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| Status |
Public on Jul 08, 2020 |
| Title |
lncRNA DIGIT and BRD3 protein form phase-separated condensates to regulate endoderm differentiation |
| Organism |
Homo sapiens |
| Experiment type |
Genome binding/occupancy profiling by high throughput sequencing
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| Summary |
Gene programs that control differentiation are regulated through the interplay between DNA, RNA, and protein. Cooperation among these fundamental cellular components can occur through highly structured interactions connecting domains formed by specific sequences of nucleotides, ribonucleotides, and/or amino acids and also through the assembly of biomolecular condensates. Here, we show that endoderm differentiation is regulated through the interaction of the long noncoding (lnc) RNA DIGITand the bromodomain and extra-terminal (BET) domain family protein BRD3. BRD3 forms phase-separated condensates that contain DIGIT, occupies enhancers of endoderm transcription factors, and is required for endoderm differentiation. Purified BRD3 binds to acetylated histone H3 lysine 18 (H3K18ac) in vitro and occupies regions of the genome enriched in H3K18ac during endoderm differentiation, including the key transcription factors that regulate endoderm differentiation. DIGIT is also enriched in regions of H3K18ac, and depletion of DIGIT results in decreased recruitment of BRD3 to these regions. Our findings support a model where cooperation between DIGIT and BRD3 at regions of H3K18ac regulates the transcription factors that drive endoderm differentiation and suggest a broader role for protein-lncRNA phase-separated condensates as regulators of transcription in development.
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| Overall design |
BRD3 ChIP-seq was performed and analyzed to define the regions of the human genome occupied by BRD3 in human embryonic stem cells (hESCs) and after four days of endoderm differentiation.
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| Contributor(s) |
Daneshvar K, Zhou C, Kratkiewicz AJ, Moran SP, Mullen AC |
| Citation(s) |
32895492 |
| |
| Submission date |
Feb 16, 2019 |
| Last update date |
Oct 07, 2020 |
| Contact name |
Alan C. Mullen |
| E-mail(s) |
mullenlabmgh@gmail.com
|
| Organization name |
Massachusetts General Hospital
|
| Department |
Department of Medicine
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| Street address |
55 Fruit St.
|
| City |
Boston |
| State/province |
MA |
| ZIP/Postal code |
02135 |
| Country |
USA |
| |
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| Platforms (1) |
| GPL11154 |
Illumina HiSeq 2000 (Homo sapiens) |
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| Samples (6)
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| GSM3610697 |
H1_input: ChIP-seq WCE H1 hESC |
| GSM3610698 |
DE_input: ChIP-seq WCE H1 hESC differentiated to definitive endoderm for 4 days |
| GSM3610699 |
H1_BRD3IP_rep1: BRD3 ChIP-seq H1 hESC |
| GSM3610700 |
H1_BRD3IP_rep2: BRD3 ChIP-seq H1 hESC |
| GSM3610701 |
DE_BRD3IP_rep1: BRD3 ChIP-seq H1 hESC differentiated to definitive endoderm for 4 days |
| GSM3610702 |
DE_BRD3IP_rep2: BRD3 ChIP-seq H1 hESC differentiated to definitive endoderm for 4 days |
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| Relations |
| BioProject |
PRJNA522865 |
| SRA |
SRP186093 |
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