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PMID: 21423168 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

A long noncoding RNA maintains active chromatin to coordinate homeotic gene expression.

Nature ·Vol. 472 ·No. 7341 ·2011-04-07 ·Pages 120-4

Wang KC, Yang YW, Liu B, Sanyal A, Corces-Zimmerman R, Chen Y, Lajoie BR, Protacio A, Flynn RA, Gupta RA, Wysocka J, Lei M, Dekker J, Helms JA, Chang HY

Abstract

The genome is extensively transcribed into long intergenic noncoding RNAs (lincRNAs), many of which are implicated in gene silencing. Potential roles of lincRNAs in gene activation are much less understood. Development and homeostasis require coordinate regulation of neighbouring genes through a process termed locus control. Some locus control elements and enhancers transcribe lincRNAs, hinting at possible roles in long-range control. In vertebrates, 39 Hox genes, encoding homeodomain transcription factors critical for positional identity, are clustered in four chromosomal loci; the Hox genes are expressed in nested anterior-posterior and proximal-distal patterns colinear with their genomic position from 3' to 5'of the cluster. Here we identify HOTTIP, a lincRNA transcribed from the 5' tip of the HOXA locus that coordinates the activation of several 5' HOXA genes in vivo. Chromosomal looping brings HOTTIP into close proximity to its target genes. HOTTIP RNA binds the adaptor protein WDR5 directly and targets WDR5/MLL complexes across HOXA, driving histone H3 lysine 4 trimethylation and gene transcription. Induced proximity is necessary and sufficient for HOTTIP RNA activation of its target genes. Thus, by serving as key intermediates that transmit information from higher order chromosomal looping into chromatin modifications, lincRNAs may organize chromatin domains to coordinate long-range gene activation.

MeSH Terms
Animals Cell Line Cells, Cultured Chromatin/genetics,metabolism DNA, Intergenic/genetics Embryo, Mammalian/metabolism Fibroblasts/metabolism Gene Expression Regulation, Developmental/genetics Gene Knockdown Techniques Genes, Homeobox/genetics Histone-Lysine N-Methyltransferase/metabolism Histones/chemistry,metabolism Humans Intracellular Signaling Peptides and Proteins Lysine/metabolism Methylation Mice Molecular Sequence Data Multigene Family/genetics Organ Specificity RNA, Untranslated/genetics Transcription, Genetic
Chemicals
Chromatin DNA, Intergenic Histones Intracellular Signaling Peptides and Proteins RNA, Untranslated WDR5 protein, human Histone-Lysine N-Methyltransferase Lysine
Authors & Affiliations
15 authors, click to expand affiliations / ORCID
Wang Kevin C
Howard Hughes Medical Institute, Program in Epithelial Biology, Stanford University School of Medicine, Stanford, California 94305, USA.
Yang Yul W
Liu Bo
Sanyal Amartya
Corces-Zimmerman Ryan
Chen Yong
Lajoie Bryan R
Protacio Angeline
Flynn Ryan A
Gupta Rajnish A
Wysocka Joanna
Lei Ming
Dekker Job
Helms Jill A
Chang Howard Y
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Article Info
Journal
Nature
Abbr.
Nature
ISSN
1476-4687
Published
2011-04-07
Epub
2011-00-20
Pages
120-4
Language
English
Region
England
NLM ID
0410462
PMCID
PMC3670758
Subset
IM
Grants
NHGRI NIH HHS · HG003143 · United States
NHGRI NIH HHS · R01 HG003143 · United States
Howard Hughes Medical Institute · United States
NHGRI NIH HHS · R01 HG003143-06S2 · United States
NHGRI NIH HHS · R01 HG003143-06S1 · United States
NHGRI NIH HHS · R01 HG003143-06 · United States
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