Cloning of Eleutherococcus senticosus calmodulin gene and effect of endophytic fungus on expression amount of gene.
- Author:
Zhaobin XING
1
;
Yuehong LONG
;
Baocai LI
;
Jinli ZHU
;
Shan HE
Author Information
- Publication Type:Journal Article
- MeSH: Calmodulin; chemistry; genetics; metabolism; Cloning, Molecular; Eleutherococcus; classification; genetics; metabolism; microbiology; Endophytes; physiology; Fungi; physiology; Gene Expression Regulation, Plant; Molecular Sequence Data; Phylogeny; Plant Proteins; chemistry; genetics; metabolism
- From: China Journal of Chinese Materia Medica 2012;37(15):2267-2271
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo clone calmodulin (CaM) gene in Eleutherococcus senticosus, and study the effect of endophytic fungi on expression amount of CaM gene.
METHODThe CaM full length cDNA sequence was cloned by rapid amplification of cDNA ends (RACE). The gene was analyzed and corresponding structure and functions were predicted by the bioinformatics methods. The expression amount of CaM gene affected of endophytic fungus P116-1a, P116-1b, P1094 and P312-1 was detected by RT-PCR.
RESULTThe full length of CaM cDNA was 856 bp containing an ORF of 450 bp that encoded a protein of 149 amino acids. The homologous of predicted protein was almost 100% with plants like Panax ginseng and Daucus carota. RT-PCR results showed that endophytic fungus improved CaM expression amount significantly (P<0.05). The highest expression amount of CaM occurred 90 d after reinoculated with endophytic fungi P1094, up to 2.96 times of the control.
CONCLUSIONThe CaM gene of E. senticosus was successfully cloned for the first time. The results demonstrated that endophytic fungus of E. senticosus improved CaM expression amount significantly.
