Literature DB >> 11691846

A short pseudoautosomal region in laboratory mice.

J Perry1, S Palmer, A Gabriel, A Ashworth.   

Abstract

The pseudoautosomal region (PAR) of mammalian sex chromosomes is a small region of sequence identity that is the site of an obligatory pairing and recombination event between the X and Y chromosomes during male meiosis. During female meiosis, X chromosomes can pair and recombine along their entire length; recombination in the PAR is therefore approximately 10x greater in male meiosis compared with female meiosis. A consequence of the presence of the PAR in two copies in males and females is that genes in the region escape the process of X-inactivation. Although the structure and gene content of the human PAR at Xq/Yq is well understood, the mouse PAR, which appears to be of independent evolutionary origin, is poorly characterized. Here we describe a yeast artificial chromosome (YAC) contig covering the distal part of the mouse X chromosome, which we have used to define the pseudoautosomal boundary, that is, the point of divergence of X-specific and X-Y-identical sequences. In addition, we have investigated the size of the mouse PAR by integrating a unique restriction endonuclease recognition site just proximal to the pseudoautosomal boundary by homologous recombination. Restriction digestion of this modified DNA and pulsed field gel electrophoresis reveal that the PAR in these cells is approximately 700 kb. Thus, the mouse PAR, although small in size, has retained essential sex chromosome pairing functions despite its rapid rate of evolution.

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Year:  2001        PMID: 11691846      PMCID: PMC311143          DOI: 10.1101/gr.203001

Source DB:  PubMed          Journal:  Genome Res        ISSN: 1088-9051            Impact factor:   9.043


  44 in total

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Journal:  Hum Mol Genet       Date:  1997-08       Impact factor: 6.150

2.  A gene spans the pseudoautosomal boundary in mice.

Authors:  S Palmer; J Perry; D Kipling; A Ashworth
Journal:  Proc Natl Acad Sci U S A       Date:  1997-10-28       Impact factor: 11.205

3.  Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndrome.

Authors:  E Rao; B Weiss; M Fukami; A Rump; B Niesler; A Mertz; K Muroya; G Binder; S Kirsch; M Winkelmann; G Nordsiek; U Heinrich; M H Breuning; M B Ranke; A Rosenthal; T Ogata; G A Rappold
Journal:  Nat Genet       Date:  1997-05       Impact factor: 38.330

4.  Genetic homology and crossing over in the X and Y chromosomes of Mammals.

Authors:  P S Burgoyne
Journal:  Hum Genet       Date:  1982       Impact factor: 4.132

5.  Gene duplications as a recurrent theme in the evolution of the human pseudoautosomal region 1: isolation of the gene ASMTL.

Authors:  K Ried; E Rao; K Schiebel; G A Rappold
Journal:  Hum Mol Genet       Date:  1998-10       Impact factor: 6.150

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Journal:  Hum Mol Genet       Date:  1997-01       Impact factor: 6.150

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

Authors:  J Perry; S Feather; A Smith; S Palmer; A Ashworth
Journal:  Hum Mol Genet       Date:  1998-02       Impact factor: 6.150

8.  Differentially regulated and evolved genes in the fully sequenced Xq/Yq pseudoautosomal region.

Authors:  A Ciccodicola; M D'Esposito; T Esposito; F Gianfrancesco; C Migliaccio; M G Miano; M R Matarazzo; M Vacca; A Franzè; M Cuccurese; M Cocchia; A Curci; A Terracciano; A Torino; S Cocchia; G Mercadante; E Pannone; N Archidiacono; M Rocchi; D Schlessinger; M D'Urso
Journal:  Hum Mol Genet       Date:  2000-02-12       Impact factor: 6.150

9.  Differential expression pattern of XqPAR-linked genes SYBL1 and IL9R correlates with the structure and evolution of the region.

Authors:  M D'Esposito; M R Matarazzo; A Ciccodicola; M Strazzullo; R Mazzarella; N A Quaderi; H Fujiwara; M S Ko; L B Rowe; A Ricco; N Archidiacono; M Rocchi; D Schlessinger; M D'Urso
Journal:  Hum Mol Genet       Date:  1997-10       Impact factor: 6.150

10.  Opitz G/BBB syndrome, a defect of midline development, is due to mutations in a new RING finger gene on Xp22.

Authors:  N A Quaderi; S Schweiger; K Gaudenz; B Franco; E I Rugarli; W Berger; G J Feldman; M Volta; G Andolfi; S Gilgenkrantz; R W Marion; R C Hennekam; J M Opitz; M Muenke; H H Ropers; A Ballabio
Journal:  Nat Genet       Date:  1997-11       Impact factor: 38.330

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  64 in total

1.  Chromatin configuration and epigenetic landscape at the sex chromosome bivalent during equine spermatogenesis.

Authors:  Claudia Baumann; Christopher M Daly; Sue M McDonnell; Maria M Viveiros; Rabindranath De La Fuente
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2.  Hybrid breakdown caused by substitution of the X chromosome between two mouse subspecies.

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Journal:  Genetics       Date:  2004-02       Impact factor: 4.562

3.  Synapsis, recombination, and chromatin remodeling in the XY body of armadillos.

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4.  Clcn4-2 genomic structure differs between the X locus in Mus spretus and the autosomal locus in Mus musculus: AT motif enrichment on the X.

Authors:  Di Kim Nguyen; Fan Yang; Rajinder Kaul; Can Alkan; Anthony Antonellis; Karen F Friery; Baoli Zhu; Pieter J de Jong; Christine M Disteche
Journal:  Genome Res       Date:  2011-01-31       Impact factor: 9.043

5.  Chromosomal rearrangement interferes with meiotic X chromosome inactivation.

Authors:  David Homolka; Robert Ivanek; Jana Capkova; Petr Jansa; Jiri Forejt
Journal:  Genome Res       Date:  2007-08-23       Impact factor: 9.043

Review 6.  Mouse model systems to study sex chromosome genes and behavior: relevance to humans.

Authors:  Kimberly H Cox; Paul J Bonthuis; Emilie F Rissman
Journal:  Front Neuroendocrinol       Date:  2014-01-02       Impact factor: 8.606

7.  Telomeric TERB1-TRF1 interaction is crucial for male meiosis.

Authors:  Juanjuan Long; Chenhui Huang; Yanyan Chen; Ying Zhang; Shaohua Shi; Ligang Wu; Yie Liu; Chengyu Liu; Jian Wu; Ming Lei
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8.  Difference between random and imprinted X inactivation in common voles.

Authors:  Elena V Dementyeva; Alexander I Shevchenko; Olga V Anopriyenko; Nina A Mazurok; Eugeny A Elisaphenko; Tatyana B Nesterova; Neil Brockdorff; Suren M Zakian
Journal:  Chromosoma       Date:  2010-05-15       Impact factor: 4.316

9.  Hybrid Sterility with Meiotic Metaphase Arrest in Intersubspecific Mouse Crosses.

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Journal:  J Hered       Date:  2019-03-05       Impact factor: 2.645

10.  Characterization of the bovine pseudoautosomal boundary: Documenting the evolutionary history of mammalian sex chromosomes.

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Journal:  Genome Res       Date:  2008-11-03       Impact factor: 9.043

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