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Conidial Morphogenesis and Septin-Mediated Plant Infection Require Smo1, a Ras GTPase-Activating Protein in Magnaporthe oryzae.


ABSTRACT: The pathogenic life cycle of the rice blast fungus Magnaporthe oryzae involves a series of morphogenetic changes, essential for its ability to cause disease. The smo mutation was identified > 25 years ago, and affects the shape and development of diverse cell types in M. oryzae, including conidia, appressoria, and asci. All attempts to clone the SMO1 gene by map-based cloning or complementation have failed over many years. Here, we report the identification of SMO1 by a combination of bulk segregant analysis and comparative genome analysis. SMO1 encodes a GTPase-activating protein, which regulates Ras signaling during infection-related development. Targeted deletion of SMO1 results in abnormal, nonadherent conidia, impaired in their production of spore tip mucilage. Smo1 mutants also develop smaller appressoria, with a severely reduced capacity to infect rice plants. SMO1 is necessary for the organization of microtubules and for septin-dependent remodeling of the F-actin cytoskeleton at the appressorium pore. Smo1 physically interacts with components of the Ras2 signaling complex, and a range of other signaling and cytoskeletal components, including the four core septins. SMO1 is therefore necessary for the regulation of RAS activation required for conidial morphogenesis and septin-mediated plant infection.

SUBMITTER: Kershaw MJ 

PROVIDER: S-EPMC6325701 | biostudies-literature | 2019 Jan

REPOSITORIES: biostudies-literature

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Conidial Morphogenesis and Septin-Mediated Plant Infection Require Smo1, a Ras GTPase-Activating Protein in <i>Magnaporthe oryzae</i>.

Kershaw Michael J MJ   Basiewicz Magdalena M   Soanes Darren M DM   Yan Xia X   Ryder Lauren S LS   Csukai Michael M   Oses-Ruiz Miriam M   Valent Barbara B   Talbot Nicholas J NJ  

Genetics 20181116 1


The pathogenic life cycle of the rice blast fungus <i>Magnaporthe oryzae</i> involves a series of morphogenetic changes, essential for its ability to cause disease. The <i>smo</i> mutation was identified > 25 years ago, and affects the shape and development of diverse cell types in <i>M. oryzae</i>, including conidia, appressoria, and asci. All attempts to clone the <i>SMO1</i> gene by map-based cloning or complementation have failed over many years. Here, we report the identification of <i>SMO1  ...[more]

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