Nucleotide sequence of a cDNA clone encoding chloroplast fructose-1,6-bisphosphatase from Arabidopsis thaliana.
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Amino Acid Sequence↗
Biomedical subjects
C A Raines
Publications and source records attributed to C A Raines.
The chloroplast FBPase gene of wheat: structure and expression of the promoter in photosynthetic and meristematic cells of transgenic tobacco plants.
A gene encoding chloroplast fructose-1,6-bisphosphatase (FBPase) was isolated from a genomic library of wheat DNA. Comparison of the gene sequence obtained with that of a wheat cDNA clone revealed the presence of three introns, each less than 100 bases in length. One of these introns lies in a region that may be involved in the light activation of FBPase catalytic activity. Chimeric gene constructs comprising 1673 bp of the upstream FBPase promoter region in a transcriptional fusion to the beta-glucuronidase (GUS) reporter gene were used to investigate expression in transgenic tobacco plants. Histochemical localization of GUS activity revealed high levels of expression driven by the FBPase promoter sequences in photosynthetically active tissues and, unexpectedly, also in the meristematic regions of shoots, lateral buds and roots. The biological significance of FBPase expression in meristematic regions is not yet clear but this pattern of expression may be explained by the presence in the FBPase promoter of a short DNA sequence motif which is also found in the CaMV 35S viral promoter.
Amino Acid Sequence↗
Wheat phosphoglycerate kinase: evidence for recombination between the genes for the chloroplastic and cytosolic enzymes.
We have isolated and sequenced cDNA clones containing the entire coding region of both the chloroplast and cytosolic versions of phosphoglycerate kinase from wheat. Comparison of these sequences reveals a higher than expected level of similarity between the nucleic acids and encoded proteins. Analysis of this data in relation to that for phosphoglycerate kinase sequences of mammals, prokaryotes and yeasts suggests that the wheat genes have recombined. This has resulted in the chloroplast and cytosolic kinases being more similar to each other than would be expected if the chloroplast enzyme had evolved directly from that of a prokaryotic progenitor.
Amino Acid Sequence↗
Complete coding sequence of wheat phosphoribulokinase: developmental and light-dependent expression of the mRNA.
We have isolated and sequenced a cDNA clone which contains the entire coding sequence of the precursor to a subunit of wheat phosphoribulokinase (PRKase). (The enzyme is a homodimer). The cDNA contains 1533 bp and has an open reading frame of 1212 nucleotides. This encodes a protein with an amino-terminal transit sequence of 53 amino acids, while the part that forms the mature protein contains 351 amino acids and has a molecular weight of 39,200 daltons. A comparison of the wheat amino acid sequence with that already known for the mature protein of spinach reveals that there are identical residues in 86% of the positions but their transit peptides differ substantially from one another. The mature wheat and spinach proteins are identical in a segment of over 50 amino acids near the amino-terminus which is the region believed to be involved in ATP binding and in regulation by light of the catalytic activity of the enzyme. We further demonstrate that the expression of PRKase mRNA in wheat leaves is regulated in a developmental, tissue-specific and light dependent manner. We also show that the light-induced increase in the steady-state levels of this mRNA is dependent on the developmental stage of the leaf.
Amino Acid Sequence↗
Chloroplast fructose-1,6-bisphosphatase: the product of a mosaic gene.
We show here that light stimulates the expression of nuclear genes in wheat leaves for chloroplast fructose-1,6-bisphosphatase (FBPase) and describe a sequence of amino acids in this enzyme which may be responsible, via thioredoxin, for the light regulation of its activity. This data results from (a) our isolation and characterization of a cDNA of this enzyme which contains its entire coding sequence, and (b) our use of this cDNA as a probe to detect mRNA levels in wheat plants subjected to different light regimes. The similarity in amino acid sequence of the encoded enzyme from diverse sources suggests that the FBPase genes all had a common origin. However, their control sequences have been adjusted so that they are appropriately expressed and their coding sequences modified so that the enzymic activity of their products are suitably regulated in the particular cellular environment in which they must function. The light-activated regulatory sequences in the gene for the chloroplast protein have probably come together by a shuffling of DNA segments.
Amino Acid Sequence↗