Using multiplex PCR to analyze the breakpoint of a severe Y-chromosome deletion.
- Author:
Xiao-su XIAO
1
;
Xiao-yi LIU
;
Yong-qiang WANG
;
Yi ZHOU
;
Li OUYANG
;
Xu ZHANG
;
Zhi-ming CAI
Author Information
- Publication Type:Journal Article
- MeSH: Azoospermia; diagnosis; genetics; Chromosome Breakage; Chromosome Deletion; Chromosomes, Human, Y; genetics; Humans; Male; Polymerase Chain Reaction; methods; Reproducibility of Results; Sensitivity and Specificity
- From: Chinese Journal of Medical Genetics 2005;22(5):560-562
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo elucidate the relationship between azoospermia factor(AZF) microdeletion of Y chromosome and azoospermia, the exact breakpoint of a severe Y-chromosome deletion was determined according to the physical map of AZF.
METHODSMultiplex polymerase chain reaction was used to amplify fifteen sequence tagged sites (STS), namely sY82, sY84, sY86 in AZFa, sY124, sY127, sY128, sY133, sY134, sY143 in AZFb, sY239, sY242 sY254, sY255 in AZFc, and sY145, sY152 in AZFd; sex-determining region Y(SRY) was taken as an internal control. And then sY82,sY86,sY85,sY84 were further analyzed using the sample of the patient who had Y-chromosome deletion by G band analysis to map the breakpoint at molecular level.
RESULTSAll 15 STS and sY85 were amplified in positive control while only sY82, sY86 were amplified in the clinical sample, thus the breakpoint was found to be between sY86 and sY85.
CONCLUSIONThis study on the patient provided the direct biomolecular evidence of the exact breakpoint of the severe Y-chromosome deletion and established the deletion map of acrocentric chromosome. It also proved that the patient's azoospermia was due to the deletion of AZF.
