EVIDENCE FOR A NOVEL EXON IN THE CODING REGION OF THE ADENOMATOUS POLYPOSIS-COLI (APC) GENE

被引:22
|
作者
XIA, L
STDENIS, KA
BAPAT, B
机构
[1] UNIV TORONTO,MT SINAI HOSP,DEPT PATHOL,TORONTO,ON M5G 1X5,CANADA
[2] UNIV TORONTO,MT SINAI HOSP,DEPT SURG,TORONTO,ON M5G 1X5,CANADA
[3] UNIV TORONTO,MT SINAI HOSP,STEVE ATANAS STAVRO FAMILAL GI CANC REGISTRY,TORONTO,ON M5G 1X5,CANADA
[4] UNIV TORONTO,MT SINAI HOSP,SAMUEL LUNENFELD RES INST,TORONTO,ON M5G 1X5,CANADA
关键词
D O I
10.1006/geno.1995.1195
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Germline mutations of the tumor suppressor gene APC cause familial adenomatous polyposis. Somatic APC alterations are involved in several sporadic neoplasms, including colorectal, duodenal, gastric, and esophageal carcinoma. The APC mRNA is encoded by 15 exons. Additional transcripts have been reported, due to alternative splicing of coding as well as noncoding regions. Two mRNA isoforms occur due to a deletion of exon 7 or a partial deletion of exon 9. We have identified a novel exon, flanked by APC exons 10 and 11, which is expressed as an alternatively transcribed product of the gene. Further, we have shown that the novel exon consists of a heptad repeat motif and is conserved across species. (C) 1995 Academic Press, Inc.
引用
收藏
页码:589 / 591
页数:3
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