IDENTIFICATION AND CHARACTERIZATION OF THE FAMILIAL ADENOMATOUS POLYPOSIS-COLI GENE

被引:2342
作者
GRODEN, J
THLIVERIS, A
SAMOWITZ, W
CARLSON, M
GELBERT, L
ALBERTSEN, H
JOSLYN, G
STEVENS, J
SPIRIO, L
ROBERTSON, M
SARGEANT, L
KRAPCHO, K
WOLFF, E
BURT, R
HUGHES, JP
WARRINGTON, J
MCPHERSON, J
WASMUTH, J
LEPASLIER, D
ABDERRAHIM, H
COHEN, D
LEPPERT, M
WHITE, R
机构
[1] UNIV UTAH,HLTH SCI CTR,HOWARD HUGHES MED INST,SALT LAKE CITY,UT 84132
[2] UNIV UTAH,HLTH SCI CTR,DEPT PATHOL,SALT LAKE CITY,UT 84132
[3] UNIV UTAH,HLTH SCI CTR,DEPT MED,DIV GASTROENTEROL,SALT LAKE CITY,UT 84132
[4] ST MARKS HOSP,SALT LAKE CITY,UT 84117
[5] UNIV CALIF IRVINE,COLL MED,DEPT BIOL CHEM,IRVINE,CA 92717
[6] CTR ETUD POLYMORPHISME HUMAIN,F-75010 PARIS,FRANCE
关键词
D O I
10.1016/0092-8674(81)90021-0
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
DNA from 61 unrelated patients with adenomatous polyposis coli (APC) was examined for mutations in three genes (DP1, SRP19, and DP2.5) located within a 100 kb region deleted in two of the patients. The intron-exon boundary sequences were defined for each of these genes, and single-strand conformation polymorphism analysis of exons from DP2.5 identified four mutations specific to APC patients. Each of two aberrant alleles contained a base substitution changing an amino acid to a stop codon in the predicted peptide; the other mutations were small deletions leading to frameshifts. Analysis of DNA from parents of one of these patients showed that his 2 bp deletion is a new mutation; furthermore, the mutation was transmitted to two of his children. These data have established that DP2.5 is the APC gene.
引用
收藏
页码:589 / 600
页数:12
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