Literature DB >> 9344660

Multiple functional copies of the RBM gene family, a spermatogenesis candidate on the human Y chromosome.

N N Chai1, E C Salido, P H Yen.   

Abstract

The RBM (RNA-binding motif) gene family on the human Y chromosome encodes proteins with an RNA-binding domain. Its exclusive expression in germ cells and its partial deletion in some azoospermic or severely oligospermic males provide evidence of a role for RBM genes in spermatogenesis. There are approximately 30 RBM genes, found on both arms of the Y chromosome. Two RBM cDNA clones with slightly different sequences have been reported. To investigate the number of functional genes, we studied RBM expression by use of RT-PCR of RBM transcripts and by characterizing numerous RBM cDNA clones. A total of 27 RT-PCR and 19 cDNA clones were sequenced. Whereas the RT-PCR clones pointed to the existence of at least six RBM subfamilies (RBMI to RBMVI), the cDNA clones indicated that only RBMI is actively transcribed and encodes functional proteins. A total of six RBMI genes were identified, which produce four polypeptides due to some silent base substitutions. The transcripts of each gene are alternatively spliced to generate protein isoforms with three or four SRGY boxes, thus greatly increasing the complexity of the products of the RBM gene family. We also provide evidence suggesting that a 5-bp deletion in a previously reported RBM cDNA clone represents a processing irregularity. Copyright 1997 Academic Press.

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Year:  1997        PMID: 9344660     DOI: 10.1006/geno.1997.4944

Source DB:  PubMed          Journal:  Genomics        ISSN: 0888-7543            Impact factor:   5.736


  11 in total

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Review 2.  The role of human and mouse Y chromosome genes in male infertility.

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Review 5.  Molecular insights into the causes of male infertility.

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6.  Idiopathic cases of male infertility from a region in India show low incidence of Y-chromosome microdeletion.

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7.  Human Y-chromosome variation and male dysfunction.

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8.  A comparative study of Y chromosome microdeletions in infertile males from two Chinese populations.

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9.  Spontaneous transmission from a father to his son of a Y chromosome microdeletion involving the deleted in azoospermia (DAZ) gene.

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Review 10.  Genetic dissection of the AZF regions of the human Y chromosome: thriller or filler for male (in)fertility?

Authors:  Paulo Navarro-Costa; Carlos E Plancha; João Gonçalves
Journal:  J Biomed Biotechnol       Date:  2010-06-30
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