Definition of regulatory network elements for T cell development by perturbation analysis with PU.1 and GATA-3

被引:67
作者
Anderson, MK
Hernandez-Hoyos, G
Dionne, CJ
Arias, AM
Chen, D
Rothenberg, EV [1 ]
机构
[1] CALTECH, Div Biol, Pasadena, CA 91125 USA
[2] Genencor Int Inc, Palo Alto, CA 94304 USA
关键词
T cell development; fetal thymus organ culture; GATA-3; PU.1; Ets family; retroviral transduction; IL-7; receptor; c-Myb; HES-1; pre-TCR;
D O I
10.1006/dbio.2002.0674
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
PU.1 and GATA-3 are transcription factors that are required for development of T cell progenitors from the earliest stages. Neither one is a simple positive regulator for T lineage specification, however. When expressed at elevated levels at early stages of T cell development, each of these transcription factors blocks T cell development within a different, characteristic time window, with GATA-3 overexpression initially inhibiting at an earlier stage than PU.1. These perturbations are each associated with a distinct spectrum of changes in the regulation of genes needed for T cell development. Both transcription factors can interfere with expression of the Rag-1 and Rag-2 recombinases, while GATA-3 notably blocks PU.1 and IL-7Ralpha expression, and PU.1 reduces expression of HES-1 and c-Myb. A first-draft assembly of the regulatory targets of these two factors is presented as a provisional gene network. The target genes identified here provide insight into the basis of the effects of GATA-3 or PU.1 overexpression and into the regulatory changes that distinguish the developmental time windows for these effects. (C) 2002 Elsevier Science (USA).
引用
收藏
页码:103 / 121
页数:19
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