|
|
GEO help: Mouse over screen elements for information. |
|
Status |
Public on Jun 12, 2009 |
Title |
Genome-wide Analysis of Histone Methylations in Memory CD8+ T Cells |
Organism |
Homo sapiens |
Experiment type |
Genome binding/occupancy profiling by high throughput sequencing
|
Summary |
Histone methylations play a major role in regulating the chromatin state and gene expression, yet little is known about their involvement in differential gene expression and function of memory CD8 T cells. Here, we report a genome-wide analysis of two histone H3 methylations (H3K4me3 and H3K27me3) and gene expression in naïve, central (TCM) and effector (TEM) memory CD8 T cells. Analysis of 16,314 annotated genes in CD8 T cell subsets revealed that gene expression were positively correlated with the levels of H3K4me3 and negatively correlated with the levels of H3K27me3 in these gene loci. The correlation between differential H3K4me3 orH3K27me3 levels with gene expressions in memory CD8 T cells displayed four distinct modes: repressive, active, poised, and bivalent, reflecting their complex regulation and different function of these genes. Furthermore, accessible chromatin states of different gene loci were preferentially influenced by different histone modifications as demonstrated here high levels of H3K9ac found in active gene loci without high levels of H3K4me3. These findings reveal a histone methylation based complex regulation of differential gene expression in memory CD8 T cells. Thus, change of chromatin structure mediated by histone methylation may serve a fundamental basis for the rapid transcriptional response of memory CD8 T cells.
|
|
|
Overall design |
genome-wide analysis of two histone H3 methylations (H3K4me3 and H3K27me3) in naïve, central (TCM) and effector (TEM) memory CD8 T cells.
|
|
|
Contributor(s) |
Araki Y, Wang Z, Zang C, Wood W, Schones DE, Cui K, Roh T, Lhotsky B, Wersto R, Peng W, Becker K, Zhao K, Weng N |
Citation(s) |
19523850 |
|
Submission date |
Aug 29, 2008 |
Last update date |
May 15, 2019 |
Contact name |
Chongzhi Zang |
Organization name |
University of Virginia
|
Street address |
P. O. Box 800717
|
City |
Charlottesville |
State/province |
VA |
ZIP/Postal code |
22908 |
Country |
USA |
|
|
Platforms (1) |
GPL9052 |
Illumina Genome Analyzer (Homo sapiens) |
|
Samples (6)
|
|
Relations |
SRA |
SRP000828 |
BioProject |
PRJNA113077 |
Supplementary file |
Size |
Download |
File type/resource |
GSE12616_RAW.tar |
340.8 Mb |
(http)(custom) |
TAR (of BED, GRAPH) |
SRA Run Selector |
Raw data are available in SRA |
Processed data provided as supplementary file |
|
|
|
|
|