A novel universal multiplex PCR improves detection of AZFc Y-chromosome microdeletions

J Assist Reprod Genet. 2014 May;31(5):613-20. doi: 10.1007/s10815-014-0204-5. Epub 2014 Mar 11.

Abstract

Purpose: To determine the frequencies and the characteristics of Y chromosome microdeletions (pl) in infertile men from central China to perform appropriate therapeutic choices by updated multiplex-PCR.

Methods: In this study, we established a novel universal primer-multiplex-PCR (U-M-PCR) method to overcome the disadvantages of traditional multiplex PCR (M-PCR). We chose 15 sequence-tagged sites (STS) for detection of Y chromosome microdeletions. 540 infertile male patients and 100 healthy male controls were selected in the study.

Results: Of the 540 male infertility patients, 48 Y-chromosome microdeletions were detected, with a total deletion rate of 8.9 %. Of these deletions, the rate of AZFa deletions (sY84) was 0.5 % (3/540), the rate of AZFb deletions (sY143) was 0.7 % (4/540) and the rate of AZFc deletions (sY242, sY254 and sY255) was 7.6 % (41/540). Compared with AZF deletion rates by M-PCR, we found U-M-PCR could detect AZFc deletion more specifically (1.0 % & 7.6 %). No Y-chromosome microdeletions were detected in the 100 males with normal semen (the control group).

Conclusions: U-M-PCR method was more specific to detect AZFc microdeletions. It is necessary to use the U-M-PCR method to offer genetic screening and counseling to infertile men prior to intracytoplasmic sperm injection (ICSI) or in-vitro fertilization (IVF).

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Asian People / genetics
  • Case-Control Studies
  • Chromosome Deletion
  • Chromosomes, Human, Y / genetics
  • DNA Primers
  • Humans
  • Infertility, Male
  • Male
  • Multiplex Polymerase Chain Reaction / methods*
  • Sequence Tagged Sites
  • Sex Chromosome Aberrations
  • Sex Chromosome Disorders of Sex Development / genetics*

Substances

  • DNA Primers

Supplementary concepts

  • Male sterility due to Y-chromosome deletions