Genomic organization, sequence analysis and expression of all five genes encoding the small subunit of ribulose-1,5-bisphosphate carboxylase/oxygenase from tomato
0301 basic medicine
2. Zero hunger
Base Sequence
Transcription, Genetic
Macromolecular Substances
Ribulose-Bisphosphate Carboxylase
Molecular Sequence Data
Nucleotide Sequence
Life Sciences
Nucleic Acid Hybridization
Cell Biology
Plants
Differential Expression
Biochemistry
Tomato
Ribulose-1,5-bisphosphate Carboxylase
03 medical and health sciences
Genes
Multigene Family
Health Sciences
Genetics
Amino Acid Sequence
General
Microbial Genetics and Genomics
DOI:
10.1007/bf00329650
Publication Date:
2004-10-23T13:11:16Z
AUTHORS (5)
ABSTRACT
We have cloned and sequenced all five members of the gene family for the small subunit (rbcS) of ribulose-1,5-bisphosphate carboxylase/oxygenase from tomato, Lycopersicon esculentum cv. VFNT LA 1221 cherry line. Two of the five genes, designated Rbcs-1 and Rbcs-2, are present as single genes at individual loci. Three genes, designated Rbcs-3A, Rbcs-3B and Rbcs-3C, are organized in a tandem array within 10 kb at a third independent locus. The Rbcs-2 gene contains three introns; all the other members of the tomato gene family contain two introns. The coding sequence of Rbcs-1 differs by 14.0% from that of Rbcs-2 and by 13.3% from that of Rbcs-3 genes. Rbcs-2 shows 10.4% divergence from Rbcs-3. The exon and intron sequences of Rbcs-3A are identical to those of Rbcs-3C, and differ by 1.9% from those of Rbcs-3B. Nucleotide sequence analysis suggests that the five rbcS genes encode four different precursors, and three different mature polypeptides. S1 nuclease mapping of the 5' end of rbcS mRNAs revealed that the mRNA leader sequences vary in length from 8 to 75 nucleotides. Northern analysis using gene-specific oligonucleotide probes from the 3' non-coding region of each gene reveals a four to five-fold difference among the five genes in maximal steady-state mRNA levels in leaves.
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