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Syst Biol Reprod Med. 2011 Feb;57(1-2):3-16. doi: 10.3109/19396368.2010.527427. Epub 2011 Jan 6.

Structural variation of the human genome: mechanisms, assays, and role in male infertility.

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1
Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030-3498, USA.

Abstract

Genomic disorders are defined as diseases caused by rearrangements of the genome incited by a genomic architecture that conveys instability. Y-chromosome related dysfunctions such as male infertility are frequently associated with gross DNA rearrangements resulting from its peculiar genomic architecture. The Y-chromosome has evolved into a highly specialized chromosome to perform male functions, mainly spermatogenesis. Direct and inverted repeats, some of them palindromes with highly identical nucleotide sequences that can form DNA cruciform structures, characterize the genomic structure of the Y-chromosome long arm. Some particular Y chromosome genomic deletions can cause spermatogenic failure likely because of removal of one or more transcriptional units with a potential role in spermatogenesis. We describe mechanisms underlying the formation of human genomic rearrangements on autosomes and review Y-chromosome deletions associated with male infertility.

PMID:
21210740
PMCID:
PMC3179416
DOI:
10.3109/19396368.2010.527427
[Indexed for MEDLINE]
Free PMC Article
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