Isolation and Expression Analysis of PeDWF1 in Phyllostachys edulis
- Authors: Wang S.N.1, Xu H.1, Sun H.Y.1, Zhao H.S.1, Yang Y.H.1,2, Gao Z.M.1
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Affiliations:
- State Forestry Administration Key Open Laboratory on the Science and Technology of Bamboo and Rattan, Institute of Gene Science for Bamboo and Rattan Resources
- College of Horticulture
- Issue: Vol 65, No 5 (2018)
- Pages: 762-769
- Section: Research Papers
- URL: https://journal-vniispk.ru/1021-4437/article/view/180242
- DOI: https://doi.org/10.1134/S1021443718050175
- ID: 180242
Cite item
Abstract
Brassinosteroids (BRs) are steroidal hormones that play crucial roles in various processes of plant growth and development. DWF1 encodes a delta(24)-sterol reductase that participates in one of the early stage in the brassinosteroids’ biosynthetic pathway: the conversion of 24-methylenecholesterol to campesterol. Here we report the isolation and expression of one DWF1 homologous gene, PeDWF1, in moso bamboo (Phyllostachys edulis (Carrière) J. Houz.). Sequence analysis revealed that the open reading frame of PeDWF1 was 1686-bp encoding a protein composed of 561 amino acid residues with a calculated molecular weight of 65.1 kD and a theoretic isoelectric point of 8.32. Phylogenetic analysis indicated that PeDWF1 was very close to the cell elongation protein Dwarf1 in rice (Oryza sativa). Furthermore, transient expression of a PeDWF1::GFP fusion protein showed that PeDWF1 was an integral membrane protein most probably associated with the endoplasmic reticulum similar to Dwarf1. Tissue specific expression analysis showed that PeDWF1 was constitutively expressed in moso bamboo with the highest level in shoots and the lowest level in mature leaves. In the early growing stage of shoots, the expression level of PeDWF1 had a rising trend with the increasing height of shoots. These results indicated that PeDWF1 might be involved in the regulation of shoot development by participating in BRs biosynthesis. Moreover, PeDWF1 was heterologously expressed in Escherichia coli and the recombinant protein was about 65 kD, which facilitated further study on the gene function of PeDWF1 in bamboo.
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About the authors
S. N. Wang
State Forestry Administration Key Open Laboratory on the Science and Technology of Bamboo and Rattan, Institute of Gene Science for Bamboo and Rattan Resources
Email: gaozhimin@icbr.ac.cn
China, Beijing, 100102
H. Xu
State Forestry Administration Key Open Laboratory on the Science and Technology of Bamboo and Rattan, Institute of Gene Science for Bamboo and Rattan Resources
Email: gaozhimin@icbr.ac.cn
China, Beijing, 100102
H. Y. Sun
State Forestry Administration Key Open Laboratory on the Science and Technology of Bamboo and Rattan, Institute of Gene Science for Bamboo and Rattan Resources
Email: gaozhimin@icbr.ac.cn
China, Beijing, 100102
H. S. Zhao
State Forestry Administration Key Open Laboratory on the Science and Technology of Bamboo and Rattan, Institute of Gene Science for Bamboo and Rattan Resources
Email: gaozhimin@icbr.ac.cn
China, Beijing, 100102
Y. H. Yang
State Forestry Administration Key Open Laboratory on the Science and Technology of Bamboo and Rattan, Institute of Gene Science for Bamboo and Rattan Resources; College of Horticulture
Email: gaozhimin@icbr.ac.cn
China, Beijing, 100102; Baoding, 071001
Z. M. Gao
State Forestry Administration Key Open Laboratory on the Science and Technology of Bamboo and Rattan, Institute of Gene Science for Bamboo and Rattan Resources
Author for correspondence.
Email: gaozhimin@icbr.ac.cn
China, Beijing, 100102
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