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Lhx2/Ldb1-mediated trans interactions regulate olfactory receptor choice

The genome is partitioned into topologically associated domains (TADs) and genomic compartments of shared chromatin valance. This architecture is constrained by the DNA polymer, which precludes genic interactions between chromosomes. Here, we report a dramatic divergence from this pattern of nuclear...

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Autores principales: Monahan, K, Horta, A, Lomvardas, S
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6436840/
https://www.ncbi.nlm.nih.gov/pubmed/30626972
http://dx.doi.org/10.1038/s41586-018-0845-0
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author Monahan, K
Horta, A
Lomvardas, S
author_facet Monahan, K
Horta, A
Lomvardas, S
author_sort Monahan, K
collection PubMed
description The genome is partitioned into topologically associated domains (TADs) and genomic compartments of shared chromatin valance. This architecture is constrained by the DNA polymer, which precludes genic interactions between chromosomes. Here, we report a dramatic divergence from this pattern of nuclear organization that occurs in mouse olfactory sensory neurons (OSNs). In situ HiC on FAC-sorted OSNs and their progenitors shows that olfactory receptor (OR) gene clusters from 18 chromosomes make specific and robust interchromosomal contacts that increase with differentiation. These contacts are orchestrated by intergenic OR enhancers, the Greek Islands, which first contribute to the formation of OR compartments and then form a multi-chromosomal super-enhancer that associates with the single active OR. Greek Island-bound transcription factor Lhx2 and adaptor protein Ldb1 regulate the assembly and maintenance of OR compartments, Greek Island hubs, and OR transcription, providing mechanistic insight and functional support for the role of trans interactions in gene expression.
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spelling pubmed-64368402019-07-09 Lhx2/Ldb1-mediated trans interactions regulate olfactory receptor choice Monahan, K Horta, A Lomvardas, S Nature Article The genome is partitioned into topologically associated domains (TADs) and genomic compartments of shared chromatin valance. This architecture is constrained by the DNA polymer, which precludes genic interactions between chromosomes. Here, we report a dramatic divergence from this pattern of nuclear organization that occurs in mouse olfactory sensory neurons (OSNs). In situ HiC on FAC-sorted OSNs and their progenitors shows that olfactory receptor (OR) gene clusters from 18 chromosomes make specific and robust interchromosomal contacts that increase with differentiation. These contacts are orchestrated by intergenic OR enhancers, the Greek Islands, which first contribute to the formation of OR compartments and then form a multi-chromosomal super-enhancer that associates with the single active OR. Greek Island-bound transcription factor Lhx2 and adaptor protein Ldb1 regulate the assembly and maintenance of OR compartments, Greek Island hubs, and OR transcription, providing mechanistic insight and functional support for the role of trans interactions in gene expression. 2019-01-09 2019-01 /pmc/articles/PMC6436840/ /pubmed/30626972 http://dx.doi.org/10.1038/s41586-018-0845-0 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Monahan, K
Horta, A
Lomvardas, S
Lhx2/Ldb1-mediated trans interactions regulate olfactory receptor choice
title Lhx2/Ldb1-mediated trans interactions regulate olfactory receptor choice
title_full Lhx2/Ldb1-mediated trans interactions regulate olfactory receptor choice
title_fullStr Lhx2/Ldb1-mediated trans interactions regulate olfactory receptor choice
title_full_unstemmed Lhx2/Ldb1-mediated trans interactions regulate olfactory receptor choice
title_short Lhx2/Ldb1-mediated trans interactions regulate olfactory receptor choice
title_sort lhx2/ldb1-mediated trans interactions regulate olfactory receptor choice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6436840/
https://www.ncbi.nlm.nih.gov/pubmed/30626972
http://dx.doi.org/10.1038/s41586-018-0845-0
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