» Articles » PMID: 21353562

Long- and Short-range Transcriptional Repressors Induce Distinct Chromatin States on Repressed Genes

Overview
Journal Curr Biol
Publisher Cell Press
Specialty Biology
Date 2011 Mar 1
PMID 21353562
Citations 35
Authors
Affiliations
Soon will be listed here.
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.

Citing Articles

Optogenetic dissection of transcriptional repression in a multicellular organism.

Zhao J, Lammers N, Alamos S, Kim Y, Martini G, Garcia H Nat Commun. 2024; 15(1):9263.

PMID: 39461978 PMC: 11513125. DOI: 10.1038/s41467-024-53539-0.


A regulatory role for the unstructured C-terminal domain of the CtBP transcriptional corepressor.

Raicu A, Suresh M, Arnosti D J Biol Chem. 2023; 300(1):105490.

PMID: 38000659 PMC: 10788531. DOI: 10.1016/j.jbc.2023.105490.


Long-range repression by ecdysone receptor on complex enhancers of the insulin receptor gene.

Thompson K, Suber W, Nicholas R, Arnosti D Fly (Austin). 2023; 17(1):2242238.

PMID: 37621079 PMC: 10461493. DOI: 10.1080/19336934.2023.2242238.


How enhancers regulate wavelike gene expression patterns.

Mau C, Rudolf H, Strobl F, Schmid B, Regensburger T, Palmisano R Elife. 2023; 12.

PMID: 37432987 PMC: 10368423. DOI: 10.7554/eLife.84969.


Long-range repression by ecdysone receptor on complex enhancers of the insulin receptor gene.

Thompson K, Suber W, Nicholas R, Arnosti D bioRxiv. 2023; .

PMID: 37293119 PMC: 10245858. DOI: 10.1101/2023.05.23.541945.


References
1.
Clyde D, Corado M, Wu X, Pare A, Papatsenko D, Small S . A self-organizing system of repressor gradients establishes segmental complexity in Drosophila. Nature. 2003; 426(6968):849-53. DOI: 10.1038/nature02189. View

2.
Ish-Horowicz D, Pinchin S . Pattern abnormalities induced by ectopic expression of the Drosophila gene hairy are associated with repression of ftz transcription. Cell. 1987; 51(3):405-15. DOI: 10.1016/0092-8674(87)90636-2. View

3.
Calhoun V, Levine M . Long-range enhancer-promoter interactions in the Scr-Antp interval of the Drosophila Antennapedia complex. Proc Natl Acad Sci U S A. 2003; 100(17):9878-83. PMC: 187872. DOI: 10.1073/pnas.1233791100. View

4.
Ardehali M, Yao J, Adelman K, Fuda N, Petesch S, Webb W . Spt6 enhances the elongation rate of RNA polymerase II in vivo. EMBO J. 2009; 28(8):1067-77. PMC: 2683705. DOI: 10.1038/emboj.2009.56. View

5.
Li L, Arnosti D . Fine mapping of chromatin structure in Drosophila melanogaster embryos using micrococcal nuclease. Fly (Austin). 2010; 4(3):213-5. PMC: 3322504. DOI: 10.4161/fly.4.3.12200. View