Literature DB >> 9425238

The human FXY gene is located within Xp22.3: implications for evolution of the mammalian X chromosome.

J Perry1, S Feather, A Smith, S Palmer, A Ashworth.   

Abstract

It has been proposed that the pseudoautosomal region of mammals has evolved by sequential addition of autosomal material onto the X and Y chromosomes followed by movement of the pseudoautosomal boundary to create X-unique regions. We have previously described a gene, Fxy , that spans the pseudoautosomal boundary in mice such that the first three exons of the gene are located on the X chromosome, but the remainder of the gene is located on both X and Y chromosomes. Therefore, this gene might be in a state of transition between pseudoautosomal and X-unique locations. In support of this theory we show here that the human FXY gene is located in Xp22.3 in humans, proximal to the pseudoautosomal boundary.

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Year:  1998        PMID: 9425238     DOI: 10.1093/hmg/7.2.299

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


  6 in total

1.  Validation of mRNA/EST-based gene predictions in human Xp11.4 revealed differences to the organization of the orthologous mouse locus.

Authors:  Gaiping Wen; Juliane Ramser; Stefan Taudien; Ulrike Gausmann; Karin Blechschmidt; Adam Frankish; Jennifer Ashurst; Alfons Meindl; Matthias Platzer
Journal:  Mamm Genome       Date:  2005-12-08       Impact factor: 2.957

2.  A short pseudoautosomal region in laboratory mice.

Authors:  J Perry; S Palmer; A Gabriel; A Ashworth
Journal:  Genome Res       Date:  2001-11       Impact factor: 9.043

Review 3.  The MID1 gene product in physiology and disease.

Authors:  Rossella Baldini; Martina Mascaro; Germana Meroni
Journal:  Gene       Date:  2020-04-10       Impact factor: 3.688

4.  The Human Pseudoautosomal Region (PAR): Origin, Function and Future.

Authors:  A Helena Mangs; Brian J Morris
Journal:  Curr Genomics       Date:  2007-04       Impact factor: 2.236

5.  Differential divergence of three human pseudoautosomal genes and their mouse homologs: implications for sex chromosome evolution.

Authors:  F Gianfrancesco; R Sanges; T Esposito; S Tempesta; E Rao; G Rappold; N Archidiacono; J A Graves; A Forabosco; M D'Urso
Journal:  Genome Res       Date:  2001-12       Impact factor: 9.043

6.  Mid1/Mid2 expression in craniofacial development and a literature review of X-linked opitz syndrome.

Authors:  Bijun Li; Tianhong Zhou; Yi Zou
Journal:  Mol Genet Genomic Med       Date:  2015-12-12       Impact factor: 2.183

  6 in total

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