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非典型脊椎动物GATA蛋白TRPS1的转录抑制与发育功能

Transcriptional repression and developmental functions of the atypical vertebrate GATA protein TRPS1.

作者信息

Malik T H, Shoichet S A, Latham P, Kroll T G, Peters L L, Shivdasani R A

机构信息

Department of Adult Oncology, Dana-Farber Cancer Institute, Brigham & Women's Hospital and Harvard Medical School, Boston, MA, USA.

出版信息

EMBO J. 2001 Apr 2;20(7):1715-25. doi: 10.1093/emboj/20.7.1715.

Abstract

Known vertebrate GATA proteins contain two zinc fingers and are required in development, whereas invertebrates express a class of essential proteins containing one GATA-type zinc finger. We isolated the gene encoding TRPS1, a vertebrate protein with a single GATA-type zinc finger. TRPS1 is highly conserved between Xenopus and mammals, and the human gene is implicated in dominantly inherited tricho-rhino-phalangeal (TRP) syndromes. TRPS1 is a nuclear protein that binds GATA sequences but fails to transactivate a GATA-dependent reporter. Instead, TRPS1 potently and specifically represses transcriptional activation mediated by other GATA factors. Repression does not occur from competition for DNA binding and depends on a C-terminal region related to repressive domains found in Ikaros proteins. During mouse development, TRPS1 expression is prominent in sites showing pathology in TRP syndromes, which are thought to result from TRPS1 haploinsufficiency. We show instead that truncating mutations identified in patients encode dominant inhibitors of wild-type TRPS1 function, suggesting an alternative mechanism for the disease. TRPS1 is the first example of a GATA protein with intrinsic transcriptional repression activity and possibly a negative regulator of GATA-dependent processes in vertebrate development.

摘要

已知的脊椎动物GATA蛋白含有两个锌指结构,在发育过程中是必需的,而无脊椎动物表达一类含有一个GATA型锌指的必需蛋白。我们分离出了编码TRPS1的基因,TRPS1是一种具有单个GATA型锌指的脊椎动物蛋白。TRPS1在非洲爪蟾和哺乳动物之间高度保守,人类基因与显性遗传的毛发 - 鼻 - 指(趾)综合征(TRP)有关。TRPS1是一种核蛋白,它能结合GATA序列,但不能激活依赖GATA的报告基因。相反,TRPS1能有效且特异性地抑制由其他GATA因子介导的转录激活。这种抑制并非源于对DNA结合的竞争,而是依赖于与Ikaros蛋白中发现的抑制结构域相关的C末端区域。在小鼠发育过程中,TRPS1在TRP综合征中出现病理变化的部位表达显著,而TRP综合征被认为是由TRPS1单倍体不足引起的。相反,我们发现患者中鉴定出的截短突变编码野生型TRPS1功能的显性抑制剂,这提示了该疾病的另一种机制。TRPS1是具有内在转录抑制活性的GATA蛋白的首个例子,可能是脊椎动物发育中GATA依赖过程的负调节因子。

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