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首页> 外文期刊>Eukaryotic cell >Architecture of the Sporulation-Specific Cdc14 Promoter from the Oomycete Phytophthora infestans
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Architecture of the Sporulation-Specific Cdc14 Promoter from the Oomycete Phytophthora infestans

机译:马铃薯疫霉菌的孢子特异性Cdc14启动子的体系结构

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The Cdc14 gene of Phytophthora infestans is transcribed specifically during sporulation, with no mRNA detectable in vegetative hyphae, and is required for sporangium development. To unravel the mechanisms regulating its transcription, mutated Cdc14 promoters plus chimeras of selected Cdc14 sequences and a minimal promoter were tested in stable transformants. This revealed that a tandem repeat of three copies of the motif CTYAAC, located between 67 and 90 nucleotides (nt) upstream of the major transcription start site, is sufficient to determine sporulation-specific expression. All three repeats need to be present for activity, suggesting that they bind a transcription factor through a cooperative mechanism. Electrophoretic mobility shift assays indicated that the CTYAAC repeats are specifically bound by a protein in nuclear extracts. Evidence was also obtained for a second region within the promoter that activates Cdc14 transcription during sporulation which does not involve those repeats. The CTYAAC motif also affects the specificity of transcription initiation. Wild-type Cdc14 is transcribed from a major start site and minor site(s) located about 100 nt upstream of the major site. However, stepwise mutations through the CTYAAC triad caused a graded shift to the upstream sites, as did mutating bases surrounding the major start site; transcripts initiated from the upstream site remained sporulation specific. Replacing the Cdc14 initiation region with the Inr-like region of the constitutive Piexo1 gene had no apparent effect on the pattern of transcription. Therefore, this study reports the first motif determining sporulation-induced transcription in oomycetes and helps define oomycete core promoters.
机译:疫霉菌 Cdc14 基因是在孢子形成过程中特异性转录的,营养菌丝中没有检测到mRNA,是孢子囊发育所必需的。为了弄清调节其转录的机制,在稳定的转化子中测试了突变的 Cdc14 启动子以及选定的 Cdc14 序列的嵌合体和最小启动子。这揭示了位于主要转录起始位点上游67和90个核苷酸(nt)之间的三个拷贝的CTYAAC基序的串联重复足以确定孢子特异性表达。所有三个重复序列都需要存在才能发挥活性,这表明它们通过协作机制结合转录因子。电泳迁移率变动分析表明,CTYAAC重复序列被核提取物中的蛋白质特异性结合。还获得了启动子内第二个区域的证据,该区域在孢子形成过程中激活了 Cdc14 转录,而这些区域不涉及这些重复。 CTYAAC基序也影响转录起始的特异性。野生型 Cdc14 是从主要起始站点和次要站点(位于主要站点上游约100 nt)转录的。然而,通过CTYAAC三联体的逐步突变导致了向上游位点的逐步转移,主要起始位点周围的突变碱基也是如此。从上游位点开始的转录本仍具有孢子特异性。用组成型 Piexo1 基因的Inr-like区域代替 Cdc14 起始区域对转录模式没有明显影响。因此,这项研究报告了第一个确定卵母细胞中孢子诱导转录的基序,并有助于定义卵母细胞核心启动子。

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