4.5 Article

The BardetBiedl syndrome-related protein CCDC28B modulates mTORC2 function and interacts with SIN1 to control cilia length independently of the mTOR complex

期刊

HUMAN MOLECULAR GENETICS
卷 22, 期 20, 页码 4031-4042

出版社

OXFORD UNIV PRESS
DOI: 10.1093/hmg/ddt253

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资金

  1. ANII-Innova
  2. Genzyme Renal Innovations Program (GRIP)
  3. NIH [HD04260, DK072301]
  4. EU-FP7 [SYS-CILIA-241955]
  5. 'Programa de Desarrollo de las Ciencias Basicas', PEDECIBA
  6. Agencia Nacional de Investigacion e Innovacion (ANII), Uruguay
  7. Comision Academica de Postgrado, Universidad de la Republica, Uruguay

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CCDC28B encodes a coiled coil domain-containing protein involved in ciliogenesis that was originally identified as a second site modifier of the ciliopathy BardetBiedl syndrome. We have previously shown that the depletion of CCDC28B leads to shortened cilia; however, the mechanism underlying how this protein controls ciliary length is unknown. Here, we show that CCDC28B interacts with SIN1, a component of the mTOR complex 2 (mTORC2), and that this interaction is important both in the context of mTOR signaling and in a hitherto unknown, mTORC-independent role of SIN1 in cilia biology. We show that CCDC28B is a positive regulator of mTORC2, participating in its assembly/stability and modulating its activity, while not affecting mTORC1 function. Further, we show that Ccdc28b regulates cilia length in vivo, at least in part, through its interaction with Sin1. Importantly, depletion of Rictor, another core component of mTORC2, does not result in shortened cilia. Taken together, our findings implicate CCDC28B in the regulation of mTORC2, and uncover a novel function of SIN1 regulating cilia length that is likely independent of mTOR signaling.

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