Suppr超能文献

里氏木霉和黑曲霉中编码蛋白激酶C同源物的基因(pkc1和pkcA)的克隆与特性分析

Cloning and characterisation of genes (pkc1 and pkcA) encoding protein kinase C homologues from Trichoderma reesei and Aspergillus niger.

作者信息

Morawetz R, Lendenfeld T, Mischak H, Mühlbauer M, Gruber F, Goodnight J, de Graaff L H, Visser J, Mushinski J F, Kubicek C P

机构信息

Abteilung für Mikrobielle Biochemie, Institut für Biochemische Technologie und Mikrobiologie, TU Wein, Austria.

出版信息

Mol Gen Genet. 1996 Jan 15;250(1):17-28. doi: 10.1007/BF02191821.

Abstract

Oligonucleotides, designed on the basis of conserved flanking amino acid sequence segments within the catalytic domain of eukaryotic protein kinase C (PKC) proteins, were used as primers for polymerase chain reactions to amplify a 427-bp chromosomal DNA fragment from the filamentous fungus Trichoderma reesei. This fragment was then used to isolate genes encoding PKC homologues of T. reesei and Aspergillus niger (pkc1 and pkcA, respectively). The genes contain six (T. reesei) and eight (A. niger) introns, which exhibit notable conservation in position with those found in the corresponding Schizosaccharomyces pombe pkc1+ and Drosophila melanogaster dPKC53Ebr genes. A single 4.2-kb transcript was detected in Northern analyses. The deduced PKC1 (T.reesei, 126 kDa) and PKCA (A. niger, 122 kDa) amino acid sequences reveal domains homologous to the C1 and C3/C4 domains of PKC-related proteins, but lack typical Ca(2+)-binding (C2) domains. Both contain a large, extended N-terminus, which shares a high degree of similarity with the corresponding regions of Saccharomyces cerevisiae PKC1 and S. pombe pkc1+ and pkc2+ proteins, but which is not present in PKCs of Dictyostelium or higher eukaryotes. This extended region can be divided into three subdomains; the N-terminal one contains a hydrophobic helix-turn-helix motif, whereas the C-terminal one contains potential targets for proteolytic processing. A polyclonal antiserum raised against the pseudosubstrate-binding domain of PKC1 recognizes in T. reesei a 115-120 kDa protein in Western blots. Expression of pkc1 cDNA in insect cells directs the synthesis of a PKC1 protein of similar size. The T. reesei PKC1 protein was partially purified and some of its properties examined: it is stimulated about twofold by phospholipids or phorbol esters but is not stimulated by Ca2+. We conclude that these PKC proteins from filamentous fungi represent the Ca(2+)-insensitive fungal homologues of the nPKC family.

摘要

基于真核蛋白激酶C(PKC)蛋白催化结构域内保守的侧翼氨基酸序列片段设计的寡核苷酸,被用作聚合酶链反应的引物,以从丝状真菌里氏木霉中扩增出一个427 bp的染色体DNA片段。然后利用该片段分离编码里氏木霉和黑曲霉PKC同源物的基因(分别为pkc1和pkcA)。这些基因含有六个(里氏木霉)和八个(黑曲霉)内含子,其位置与相应的粟酒裂殖酵母pkc1 +和黑腹果蝇dPKC53Ebr基因中的内含子具有显著的保守性。在Northern分析中检测到单一的4.2 kb转录本。推导的PKC1(里氏木霉,126 kDa)和PKCA(黑曲霉,122 kDa)氨基酸序列显示出与PKC相关蛋白的C1和C3/C4结构域同源的结构域,但缺乏典型的Ca(2 +)结合(C2)结构域。两者都含有一个大的、延伸的N端,与酿酒酵母PKC1以及粟酒裂殖酵母pkc1 +和pkc2 +蛋白的相应区域具有高度相似性,但在盘基网柄菌或高等真核生物的PKC中不存在。这个延伸区域可分为三个亚结构域;N端亚结构域包含一个疏水的螺旋-转角-螺旋基序,而C端亚结构域包含蛋白水解加工的潜在靶点。针对PKC1的假底物结合结构域产生的多克隆抗血清在蛋白质印迹中识别里氏木霉中一种115 - 120 kDa的蛋白质。pkc1 cDNA在昆虫细胞中的表达指导合成大小相似的PKC1蛋白。里氏木霉PKC1蛋白被部分纯化并检测了其一些特性:它受到磷脂或佛波酯的约两倍刺激,但不受Ca2 +刺激。我们得出结论,这些来自丝状真菌的PKC蛋白代表nPKC家族的Ca(2 +)不敏感真菌同源物。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验