Finnegan P M, Suzuki S, Ludwig M, Burnell J N
Division of Biochemistry and Molecular Biology, Faculty of Science, Australian National University, Canberra, Australian Capital Territory 0200, Australia.
Plant Physiol. 1999 Aug;120(4):1033-42. doi: 10.1104/pp.120.4.1033.
Previous screening of a cDNA library of leaf poly(A(+)) RNA from Urochloa panicoides, a phosphoenolpyruvate carboxykinase (PCK)-type C(4) monocot, led to the characterization of cDNAs encoding the U. panicoides PCK subunit PCK1. A second PCK sequence, designated PCK2, has now been found by rescreening the library. The deduced PCK2 polypeptide is 626 residues in length, has a predicted molecular mass of 68,686 D, and is 96% identical to the deduced PCK1 sequence. Isolation and characterization of genomic DNA fragments revealed that the PCK1 and PCK2 genes are each closely linked to another PCK gene. These additional genes have been designated PCK3 and PCK4, respectively. In each case, the second gene is located upstream and in the same transcriptional orientation as the gene characterized through cDNA analysis. A reverse transcription-polymerase chain reaction assay was used to demonstrate that PCK1 and PCK2 transcripts predominate in leaves, whereas PCK3 and PCK4 transcripts predominate in roots. Moreover, accumulation of PCK1 and PCK2 transcripts is light dependent. Direct N-terminal sequencing of PCK polypeptides purified from leaves demonstrated that PCK2 is produced. These results strongly suggest that PCK1 and PCK2 are involved in the photosynthetic CO(2)-concentrating mechanism active in U. panicoides.
先前对黍稷(一种磷酸烯醇式丙酮酸羧激酶(PCK)型C4单子叶植物)叶片多聚腺苷酸(poly(A+))RNA的cDNA文库进行筛选,从而鉴定出了编码黍稷PCK亚基PCK1的cDNA。现在,通过对该文库进行重新筛选,发现了第二个PCK序列,命名为PCK2。推导的PCK2多肽长度为626个残基,预测分子量为68,686 D,与推导的PCK1序列有96%的同一性。基因组DNA片段的分离和鉴定表明,PCK1和PCK2基因各自与另一个PCK基因紧密连锁。这些额外的基因分别被命名为PCK3和PCK4。在每种情况下,第二个基因位于上游,并且与通过cDNA分析鉴定的基因转录方向相同。采用逆转录-聚合酶链反应分析来证明PCK1和PCK2转录本在叶片中占主导地位,而PCK3和PCK4转录本在根中占主导地位。此外,PCK1和PCK2转录本的积累依赖于光照。对从叶片中纯化的PCK多肽进行直接N端测序证明PCK2是有表达的。这些结果有力地表明,PCK1和PCK2参与了黍稷中活跃的光合CO2浓缩机制。