Hervás-Aguilar América, Rodríguez José M, Tilburn Joan, Arst Herbert N, Peñalva Miguel A
Departamento de Microbiología Molecular, Centro de Investigaciones Biológicas, Consejo Superior de Investigaciones Científicas, Madrid 28040, Spain.
J Biol Chem. 2007 Nov 30;282(48):34735-47. doi: 10.1074/jbc.M706723200. Epub 2007 Oct 1.
The 72-kDa zinc finger transcription factor PacC, distantly related to Ci/Gli developmental regulators, undergoes two-step proteolytic processing in response to alkaline ambient pH. "Signaling protease" cleavage of PacC(72) removes a processing-inhibitory C-terminal domain, making its truncated PacC(53) product accessible to a second "processing" protease, yielding PacC(27). Features of the processing proteolysis suggested the proteasome as a candidate protease. We constructed, using gene replacements, two missense active site mutations in preB, the Aspergillus nidulans orthologue of Saccharomyces cerevisiae PRE2 encoding the proteasome beta5 subunit. preB1(K101A) is lethal. Viable preB2(K101R) impairs growth and, like its equivalent pre2(K108R) in yeast, impairs chymotryptic activity. pre2(K108R) and preB2(K101R) active site mutations consistently shift position of the scissile bonds when PacC is processed in S. cerevisiae and A. nidulans, respectively, indicating that PacC must be a direct substrate of the proteasome. preB2(K101R) leads to a 2-3-fold elevation in NimE mitotic cyclin levels but appears to result in PacC instability, suggesting an altered balance between processing and degradation. preB2(K101R) compensates the marked impairment in PacC(27) formation resulting from deletion of the processing efficiency determinant in PacC, further indicating direct proteasomal involvement in the formation of PacC(27). Deletion of a Gly-Pro-Ala-rich region within this processing efficiency determinant markedly destabilizes PacC. Arg substitutions of Lys residues within this efficiency determinant and nearby show that they cooperate to promote PacC processing. A quadruple Lys-to-Arg substitution (4K-->R) impairs formation of PacC(27) and leads to persistence of PacC(53). Wild-type PacC(53) becomes multiply phosphorylated upon alkaline pH exposure. Processing-impaired 4K-->R PacC(53) becomes excessively phosphorylated.
72 kDa的锌指转录因子PacC与Ci/Gli发育调节因子有较远的亲缘关系,在碱性环境pH条件下会经历两步蛋白水解过程。PacC(72)的“信号蛋白酶”切割去除了一个加工抑制性C末端结构域,使其截短的PacC(53)产物能够被第二种“加工”蛋白酶作用,产生PacC(27)。加工蛋白水解的特征表明蛋白酶体是一种候选蛋白酶。我们利用基因替换在preB中构建了两个错义活性位点突变,preB是酿酒酵母PRE2在构巢曲霉中的同源物,编码蛋白酶体β5亚基。preB1(K101A)是致死性的。可存活的preB2(K101R)损害生长,并且与其在酵母中的等效物pre2(K108R)一样,损害胰凝乳蛋白酶活性。pre2(K108R)和preB2(K101R)活性位点突变分别在酿酒酵母和构巢曲霉中加工PacC时一致地改变了可裂键的位置,表明PacC必定是蛋白酶体的直接底物。preB2(K101R)导致NimE有丝分裂周期蛋白水平升高2至3倍,但似乎导致PacC不稳定,表明加工和降解之间的平衡发生了改变。preB2(K...