Gingrich J C, Hallick R B
J Biol Chem. 1985 Dec 25;260(30):16162-8.
The polypeptide product of the gene for the large subunit of ribulose-1,5-bisphosphate carboxylase from Euglena gracilis based on the DNA sequence of the chloroplast-encoded gene is described. The large subunit polypeptide of 475 codons is co-linear with the homologous polypeptides from other chloroplasts and cyanobacteria. The amino acid sequence is 92% homologous to that of Chlamydomonas, 84% homologous to spinach, 82% homologous to maize, and 80% homologous to that of the cyanobacterium Anabaena variabilis. Known functional domains of the protein are coded by the larger exons of the gene. Introns in the gene generally occur at coding sequences specifying hydrophilic, presumably surface exposed, regions of the polypeptide. The location of some of the introns may reflect a separation of functional domains. The 5'- and 3'-ends of the rbcL transcript were determined by primer extension sequencing using reverse transcriptase and S1 nuclease protection, respectively. The transcribed but untranslated sequences are quite distinct from those from other rbcL loci.
基于叶绿体编码基因的DNA序列,描述了来自纤细裸藻的1,5-二磷酸核酮糖羧化酶大亚基基因的多肽产物。由475个密码子组成的大亚基多肽与来自其他叶绿体和蓝细菌的同源多肽是共线性的。其氨基酸序列与衣藻的同源性为92%,与菠菜的同源性为84%,与玉米的同源性为82%,与蓝细菌多变鱼腥藻的同源性为80%。该蛋白质已知的功能域由基因中较大的外显子编码。基因中的内含子通常出现在编码多肽亲水性(可能位于表面)区域的编码序列中。一些内含子的位置可能反映了功能域的分隔。分别使用逆转录酶通过引物延伸测序和S1核酸酶保护法确定了rbcL转录本的5'端和3'端。转录但未翻译的序列与其他rbcL基因座的序列有很大不同。