Literature DB >> 15197169

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

Karen D Tsuchiya1, John M Greally, Yajun Yi, Kevin P Noel, Jean-Pierre Truong, Christine M Disteche.   

Abstract

We have performed X-inactivation and sequence analyses on 350 kb of sequence from human Xp11.2, a region shown previously to contain a cluster of genes that escape X inactivation, and we compared this region with the region of conserved synteny in mouse. We identified several new transcripts from this region in human and in mouse, which defined the full extent of the domain escaping X inactivation in both species. In human, escape from X inactivation involves an uninterrupted 235-kb domain of multiple genes. Despite highly conserved gene content and order between the two species, Smcx is the only mouse gene from the conserved segment that escapes inactivation. As repetitive sequences are believed to facilitate spreading of X inactivation along the chromosome, we compared the repetitive sequence composition of this region between the two species. We found that long terminal repeats (LTRs) were decreased in the human domain of escape, but not in the majority of the conserved mouse region adjacent to Smcx in which genes were subject to X inactivation, suggesting that these repeats might be excluded from escape domains to prevent spreading of silencing. Our findings indicate that genomic context, as well as gene-specific regulatory elements, interact to determine expression of a gene from the inactive X-chromosome. Copyright 2004 Cold Spring Harbor Laboratory Press ISSN

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Year:  2004        PMID: 15197169      PMCID: PMC442142          DOI: 10.1101/gr.2575904

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


  58 in total

1.  Escapees on the X chromosome.

Authors:  C M Disteche
Journal:  Proc Natl Acad Sci U S A       Date:  1999-12-07       Impact factor: 11.205

2.  PipMaker--a web server for aligning two genomic DNA sequences.

Authors:  S Schwartz; Z Zhang; K A Frazer; A Smit; C Riemer; J Bouck; R Gibbs; R Hardison; W Miller
Journal:  Genome Res       Date:  2000-04       Impact factor: 9.043

3.  Molecular evidence for a relationship between LINE-1 elements and X chromosome inactivation: the Lyon repeat hypothesis.

Authors:  J A Bailey; L Carrel; A Chakravarti; E E Eichler
Journal:  Proc Natl Acad Sci U S A       Date:  2000-06-06       Impact factor: 11.205

Review 4.  Functional gene expression domains: defining the functional unit of eukaryotic gene regulation.

Authors:  N Dillon; P Sabbattini
Journal:  Bioessays       Date:  2000-07       Impact factor: 4.345

5.  Chromosomal domains and escape from X inactivation: comparative X inactivation analysis in mouse and human.

Authors:  K D Tsuchiya; H F Willard
Journal:  Mamm Genome       Date:  2000-10       Impact factor: 2.957

Review 6.  Xist RNA and the mechanism of X chromosome inactivation.

Authors:  Kathrin Plath; Susanna Mlynarczyk-Evans; Dmitri A Nusinow; Barbara Panning
Journal:  Annu Rev Genet       Date:  2002-06-11       Impact factor: 16.830

7.  Comparative genome analysis delimits a chromosomal domain and identifies key regulatory elements in the alpha globin cluster.

Authors:  J Flint; C Tufarelli; J Peden; K Clark; R J Daniels; R Hardison; W Miller; S Philipsen; K C Tan-Un; T McMorrow; J Frampton; B P Alter; A M Frischauf; D R Higgs
Journal:  Hum Mol Genet       Date:  2001-02-15       Impact factor: 6.150

8.  Comparative genome analysis of the mouse imprinted gene impact and its nonimprinted human homolog IMPACT: toward the structural basis for species-specific imprinting.

Authors:  K Okamura; Y Hagiwara-Takeuchi; T Li; T H Vu; M Hirai; M Hattori; Y Sakaki; A R Hoffman; T Ito
Journal:  Genome Res       Date:  2000-12       Impact factor: 9.043

9.  Sequence and functional comparison in the Beckwith-Wiedemann region: implications for a novel imprinting centre and extended imprinting.

Authors:  S Engemann; M Strödicke; M Paulsen; O Franck; R Reinhardt; N Lane; W Reik; J Walter
Journal:  Hum Mol Genet       Date:  2000-11-01       Impact factor: 6.150

Review 10.  Interspersed repeats and other mementos of transposable elements in mammalian genomes.

Authors:  A F Smit
Journal:  Curr Opin Genet Dev       Date:  1999-12       Impact factor: 5.578

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  33 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 novel role for Xist RNA in the formation of a repressive nuclear compartment into which genes are recruited when silenced.

Authors:  Julie Chaumeil; Patricia Le Baccon; Anton Wutz; Edith Heard
Journal:  Genes Dev       Date:  2006-08-15       Impact factor: 11.361

3.  Monoallelic expression of MAO-A in skin fibroblasts.

Authors:  N Nordquist; L Oreland
Journal:  J Neural Transm (Vienna)       Date:  2007-04-04       Impact factor: 3.575

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.  Escape from X chromosome inactivation is an intrinsic property of the Jarid1c locus.

Authors:  Nan Li; Laura Carrel
Journal:  Proc Natl Acad Sci U S A       Date:  2008-10-29       Impact factor: 11.205

6.  Clustered transcripts that escape X inactivation at mouse XqD.

Authors:  Alexandra M Lopes; Sarah E Arnold-Croop; António Amorim; Laura Carrel
Journal:  Mamm Genome       Date:  2011-07-19       Impact factor: 2.957

Review 7.  Genes that escape from X inactivation.

Authors:  Joel B Berletch; Fan Yang; Jun Xu; Laura Carrel; Christine M Disteche
Journal:  Hum Genet       Date:  2011-05-26       Impact factor: 4.132

8.  Mutations in epilepsy and intellectual disability genes in patients with features of Rett syndrome.

Authors:  Heather E Olson; Dimira Tambunan; Christopher LaCoursiere; Marti Goldenberg; Rebecca Pinsky; Emilie Martin; Eugenia Ho; Omar Khwaja; Walter E Kaufmann; Annapurna Poduri
Journal:  Am J Med Genet A       Date:  2015-04-25       Impact factor: 2.802

9.  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

10.  X chromosome inactivation and Xist evolution in a rodent lacking LINE-1 activity.

Authors:  Michael A Cantrell; Bryan C Carstens; Holly A Wichman
Journal:  PLoS One       Date:  2009-07-15       Impact factor: 3.240

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