Cloning and Expression Analysis of Drought-tolerance Related Gene Gp LEAin Grimmia pilifera
Sha We
Abstract
Sha We
Abstract
A full-length cDNA encoding late embriogenesis abundant protein(LEA)named Gp-LEA,was cloned fromGrimmia piliferathrough the method of rapid amplification of cDNA ends(RACE).The full length of this gene was 814 bp,and contained a 456 bp open reading frame which encoded a protein containing 151 amino acids.The result of bioinformatics showed that this protein was a stable protein with a function domain-LEA_2,which molecular weight was 16.612 kD and theoretical pI was 5.06,and it was not a transmembrane protein and had no signal peptide.Phylogenetic analysis indicated that this gene had the closest genetic relationship with that of Pseudotsuga menziesii.The quantitative RT-PCR results suggested that the expression of Gp-LEAgene was induced in both rehydration and dehydration,and this gene might play an important role in the two processes.
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A full-length cDNA encoding late embriogenesis abundant protein(LEA)named Gp-LEA,was cloned fromGrimmia piliferathrough the method of rapid amplification of cDNA ends(RACE).The full length of this gene was 814 bp,and contained a 456 bp open reading frame which encoded a protein containing 151 amino acids.The result of bioinformatics showed that this protein was a stable protein with a function domain-LEA_2,which molecular weight was 16.612 kD and theoretical pI was 5.06,and it was not a transmembrane protein and had no signal peptide.Phylogenetic analysis indicated that this gene had the closest genetic relationship with that of Pseudotsuga menziesii.The quantitative RT-PCR results suggested that the expression of Gp-LEAgene was induced in both rehydration and dehydration,and this gene might play an important role in the two processes.
Key concepts: Open reading frame, Complementary DNA, Gene, Biology, Signal peptide, Cloning (programming), Rapid amplification of cDNA ends, Genetics