Cloning, expression, and bioinformatics analysis of acetyl-CoA C-acetyltransferase gene in Houttuynia cordata
10.7501/j.issn.0253-2670.2015.01.021
- Author:
Yuan-Zhi YAO
1
Author Information
1. Key Laboratory of Xiangxi Medicinal Plant and Ethnobotany of Hunan Higher Education, Department of Life Sciences, Huaihua University
- Publication Type:Journal Article
- Keywords:
Acetyl-CoA C-acetyltransferase;
CDNA sequence;
Differential expression;
Houttuynia cordata Thunb.;
RT-PCR
- From:
Chinese Traditional and Herbal Drugs
2015;46(1):107-111
- CountryChina
- Language:Chinese
-
Abstract:
Objective: Acetyl-CoA C-acetyltransferase (AACT) is the initial enzyme in the terpenoid biosynthesis pathway of mevalonate (MVA), two units of acetyl-CoA were catalyzed to acetoacetyl-CoA. To clone the full length cDNA of AACT gene and carry out the bioinformatics analysis and expression analysis in order to provide the basis on resolving the mechanism of biosynthesis for terpenoid secondary metabolites from Houttuynia cordata. Methods: The cDNA sequence of AACT gene was obtained from H. cordata by using RT-PCR strategy. And the different expression of AACT gene in the rhizomes, stems, leaves, and flowers of H. cordata was analyzed by fluorescent quantitative PCR. Results: The cDNA contains a 1 218 bp open reading frame and encodes a predicted protein of 405 amino acids. No transmembrane region and signal peptide were present in AACT protein by bioinformatics prediction. Relative real-time PCR analysis indicated that AACT gene showed the highest transcript abundance in the stems and rhizomes of H. cordata lower levels in the flowers and leaves, the values of them were 1.49, 0.96, 0.20, and 0.10, respectively. Conclusion: This AACT gene is cloned from H. cordata for the first time. The results will provide a foundation for exploring the mechanism of the gene in terpenoid biosynthesis and metabolism in H. cordata.
