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AAC as a Potential Target Gene to Control Verticillium dahliae.


ABSTRACT: Verticillium dahliae invades the roots of host plants and causes vascular wilt, which seriously diminishes the yield of cotton and other important crops. The protein AAC (ADP, ATP carrier) is responsible for transferring ATP from the mitochondria into the cytoplasm. When V. dahliae protoplasts were transformed with short interfering RNAs (siRNAs) targeting the VdAAC gene, fungal growth and sporulation were significantly inhibited. To further confirm a role for VdAAC in fungal development, we generated knockout mutants (?VdACC). Compared with wild-type V. dahliae (Vd wt), ?VdAAC was impaired in germination and virulence; these impairments were rescued in the complementary strains (?VdAAC-C). Moreover, when an RNAi construct of VdAAC under the control of the 35S promoter was used to transform Nicotiana benthamiana, the expression of VdAAC was downregulated in the transgenic seedlings, and they had elevated resistance against V. dahliae. The results of this study suggest that VdAAC contributes to fungal development, virulence and is a promising candidate gene to control V. dahliae. In addition, RNAi is a highly efficient way to silence fungal genes and provides a novel strategy to improve disease resistance in plants.

SUBMITTER: Su X 

PROVIDER: S-EPMC5295020 | biostudies-literature | 2017 Jan

REPOSITORIES: biostudies-literature

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AAC as a Potential Target Gene to Control Verticillium dahliae.

Su Xiaofeng X   Rehman Latifur L   Guo Huiming H   Li Xiaokang X   Zhang Rui R   Cheng Hongmei H  

Genes 20170110 1


<i>Verticillium dahliae</i> invades the roots of host plants and causes vascular wilt, which seriously diminishes the yield of cotton and other important crops. The protein AAC (ADP, ATP carrier) is responsible for transferring ATP from the mitochondria into the cytoplasm. When <i>V. dahliae</i> protoplasts were transformed with short interfering RNAs (siRNAs) targeting the <i>VdAAC</i> gene, fungal growth and sporulation were significantly inhibited. To further confirm a role for <i>VdAAC</i> i  ...[more]

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