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Publication : Mouse germ cell-less as an essential component for nuclear integrity.

First Author  Kimura T Year  2003
Journal  Mol Cell Biol Volume  23
Issue  4 Pages  1304-15
PubMed ID  12556490 Mgi Jnum  J:81819
Mgi Id  MGI:2450042 Doi  10.1128/MCB.23.4.1304-1315.2003
Citation  Kimura T, et al. (2003) Mouse germ cell-less as an essential component for nuclear integrity. Mol Cell Biol 23(4):1304-15
abstractText  A mouse homologue of the Drosophila melanogaster germ cell-less (mgcl-1) gene is expressed ubiquitously, and its gene product is localized to the nuclear envelope based on its binding to LAP2 beta (lamina-associated polypeptide 2 beta). To elucidate the role of mgcl-1, we analyzed two mutant mouse lines that lacked mgcl-1 gene expression. Abnormal nuclear morphologies that were probably due to impaired nuclear envelope integrity were observed in the liver, exocrine pancreas, and testis. In particular, functional abnormalities were observed in testis in which the highest expression of mgcl-1 was detected. Fertility was significantly impaired in mgcl-1-null male mice, probably as a result of severe morphological abnormalities in the sperm. Electron microscopic observations showed insufficient chromatin condensation and abnormal acrosome structures in mgcl-1-null sperm. In addition, the expression patterns of transition proteins and protamines, both of which are essential for chromatin remodeling during spermatogenesis, were aberrant. Considering that the first abnormality during the process of spermatogenesis was abnormal nuclear envelope structure in spermatocytes, the mgcl-1 gene product appears to be essential for appropriate nuclear-lamina organization, which in turn is essential for normal sperm morphogenesis and chromatin remodeling.
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