Polymorphism of the D4Z4 locus associated with facioscapulohumeral muscular dystrophy 1A in Shanghai population.
- Author:
Yu-zhou ZHANG
1
;
Shun-chang SUN
;
Hua-cheng WU
;
Qi-shi FAN
;
Yong-jian SONG
;
Wen YU
;
Marc JEANPIERRE
;
J Andoni URTIZBEREA
Author Information
- Publication Type:Journal Article
- MeSH: Asian Continental Ancestry Group; genetics; Blotting, Southern; China; Chromosomes, Human, Pair 4; genetics; Electrophoresis, Gel, Pulsed-Field; Female; Genetic Linkage; Humans; Male; Muscular Dystrophy, Facioscapulohumeral; ethnology; genetics; Pedigree; Polymorphism, Genetic; Tandem Repeat Sequences; genetics
- From: Chinese Journal of Medical Genetics 2005;22(4):380-382
- CountryChina
- Language:English
-
Abstract:
OBJECTIVETo investigate the D4Z4 repeats on chromosome 4q35 in normal individuals in Shanghai and analysis the polymorphism of the D4Z4 locus.
METHODSThe length of D4Z4 repeats on chromosome 4q35 in 191 normal individuals in Shanghai was determined by pulsed-field gel electrophoresis and Southern blotting after double digestion with Eco RI and Bln I. The number of short D4Z4 repeats was counted after partial digestion with Kpn I.
RESULTSAmong 191 normal individuals in Shanghai, seventeen showed the size of D4Z4 fragments ranged from 22 to 34 kb, i.e. 8.9% of individuals had fewer numbers of D4Z4 repeats. Of these 17 individuals, sixteen showed the short D4Z4 fragment on chromosome 4q35, and one low D4Z4 fragment was correlated to 4q35--> 10q26 translocation.
CONCLUSIONThe frequency of individuals having fewer numbers of D4Z4 repeats on chromosome 4q35 in Shanghai population is higher than that in Caucasian population although the short D4Z4 fragment on chromosome 4q35 is associated with facioscapulohumeral muscular dystrophy. These findings suggest that other factors may also contribute to facioscapulohumeral muscular dystrophy.
