Literature DB >> 15979907

The sperm mitochondria-specific translocator has a key role in maternal mitochondrial inheritance.

Kenji Hayashida1, Katsuhisa Omagari, Jun-ichi Masuda, Hiroaki Hazama, Yoshiko Kadokawa, Kazuo Ohba, Shigeru Kohno.   

Abstract

The mechanism of maternal mitochondrial inheritance in animals involves the selective elimination of sperm mitochondria by the elimination factor of the egg and the sperm mitochondria-specific factor. In vitro fertilization using sperm from isogenic mice incorporating heterospecific mitochondrial DNA (mtDNA) showed that the number of PCR positives of sperm mtDNA in two-cell embryos was significantly increased following sperm incubation with anti-tetratricopeptide repeat-containing protein involved in spermatogenesis (tpis) protein, anti-translocator of mitochondrial outer membrane (Tom) 22 and anti-Tom40 antibodies. The treatment of fertilized eggs with EGTA and other endonuclease inhibitors increased the sperm mtDNA levels. We conclude that the elimination factor, which is probably an endonuclease, is selectively received by the tpis protein of the sperm mitochondrial outer membrane within the egg. It is then transported into the sperm mitochondria by Tom22 and Tom40, where it destroys the sperm mtDNA, establishing the maternal inheritance of mtDNA.

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Year:  2005        PMID: 15979907     DOI: 10.1016/j.cellbi.2004.09.016

Source DB:  PubMed          Journal:  Cell Biol Int        ISSN: 1065-6995            Impact factor:   3.612


  2 in total

1.  Hybrid male sterility is caused by mitochondrial DNA deletion.

Authors:  Kenji Hayashida; Shigeru Kohno
Journal:  Mol Biol Rep       Date:  2008-07-22       Impact factor: 2.316

Review 2.  A framework for high-resolution phenotyping of candidate male infertility mutants: from human to mouse.

Authors:  Brendan J Houston; Donald F Conrad; Moira K O'Bryan
Journal:  Hum Genet       Date:  2020-04-04       Impact factor: 5.881

  2 in total

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