Haplotype and linkage analysis in Chinese hereditary mixed polyposis syndrome.
- Author:
Hui PENG
1
;
Xia CAO
;
Hui-hua LI
;
Loi CAROL
;
Kong-weng EU
;
Jian-ping WANG
Author Information
- Publication Type:Journal Article
- MeSH: Adenomatous Polyposis Coli; genetics; Adult; Asian Continental Ancestry Group; genetics; Chromosomes, Human, Pair 6; Colorectal Neoplasms; genetics; Female; Genetic Linkage; Genetic Predisposition to Disease; Haplotypes; Humans; Male; Middle Aged; Pedigree
- From: Chinese Journal of Gastrointestinal Surgery 2005;8(4):312-315
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo investigate if hereditary mixed polyposis syndrome (HMPS) locus of two Singapore Chinese HMPS families is identical with the Ashkenazi families.
METHODSGenomic DNA was extracted, multiplex polymerase chain reaction (PCR) was used to amplify 4 microsatellite markers D15S1010, D15S1007, ACTC and D15S118 in 31 individuals from two families. The HMPS locus cosecretion of the markers on 15q13 over a region of 2.8 cM was confirmed by Haplotype and linkage analysis.
RESULTSThe disease of haplotype identified in one pedigree was not co-segregated with an affected individual while no definitive disease haplotype could be assigned for the second pedigree. The maximum two-point and multi-point LOD scores at ACTC for the two Chinese families are 0.20 (theta = 0.3) and -5.0 respectively.
CONCLUSIONSHaplotype and linkage analysis indicate that the Ashkenazi haplotypes is not associated with HMPS in Singapore Chinese families, which suggests genetic heterogeneity.