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Characterization of the protein phosphatase 2c gene from Porphyra yezoensis and functional analysis under dessicating conditionsa

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Published/Copyright: June 23, 2012

Abstract

To characterize the structure and function of the protein phosphatase 2C (PP2C) gene in Porphyra yezoensis, full-length cDNA of the locus (denoted pypp2c) was obtained by electronic cloning, rapid amplification of cDNA ends, and reverse-transcription PCR. The nucleotide sequence of PyPP2C was 1988 bp, including a 5′-untranslated region (UTR) of 301 bp, a 3′-UTR of 256 bp, and an open reading frame of 1431 bp that can be translated into 476 amino acids with a molecular mass of 50.96 kDa and a putative isoelectric point of 8.34. The amino acids had 30–36% identity with those encoded by PP2C genes in protozoa and higher plants. A PP2C-like catalytic domain was found in the 57–397 region, and several residues involved in the metal ion binding sites were conserved. mRNA expression levels in the three life stages of leafy thalli, filaments, and conchospores were examined by real-time fluorescent quantitative PCR. Highest expression of pypp2c occurred in conchospores. Gene expression levels were similar among the three life stages. pypp2c expression at different thallus relative water contents (RWCs) varied, with the highest expression occurring at 60% RWC.


Corresponding author

Received: 2011-9-25
Accepted: 2012-4-19
Published Online: 2012-06-23
Published in Print: 2012-08-01

©2012 by Walter de Gruyter Berlin Boston

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