Loading…
Cloning and functional characterization of the peptide deformylase encoding gene EuPDF1B from Eucommia ulmoides Oliv
Peptide deformylase can catalyse the removal of formyl groups from the N-terminal formyl methionine of the primary polypeptide chain. The peptide deformylase genes of a few herbaceous plants have been studied to some extent, but the peptide deformylase genes of woody plants have not been studied. In...
Saved in:
Published in: | Scientific reports 2024-05, Vol.14 (1), p.11587-11587, Article 11587 |
---|---|
Main Authors: | , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Summary: | Peptide deformylase can catalyse the removal of formyl groups from the N-terminal formyl methionine of the primary polypeptide chain. The peptide deformylase genes of a few herbaceous plants have been studied to some extent, but the peptide deformylase genes of woody plants have not been studied. In this study, we isolated
EuPDF1B
from
Eucommia ulmoides
Oliv. The full-length sequence of
EuPDF1B
is 1176 bp long with a poly-A tail and contains an open reading frame of 831 bp that encodes a protein of 276 amino acids. EuPDF1B was localized to the chloroplast. qRT‒PCR analysis revealed that this gene was expressed in almost all tissues tested but mainly in mature leaves. Moreover, the expression of
EuPDF1B
was enhanced by ABA, MeJA and GA and inhibited by shading treatment. The expression pattern of
EuPDF1B
was further confirmed in EuPDF1Bp: GUS transgenic tobacco plants. Among all the transgenic tobacco plants, EuPDF1Bp-3 showed the highest GUS histochemical staining and activity in different tissues. This difference may be related to the presence of enhancer elements in the region from − 891 bp to − 236 bp of the
EuPDF1B
promoter. In addition, the expression of the chloroplast gene
psbA
and the net photosynthetic rate, fresh weight and height of tobacco plants overexpressing
EuPDF1B
were greater than those of the wild-type tobacco plants, suggesting that
EuPDF1B
may promote the growth of transgenic tobacco plants. This is the first time that
PDF
and its promoter have been cloned from woody plants, laying a foundation for further analysis of the function of
PDF
and the regulation of its expression. |
---|---|
ISSN: | 2045-2322 2045-2322 |
DOI: | 10.1038/s41598-024-62512-2 |