Gowri G, Paiva N L, Dixon R A
Plant Biology Division, Samuel Roberts Noble Foundation, Ardmore, OK 73402.
Plant Mol Biol. 1991 Sep;17(3):415-29. doi: 10.1007/BF00040636.
An expression library containing cDNAs derived from transcripts from fungal elicitor-treated alfalfa cell suspension cultures was screened with an antiserum raised against phenylalanine ammonia-lyase (PAL) from alfalfa. A single immunoreactive clone was isolated which encoded a full-length PAL cDNA (APAL1) consisting of a 2175 bp open reading frame, 96 bp 5'-untranslated leader and 128 bp 3'-non-coding region. The deduced amino acid sequence was 86.5% similar to that of the PAL2 gene of bean, and encoded a polypeptide of Mr 78,865. A second PAL cDNA species was isolated, whose 3'-untranslated region was 86% identical to that of APAL1. Southern blot analysis indicated that PAL is encoded by a small multigene family in alfalfa. PAL transcript levels were rapidly and massively induced, and preceded increased PAL extractable activity, on exposure of alfalfa suspension cells to elicitor from baker's yeast. PAL transcripts were most abundant in roots, stems and petioles during growth and development of alfalfa seedlings. These studies provide the basis for an examination of the developmental and environmental control of a key enzyme of phenylpropanoid synthesis in a plant species which is readily amenable to stable genetic transformation.
用一种针对紫花苜蓿苯丙氨酸解氨酶(PAL)产生的抗血清,筛选了一个表达文库,该文库包含来自真菌激发子处理的紫花苜蓿细胞悬浮培养物转录本的cDNA。分离出一个单一的免疫反应性克隆,它编码一个全长PAL cDNA(APAL1),由一个2175 bp的开放阅读框、96 bp的5'-非翻译前导序列和128 bp的3'-非编码区组成。推导的氨基酸序列与菜豆PAL2基因的序列有86.5%的相似性,编码一个Mr为78,865的多肽。分离出第二个PAL cDNA种类,其3'-非编码区与APAL1的3'-非编码区有86%的同一性。Southern杂交分析表明,PAL在紫花苜蓿中由一个小的多基因家族编码。当紫花苜蓿悬浮细胞暴露于面包酵母的激发子时,PAL转录水平迅速大量诱导,并先于PAL可提取活性的增加。在紫花苜蓿幼苗的生长和发育过程中,PAL转录本在根、茎和叶柄中最为丰富。这些研究为在一个易于进行稳定遗传转化的植物物种中,研究苯丙烷类合成关键酶的发育和环境调控提供了基础。