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Core Promoter Structure in the Oomycete Phytophthora infestans

机译:卵菌疫霉菌的核心启动子结构

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We have investigated the core promoter structure of the oomycete Phytophthora infestans. The transcriptional start sites (TSS) of three previously characterized P. infestans genes, Piexo1, Piexo3, and Piendo1, were determined by primer extension analyses. The TSS regions were homologous to a previously identified 16-nucleotide (nt) core sequence that overlaps the TSS in most oomycete genes. The core promoter regions of Piexo1 and Piendo1 were investigated by using a transient protoplast expression assay and the reporter gene β-glucuronidase. Mutational analyses of the promoters of Piexo1 and Piendo1 showed that there is a putative core promoter element encompassing the TSS (?2 to + 5) that has high sequence and functional homology to a known core promoter element present in other eukaryotes, the initiator element (Inr). Downstream and flanking the Inr is a highly conserved oomycete promoter region (+7 to + 15), hereafter referred to as FPR (flanking promoter region), which is also important for promoter function. The importance of the 19-nt core promoter region (Inr and FPR) in Piexo1 and Piendo1 was further investigated through electrophoretic mobility shift assays (EMSA). The EMSA studies showed that (i) both core promoters were able to specifically bind a protein or protein complex in a P. infestans whole-cell protein extract and (ii) the same mutations that reduced binding of the EMSA complex also reduced β-glucuronidase (GUS) levels in transient expression assays. The consistency of results obtained using two different assays (GUS transient assays [in vivo] and EMSA studies [in vitro]) supports a convergence of inference about the relative importance of specific nucleotides within the 19-nt core promoter region.
机译:我们研究了卵菌 Phytophthora infestans 的卵母细胞的核心启动子结构。三个先前表征的 P的转录起始位点(TSS)。通过引物延伸分析确定了infestans 基因, Piexo1 Piexo3 Piendo1 。 TSS区与先前鉴定的16个核苷酸(nt)核心序列同源,该序列在大多数卵菌基因中与TSS重叠。通过瞬时原生质体表达检测和报道基因β-葡萄糖醛酸苷酶研究了 Piexo1 Piendo1 的核心启动子区域。对 Piexo1 Piendo1 启动子的突变分析表明,存在一个推定的核心启动子元件,包含TSS(?2至+ 5),与TSS具有高序列和功能同源性。存在于其他真核生物中的已知核心启动子元件,即引发剂元件(Inr)。 Inr的下游和侧翼是高度保守的卵菌启动子区(+7至+ 15),以下称为FPR(侧翼启动子区),这对启动子功能也很重要。通过电泳迁移率迁移分析(EMSA)进一步研究了 Piexo1 Piendo1 中19-nt核心启动子区域(Inr和FPR)的重要性。 EMSA研究表明(i)两个核心启动子都能够特异性结合 P中的蛋白质或蛋白质复合物。侵染全细胞蛋白提取物和(ii)减少EMSA复合物结合的相同突变也降低了瞬时表达测定法中的β-葡萄糖醛酸苷酶(GUS)水平。使用两种不同的测定(GUS瞬态测定[体内]和EMSA研究[体外])获得的结果的一致性,支持了19-nt核心启动子区域内特定核苷酸相对重要性的推断的融合。

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