Drake R, John I, Farrell A, Cooper W, Schuch W, Grierson D
Department of Physiology and Environmental Science, University of Nottingham, Loughborough, UK.
Plant Mol Biol. 1996 Feb;30(4):755-67. doi: 10.1007/BF00019009.
Several cDNAs for mRNAs that change in abundance during tomato leaf senescence were isolated. In this paper we report molecular cloning and expression analysis of two cysteine proteases. SENU2 is identical to the cDNA C14 which encodes a cysteine protease previously shown to be expressed in response to extremes of temperature in tomato fruit [43]. SENU3 cDNA clone was 1.2 kb in length and hybridized to a transcript of 1.4 kb which suggested that the clone was not full-length. The missing 5' end was isolated using rapid amplification of cDNA ends (RACE). Southern blot analysis of tomato genomic DNA indicates that SENU3 is encoded by a single or low copy gene. SENU3 was also shown to have significant homology with known cysteine proteases. These two senescence-associated cysteine proteases are also expressed during other developmental processes, including seed germination, consistent with a role in protein turnover. SENU2 and SENU3 mRNAs were detectable in young fully expanded leaves and increased in abundance with leaf age, reaching a maximum during the later stages of visible leaf senescence. Such a pattern of expression suggests that the onset of leaf senescence is a gradual event. Analysis of senescence in transgenic plants deficient in ethylene biosynthesis, in which leaf senescence is delayed, indicated that enhanced accumulation of SENU2 and SENU3 mRNA was similarly delayed but not prevented.
分离出了几个在番茄叶片衰老过程中丰度发生变化的mRNA的cDNA。在本文中,我们报道了两种半胱氨酸蛋白酶的分子克隆和表达分析。SENU2与cDNA C14相同,C14编码一种半胱氨酸蛋白酶,先前已证明该蛋白酶在番茄果实中对极端温度有响应时表达[43]。SENU3 cDNA克隆长度为1.2 kb,与1.4 kb的转录本杂交,这表明该克隆不是全长的。使用cDNA末端快速扩增(RACE)分离出缺失的5'末端。番茄基因组DNA的Southern印迹分析表明,SENU3由单拷贝或低拷贝基因编码。SENU3还显示与已知的半胱氨酸蛋白酶有显著同源性。这两种与衰老相关的半胱氨酸蛋白酶在包括种子萌发在内的其他发育过程中也有表达,这与它们在蛋白质周转中的作用一致。在幼嫩完全展开的叶片中可检测到SENU2和SENU3 mRNA,其丰度随叶龄增加,在叶片明显衰老的后期达到最大值。这种表达模式表明叶片衰老的开始是一个渐进的过程。对乙烯生物合成缺陷的转基因植物中的衰老进行分析,其中叶片衰老延迟,结果表明SENU2和SENU3 mRNA的积累增强同样延迟但未被阻止。