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Characterization of a full-length cDNA clone encoding glutamine synthetase from rubber tree latex

By: Contributor(s): Material type: TextTextPublication details: Plant Physiology and Biochemstry 1997Description: 85-93Subject(s): Online resources: Summary: A full-length cDNA clone (HbGS) encoding glutamine synthetase [glutamate-ammonia ligase] (GS, EC 6.3.1.2) was isolated from a lambda Zap II library of ethylene-treated Hevea brasiliensis latex. Sequence analysis of this clone revealed an open reading frame corresponding to a 356 amino acid polypeptide. The deduced amino acid sequence showeed 80-96;and 76;identity respectively with cytosolic and chloroplastic GS published sequences. These homologies and the lack of a N-terminal leader peptide sequence strongly suggested that this clone encodes a cytosolic glutamine synthetase. Southern blot analysis demonstrated the existence of an intron(s) and suggested that the rubber tree GS is encoded by a small multigene family. The short-term kinetics of ethylene action on gene expression revealed marked accumulation of the corresponding GS mRNA in the latex cells of ethylene-treated newly tapped trees, compared with non-treated controls. Additionally, tapping itself was shown to slightly stimulate GS gene expression.
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Item type Current library Vol info Status
Journals Journals RRII Library Physiology Volume 35, Issue 2 Journals
Total holds: 0

Source Year: 1997

A full-length cDNA clone (HbGS) encoding glutamine synthetase [glutamate-ammonia ligase] (GS, EC 6.3.1.2) was isolated from a lambda Zap II library of ethylene-treated Hevea brasiliensis latex. Sequence analysis of this clone revealed an open reading frame corresponding to a 356 amino acid polypeptide. The deduced amino acid sequence showeed 80-96;and 76;identity respectively with cytosolic and chloroplastic GS published sequences. These homologies and the lack of a N-terminal leader peptide sequence strongly suggested that this clone encodes a cytosolic glutamine synthetase. Southern blot analysis demonstrated the existence of an intron(s) and suggested that the rubber tree GS is encoded by a small multigene family. The short-term kinetics of ethylene action on gene expression revealed marked accumulation of the corresponding GS mRNA in the latex cells of ethylene-treated newly tapped trees, compared with non-treated controls. Additionally, tapping itself was shown to slightly stimulate GS gene expression.

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