Simard C, Lemieux C, Bellemare G
Département de biochimie, Faculté des sciences et de génie, Université Laval, Québec, Canada.
Curr Genet. 1988 Nov;14(5):461-70. doi: 10.1007/BF00521270.
We have isolated and characterized a full-length cDNA clone encoding the precursor of the small subunit (pSU) of ribulose-1,5-bisphosphate carboxylase/oxygenase (RUBISCO) from the green alga, Chlamydomonas moewusii. Comparison with the C. reinhardtii rbcS1 gene sequence reveals that both small subunit (SS) coding regions are 75% homologous and that their predicted mature polypeptide chains are each composed of 140 amino acids. In contrast, their transit peptides appear to be divergent. We also show that transcription of the C. moewusii rbcS gene(s) which generates a 1,230 and a 930 base mRNA species are light-stimulated/or accumulated during the light period of the cell cycle. Finally, the SS polypeptide sequences of fifteen different photosynthetic organisms are compared; this analysis reveals at least five well-conserved polypeptide domains.
我们已经从绿藻莱茵衣藻中分离并鉴定了一个全长cDNA克隆,该克隆编码1,5-二磷酸核酮糖羧化酶/加氧酶(RUBISCO)小亚基(pSU)的前体。与莱茵衣藻rbcS1基因序列比较发现,两个小亚基(SS)编码区的同源性为75%,且它们预测的成熟多肽链均由140个氨基酸组成。相比之下,它们的转运肽似乎存在差异。我们还表明,莱茵衣藻rbcS基因转录产生1230和930个碱基的mRNA种类,在细胞周期的光照期受到光刺激/积累。最后,比较了15种不同光合生物的SS多肽序列;该分析揭示了至少5个保守的多肽结构域。