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| Status |
Public on Jan 31, 2011 |
| Title |
Global Mapping of H3K4me1 and H3K4me3 in human CD4+CD25+FOXP3+ Treg cells |
| Organism |
Homo sapiens |
| Experiment type |
Genome binding/occupancy profiling by high throughput sequencing
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| Summary |
Regulatory T cells (Treg) contribute to the crucial immunological processes of self-tolerance and immune homeostasis. However, the mechanisms underlying Treg function and cell fate decisions to differentiate between Treg and conventional T cells (Tconv) remain to be fully elucidated, especially at the histone modification level. Covalent modifications of histones establish and maintain chromatin structure, and regulate gene transcription events by facilitating access to cis-elements by trans-acting factors during mammalian development and cellular differentiation. We aimed to investigate the role of the methylation form of histone modification as related to Treg function and phenotype. High-resolution maps of the genome-wide distribution of monomethylated histone H3 lysine 4, H3K4me1, and the trimethylated form H3K4me3 were generated for human activated conventional CD4+CD25+FOXP3- T cells (aTconv) and CD4+CD25+FOXP3+ regulatory T cells (Treg) by sequencing using the Solexa 1G Genetic Analyzer. We found 2115 H3K4me3 regions corresponding to proximal promoter regions; the genes associated with these regions in Treg cells included the crucial transcription factor forkhead box P3 (FOXP3) and the chemokine receptor CCR7. We also identified 41024 Treg cell type-specific H3K4me1 regions. The majority of the H3K4me1 regions differing between the Treg and aTconv cells were located at promoter-distal sites, some of which were selected and consolidated to further examine enhancer activity in in vitro reporter gene assays. The findings from our study provide a comprehensive genome-wide dataset of lineage-specific H3K4me1 and H3K4me3 patterns in Treg and aTconv cells, which may control the differentiation decision, lineage commitment and cell type-specific gene regulation. This basic principle is likely not confined to the two closely-related T cell populations, but may apply generally to somatic cell lineages in adult organisms.
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| Overall design |
Genome-wide distribution of monomethylated histone H3 lysine 4, H3K4me1, and the trimethylated form H3K4me3 in human activated conventional CD4+CD25+FOXP3- T cells (aTconv) and CD4+CD25+FOXP3+ regulatory T cells (Treg) (5 samples in total)
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| Contributor(s) |
Tian Y, Jia Z, Wang J, Song J, Huang Z, Zheng Y, Fu X, Tang Y, Yang D, Tang J, Wang Q, Tian Z, Zhang Y, Wu Y, Ni B |
| Citation(s) |
22132139 |
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| Submission date |
Jan 04, 2011 |
| Last update date |
May 15, 2019 |
| Contact name |
Ni Bing |
| E-mail(s) |
nibingxi@yahoo.com
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| Phone |
+86-23-68772348
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| Fax |
+86-23-68772348
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| Organization name |
PLA, Third Military Medical University
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| Department |
Institute of Immunology
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| Street address |
PLA, Third Military Medical University
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| City |
Chongqing |
| ZIP/Postal code |
400038 |
| Country |
China |
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| Platforms (1) |
| GPL9052 |
Illumina Genome Analyzer (Homo sapiens) |
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| Samples (5)
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| Relations |
| SRA |
SRP005179 |
| BioProject |
PRJNA136807 |
| Supplementary file |
Size |
Download |
File type/resource |
| GSE26427_RAW.tar |
117.6 Mb |
(http)(custom) |
TAR (of BED, TAR, TXT) |
SRA Run Selector |
| Raw data are available in SRA |
| Processed data provided as supplementary file |
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