The prognostic role of the extent of Y microdeletion on spermatogenesis and maturity of Sertoli cells
Open Access
- 1 March 2001
- journal article
- review article
- Published by Oxford University Press (OUP) in Human Reproduction
- Vol. 16 (3) , 399-402
- https://doi.org/10.1093/humrep/16.3.399
Abstract
Substantial involvement of the Y chromosome in sexual development and spermatogenesis has been demonstrated. Over the last decade, varying extent of Y chromosome microdeletions have been identified among infertile patients with azoospermia or oligozoospermia. These microdeletions were clustered in three main regions named AZFa, AZFb, and AZFc. Analysis of the Y chromosome microdeletion was found to be of prognostic value in cases of infertility, both in terms of clinical management as well as for understanding the aetiology of the spermatogenesis impairment. However, the accumulated data are difficult to analyse, due to the variable extent of these deletions, the different sequence-tagged sites (STS) used to detect the microdeletions, and the non-uniformity of the histological terminology used by different investigators. This debate discusses the chances of finding testicular spermatozoa in men with a varying extent of Y chromosome microdeletions. The genotype and germ cell findings in men with AZFa microdeletions as well as those that include more than a single AZF region are reviewed, as is the effect of Y chromosome AZF microdeletions on the maturity of the Sertoli cells.Keywords
This publication has 29 references indexed in Scilit:
- A High Frequency of Y Chromosome Deletions in Males with Nonidiopathic InfertilityJournal of Clinical Endocrinology & Metabolism, 1999
- Functional Coherence of the Human Y ChromosomeScience, 1997
- Screening for deletions of the Y chromosome involving the DAZ (Deleted in AZoospermia) gene in azoospermia and severe oligozoospermiaFertility and Sterility, 1997
- The Drosophila developmental gene fat facets has a human homologue in Xp11.4 which escapes X-inactivation and has related sequences on Yq11.2 [published erratum appears in Hum Mol Genet 1997 Feb;6(2):334-5]Human Molecular Genetics, 1996
- Human Y chromosome azoospermia factors (AZF) mapped to different subregions in Yq11Human Molecular Genetics, 1996
- The incidence and possible relevance of Y-linked microdeletions in babies born after intracytoplasmic sperm injection and their infertile fathersMolecular Human Reproduction, 1996
- Polymerase chain reaction screening for Y chromosome microdeletions: a first step towards the diagnosis of genetically-determined spermatogenic failure in menMolecular Human Reproduction, 1996
- Diverse spermatogenic defects in humans caused by Y chromosome deletions encompassing a novel RNA–binding protein geneNature Genetics, 1995
- Intermediate filaments in sertoli cellsMicroscopy Research and Technique, 1992
- Expression of cytokeratins 8 and 18 in human Sertoli cells of immature and atrophic seminiferous tubules*Differentiation, 1990