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c-di-GMP Arms an Anti-σ to Control Progression of Multicellular Differentiation in Streptomyces
Streptomyces are our primary source of antibiotics, produced concomitantly with the transition from vegetative growth to sporulation in a complex developmental life cycle. We previously showed that the signaling molecule c-di-GMP binds BldD, a master repressor, to control initiation of development....
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cell Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7005675/ https://www.ncbi.nlm.nih.gov/pubmed/31810759 http://dx.doi.org/10.1016/j.molcel.2019.11.006 |
Sumario: | Streptomyces are our primary source of antibiotics, produced concomitantly with the transition from vegetative growth to sporulation in a complex developmental life cycle. We previously showed that the signaling molecule c-di-GMP binds BldD, a master repressor, to control initiation of development. Here we demonstrate that c-di-GMP also intervenes later in development to control differentiation of the reproductive hyphae into spores by arming a novel anti-σ (RsiG) to bind and sequester a sporulation-specific σ factor (σ(WhiG)). We present the structure of the RsiG-(c-di-GMP)(2)-σ(WhiG) complex, revealing an unusual, partially intercalated c-di-GMP dimer bound at the RsiG-σ(WhiG) interface. RsiG binds c-di-GMP in the absence of σ(WhiG), employing a novel E(X)(3)S(X)(2)R(X)(3)Q(X)(3)D motif repeated on each helix of a coiled coil. Further studies demonstrate that c-di-GMP is essential for RsiG to inhibit σ(WhiG). These findings reveal a newly described control mechanism for σ-anti-σ complex formation and establish c-di-GMP as the central integrator of Streptomyces development. |
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