Unknown

Dataset Information

0

Cep63 and cep152 cooperate to ensure centriole duplication.


ABSTRACT: Centrosomes consist of two centrioles embedded in pericentriolar material and function as the main microtubule organising centres in dividing animal cells. They ensure proper formation and orientation of the mitotic spindle and are therefore essential for the maintenance of genome stability. Centrosome function is crucial during embryonic development, highlighted by the discovery of mutations in genes encoding centrosome or spindle pole proteins that cause autosomal recessive primary microcephaly, including Cep63 and Cep152. In this study we show that Cep63 functions to ensure that centriole duplication occurs reliably in dividing mammalian cells. We show that the interaction between Cep63 and Cep152 can occur independently of centrosome localisation and that the two proteins are dependent on one another for centrosomal localisation. Further, both mouse and human Cep63 and Cep152 cooperate to ensure efficient centriole duplication by promoting the accumulation of essential centriole duplication factors upstream of SAS-6 recruitment and procentriole formation. These observations describe the requirement for Cep63 in maintaining centriole number in dividing mammalian cells and further establish the order of events in centriole formation.

SUBMITTER: Brown NJ 

PROVIDER: S-EPMC3728344 | biostudies-literature | 2013

REPOSITORIES: biostudies-literature

altmetric image

Publications

Cep63 and cep152 cooperate to ensure centriole duplication.

Brown Nicola J NJ   Marjanović Marko M   Lüders Jens J   Stracker Travis H TH   Costanzo Vincenzo V  

PloS one 20130730 7


Centrosomes consist of two centrioles embedded in pericentriolar material and function as the main microtubule organising centres in dividing animal cells. They ensure proper formation and orientation of the mitotic spindle and are therefore essential for the maintenance of genome stability. Centrosome function is crucial during embryonic development, highlighted by the discovery of mutations in genes encoding centrosome or spindle pole proteins that cause autosomal recessive primary microcephal  ...[more]

Similar Datasets

| S-EPMC7189096 | biostudies-literature
| S-EPMC2983069 | biostudies-literature
| S-EPMC7836272 | biostudies-literature
| S-EPMC2171251 | biostudies-literature