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一种新型盘基网柄菌前孢子特异性基因PspB的特性分析揭示了保守的调控序列。

Characterization of a novel Dictyostelium discoideum prespore-specific gene, PspB, reveals conserved regulatory sequences.

作者信息

Powell-Coffman J A, Firtel R A

机构信息

Department of Biology, University of California, San Diego, La Jolla 92093-0634.

出版信息

Development. 1994 Jun;120(6):1601-11. doi: 10.1242/dev.120.6.1601.

Abstract

While Dictyostelium discoideum has been studied as a developmental system for decades, and many regulatory proteins have been cloned, the molecular mechanisms of cell-type-specific gene expression are poorly understood. In this paper we characterize a novel prespore gene, PspB, and undertake a comparative analysis of the regulatory regions in prespore-specific D. discoideum promoters. Sequence alignment of the PSPB gene product with other prespore-specific proteins identifies a conserved, repeated 12 amino acid cysteine-containing motif that may be involved in spore coat function or assembly. Analysis of the PspB promoter identifies two domains essential for developmentally induced promoter activity. The first region includes two CA-rich elements (CAEs) that we show to be functionally homologous to the cAMP-inducible elements previously identified in the SP60 (cotC) promoter. The PspB CAEs compete with the SP60 (cotC) CAEs for binding in vitro to a developmentally regulated nuclear activity. We identify this activity as G-box Binding Factor, a developmentally induced transcription factor. The PspB CAEs and adjacent nucleotides direct a very low level of prespore-enriched expression, but high levels of cell-type-specific expression requires a second promoter region: a 46-bp AT-rich sequence that does not resemble the CAEs or any other previously described late gene promoter elements. Comparison of the PspB AT element with regulatory regions of the SP60 (cotC), SP70 (cotB), and D19 (pspA) promoters reveals an extensive consensus sequence. We suggest that these AT-rich sequences may represent a common regulatory element (or elements) required for prespore gene activation.

摘要

几十年来,盘基网柄菌一直作为一种发育系统被研究,许多调控蛋白已被克隆,但细胞类型特异性基因表达的分子机制仍知之甚少。在本文中,我们对一个新的前孢子基因PspB进行了表征,并对盘基网柄菌前孢子特异性启动子的调控区域进行了比较分析。PSPB基因产物与其他前孢子特异性蛋白的序列比对确定了一个保守的、重复的含12个氨基酸的半胱氨酸基序,该基序可能参与孢子壁的功能或组装。对PspB启动子的分析确定了两个对发育诱导型启动子活性至关重要的结构域。第一个区域包括两个富含CA的元件(CAEs),我们证明它们在功能上与先前在SP60(cotC)启动子中鉴定的cAMP诱导元件同源。PspB CAEs在体外与SP60(cotC)CAEs竞争结合一种受发育调控的核活性。我们将这种活性鉴定为G-box结合因子,一种受发育诱导的转录因子。PspB CAEs和相邻核苷酸指导极低水平的前孢子富集表达,但高水平的细胞类型特异性表达需要第二个启动子区域:一个46bp的富含AT的序列,它与CAEs或任何其他先前描述的晚期基因启动子元件不同。将PspB AT元件与SP60(cotC)、SP70(cotB)和D19(pspA)启动子的调控区域进行比较,发现了一个广泛的共有序列。我们认为这些富含AT的序列可能代表前孢子基因激活所需的一个或多个共同调控元件。

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