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通过对PU.1和GATA-3进行扰动分析来定义T细胞发育的调控网络元件。

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

作者信息

Anderson Michele K, Hernandez-Hoyos Gabriela, Dionne Christopher J, Arias Alexandra M, Chen Dan, Rothenberg Ellen V

机构信息

Division of Biology, California Institute of Technology, Pasadena 91125, USA.

出版信息

Dev Biol. 2002 Jun 1;246(1):103-21. doi: 10.1006/dbio.2002.0674.

Abstract

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.

摘要

PU.1和GATA-3是从最早阶段开始T细胞祖细胞发育所必需的转录因子。然而,它们都不是T细胞谱系特化的简单正调控因子。在T细胞发育早期阶段高水平表达时,这两种转录因子中的每一种都会在不同的特征性时间窗口内阻断T细胞发育,GATA-3过表达最初比PU.1在更早阶段起抑制作用。这些干扰各自与T细胞发育所需基因调控的不同变化谱相关。两种转录因子都能干扰Rag-1和Rag-2重组酶的表达,而GATA-3特别阻断PU.1和IL-7Rα的表达,PU.1则降低HES-1和c-Myb的表达。这两种因子的调控靶点的初稿组装作为一个临时基因网络呈现。这里鉴定出的靶基因有助于深入了解GATA-3或PU.1过表达效应的基础,以及区分这些效应的发育时间窗口的调控变化。

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