Source:http://linkedlifedata.com/resource/pubmed/id/11570956
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
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pubmed:dateCreated |
2001-9-25
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pubmed:abstractText |
Recent advances in understanding of male infertility have implicated two major causative factors, oxidative stress and Y chromosome deletions. A major cause of oxidative stress appears to be the high rate of reactive oxygen species generation associated with the retention of excess residual cytoplasm in the sperm midpiece. Other possible causes include the redox cycling of xenobiotics, and antioxidant depletion or apoptosis. Oxidative stress induces peroxidative damage in the sperm plasma membrane and DNA damage in both the mitochondrial and nuclear genomes. Nuclear DNA damage in the germ line of the father may be associated with pathology in the offspring, including childhood cancer and infertility. Gene deletions on the non-recombining region of the Y chromosome account for the infertility observed in about 15% of patients with azoospermia and 5-10% of subjects with severe oligozoospermia. The Y chromosome is particularly susceptible to gene deletions because of the inability of the haploid genome to deploy recombination repair in retrieving lost genetic information. Aberrant recombination, defective chromatin packaging, abortive apoptosis and oxidative stress may all be involved in the aetiology of DNA damage in the germ line. The factors responsible for Y chromosome deletions in spermatozoa remain unresolved but may be one facet of a central reproductive problem: controlling the amount of oxidative stress experienced by germ cells during their differentiation and maturation in the male reproductive tract.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
1470-1626
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
122
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
497-506
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pubmed:dateRevised |
2007-11-15
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pubmed:meshHeading |
pubmed-meshheading:11570956-Animals,
pubmed-meshheading:11570956-Cell Differentiation,
pubmed-meshheading:11570956-DNA Damage,
pubmed-meshheading:11570956-DNA Fragmentation,
pubmed-meshheading:11570956-DNA Replication,
pubmed-meshheading:11570956-Evolution, Molecular,
pubmed-meshheading:11570956-Gene Deletion,
pubmed-meshheading:11570956-Humans,
pubmed-meshheading:11570956-Infertility, Male,
pubmed-meshheading:11570956-Male,
pubmed-meshheading:11570956-Oncogenes,
pubmed-meshheading:11570956-Oxidative Stress,
pubmed-meshheading:11570956-Precursor Cell Lymphoblastic Leukemia-Lymphoma,
pubmed-meshheading:11570956-Spermatogenesis,
pubmed-meshheading:11570956-Spermatozoa,
pubmed-meshheading:11570956-Y Chromosome
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pubmed:year |
2001
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pubmed:articleTitle |
Oxidative stress, DNA damage and the Y chromosome.
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pubmed:affiliation |
School of Biological and Chemical Sciences, Centre for Life Sciences, University of Newcastle, University Drive, Callaghan, NSW 23008, Australia. jaitken@mail.newcastle.edu.au
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pubmed:publicationType |
Journal Article,
Review,
Research Support, Non-U.S. Gov't
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