Literature DB >> 9671743

Chromosomal basis of X chromosome inactivation: identification of a multigene domain in Xp11.21-p11.22 that escapes X inactivation.

A P Miller1, H F Willard.   

Abstract

A number of genes have been identified that escape mammalian X chromosome inactivation and are expressed from both active and inactive X chromosomes. The basis for escape from inactivation is unknown and, a priori, could be a result of local factors that act in a gene-specific manner or of chromosomal control elements that act regionally. Models invoking the latter predict that such genes should be clustered in specific domains on the X chromosome, rather than distributed at random along the length of the X. To distinguish between these possibilities, we have constructed a transcription map composed of at least 23 distinct expressed sequences in an approximately 5.5-megabase region on the human X chromosome spanning Xp11.21-p11.22. The inactivation status of these transcribed sequences has been determined in a somatic cell hybrid system and correlated with the position of the genes on the physical map. Although the majority of transcribed sequences in this region are subject to X inactivation, eight expressed sequences (representing at least six different genes) escape inactivation, and all are localized to within a region of less than 370 kb. Genes located both distal and proximal to this cluster are subject to inactivation, thereby defining a unique multigene domain on the proximal short arm that is transcriptionally active on the inactive X chromosome.

Entities:  

Mesh:

Year:  1998        PMID: 9671743      PMCID: PMC21141          DOI: 10.1073/pnas.95.15.8709

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  60 in total

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Authors:  Y Saitoh; U K Laemmli
Journal:  Cold Spring Harb Symp Quant Biol       Date:  1993

2.  A 6-Mb YAC contig in Xp22.1-p22.2 spanning the DXS69E, XE59, GLRA2, PIGA, GRPR, CALB3, and PHKA2 genes.

Authors:  T Alitalo; F Francis; J Kere; H Lehrach; D Schlessinger; H F Willard
Journal:  Genomics       Date:  1995-02-10       Impact factor: 5.736

3.  Three genes that escape X chromosome inactivation are clustered within a 6 Mb YAC contig and STS map in Xp11.21-p11.22.

Authors:  A P Miller; K Gustashaw; D J Wolff; S H Rider; A P Monaco; B Eble; D Schlessinger; J L Gorski; G J van Ommen; J Weissenbach
Journal:  Hum Mol Genet       Date:  1995-04       Impact factor: 6.150

4.  Genomic imprinting of Mash2, a mouse gene required for trophoblast development.

Authors:  F Guillemot; T Caspary; S M Tilghman; N G Copeland; D J Gilbert; N A Jenkins; D J Anderson; A L Joyner; J Rossant; A Nagy
Journal:  Nat Genet       Date:  1995-03       Impact factor: 38.330

5.  Identification of two alternative fusion genes, SYT-SSX1 and SYT-SSX2, in t(X;18)(p11.2;q11.2)-positive synovial sarcomas.

Authors:  B de Leeuw; M Balemans; D Olde Weghuis; A Geurts van Kessel
Journal:  Hum Mol Genet       Date:  1995-06       Impact factor: 6.150

6.  Parental imprinting of the Mas protooncogene in mouse.

Authors:  A J Villar; R A Pedersen
Journal:  Nat Genet       Date:  1994-12       Impact factor: 38.330

Review 7.  Escape from X inactivation in human and mouse.

Authors:  C M Disteche
Journal:  Trends Genet       Date:  1995-01       Impact factor: 11.639

8.  The DXS423E gene in Xp11.21 escapes X chromosome inactivation.

Authors:  C J Brown; A P Miller; L Carrel; J L Rupert; K E Davies; H F Willard
Journal:  Hum Mol Genet       Date:  1995-02       Impact factor: 6.150

9.  Trophinin and tastin, a novel cell adhesion molecule complex with potential involvement in embryo implantation.

Authors:  M N Fukuda; T Sato; J Nakayama; G Klier; M Mikami; D Aoki; S Nozawa
Journal:  Genes Dev       Date:  1995-05-15       Impact factor: 11.361

10.  Identification of a novel paternally expressed gene in the Prader-Willi syndrome region.

Authors:  R Wevrick; J A Kerns; U Francke
Journal:  Hum Mol Genet       Date:  1994-10       Impact factor: 6.150

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  27 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

Review 2.  Genomic imprinting: implications for human disease.

Authors:  J G Falls; D J Pulford; A A Wylie; R L Jirtle
Journal:  Am J Pathol       Date:  1999-03       Impact factor: 4.307

3.  The molecular basis of X-linked spondyloepiphyseal dysplasia tarda.

Authors:  A K Gedeon; G E Tiller; M Le Merrer; S Heuertz; L Tranebjaerg; D Chitayat; S Robertson; I A Glass; R Savarirayan; W G Cole; D L Rimoin; B G Kousseff; H Ohashi; B Zabel; A Munnich; J Gecz; J C Mulley
Journal:  Am J Hum Genet       Date:  2001-05-08       Impact factor: 11.025

4.  DNA methylation has a local effect on transcription and histone acetylation.

Authors:  Ryan A Irvine; Iping G Lin; Chih-Lin Hsieh
Journal:  Mol Cell Biol       Date:  2002-10       Impact factor: 4.272

5.  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

6.  Does the HSD17B10 gene escape from X-inactivation?

Authors:  Xue-Ying He; Carl Dobkin; Song-Yu Yang
Journal:  Eur J Hum Genet       Date:  2010-11-17       Impact factor: 4.246

7.  A recurrent RNA-splicing mutation in the SEDL gene causes X-linked spondyloepiphyseal dysplasia tarda.

Authors:  G E Tiller; V L Hannig; D Dozier; L Carrel; K C Trevarthen; W R Wilcox; S Mundlos; J L Haines; A K Gedeon; J Gecz
Journal:  Am J Hum Genet       Date:  2001-04-26       Impact factor: 11.025

8.  X-chromosome genetic association test accounting for X-inactivation, skewed X-inactivation, and escape from X-inactivation.

Authors:  Jian Wang; Robert Yu; Sanjay Shete
Journal:  Genet Epidemiol       Date:  2014-07-08       Impact factor: 2.135

9.  Multiple spatially distinct types of facultative heterochromatin on the human inactive X chromosome.

Authors:  Brian P Chadwick; Huntington F Willard
Journal:  Proc Natl Acad Sci U S A       Date:  2004-12-01       Impact factor: 11.205

10.  The impact of local genome sequence on defining heterochromatin domains.

Authors:  Bayly S Wheeler; Jared A Blau; Huntington F Willard; Kristin C Scott
Journal:  PLoS Genet       Date:  2009-04-10       Impact factor: 5.917

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