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Sequence Characteristics and Transcripts of rbcS Genes from Brassica napus : Temporal and Spatial Expression During Crucifer Seedling Morphogenesis *
Author(s) -
Fiebig C.,
Kretzschmar F.,
Sprenger I.,
Link G.
Publication year - 1990
Publication title -
botanica acta
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.871
H-Index - 87
eISSN - 1438-8677
pISSN - 0932-8629
DOI - 10.1111/j.1438-8677.1990.tb00158.x
Subject(s) - biology , brassica , sinapis , complementary dna , gene , microbiology and biotechnology , cotyledon , gene expression , genetics , botany
The small subunit of ribulose‐1,5‐bisphosphate carboxylase/oxygenase is encoded by a nuclear multigene family ( rbcS genes). We have cloned and characterized three rbcS cDNA sequences from Brassica napus . These cDNA clones all appear to encode the same protein, but they differ in their nucleotide sequence, which has been exploited in the construction of clone‐specific oligonucleotides as selective hybridization probes. By using a nonselective RNA probe, the temporal expression of the entire rbcS gene family was analyzed during seedling development of Brassica napus and of Sinapis alba . In both crucifer species, rbcS transcripts show transient peak levels and then decrease, although to a different degree. Only a moderate (twofold) difference in transcript pool sizes is observed in light‐grown versus dark‐grown seedlings at the time of peak levels, while a much higher light/dark ratio is found in late‐stage seedlings. The oligonucleotide probes reveal three subsets of transcripts which differ in their accumulation kinetics and light/dark ratio. Assessment of the spatial distribution by using in situ hybridization indicates that rbcS transcripts are uniformly localized in cross‐sections of cotyledons from either light‐grown or dark‐grown seedlings, whereas they are undetectable in root sections.