Osakabe K, Koyama H, Kawai S, Katayama Y, Morohoshi N
Laboratory of Wood Chemistry, Faculty of Agriculture, Tokyo University of Agriculture and Technology, Japan.
Plant Mol Biol. 1995 Jul;28(4):677-89. doi: 10.1007/BF00021193.
A genomic library was prepared from Populus kitakamiensis and screened with the cDNA for an anionic peroxidase from P. kitakamiensis. One genomic clone was isolated that contained two tandemly oriented genes for anionic peroxidases, prxA3a and prxA4a. Both genes consisted of four exons and three introns; the introns had consensus nucleotides, namely, GT and AG, at their 5' and 3' ends, respectively. The prxA3a and prxA4a genes encoded 347 and 343 amino acid residues, respectively, including putative signal sequences at the amino-termini. Putative promoters and polyadenylation signals were found in the flanking regions of both genes. The sequence of the coding region of prxA3a was completely identical to that of the cDNA clone pA3, whereas the sequence of the coding region of prxA4a was only 73% identical to that of the cDNA clone pA3. Northern blot analysis showed that the patterns of expression of the mRNAs that corresponded to prxA3a and prxA4a differed in stems of P. kitakamiensis.
从北日本山杨(Populus kitakamiensis)制备了基因组文库,并用北日本山杨阴离子过氧化物酶的cDNA进行筛选。分离出一个基因组克隆,其中包含两个串联排列的阴离子过氧化物酶基因,prxA3a和prxA4a。这两个基因均由四个外显子和三个内含子组成;内含子在其5'和3'末端分别具有共有核苷酸,即GT和AG。prxA3a和prxA4a基因分别编码347和343个氨基酸残基,在氨基末端包括推定的信号序列。在两个基因的侧翼区域发现了推定的启动子和聚腺苷酸化信号。prxA3a编码区的序列与cDNA克隆pA3的序列完全相同,而prxA4a编码区的序列与cDNA克隆pA3的序列仅73%相同。Northern印迹分析表明,与prxA3a和prxA4a相对应的mRNA在北日本山杨茎中的表达模式不同。