 1991
Cited by 2,358

Abstract

Recent studies suggest that one or more genes on chromosome 5q21 are important for the development of colorectal cancers, particularly those associated with familial adenomatous polyposis (FAP). To facilitate the identification of genes from this locus, a portion of the region that is tightly linked to FAP was cloned. Six contiguous stretches of sequence (contigs) containing approximately 5.5 Mb of DNA were isolated. Subclones from these contigs were used to identify and position six genes, all of which were expressed in normal colonic mucosa. Two of these genes (APC and MCC) are likely to contribute to colorectal tumorigenesis. The MCC gene had previously been identified by virtue of its mutation in human colorectal tumors. The APC gene was identified in a contig initiated from the MCC gene and was found to encode an unusually large protein. These two closely spaced genes encode proteins predicted to contain coiled-coil regions. Both genes were also expressed in a wide variety of tissues. Further studies of MCC and APC and their potential interaction should prove useful for understanding colorectal neoplasia.


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