TY - JOUR
T1 - Phosphoenolpyruvate carboxykinase in the C4 monocot Urochloa panicoides is encoded four differentially expressed genes
AU - Finnegan, Patrick M.
AU - Suzuki, Shoichi
AU - Ludwig, Martha
AU - Burnell, James N.
PY - 1999/8
Y1 - 1999/8
N2 - Previous screening of a cDNA library of leaf poly(A+) RNA from Urochloa panicoides, a phosphoenolpyruvate carboxykinase (PCK)type C4 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 CO2-concentrating mechanism active in U. panicoides.
AB - Previous screening of a cDNA library of leaf poly(A+) RNA from Urochloa panicoides, a phosphoenolpyruvate carboxykinase (PCK)type C4 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 CO2-concentrating mechanism active in U. panicoides.
UR - http://www.scopus.com/inward/record.url?scp=0033179932&partnerID=8YFLogxK
U2 - 10.1104/pp.120.4.1033
DO - 10.1104/pp.120.4.1033
M3 - Article
SN - 0032-0889
VL - 120
SP - 1033
EP - 1041
JO - Plant Physiology
JF - Plant Physiology
IS - 4
ER -