4.8 Article

Tobacco calmodulin-like protein provides secondary defense by binding to and directing degradation of virus RNA silencing suppressors

Publisher

NATL ACAD SCIENCES
DOI: 10.1073/pnas.1201628109

Keywords

innate immunity; arms race; ubiquitin-26S proteasome

Funding

  1. Japan Society for the Promotion of Science
  2. Ministry of Education, Culture, Sports, Science, and Technology of Japan [17780032, 18108001, 20688002]
  3. Northern Advancement Center for Science and Technology of Hokkaido, Japan
  4. National Institutes of Health [GM068743]
  5. Grants-in-Aid for Scientific Research [23780305, 18108001, 17780032, 20688002, 24880005] Funding Source: KAKEN

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RNA silencing (RNAi) induced by virus-derived double-stranded RNA (dsRNA), which is in a sense regarded as a pathogen-associated molecular pattern (PAMP) of viruses, is a general plant defense mechanism. To counteract this defense, plant viruses express RNA silencing suppressors (RSSs), many of which bind to dsRNA and attenuate RNAi. We showed that the tobacco calmodulin-like protein, rgs-CaM, counterattacked viral RSSs by binding to their dsRNA-binding domains and sequestering them from inhibiting RNAi. Autophagy-like protein degradation seemed to operate to degrade RSSs with the sacrifice of rgs-CaM. These RSSs could thus be regarded as secondary viral PAMPs. This study uncovered a unique defense system in which an rgs-CaM-mediated countermeasure against viral RSSs enhanced host antiviral RNAi in tobacco.

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