Koehler S M, Ho T H
Department of Biology, Washington University, St. Louis, Missouri 63130.
Plant Cell. 1990 Aug;2(8):769-83. doi: 10.1105/tpc.2.8.769.
Barley aleurone layers synthesize and secrete several proteases in response to gibberellic acid (GA3). Two major cysteine proteinases designated EP-A (37,000 M(r)) and EP-B (30,000 M(r)) have been described [Koehler and Ho (1988). Plant Physiol. 87, 95-103]. We now report the cDNA cloning of EP-B and describe the post-translational processing and hormonal regulation of both cysteine proteinases. Three cDNAs for cysteine proteinases were cloned from GA3-induced barley aleurone layers. Genomic DNA gel blot analysis indicated that these are members of a small gene family with no more than four to five different genes. The proteins encoded by two of these clones, pHVEP1 and 4, are 98% similar to each other and are isozymes of EP-B. The proteins contain large preprosequences followed by the amino acid sequence described as the mature N terminus of purified EP-B, and are antigenic to EP-B antiserum. The results of pulse-chase experiments indicated that the post-translational processing of large prosequences proceeds in a multistep fashion to produce the mature enzymes. Processing intermediates for EP-B are observed both in the aleurone layers and surrounding incubation medium, but only mature EP-A is secreted. The regulation of synthesis of EP-A, EP-B, and other aleurone cysteine proteinases was compared at the protein and mRNA levels. We conclude that barley aleurone cysteine proteinases are differentially regulated with respect to their temporal and hormonally induced expression.
大麦糊粉层会响应赤霉素(GA3)合成并分泌多种蛋白酶。已描述了两种主要的半胱氨酸蛋白酶,分别命名为EP - A(分子量37,000)和EP - B(分子量30,000)[Koehler和Ho(1988年)。《植物生理学》87卷,95 - 103页]。我们现在报告EP - B的cDNA克隆,并描述这两种半胱氨酸蛋白酶的翻译后加工及激素调节。从GA3诱导的大麦糊粉层中克隆到了三个半胱氨酸蛋白酶的cDNA。基因组DNA凝胶印迹分析表明,这些是一个小基因家族的成员,该家族不超过四到五个不同的基因。其中两个克隆,即pHVEP1和4所编码的蛋白质彼此相似度为98%,是EP - B的同工酶。这些蛋白质含有大的前原序列,其后是被描述为纯化后的EP - B成熟N端的氨基酸序列,并且与EP - B抗血清具有抗原性。脉冲追踪实验结果表明,大前序列的翻译后加工以多步骤方式进行,以产生成熟酶。在糊粉层和周围的孵育培养基中均观察到了EP - B的加工中间体,但仅分泌成熟的EP - A。在蛋白质和mRNA水平上比较了EP - A、EP - B和其他糊粉层半胱氨酸蛋白酶的合成调节。我们得出结论,大麦糊粉层半胱氨酸蛋白酶在其时间和激素诱导表达方面受到差异调节。