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盘基网柄菌STAT蛋白Dd-STATa在内部基盘细胞分化中发挥作用的证据以及对这些细胞中表达所必需的启动子元件的鉴定。

Evidence that the Dictyostelium STAT protein Dd-STATa plays a role in the differentiation of inner basal disc cells and identification of a promoter element essential for expression in these cells.

作者信息

Shimada Nao, Maruo Toshinari, Maeda Mineko, Urushihara Hideko, Kawata Takefumi

机构信息

Department of Biology, Faculty of Science, Toho University, Funabashi, Chiba 274-8510, Japan.

出版信息

Differentiation. 2005 Feb;73(1):50-60. doi: 10.1111/j.1432-0436.2005.07301001.x.

Abstract

Dd-STATa, a Dictyostelium homolog of the metazoan STAT (signal transducers and activators of transcription) proteins, is necessary in the slug for correct entry into culmination. Dd-STATa-null mutant fails to culminate and its phenotype correlates with the loss of a funnel-shaped core region, the pstAB core region, which expresses both the ecmA and ecmB genes. To understand how the differentiation of pstAB core cells is regulated, we identified an EST that is expressed in the core cells of normal slugs but down-regulated in the Dd-STATa-null mutant. This EST, SSK348, encodes a close homolog of the Dictyostelium acetyl-CoA synthetase (ACS). A promoter fragment of the cognate gene, aslA (acetyl-CoA synthetase-like A), was fused to a lacZ reporter and the expression pattern determined. As expected from the behavior of the endogenous aslA gene, the aslA::lacZ fusion gene is not expressed in Dd-STATa-null slugs. In parental cells, the aslA promoter is first activated in the funnel-shaped core cells located at the slug anterior, the "pstAB core." During culmination, the pstAB core cells move down, through the prespore cells, to form the inner part of the basal disc. As the spore mass climbs the stalk, the aslA gene comes to be expressed in cells of the upper and lower cups, structures that cradle the spore head. Deletion and point mutation analyses of the promoter identified an AT-rich sequence that is necessary for expression in the pstAB core. This acts in combination with repressor regions that prevent ectopic aslA expression in the pre-stalk regions of slugs and the stalks of culminants. Thus, this study confirms that Dd-STATa is necessary for the differentiation of pstAB core cells, by showing that it is needed for the activation of the aslA gene. It also identifies aslA promoter elements that are likely to be regulated, directly or indirectly, by Dd-STATa.

摘要

Dd-STATa是后生动物STAT(信号转导子和转录激活子)蛋白在盘基网柄菌中的同源物,在蛞蝓体中对于正确进入发育 culmination 阶段是必需的。Dd-STATa基因敲除突变体无法完成发育 culmination,其表型与漏斗状核心区域(即pstAB核心区域)的缺失相关,该区域表达ecmA和ecmB基因。为了了解pstAB核心细胞的分化是如何调控的,我们鉴定了一个在正常蛞蝓体的核心细胞中表达但在Dd-STATa基因敲除突变体中下调的EST。这个EST,SSK348,编码盘基网柄菌乙酰辅酶A合成酶(ACS)的一个紧密同源物。同源基因aslA(类乙酰辅酶A合成酶A)的启动子片段与lacZ报告基因融合,并确定其表达模式。正如内源性aslA基因的表现所预期的那样,aslA::lacZ融合基因在Dd-STATa基因敲除的蛞蝓体中不表达。在亲本细胞中,aslA启动子首先在位于蛞蝓体前部的漏斗状核心细胞(“pstAB核心”)中被激活。在发育 culmination 过程中,pstAB核心细胞向下移动,穿过前孢子细胞,形成基盘的内部。当孢子团爬上柄时,aslA基因开始在上杯和下杯的细胞中表达,上杯和下杯是包围孢子头的结构。对启动子的缺失和点突变分析确定了一个富含AT的序列,该序列对于在pstAB核心中的表达是必需的。它与抑制区域共同作用,防止aslA在蛞蝓体的柄前区域和发育 culminant 的柄中异位表达。因此,这项研究通过表明Dd-STATa是激活aslA基因所必需的,证实了Dd-STATa对于pstAB核心细胞的分化是必需的。它还鉴定了可能直接或间接受Dd-STATa调控的aslA启动子元件。

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