Literature DB >> 11243412

The 5' repeat elements of the mouse Xist gene inhibit the transcription of X-linked genes.

N Allaman-Pillet1, A Djemaï, C Bonny, D F Schorderet.   

Abstract

X chromosome inactivation in mammals requires the Xist gene, which is exclusively expressed from the inactive X chromosome (Xi). The large heterogeneous Xist nuclear RNA colocalizes with Xi, most likely through nuclear protein interactions. The 5' region of the Xist RNA contains a series of well-conserved tandem repeats known to bind heteronuclear proteins in vitro and to enhance human XIST transcription. We show in an in vitro system that the conserved repeat element located in the 5' region of the mouse Xist gene (Xcr) represses three X-linked genes but has no effect on the autosomal genes Aprt, Ins, and the viral SV40 gene. The repression effect is not mediated by the conserved core sequence (Ccs) of Xcr, but requires the presence of the complete Xcr. This Xcr effect on X-linked genes suggests that Xcr transcript recognizes the genes to be silenced and is involved in the spreading of X inactivation.

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Year:  2000        PMID: 11243412      PMCID: PMC5964931          DOI: 10.3727/000000001783992632

Source DB:  PubMed          Journal:  Gene Expr        ISSN: 1052-2166


  32 in total

1.  roX1 RNA paints the X chromosome of male Drosophila and is regulated by the dosage compensation system.

Authors:  V H Meller; K H Wu; G Roman; M I Kuroda; R L Davis
Journal:  Cell       Date:  1997-02-21       Impact factor: 41.582

2.  Lack of inactivation of a mouse X-linked gene physically separated from the inactivation centre.

Authors:  M F Lyon; J Zenthon; E P Evans; M D Burtenshaw; K A Wareham; E D Williams
Journal:  J Embryol Exp Morphol       Date:  1986-09

3.  The location of Cattanach's translocation in the X-chromosome linkage map of the mouse.

Authors:  B M Cattanach
Journal:  Genet Res       Date:  1966-10       Impact factor: 1.588

4.  Tsix, a gene antisense to Xist at the X-inactivation centre.

Authors:  J T Lee; L S Davidow; D Warshawsky
Journal:  Nat Genet       Date:  1999-04       Impact factor: 38.330

5.  An imprinted mouse transcript homologous to the human imprinted in Prader-Willi syndrome (IPW) gene.

Authors:  R Wevrick; U Francke
Journal:  Hum Mol Genet       Date:  1997-02       Impact factor: 6.150

6.  The human XIST gene: analysis of a 17 kb inactive X-specific RNA that contains conserved repeats and is highly localized within the nucleus.

Authors:  C J Brown; B D Hendrich; J L Rupert; R G Lafrenière; Y Xing; J Lawrence; H F Willard
Journal:  Cell       Date:  1992-10-30       Impact factor: 41.582

7.  Localization of the X inactivation centre on the human X chromosome in Xq13.

Authors:  C J Brown; R G Lafreniere; V E Powers; G Sebastio; A Ballabio; A L Pettigrew; D H Ledbetter; E Levy; I W Craig; H F Willard
Journal:  Nature       Date:  1991-01-03       Impact factor: 49.962

8.  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

9.  Disruption of imprinting caused by deletion of the H19 gene region in mice.

Authors:  P A Leighton; R S Ingram; J Eggenschwiler; A Efstratiadis; S M Tilghman
Journal:  Nature       Date:  1995-05-04       Impact factor: 49.962

10.  RNA annealing activities in HeLa nuclei.

Authors:  D S Portman; G Dreyfuss
Journal:  EMBO J       Date:  1994-01-01       Impact factor: 11.598

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  1 in total

1.  Antisense transcription through the Xist locus mediates Tsix function in embryonic stem cells.

Authors:  S Luikenhuis; A Wutz; R Jaenisch
Journal:  Mol Cell Biol       Date:  2001-12       Impact factor: 4.272

  1 in total

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