A genome wide transcriptional model of the complex response to pre-TCR signalling during thymocyte differentiation

被引：16

作者：

Sahni, Hemant ^{[1
]}

Ross, Susan ^{[1
]}

Barbarulo, Alessandro ^{[1
]}

Solanki, Anisha ^{[1
]}

Lau, Ching-In ^{[1
]}

Furmanski, Anna ^{[1
]}

Saldana, Jose Ignacio ^{[1
]}

Ono, Masahiro ^{[1
]}

Hubank, Mike ^{[1
]}

Barenco, Martino ^{[1
]}

Crompton, Tessa ^{[1
]}

机构：

[1] UCL, Inst Child Hlth, London WC1N 1EH, England

来源：

ONCOTARGET | 2015年 / 6卷 / 30期

基金：

英国生物技术与生命科学研究理事会; 英国惠康基金;

关键词：

pre-TCR; thymus; foetal thymic organ cultures; DP; genome wide transcriptional modelling; Immunology Section; Immune response; Immunity; ACUTE LYMPHOBLASTIC-LEUKEMIA; T-CELL DEVELOPMENT; EXPRESSION; PROLIFERATION; ACTIVATION; MICE; IL-7;

D O I：

10.18632/oncotarget.5796

中图分类号：

R73 [肿瘤学];

学科分类号：

100214 ;

摘要：

Developing thymocytes require pre-TCR signalling to differentiate from CD4-CD8- double negative to CD4+CD8+ double positive cell. Here we followed the transcriptional response to pre-TCR signalling in a synchronised population of differentiating double negative thymocytes. This time series analysis revealed a complex transcriptional response, in which thousands of genes were up and downregulated before changes in cell surface phenotype were detected. Genome-wide measurement of RNA degradation of individual genes showed great heterogeneity in the rate of degradation between different genes. We therefore used time course expression and degradation data and a genome wide transcriptional modelling (GWTM) strategy to model the transcriptional response of genes up-regulated on pre-TCR signal transduction. This analysis revealed five major temporally distinct transcriptional activities that up regulate transcription through time, whereas downregulation of expression occurred in three waves. Our model thus placed known regulators in a temporal perspective, and in addition identified novel candidate regulators of thymocyte differentiation.

引用

页码：28646 / 28660

页数：15

共 54 条

[1] Constitutive pre-TCR signaling promotes differentiation through Ca2+ mobilization and activation of NF-κB and NFAT [J].