» Articles » PMID: 32052053

The Drosophila MLR COMPASS Complex is Essential for Programming Cis-regulatory Information and Maintaining Epigenetic Memory During Development

Overview
Specialty Biochemistry
Date 2020 Feb 14
PMID 32052053
Citations 3
Authors
Affiliations
Soon will be listed here.
Abstract

The MLR COMPASS complex monomethylates H3K4 that serves to epigenetically mark transcriptional enhancers to drive proper gene expression during animal development. Chromatin enrichment analyses of the Drosophila MLR complex reveals dynamic association with promoters and enhancers in embryos with late stage enrichments biased toward both active and poised enhancers. RNAi depletion of the Cmi (also known as Lpt) subunit that contains the chromatin binding PHD finger domains attenuates enhancer functions, but unexpectedly results in inappropriate enhancer activation during stages when hormone responsive enhancers are poised, revealing critical epigenetic roles involved in both the activation and repression of enhancers depending on developmental context. Cmi is necessary for robust H3K4 monomethylation and H3K27 acetylation that mark active enhancers, but not for the chromatin binding of Trr, the MLR methyltransferase. Our data reveal two likely major regulatory modes of MLR function, contributions to enhancer commissioning in early embryogenesis and bookmarking enhancers to enable rapid transcriptional re-activation at subsequent developmental stages.

Citing Articles

Epigenetic disruption of the RARγ complex impairs its function to bookmark AR enhancer interactions required for enzalutamide sensitivity in prostate cancer.

Wani S, Hussain S, Gray J, Nayak D, Tang H, Perez L bioRxiv. 2024; .

PMID: 38168185 PMC: 10760102. DOI: 10.1101/2023.12.15.571947.


New twists of a TAIL: novel insights into the histone binding properties of a highly conserved PHD finger cluster within the MLR family of H3K4 mono-methyltransferases.

Zraly C, Schultz R, Diaz M, Dingwall A Nucleic Acids Res. 2023; 51(18):9672-9689.

PMID: 37638761 PMC: 10570056. DOI: 10.1093/nar/gkad698.


Notch-dependent and -independent transcription are modulated by tissue movements at gastrulation.

Falo-Sanjuan J, Bray S Elife. 2022; 11.

PMID: 35583918 PMC: 9183233. DOI: 10.7554/eLife.73656.

References
1.
Dorighi K, Swigut T, Henriques T, Bhanu N, Scruggs B, Nady N . Mll3 and Mll4 Facilitate Enhancer RNA Synthesis and Transcription from Promoters Independently of H3K4 Monomethylation. Mol Cell. 2017; 66(4):568-576.e4. PMC: 5662137. DOI: 10.1016/j.molcel.2017.04.018. View

2.
Dhar S, Lee S, Kan P, Voigt P, Ma L, Shi X . Trans-tail regulation of MLL4-catalyzed H3K4 methylation by H4R3 symmetric dimethylation is mediated by a tandem PHD of MLL4. Genes Dev. 2012; 26(24):2749-62. PMC: 3533079. DOI: 10.1101/gad.203356.112. View

3.
Lintas C, Persico A . Unraveling molecular pathways shared by Kabuki and Kabuki-like syndromes. Clin Genet. 2017; 94(3-4):283-295. DOI: 10.1111/cge.12983. View

4.
Oh H, Slattery M, Ma L, Crofts A, White K, Mann R . Genome-wide association of Yorkie with chromatin and chromatin-remodeling complexes. Cell Rep. 2013; 3(2):309-18. PMC: 3633442. DOI: 10.1016/j.celrep.2013.01.008. View

5.
Pherson M, Misulovin Z, Gause M, Dorsett D . Cohesin occupancy and composition at enhancers and promoters are linked to DNA replication origin proximity in . Genome Res. 2019; 29(4):602-612. PMC: 6442380. DOI: 10.1101/gr.243832.118. View