Literature DB >> 7951230

A novel X gene with a widely transcribed Y-linked homologue escapes X-inactivation in mouse and human.

A I Agulnik1, M J Mitchell, M G Mattei, G Borsani, P A Avner, J L Lerner, C E Bishop.   

Abstract

A new gene, designated Smcx, was cloned from the mouse X chromosome by its homology to the Y located gene Smcy. Using direct in situ hybridisation Smcx was mapped to the distal end of the mouse X chromosome (XF2-XF4) and its human homologue, SMCX, was mapped to proximal Xp (Xp11.1-Xp11.2). Further meiotic mapping in the mouse placed Smcx in the Plp-Pdha1 interval. As Smcx/SMCX have widely expressed homologues on the Y chromosome, they appeared good candidates for genes that escape X-inactivation. In the human we show this to be the case as SMCX is expressed in hamster-human hybrids containing either an active or inactive human X chromosome. Two alleles of Smcx were found to be expressed in T(16;X)16H female mice despite the intact X chromosome being inactive in all cells. This indicates that Smcx is also not subject to X-inactivation and provides the first example of a gene that is expressed from inactive and active X chromosomes in the mouse.

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Year:  1994        PMID: 7951230     DOI: 10.1093/hmg/3.6.879

Source DB:  PubMed          Journal:  Hum Mol Genet        ISSN: 0964-6906            Impact factor:   6.150


  54 in total

1.  Promoter-specific hypoacetylation of X-inactivated genes.

Authors:  S L Gilbert; P A Sharp
Journal:  Proc Natl Acad Sci U S A       Date:  1999-11-23       Impact factor: 11.205

Review 2.  Sex Chromosome Genetics '99. Male infertility and the Y chromosome.

Authors:  K McElreavey; C Krausz
Journal:  Am J Hum Genet       Date:  1999-04       Impact factor: 11.025

3.  Comparative sequence and x-inactivation analyses of a domain of escape in human xp11.2 and the conserved segment in mouse.

Authors:  Karen D Tsuchiya; John M Greally; Yajun Yi; Kevin P Noel; Jean-Pierre Truong; Christine M Disteche
Journal:  Genome Res       Date:  2004-06-14       Impact factor: 9.043

4.  Familial molar tissues due to mutations in the inflammatory gene, NALP7, have normal postzygotic DNA methylation.

Authors:  Ugljesa Djuric; Osman El-Maarri; Barbara Lamb; Rork Kuick; Muheiddine Seoud; Philippe Coullin; Johannes Oldenburg; Samir Hanash; Rima Slim
Journal:  Hum Genet       Date:  2006-07-28       Impact factor: 4.132

5.  Comparative methylation analysis of murine transgenes that undergo or escape X-chromosome inactivation.

Authors:  M A Goldman; P S Reeves; C M Wirth; W J Zupko; M A Wong; S Edelhoff; C M Disteche
Journal:  Chromosome Res       Date:  1998-08       Impact factor: 5.239

6.  Transcription precedes loss of Xist coating and depletion of H3K27me3 during X-chromosome reprogramming in the mouse inner cell mass.

Authors:  Lucy H Williams; Sundeep Kalantry; Joshua Starmer; Terry Magnuson
Journal:  Development       Date:  2011-04-06       Impact factor: 6.868

7.  Smcx lies distal to DXHX674 and DXHX679 on the mouse X chromosome.

Authors:  S H Laval; H J Blair; M J Mitchell; Y Boyd
Journal:  Mamm Genome       Date:  1996-07       Impact factor: 2.957

Review 8.  The great escape.

Authors:  C M Disteche
Journal:  Am J Hum Genet       Date:  1997-06       Impact factor: 11.025

Review 9.  H-Y antigens.

Authors:  U Müller
Journal:  Hum Genet       Date:  1996-06       Impact factor: 4.132

10.  Transcriptional changes in response to X chromosome dosage in the mouse: implications for X inactivation and the molecular basis of Turner Syndrome.

Authors:  Alexandra M Lopes; Paul S Burgoyne; Andrew Ojarikre; Julien Bauer; Carole A Sargent; António Amorim; Nabeel A Affara
Journal:  BMC Genomics       Date:  2010-02-01       Impact factor: 3.969

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