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Publication : Characterization of genes encoding translation initiation factor eIF-2gamma in mouse and human: sex chromosome localization, escape from X-inactivation and evolution.

First Author  Ehrmann IE Year  1998
Journal  Hum Mol Genet Volume  7
Issue  11 Pages  1725-37
PubMed ID  9736774 Mgi Jnum  J:50115
Mgi Id  MGI:1289924 Doi  10.1093/hmg/7.11.1725
Citation  Ehrmann IE, et al. (1998) Characterization of genes encoding translation initiation factor eIF-2gamma in mouse and human: sex chromosome localization, escape from X-inactivation and evolution. Hum Mol Genet 7(11):1725-37
abstractText  The Delta Sxr(b) interval of the mouse Y chromosome is critical for spermatogenesis and expression of the male- specific minor transplantation antigen H-Y. Several genes have been mapped to this interval and each has a homologue on the X chromosome. Four, Zfy1, Zfy2 Ube1y and Dffry, are expressed specifically in the testis and their X homologues are not transcribed from tf ie inactive X chromosome. A further two, Smcy and Uty, are ubiquitously expressed and their X homologues escape X-inactivation. Here we report the identification of another gene from this region of the mouse Y chromosome. It encodes the highly conserved eukaryotic translation initiation factor elF-2 gamma. In the mouse this gene is ubiquitously expressed, has an X chromosome homologue which maps close to Dmd and escapes X-inactivation. The coding regions of the X and Y genes show 86% nucleotide identity and encode putative products with 98% amino acid identity. In humans, the elF-2 gamma structural gene is located on the X chromosome at Xp21 and this also escapes X-inactivation. However, there is no evidence of a Y copy of this gene in humans. We have identified autosomal retroposons of elF-2 gamma in both humans and mice and an additional retroposon on the X chromosome in some mouse strains. Ark blot analysis of eutherian and metatherian genomic DNA indicates that X-Y homologues are present in all species tested except simian primates and kangaroo and that retroposons are common to a wide range of mammals. These results shed light on the evolution of X-Y homologous genes.
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