The bardet-biedl syndrome-related protein CCDC28b modulates mTORC2 function and interacts with SIN1 to control cilia length independently of the mTOR complex

Magdalena Cardenas-rodriguez, Florencia Irigoín, Daniel P.S. Osborn, Cecilia Gascue, Elias Nicholas Katsanis, Philip L. Beales, Jose L. Badano*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

21 Scopus citations

Abstract

CCDC28Bencodes a coiled coil domain-containing protein involved in ciliogenesis thatwasoriginally identified as a secondsite modifier of the ciliopathy Bardet-Biedl syndrome.We have previouslyshownthat 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.

Original languageEnglish (US)
Article numberddt253
Pages (from-to)4031-4042
Number of pages12
JournalHuman molecular genetics
Volume22
Issue number20
DOIs
StatePublished - Oct 2013

ASJC Scopus subject areas

  • Molecular Biology
  • Genetics
  • Genetics(clinical)

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