Gene diagnosis of autosomal dominant polycystic kidney disease type 2 using microsatellite DNA tightly linked to polycystic kidney disease gene 2.
- Author:
Wei-li ZHANG
1
;
Dian-yong ZHANG
;
Yu-mei WU
;
Tian-mei SUN
;
Chang-lin MEI
Author Information
- Publication Type:Journal Article
- MeSH: Female; Genetic Linkage; Humans; Male; Microsatellite Repeats; genetics; Mutation; Polycystic Kidney, Autosomal Dominant; diagnosis; genetics; TRPP Cation Channels; genetics
- From: Chinese Journal of Medical Genetics 2004;21(4):325-328
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo use microsatellite DNA tightly linked to polycystic kidney disease gene 2 in the gene diagnosis of autosomal dominant polycystic kidney disease type 2.
METHODSMicrosatellite DNA of D4S1534, D4S1542, D4S1563,D4S2460 and D4S423 were amplified with PCR and the fragments of products were analyzed by capillary electrophoresis and Genescan and Genotyper software, and then gene diagnosis of the pedigrees was made by linkage analysis.
RESULTSThree families were found to be linked to PKD2 in 20 families. Two carriers of PKD2 mutation were revealed by linkage analysis.
CONCLUSIONGene diagnosis can be done for PKD2 mutation carriers prior to cytogenesis. Linkage analysis is a rapid, simple method for studying the heterogeneity of polycystic kidney disease and for diagnosing the disease at the molecular level.
