Literature DB >> 21353562

Long- and short-range transcriptional repressors induce distinct chromatin states on repressed genes.

Li M Li1, David N Arnosti.   

Abstract

Transcriptional repression is essential for establishing precise patterns of gene expression during development. Repressors governing early Drosophila segmentation can be classified as short- or long-range factors based on their ranges of action, acting either locally to quench adjacent activators or broadly to silence an entire locus. Paradoxically, these repressors recruit common corepressors, Groucho and CtBP, despite their different ranges of repression. To reveal the mechanisms underlying these two distinct modes of repression, we performed chromatin analysis using the prototypical long-range repressor Hairy and the short-range repressor Knirps. Chromatin immunoprecipitation and micrococcal nuclease mapping studies reveal that Knirps causes local changes of histone density and acetylation, and the inhibition of activator recruitment, without affecting the recruitment of basal transcriptional machinery. In contrast, Hairy induces widespread histone deacetylation and inhibits the recruitment of basal machinery without inducing chromatin compaction. Our study provides detailed mechanistic insight into short- and long-range repression on selected endogenous target genes and suggests that the transcriptional corepressors can be differentially deployed to mediate chromatin changes in a context-dependent manner.
Copyright © 2011 Elsevier Ltd. All rights reserved.

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Year:  2011        PMID: 21353562      PMCID: PMC3061390          DOI: 10.1016/j.cub.2011.01.054

Source DB:  PubMed          Journal:  Curr Biol        ISSN: 0960-9822            Impact factor:   10.834


  36 in total

Review 1.  Transcriptional repression: the long and the short of it.

Authors:  A J Courey; S Jia
Journal:  Genes Dev       Date:  2001-11-01       Impact factor: 11.361

2.  Quantitative contributions of CtBP-dependent and -independent repression activities of Knirps.

Authors:  Paolo Struffi; Maria Corado; Meghana Kulkarni; David N Arnosti
Journal:  Development       Date:  2004-05       Impact factor: 6.868

3.  The histone modification pattern of active genes revealed through genome-wide chromatin analysis of a higher eukaryote.

Authors:  Dirk Schübeler; David M MacAlpine; David Scalzo; Christiane Wirbelauer; Charles Kooperberg; Fred van Leeuwen; Daniel E Gottschling; Laura P O'Neill; Bryan M Turner; Jeffrey Delrow; Stephen P Bell; Mark Groudine
Journal:  Genes Dev       Date:  2004-06-01       Impact factor: 11.361

Review 4.  The initiation of pair-rule stripes in the Drosophila blastoderm.

Authors:  S Small; M Levine
Journal:  Curr Opin Genet Dev       Date:  1991-08       Impact factor: 5.578

5.  The caudal gene product is a direct activator of fushi tarazu transcription during Drosophila embryogenesis.

Authors:  C R Dearolf; J Topol; C S Parker
Journal:  Nature       Date:  1989-09-28       Impact factor: 49.962

6.  Fine mapping of chromatin structure in Drosophila melanogaster embryos using micrococcal nuclease.

Authors:  Li M Li; David N Arnosti
Journal:  Fly (Austin)       Date:  2010-07-01       Impact factor: 2.160

7.  A self-organizing system of repressor gradients establishes segmental complexity in Drosophila.

Authors:  Dorothy E Clyde; Maria S G Corado; Xuelin Wu; Adam Paré; Dmitri Papatsenko; Stephen Small
Journal:  Nature       Date:  2003-12-18       Impact factor: 49.962

8.  Pattern abnormalities induced by ectopic expression of the Drosophila gene hairy are associated with repression of ftz transcription.

Authors:  D Ish-Horowicz; S M Pinchin
Journal:  Cell       Date:  1987-11-06       Impact factor: 41.582

9.  Control elements of the Drosophila segmentation gene fushi tarazu.

Authors:  Y Hiromi; A Kuroiwa; W J Gehring
Journal:  Cell       Date:  1985-12       Impact factor: 41.582

10.  Groucho is required for Drosophila neurogenesis, segmentation, and sex determination and interacts directly with hairy-related bHLH proteins.

Authors:  Z Paroush; R L Finley; T Kidd; S M Wainwright; P W Ingham; R Brent; D Ish-Horowicz
Journal:  Cell       Date:  1994-12-02       Impact factor: 41.582

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  28 in total

1.  Multiple enhancers ensure precision of gap gene-expression patterns in the Drosophila embryo.

Authors:  Michael W Perry; Alistair N Boettiger; Michael Levine
Journal:  Proc Natl Acad Sci U S A       Date:  2011-08-08       Impact factor: 11.205

2.  The Central Region of the Drosophila Co-repressor Groucho as a Regulatory Hub.

Authors:  Pak N Kwong; Michael Chambers; Ajay A Vashisht; Wiam Turki-Judeh; Tak Yu Yau; James A Wohlschlegel; Albert J Courey
Journal:  J Biol Chem       Date:  2015-10-19       Impact factor: 5.157

Review 3.  Enhancer biology and enhanceropathies.

Authors:  Edwin Smith; Ali Shilatifard
Journal:  Nat Struct Mol Biol       Date:  2014-03       Impact factor: 15.369

4.  Zygotic pioneer factor activity of Odd-paired/Zic is necessary for late function of the Drosophila segmentation network.

Authors:  Isabella V Soluri; Lauren M Zumerling; Omar A Payan Parra; Eleanor G Clark; Shelby A Blythe
Journal:  Elife       Date:  2020-04-29       Impact factor: 8.140

5.  The snail repressor inhibits release, not elongation, of paused Pol II in the Drosophila embryo.

Authors:  Jacques P Bothma; Joe Magliocco; Michael Levine
Journal:  Curr Biol       Date:  2011-09-14       Impact factor: 10.834

6.  Identification of genomic enhancers through spatial integration of single-cell transcriptomics and epigenomics.

Authors:  Carmen Bravo González-Blas; Xiao-Jiang Quan; Ramon Duran-Romaña; Ibrahim Ihsan Taskiran; Duygu Koldere; Kristofer Davie; Valerie Christiaens; Samira Makhzami; Gert Hulselmans; Maxime de Waegeneer; David Mauduit; Suresh Poovathingal; Sara Aibar; Stein Aerts
Journal:  Mol Syst Biol       Date:  2020-05       Impact factor: 11.429

7.  Hairy and Groucho mediate the action of juvenile hormone receptor Methoprene-tolerant in gene repression.

Authors:  Tusar T Saha; Sang Woon Shin; Wei Dou; Sourav Roy; Bo Zhao; Yuan Hou; Xue-Li Wang; Zhen Zou; Thomas Girke; Alexander S Raikhel
Journal:  Proc Natl Acad Sci U S A       Date:  2016-01-07       Impact factor: 11.205

Review 8.  The embryo as a laboratory: quantifying transcription in Drosophila.

Authors:  Thomas Gregor; Hernan G Garcia; Shawn C Little
Journal:  Trends Genet       Date:  2014-07-06       Impact factor: 11.639

9.  Extensive polymerase pausing during Drosophila axis patterning enables high-level and pliable transcription.

Authors:  Abbie Saunders; Leighton J Core; Catherine Sutcliffe; John T Lis; Hilary L Ashe
Journal:  Genes Dev       Date:  2013-05-15       Impact factor: 11.361

10.  Novel alterations in the epigenetic signature of MeCP2-targeted promoters in lymphocytes of Rett syndrome patients.

Authors:  Tobias Lilja; Karolina Wallenborg; Karin Björkman; Margareta Albåge; Maud Eriksson; Hugo Lagercrantz; Malin Rohdin; Ola Hermanson
Journal:  Epigenetics       Date:  2013-01-24       Impact factor: 4.528

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