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GATA蛋白的Friend U形在果蝇中作为造血肿瘤抑制因子发挥作用。

The Friend of GATA protein U-shaped functions as a hematopoietic tumor suppressor in Drosophila.

作者信息

Sorrentino Richard Paul, Tokusumi Tsuyoshi, Schulz Robert A

机构信息

Department of Biochemistry and Molecular Biology, The University of Texas M. D. Anderson Cancer Center, 1515 Holcombe Boulevard, Houston, TX 77030, USA.

出版信息

Dev Biol. 2007 Nov 15;311(2):311-23. doi: 10.1016/j.ydbio.2007.08.011. Epub 2007 Aug 16.

Abstract

Drosophila has emerged as an important model system to discover and analyze genes controlling hematopoiesis. One regulatory network known to control hemocyte differentiation is the Janus kinase (JAK)/Signal Transducer and Activator of Transcription (STAT) signal-transduction pathway. A constitutive activation mutation of the Janus kinase Hopscotch (hopscotch(Tumorous-lethal); hop(Tum-l)) results in a leukemia-like over-proliferation of hemocytes and copious differentiation of lamellocytes during larval stages. Here we show that the Friend of GATA (FOG) protein U-shaped (Ush) is expressed in circulating and lymph gland hemocytes, where it plays a critical role in controlling blood cell proliferation and differentiation. Our findings demonstrate that a reduction in ush function results in hematopoietic phenotypes strikingly similar to those observed in hop(Tum-l) animals. These include lymph gland hypertrophy, increased circulating hemocyte concentration, and abundant production of lamellocytes. Forced expression of N-terminal truncated versions of Ush likewise leads to larvae with severe hematopoietic anomalies. In contrast, expression of wild-type Ush results in a strong suppression of hop(Tum-l) phenotypes. Taken together, our findings demonstrate that U-shaped acts to control larval hemocyte proliferation and suppress lamellocyte differentiation, likely regulating hematopoietic events downstream of Hop kinase activity. Such functions appear to be facilitated through Ush interaction with the hematopoietic GATA factor Serpent (Srp).

摘要

果蝇已成为发现和分析控制造血作用基因的重要模型系统。已知控制血细胞分化的一个调控网络是Janus激酶(JAK)/信号转导子与转录激活子(STAT)信号转导途径。Janus激酶跳房子(hopscotch(Tumorous-lethal); hop(Tum-l))的组成型激活突变会导致血细胞出现白血病样过度增殖,并且在幼虫阶段会大量分化出扁平细胞。在此我们表明,GATA结合因子(FOG)蛋白U型(Ush)在循环血细胞和淋巴腺血细胞中表达,它在控制血细胞增殖和分化中起关键作用。我们的研究结果表明,ush功能的降低会导致造血表型,与在hop(Tum-l)动物中观察到的表型惊人地相似。这些表型包括淋巴腺肥大、循环血细胞浓度增加以及大量产生扁平细胞。强制表达Ush的N端截短版本同样会导致幼虫出现严重的造血异常。相反,野生型Ush的表达会强烈抑制hop(Tum-l)表型。综上所述,我们的研究结果表明,U型蛋白起到控制幼虫血细胞增殖和抑制扁平细胞分化的作用,可能在Hop激酶活性下游调节造血事件。这种功能似乎是通过Ush与造血GATA因子蛇形蛋白(Srp)的相互作用来实现的。

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