Gall-specific promoter, an alternative to the constitutive CaMV35S promoter, drives host-derived RNA interference targeting Mi-msp2 gene to confer effective nematode resistance
One of the major obligate plant parasites causing massive economic crop losses belongs to the class of root-knot nematodes (RKNs). Targeting of major nematode parasitism genes via Host Delivered-RNAi (HD-RNAi) to confer silencing is established as one of the most effective approaches to curb nematod...
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Veröffentlicht in: | Frontiers in plant science 2022-11, Vol.13, p.1007322-1007322 |
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Zusammenfassung: | One of the major obligate plant parasites causing massive economic crop losses belongs to the class of root-knot nematodes (RKNs). Targeting of major nematode parasitism genes
via
Host Delivered-RNAi (HD-RNAi) to confer silencing is established as one of the most effective approaches to curb nematode infection. Utilizing nematode-responsive root-specific (NRRS) promoters to design a dsRNA molecule targeting approach to hamper nematode parasitism. Here, a previously validated peroxidase gall specific promoter, p
At2g18140
, from
Arabidopsis
was employed to express the dsRNA construct of the nematode effector gene
Mi-msp2
from
Meloidogyne incognita
.
Arabidopsis
RNAi lines of
CaMV35S::Mi-msp2-RNAi
and p
At2g18140::Mi-msp2-RNAi
were compared with control plants to assess the decrease in plant nematode infection. When subjected to infection, the maximum reductions in the numbers of galls, females and egg masses in the
CaMV35S::Mi-msp2-RNAi
lines were 61%, 66% and 95%, respectively, whereas for the p
At2g18140::Mi-msp2-RNAi
lines, they were 63%, 68% and 100%, respectively. The reduction in transcript level ranged from 79%-82% for
CaMV35S::Mi-msp2-RNAi
and 72%-79% for the p
At2g18140::Mi-msp2-RNAi
lines. Additionally, a reduction in female size and a subsequent reduction in next-generation fecundity demonstrate the efficacy and potential of the gall specific promoter p
At2g18140
for utilization in the development of HD-RNAi constructs against RKN, as an excellent alternative to the
CaMV35S
promoter. |
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ISSN: | 1664-462X 1664-462X |
DOI: | 10.3389/fpls.2022.1007322 |