Skip to main content
Translational Andrology and Urology logoLink to Translational Andrology and Urology
. 2014 Sep;3(Suppl 1):AB188. doi: 10.3978/j.issn.2223-4683.2014.s188

AB188. Meiotic prophase I defects in an oligospermic man with Wolf-Hirschhorn syndrome with ring chromosome 4

Qi Yao 1, Liu Wang 1, Bing Yao 1, Hongliu Gao 1, Weiwei Li 1, Xinyi Xia 1, Qinghua Shi 1, Yingxia Cui 1
PMCID: PMC4708340

Abstract

Background

Ring chromosomes are often associated with spermatogenetic failure. However, the mechanism is poorly understood. We here reported a single man with severe oligospermia and a ring chromosome 4 with a microdeletion at 4p16.3.

Methods

Synapsis (asSCP3), recombination (as MLH1) and transcriptional inactivation (as BRCA1) in a testicular biopsy were examined by fluorescence immunostaining.

Results

In the oligospermia patient, 35.4% of spermatocytes were in zygotene phase compared with 5.2% in controls. The patient had a significantly reduced recombination frequency with mean of 45.9 MLH1 foci/cell compared with 47.8 in controls. In the patient, chromosome 4 in all pachytene cells displayed loop formation with varying degrees of unpaired regions. BRCA1 localized along asynapsed regions regardless of XY body association.

Conclusions

Ring chromosome 4 might affect the progression of meiosis I prophase, synapse formation, and transcriptional activation of asynapsed areas, and impair male fertility.

Keywords: Ring chromosome 4, oligospermia, synapse complex, recombination, transcriptional inactivation


Articles from Translational Andrology and Urology are provided here courtesy of AME Publications

RESOURCES