Literature DB >> 7607679

Isolation of the human MOX2 homeobox gene and localization to chromosome 7p22.1-p21.3.

M Grigoriou1, M C Kastrinaki, W S Modi, K Theodorakis, B Mankoo, V Pachnis, D Karagogeos.   

Abstract

We have isolated and characterized cDNA clones encoding a novel human homeobox gene, MOX2, the homologue of the murine mox-2 gene. The MOX2 protein contains all of the characteristic features of Mox-2 proteins of other vertebrate species, namely the homeobox, the polyhistidine stretch, and a number of potential serine/threonine phosphorylation sites. The homeodomain of MOX2 protein is identical to all other vertebrate species reported so far (rodents and amphibians). Outside the homeodomain, Mox-2 proteins share a high degree of identity, except for a few amino acid differences encountered between the human and the rodent polypeptides. A polyhistidine stretch of 12 amino acids in the N terminal region of the protein is also conserved among humans, rodents, and (only partly) amphibians. The chromosomal position of MOX2 was assigned to 7p22.1-p21.3.

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Year:  1995        PMID: 7607679     DOI: 10.1016/0888-7543(95)80174-k

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


  2 in total

1.  MEOX2 regulates nuclear factor-kappaB activity in vascular endothelial cells through interactions with p65 and IkappaBbeta.

Authors:  Yun Chen; Arnold B Rabson; David H Gorski
Journal:  Cardiovasc Res       Date:  2010-04-26       Impact factor: 10.787

2.  Mutations in MEOX1, encoding mesenchyme homeobox 1, cause Klippel-Feil anomaly.

Authors:  Jawahir Y Mohamed; Eissa Faqeih; Abdulmonem Alsiddiky; Muneera J Alshammari; Niema A Ibrahim; Fowzan S Alkuraya
Journal:  Am J Hum Genet       Date:  2013-01-03       Impact factor: 11.025

  2 in total

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