Loading…
In silico prediction of miRNAs targeting ToLCV and their regulation in susceptible and resistant tomato plants
Tomato leaf curl disease is one of the main constraints in tomato production worldwide. It is induced by viruses including Tomato leaf curl virus (ToLCV). Plant viruses can both induce and be themselves targeted by gene silencing machinery. Certain animal viruses were found to be targeted by host mi...
Saved in:
Published in: | Australasian plant pathology 2017-07, Vol.46 (4), p.379-386 |
---|---|
Main Authors: | , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Summary: | Tomato leaf curl disease is one of the main constraints in tomato production worldwide. It is induced by viruses including
Tomato leaf curl virus
(ToLCV). Plant viruses can both induce and be themselves targeted by gene silencing machinery. Certain animal viruses were found to be targeted by host miRNAs but, there is no similar experimental report for plant viruses. In this study, we investigated if tomato-encoded miRNAs target ToLCV using an in silico analysis. Results showed that ToLCV can be targeted by three tomato miRNAs, named miR156, miR159, and miR403. Following virus infection of susceptible tomato plants cv Moneymaker, miR159 and miR403 were upregulated, while miR156 was unchanged. In the plants of the resistant tomato variety PS550, that accumulated 50-fold less viral DNA and did not show disease symptoms, miR156 was upregulated, while the two others remained unchanged. In addition, the expression level of three genes known as targets of these miRNAs, i.e.
SPL6b
,
MYB33
and
AGO2a,
was measured in both susceptible and resistant tomato varieties by qRT-PCR. The possible role of the predicted miRNAs and regulation of their target genes in symptom development by ToLCV is discussed. |
---|---|
ISSN: | 0815-3191 1448-6032 |
DOI: | 10.1007/s13313-017-0500-5 |