Literature DB >> 23818637

Transgene- and locus-dependent imprinting reveals allele-specific chromosome conformations.

Nicolas Lonfat1, Thomas Montavon, David Jebb, Patrick Tschopp, Thi Hanh Nguyen Huynh, Jozsef Zakany, Denis Duboule.   

Abstract

When positioned into the integrin α-6 gene, an Hoxd9lacZ reporter transgene displayed parental imprinting in mouse embryos. While the expression from the paternal allele was comparable with patterns seen for the same transgene when present at the neighboring HoxD locus, almost no signal was scored at this integration site when the transgene was inherited from the mother, although the Itga6 locus itself is not imprinted. The transgene exhibited maternal allele-specific DNA hypermethylation acquired during oogenesis, and its expression silencing was reversible on passage through the male germ line. Histone modifications also corresponded to profiles described at known imprinted loci. Chromosome conformation analyses revealed distinct chromatin microarchitectures, with a more compact structure characterizing the maternally inherited repressed allele. Such genetic analyses of well-characterized transgene insertions associated with a de novo-induced parental imprint may help us understand the molecular determinants of imprinting.

Entities:  

Keywords:  Hox genes; architecture; enhancer; epigenetic

Mesh:

Substances:

Year:  2013        PMID: 23818637      PMCID: PMC3718164          DOI: 10.1073/pnas.1310704110

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


  54 in total

1.  Highly conserved syntenic blocks at the vertebrate Hox loci and conserved regulatory elements within and outside Hox gene clusters.

Authors:  Alison P Lee; Esther G L Koh; Alice Tay; Sydney Brenner; Byrappa Venkatesh
Journal:  Proc Natl Acad Sci U S A       Date:  2006-04-24       Impact factor: 11.205

2.  Computational and experimental identification of novel human imprinted genes.

Authors:  Philippe P Luedi; Fred S Dietrich; Jennifer R Weidman; Jason M Bosko; Randy L Jirtle; Alexander J Hartemink
Journal:  Genome Res       Date:  2007-11-30       Impact factor: 9.043

3.  Modeling Hox gene regulation in digits: reverse collinearity and the molecular origin of thumbness.

Authors:  Thomas Montavon; Jean-François Le Garrec; Michel Kerszberg; Denis Duboule
Journal:  Genes Dev       Date:  2008-02-01       Impact factor: 11.361

4.  A regulatory 'landscape effect' over the HoxD cluster.

Authors:  Patrick Tschopp; Denis Duboule
Journal:  Dev Biol       Date:  2010-12-30       Impact factor: 3.582

Review 5.  Genomic imprinting: the emergence of an epigenetic paradigm.

Authors:  Anne C Ferguson-Smith
Journal:  Nat Rev Genet       Date:  2011-07-18       Impact factor: 53.242

6.  PRMT5-mediated methylation of histone H4R3 recruits DNMT3A, coupling histone and DNA methylation in gene silencing.

Authors:  Quan Zhao; Gerhard Rank; Yuen T Tan; Haitao Li; Robert L Moritz; Richard J Simpson; Loretta Cerruti; David J Curtis; Dinshaw J Patel; C David Allis; John M Cunningham; Stephen M Jane
Journal:  Nat Struct Mol Biol       Date:  2009-02-22       Impact factor: 15.369

7.  Structure of Dnmt3a bound to Dnmt3L suggests a model for de novo DNA methylation.

Authors:  Da Jia; Renata Z Jurkowska; Xing Zhang; Albert Jeltsch; Xiaodong Cheng
Journal:  Nature       Date:  2007-08-22       Impact factor: 49.962

8.  BISMA--fast and accurate bisulfite sequencing data analysis of individual clones from unique and repetitive sequences.

Authors:  Christian Rohde; Yingying Zhang; Richard Reinhardt; Albert Jeltsch
Journal:  BMC Bioinformatics       Date:  2010-05-06       Impact factor: 3.169

Review 9.  Genomic imprinting disorders in humans: a mini-review.

Authors:  Merlin G Butler
Journal:  J Assist Reprod Genet       Date:  2009-10-21       Impact factor: 3.412

10.  Impact of copy number variations (CNVs) on long-range gene regulation at the HoxD locus.

Authors:  Thomas Montavon; Laurie Thevenet; Denis Duboule
Journal:  Proc Natl Acad Sci U S A       Date:  2012-11-07       Impact factor: 11.205

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  2 in total

1.  Implications of COMT long-range interactions on the phenotypic variability of 22q11.2 deletion syndrome.

Authors:  Michael J Zeitz; Paula P Lerner; Ferhat Ay; Eric Van Nostrand; Julia D Heidmann; William S Noble; Andrew R Hoffman
Journal:  Nucleus       Date:  2013-12-05       Impact factor: 4.197

2.  A Mouse Model for Imprinting of the Human Retinoblastoma Gene.

Authors:  Vasiliki Tasiou; Michaela Hiber; Laura Steenpass
Journal:  PLoS One       Date:  2015-08-14       Impact factor: 3.240

  2 in total

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