Uniform deletion junctions of complete azoospermia factor region c deletion in infertile men in Taiwan.
- Author:
Chao-Chin HSU
1
;
Pao-Lin KUO
;
Louise CHUANG
;
Ying-Hung LIN
;
Yen-Ni TENG
;
Yung-Ming LIN
Author Information
- Publication Type:Journal Article
- MeSH: Asian Continental Ancestry Group; genetics; Base Sequence; Chromosomes, Human, Y; genetics; DNA Primers; Deleted in Azoospermia 1 Protein; Gene Deletion; Genetic Loci; Humans; Infertility, Male; genetics; Male; Nuclear Proteins; genetics; Oligospermia; genetics; Phenotype; Polymerase Chain Reaction; Proteins; genetics; RNA-Binding Proteins; genetics; Seminal Plasma Proteins; genetics; Taiwan; Testis; anatomy & histology
- From: Asian Journal of Andrology 2006;8(2):205-211
- CountryChina
- Language:English
-
Abstract:
AIMTo determine the deletion junctions of infertile men in Taiwan with azoospermia factor region c (AZFc) deletions and to evaluate the genotype/phenotype correlation.
METHODSGenomic DNAs from 460 infertile men were examined. Bacterial artificial chromosome clones were used to verify the accuracy of polymerase chain reaction. Deletion junctions of the AZFc region were determined by analysis of sequence-tagged sites and gene-specific markers.
RESULTSComplete AZFc deletions, including BPY2, CDY1 and DAZ genes, were identified in 24 men. The proximal breakpoints were clustered between sY1197 and sY1192, and the distal breakpoints were clustered between sY1054 and sY1125 in all but one of the 24 men. The testicular phenotypes of men with complete AZFc deletion varied from oligozoospermia, to hypospermatogenesis, to maturation arrest.
CONCLUSIONWe identified a group of infertile men with uniform deletion junctions of AZFc in the Taiwan population. Despite this homogeneous genetic defect in the AZFc region, no clear genotype/phenotype correlation could be demonstrated.
