Cloning and gene functional analysis study of dynamin-related protein GeDRP1E gene in Gastrodia elata
10.16438/j.0513-4870.2023-0587
- VernacularTitle:天麻动力相关蛋白GeDRP1E基因的克隆及功能初探
- Author:
Xin FAN
1
,
2
,
3
;
Jian-hao ZHAO
4
,
5
;
Yu-chao CHEN
3
,
4
;
Zhong-yi HUA
4
;
Tian-rui LIU
4
;
Yu-yang ZHAO
4
;
Yuan YUAN
1
,
2
Author Information
1. School of Traditional Chinese Medicine, Guangdong Pharmaceutical University, Guangzhou 510006, China
2. National Key Laboratory for Quality Ensurance and Sustainable Use of Dao-Di Herbs, Beijing 100700, China
3. Agricultural Biotechnology Centre, Ningxia Academy of Agriculture and Forestry Sciences, Yinchuan 750002, China
4. National Key Laboratory for Quality Ensurance and Sustainable Use of Dao-Di Herbs, Beijing 100700, China
5. School of Pharmacy, Jiangsu University, Zhenjiang 212013, China
- Publication Type:Research Article
- Keywords:
italic>Gastrodia elata;
italic>DRP1E gene;
genetic transformation;
functional analysis;
tuber development
- From:
Acta Pharmaceutica Sinica
2024;59(2):482-488
- CountryChina
- Language:Chinese
-
Abstract:
The gene GeDRP1E encoding dynamin-related protein 1E in Gastrodia elata was cloned by specific primers which were designed based on the transcriptome data of G. elata. Bioinformatics analysis on GeDRP1E gene was carried out by using ExPASy, ClustalW, MEGA, etc. Positive transgenic Arabidopsis plant and potato minituber were obtained with the genetic transformation system of Arabidopsis and potato. The plant height and seed setting rate of transgenic Arabidopsis, and agronomic characters, such as size, weight and starch content of potato minituber of transgenic potato were tested and analyzed. And GeDRP1E gene function was preliminarily investigated. The results showed that the open reading frame of GeDRP1E gene was 1 899 bp in length and 632 amino acids residues were encoded, with a relative molecular weight of 69.90 kDa and a molecular formula of C3079H4973N883O933S19. It was predicted that the theoretical isoelectric point was 7.27, the instability coefficient was 43.34, and the average hydrophilicity index was -0.259, which was indicative of an unstable hydrophilic protein. GeDRP1E has no transmembrane structure and signal peptide, and was localized in the cytoplasm. The phylogenetic tree showed that GeDRP1E was highly homologous with DRP1E proteins of other plant species, among which GeDRP1E had the highest homology with DcDRP1E (XP_020689662.1) in Dendrobium candidum, reaching 90.05%. GeDRP1E plant expression vector pCambia1300-35Spro-GeDRP1E was constructed by double digests, and Arabidopsis complementary mutant and potato overexpression strain of GeDRP1E gene were obtained by Agrobacterium-mediated gene transformation. Compared with the Arabidopsis AtDRP1E mutant, the height and seed setting rate of the GeDRP1E complementation mutant were rescued. The minituber of GeDRP1E overexpression potato had larger size, heavier weight and higher starch content, comparing to wild-type potato. It was preliminarily induced that GeDRP1E was involved in mitochondrial morphology regulation, which related to the growth and development of Arabidopsis plants and potato miniature. The research results laid a foundation for further elucidating the molecular mechanisms underlying the growth and development of G. elata tuber development.
