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  4. Centriolar SAS-5 is required for centrosome duplication in C. elegans
 
research article

Centriolar SAS-5 is required for centrosome duplication in C. elegans

Delattre, M.
•
Leidel, S.
•
Wani, K.
Show more
2004
Nature Cell Biology

Centrosomes, the major microtubule-organizing centres (MTOCs) of animal cells, are comprised of a pair of centrioles surrounded by pericentriolar material (PCM). Early in the cell cycle, there is a single centrosome, which duplicates during S-phase to direct bipolar spindle assembly during mitosis. Although crucial for proper cell division, the mechanisms that govern centrosome duplication are not fully understood. Here, we identify the Caenorhabditis elegans gene sas-5 as essential for daughter-centriole formation. SAS-5 is a coiled-coil protein that localizes primarily to centrioles. Fluorescence recovery after photobleaching (FRAP) experiments with green fluorescent protein (GFP) fused to SAS-5 (GFP-SAS-5) demonstrated that the protein shuttles between centrioles and the cytoplasm throughout the cell cycle. Analysis of mutant alleles revealed that the presence of SAS-5 at centrioles is crucial for daughter-centriole formation and that ZYG-1, a kinase that is also essential for this process, controls the distribution of SAS-5 to centrioles. Furthermore, partial RNA-interference (RNAi)-mediated inactivation experiments suggest that both sas-5 and zyg-1 are dose-dependent regulators of centrosome duplication.

  • Details
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Type
research article
DOI
10.1038/ncb1146
PubMed ID

15232593

Author(s)
Delattre, M.
Leidel, S.
Wani, K.
Baumer, K.
Bamat, J.
Schnabel, H.
Feichtinger, R.
Schnabel, R.
Gönczy, P.  
Date Issued

2004

Published in
Nature Cell Biology
Volume

6

Issue

7

Start page

656

End page

64

Subjects

Active Transport

•

Cell Nucleus/genetics

•

Animals

•

Caenorhabditis elegans/genetics/*metabolism/ultrastructure

•

Caenorhabditis elegans Proteins/genetics/isolation &

•

purification/*metabolism

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Cell Cycle Proteins/genetics/isolation & purification/*metabolism

•

Centrioles/*metabolism/ultrastructure

•

Centrosome/*metabolism/ultrastructure

•

Gene Dosage

•

Microscopy

•

Electron

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Mitosis/*genetics

•

Molecular Sequence Data

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Protein Kinases/genetics/metabolism

•

Protein Transport/genetics

•

RNA Interference/physiology

•

Research Support

•

Non-U.S. Gov't

•

Research Support

•

U.S. Gov't

•

P.H.S.

Note

Swiss Institute for Experimental Cancer Research (ISREC), CH-1066 Epalinges/Lausanne, Switzerland.

Journal Article

Editorial or Peer reviewed

REVIEWED

Written at

EPFL

EPFL units
UPGON  
Available on Infoscience
August 24, 2006
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/233788
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