Format

Send to

Choose Destination
Cell Cycle. 2016;15(5):678-88. doi: 10.1080/15384101.2016.1147632.

STAR syndrome-associated CDK10/Cyclin M regulates actin network architecture and ciliogenesis.

Author information

1
a P2I2 group, Protein Phosphorylation and Human Disease Laboratory, Station Biologique de Roscoff, Centre National de la Recherche Scientifique (CNRS) and Université Pierre et Marie Curie (UPMC) , Roscoff , France.
2
b David H. Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology (MIT) , Cambridge , MA , USA.
3
c Proteomics Platform, Centre Hospitalier Universitaire de Québec (CHUQ) , Québec , Canada.
4
d Universitätsmedizin Göttingen, Department of Child and Adolescent Health, Division of Neuropediatrics , Göttingen , Germany.

Abstract

CDK10/CycM is a protein kinase deficient in STAR (toe Syndactyly, Telecanthus and Anogenital and Renal malformations) syndrome, which results from mutations in the X-linked FAM58A gene encoding Cyclin M. The biological functions of CDK10/CycM and etiology of STAR syndrome are poorly understood. Here, we report that deficiency of CDK10/Cyclin M promotes assembly and elongation of primary cilia. We establish that this reflects a key role for CDK10/Cyclin M in regulation of actin network organization, which is known to govern ciliogenesis. In an unbiased screen, we identified the RhoA-associated kinase PKN2 as a CDK10/CycM phosphorylation substrate. We establish that PKN2 is a bone fide regulator of ciliogenesis, acting in a similar manner to CDK10/CycM. We discovered that CDK10/Cyclin M binds and phosphorylates PKN2 on threonines 121 and 124, within PKN2's core RhoA-binding domain. Furthermore, we demonstrate that deficiencies in CDK10/CycM or PKN2, or expression of a non-phosphorylatable version of PKN2, destabilize both the RhoA protein and the actin network architecture. Importantly, we established that ectopic expression of RhoA is sufficient to override the induction of ciliogenesis resulting from CDK10/CycM knockdown, indicating that RhoA regulation is critical for CDK10/CycM's negative effect on ciliogenesis. Finally, we show that kidney sections from a STAR patient display dilated renal tubules and abnormal, elongated cilia. Altogether, these results reveal CDK10/CycM as a key regulator of actin dynamics and a suppressor of ciliogenesis through phosphorylation of PKN2 and promotion of RhoA signaling. Moreover, they suggest that STAR syndrome is a ciliopathy.

KEYWORDS:

Actin network; CDK10; Cyclin M; PKN2; RhoA; STAR syndrome; ciliogenesis

PMID:
27104747
PMCID:
PMC4846108
DOI:
10.1080/15384101.2016.1147632
[Indexed for MEDLINE]
Free PMC Article

Supplemental Content

Full text links

Icon for Taylor & Francis Icon for PubMed Central
Loading ...
Support Center