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Myb 转录因子在卵菌门疫霉属中具有新型多样化的 DNA 结合域和发育阶段特异性表达。

Myb transcription factors in the oomycete Phytophthora with novel diversified DNA-binding domains and developmental stage-specific expression.

机构信息

Department of Plant Pathology and Microbiology, University of California, Riverside, 92521, USA.

出版信息

Gene. 2010 Mar 15;453(1-2):1-8. doi: 10.1016/j.gene.2009.12.006. Epub 2010 Jan 7.

Abstract

Transcription factors containing two or three imperfect tandem repeats of the Myb DNA-binding domain (named R2R3 and R1R2R3, respectively) regulate important processes in growth and development. This study characterizes the structure, evolution, and expression of these proteins in the potato pathogen Phytophthora infestans and other oomycetes. P. infestans was found to encode five R2R3 and nine R1R2R3 transcription factor-like proteins, plus several with additional configurations of Myb domains. Sets of R2R3 and R1R2R3 orthologs are well-conserved in three Phytophthora species. Analyses of sites that bind DNA in canonical Myb transcription factors, such as mammalian c-Myb, revealed unusual diversification in the DNA recognition helices of the oomycete proteins. While oomycete R2R3 proteins contain c-Myb-like helices, R1R2R3 proteins exhibit either c-Myb-like or novel sequences. This suggests divergence in their DNA-binding specificities, which was confirmed by electrophoretic mobility shift assays. Eight of the P. infestans R2R3 and R1R2R3 genes are up-regulated during sporulation and three during zoospore release, which suggests their involvement in spore development. This is supported by the observation that an oomycete that does not form zoospores, Hyaloperonospora arabidopsidis, contains one-third fewer of these genes than Phytophthora.

摘要

含有两个或三个不完全串联重复 Myb DNA 结合域的转录因子(分别命名为 R2R3 和 R1R2R3),调节生长和发育中的重要过程。本研究描述了在马铃薯病原体致病疫霉和其他卵菌中的这些蛋白的结构、进化和表达。发现致病疫霉编码五个 R2R3 和九个 R1R2R3 转录因子样蛋白,加上几个具有额外 Myb 结构域的配置。在三个疫霉物种中,R2R3 和 R1R2R3 直系同源物的集合得到了很好的保守。对在典型 Myb 转录因子(如哺乳动物 c-Myb)中结合 DNA 的位点的分析,揭示了卵菌蛋白的 DNA 识别螺旋的异常多样化。虽然卵菌 R2R3 蛋白含有 c-Myb 样螺旋,但 R1R2R3 蛋白表现出 c-Myb 样或新序列。这表明它们在 DNA 结合特异性上存在分歧,这通过电泳迁移率变动分析得到了证实。在孢子形成过程中,8 个致病疫霉 R2R3 和 R1R2R3 基因上调,在游动孢子释放过程中,3 个基因上调,这表明它们参与了孢子发育。这一观察结果得到了支持,即不形成游动孢子的卵菌 Hyaloperonospora arabidopsidis 比疫霉少三分之一的这些基因。

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