Literature DB >> 9570953

Characterization of SCML1, a new gene in Xp22, with homology to developmental polycomb genes.

E van de Vosse1, S M Walpole, A Nicolaou, P van der Bent, A Cahn, M Vaudin, M T Ross, J Durham, R Pavitt, J Wilkinson, D Grafham, A A Bergen, G J van Ommen, J R Yates, J T den Dunnen, D Trump.   

Abstract

Using exon trapping, we have identified a new human gene in Xp22 encoding a 3-kb mRNA. Expression of this RNA is detectable in a range of tissues but is most pronounced in skeletal muscle and heart. The gene, designated "sex comb on midleg-like-1" (SCML1), maps 14 kb centromeric of marker DXS418, between DXS418 and DXS7994, and is transcribed from telomere to centromere. SCML1 spans 18 kb of genomic DNA, consists of six exons, and has a 624-bp open reading frame. The predicted 27-kDa SCML1 protein contains two domains that each have a high homology to two Drosophila transcriptional repressors of the polycomb group (PcG) genes and their homologues in mouse and human. PcG genes are known to be involved in the regulation of homeotic genes, and the mammalian homologues of the PcG genes repress the expression of Hox genes. SCML1 appears to be a new human member of this gene group and may play an important role in the control of embryonal development.

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Year:  1998        PMID: 9570953     DOI: 10.1006/geno.1998.5224

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


  13 in total

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Review 9.  MBT domain proteins in development and disease.

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10.  Adaptive evolution of SCML1 in primates, a gene involved in male reproduction.

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Journal:  BMC Evol Biol       Date:  2008-07-05       Impact factor: 3.260

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