Literature DB >> 2272520

Insights into X chromosome inactivation from studies of species variation, DNA methylation and replication, and vice versa.

B R Migeon1.   

Abstract

I am indebted to Mary Lyon as her X-inactivation hypothesis stimulated my mentor, Barton Childs, and in turn, myself, to think about the consequences of X-inactivation in heterozygous females. I often reread her original papers setting forth the single active X hypothesis, and still marvel at the concise and compelling exposition of the hypothesis and the logical predictions which seemed prophetic at my first reading, and have survived the test of time. My contribution to this Festschrift reviews evidence derived from studies of DNA methylation, species variation and DNA replication that reveals an important role for methylated CpG islands and suggests a role for late DNA replication in propagating X inactivation from one cell to its progeny. These studies also show that X inactivation is a powerful research tool for identifying the factors which program and maintain developmental processes.

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Year:  1990        PMID: 2272520     DOI: 10.1017/s0016672300035151

Source DB:  PubMed          Journal:  Genet Res        ISSN: 0016-6723            Impact factor:   1.588


  10 in total

1.  Genomic landscape of human allele-specific DNA methylation.

Authors:  Fang Fang; Emily Hodges; Antoine Molaro; Matthew Dean; Gregory J Hannon; Andrew D Smith
Journal:  Proc Natl Acad Sci U S A       Date:  2012-04-20       Impact factor: 11.205

2.  Differential underacetylation of histones H2A, H3 and H4 on the inactive X chromosome in human female cells.

Authors:  N Belyaev; A M Keohane; B M Turner
Journal:  Hum Genet       Date:  1996-05       Impact factor: 4.132

3.  Identification of TSIX, encoding an RNA antisense to human XIST, reveals differences from its murine counterpart: implications for X inactivation.

Authors:  B R Migeon; A K Chowdhury; J A Dunston; I McIntosh
Journal:  Am J Hum Genet       Date:  2001-09-12       Impact factor: 11.025

4.  Asynchronous DNA replication between 15q11.2q12 homologs: cytogenetic evidence for maternal imprinting and delayed replication.

Authors:  M S Lin; A Zhang; A Fujimoto
Journal:  Hum Genet       Date:  1995-11       Impact factor: 4.132

5.  DNA methylation of the X chromosomes of the human female: an in situ semi-quantitative analysis.

Authors:  J Bernardino; E Lamoliatte; M Lombard; A Niveleau; B Malfoy; B Dutrillaux; C A Bourgeois
Journal:  Chromosoma       Date:  1996-04       Impact factor: 4.316

6.  A potentially critical Hpa II site of the X chromosome-linked PGK1 gene is unmethylated prior to the onset of meiosis of human oogenic cells.

Authors:  J Singer-Sam; L Goldstein; A Dai; S M Gartler; A D Riggs
Journal:  Proc Natl Acad Sci U S A       Date:  1992-02-15       Impact factor: 11.205

7.  Inheritance of the fragile X syndrome: size of the fragile X premutation is a major determinant of the transition to full mutation.

Authors:  D Heitz; D Devys; G Imbert; C Kretz; J L Mandel
Journal:  J Med Genet       Date:  1992-11       Impact factor: 6.318

8.  Differential transcription of the human spermidine/spermine N1-acetyltransferase (SSAT) gene in human lung carcinoma cells.

Authors:  L Xiao; R A Casero
Journal:  Biochem J       Date:  1996-01-15       Impact factor: 3.857

9.  Distinct hypermethylation patterns occur at altered chromosome loci in human lung and colon cancer.

Authors:  M Makos; B D Nelkin; M I Lerman; F Latif; B Zbar; S B Baylin
Journal:  Proc Natl Acad Sci U S A       Date:  1992-03-01       Impact factor: 11.205

Review 10.  The distribution of genes on chromosomes: a cytological approach.

Authors:  A T Sumner; J de la Torre; L Stuppia
Journal:  J Mol Evol       Date:  1993-08       Impact factor: 2.395

  10 in total

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