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编码来自大豆疫霉的细胞外糖蛋白激发子的核苷酸序列的分子特征分析

Molecular characterization of nucleotide sequences encoding the extracellular glycoprotein elicitor from Phytophthora megasperma.

作者信息

Sacks W, Nürnberger T, Hahlbrock K, Scheel D

机构信息

Max-Planck-Institut für Züchtungsforschung, Abteilung Biochemie, Köln, Germany.

出版信息

Mol Gen Genet. 1995 Jan 6;246(1):45-55. doi: 10.1007/BF00290132.

Abstract

cDNA sequences encoding the 42 kDa glycoprotein elicitor from the oomycete, Phytophthora megasperma, that induces the defense response in parsley have been cloned and sequenced. The 5' end of the mRNA matches a consensus derived from sequences surrounding the transcription initiation sites of seven other oomycete genes. The major transcript of 1802 nucleotides contains a 529-codon open reading frame, which was predicted to encode a 57 kDa precursor protein. On the basis of peptide sequencing, the N-terminus of the mature protein is at position 163, suggesting that proteolytic processing events, in addition to signal peptide cleavage, generate the protein purified from the fungal culture filtrate. Expression studies in Escherichia coli with the cDNA as well as smaller subfragments demonstrated that a region of 47 amino acids located in the C-terminal third of the protein was sufficient to confer elicitor activity. The gene encoding the elicitor was found to be a member of a multigene family in P. megasperma. Homologous families of differing sizes were found in all eight other Phytophthora species tested, but not in other filamentous fungi including other Oomycetes. No significant similarity of the elicitor preprotein to sequences present in the databases has yet been detected.

摘要

编码来自卵菌纲大雄疫霉(Phytophthora megasperma)的42 kDa糖蛋白激发子的cDNA序列已被克隆和测序,该激发子可诱导欧芹的防御反应。mRNA的5'端与源自其他七个卵菌纲基因转录起始位点周围序列的共有序列相匹配。1802个核苷酸的主要转录本包含一个529密码子的开放阅读框,预计可编码一个57 kDa的前体蛋白。基于肽段测序,成熟蛋白的N端位于第163位,这表明除了信号肽切割外,蛋白水解加工事件还产生了从真菌培养滤液中纯化得到的蛋白。用该cDNA以及较小的亚片段在大肠杆菌中进行的表达研究表明,位于蛋白C端三分之一区域的47个氨基酸足以赋予激发子活性。发现编码该激发子的基因是大雄疫霉中一个多基因家族的成员。在所有其他八个测试的疫霉属物种中都发现了不同大小的同源家族,但在包括其他卵菌纲在内的其他丝状真菌中未发现。尚未检测到激发子前体蛋白与数据库中存在的序列有明显相似性。

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