Schwartz Ruth, Engel Isaac, Fallahi-Sichani Mohammad, Petrie Howard T, Murre Cornelis
Division of Biological Sciences, University of California at San Diego, La Jolla, CA 92093-0377, USA.
Proc Natl Acad Sci U S A. 2006 Jun 27;103(26):9976-81. doi: 10.1073/pnas.0603728103. Epub 2006 Jun 16.
In maturing T lineage cells, the helix-loop-helix protein E47 has been shown to enforce a critical proliferation and developmental checkpoint commonly referred to as beta selection. To examine how E47 regulates cellular expansion and developmental progression, we have used an E2A-deficient lymphoma cell line and DNA microarray analysis to identify immediate E47 target genes. Hierarchical cluster analysis of gene expression patterns revealed that E47 coordinately regulates the expression of genes involved in cell survival, cell cycle progression, lipid metabolism, stress response, and lymphoid maturation. These include Plcgamma2, Cdk6, CD25, Tox, Gadd45a, Gadd45b, Gfi1, Gfi1b, Socs1, Socs3, Id2, Eto2, and Xbp1. We propose a regulatory network linking Janus kinase (JAK)/signal transducer and activator of transcription (STAT)-mediated signaling, E47, and suppressor of cytokine signaling (SOCS) proteins in a common pathway. Finally, we suggest that the aberrant activation of Cdk6 in E47-deficient T lineage cells contributes to the development of lymphoid malignancy.
在成熟的T细胞谱系细胞中,螺旋-环-螺旋蛋白E47已被证明可执行一个关键的增殖和发育检查点,通常称为β选择。为了研究E47如何调节细胞扩增和发育进程,我们使用了一种E2A缺陷的淋巴瘤细胞系和DNA微阵列分析来鉴定E47的直接靶基因。基因表达模式的层次聚类分析表明,E47协同调节参与细胞存活、细胞周期进程、脂质代谢、应激反应和淋巴细胞成熟的基因表达。这些基因包括Plcgamma2、Cdk6、CD25、Tox、Gadd45a、Gadd45b、Gfi1、Gfi1b、Socs1、Socs3、Id2、Eto2和Xbp1。我们提出了一个调控网络,该网络在一个共同途径中连接了Janus激酶(JAK)/信号转导子和转录激活子(STAT)介导的信号传导、E47和细胞因子信号传导抑制因子(SOCS)蛋白。最后,我们认为E47缺陷的T细胞谱系细胞中Cdk6的异常激活促成了淋巴恶性肿瘤的发生。