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Co-Silencing of the Voltage-Gated Calcium Channel β Subunit and High-Voltage Activated α(1) Subunit by dsRNA Soaking Resulted in Enhanced Defects in Locomotion, Stylet Thrusting, Chemotaxis, Protein Secretion, and Reproduction in Ditylenchus destructor

The voltage-gated calcium channel (VGCC) β subunit (Ca(v)β) protein is a kind of cytosolic auxiliary subunit that plays an important role in regulating the surface expression and gating characteristics of high-voltage-activated (HVA) calcium channels. Ditylenchus destructor is an important plant-par...

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Detalles Bibliográficos
Autores principales: An, Mingwei, Chen, Xueling, Yang, Zhuhong, Zhou, Jianyu, Ye, Shan, Ding, Zhong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8776034/
https://www.ncbi.nlm.nih.gov/pubmed/35054970
http://dx.doi.org/10.3390/ijms23020784
Descripción
Sumario:The voltage-gated calcium channel (VGCC) β subunit (Ca(v)β) protein is a kind of cytosolic auxiliary subunit that plays an important role in regulating the surface expression and gating characteristics of high-voltage-activated (HVA) calcium channels. Ditylenchus destructor is an important plant-parasitic nematode. In the present study, the putative Ca(v)β subunit gene of D. destructor, namely, DdCa(v)β, was subjected to molecular characterization. In situ hybridization assays showed that DdCa(v)β was expressed in all nematode tissues. Transcriptional analyses showed that DdCa(v)β was expressed during each developmental stage of D. destructor, and the highest expression level was recorded in the third-stage juveniles. The crucial role of DdCa(v)β was verified by dsRNA soaking-mediated RNA interference (RNAi). Silencing of DdCa(v)β or HVA Ca(v)α(1) alone and co-silencing of the DdCa(v)β and HVA Ca(v)α(1) genes resulted in defective locomotion, stylet thrusting, chemotaxis, protein secretion and reproduction in D. destructor. Co-silencing of the HVA Ca(v)α(1) and Ca(v)β subunits showed stronger interference effects than single-gene silencing. This study provides insights for further study of VGCCs in plant-parasitic nematodes.