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PMID: 12588843 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Polarization of the C. elegans zygote proceeds via distinct establishment and maintenance phases.

Development (Cambridge, England) ·Vol. 130 ·No. 7 ·2003-04-00 ·Pages 1255-65

Cuenca AA, Schetter A, Aceto D, Kemphues K, Seydoux G

Abstract

Polarization of the C. elegans zygote along the anterior-posterior axis depends on cortically enriched (PAR) and cytoplasmic (MEX-5/6) proteins, which function together to localize determinants (e.g. PIE-1) in response to a polarizing cue associated with the sperm asters. Using time-lapse microscopy and GFP fusions, we have analyzed the localization dynamics of PAR-2, PAR-6, MEX-5, MEX-6 and PIE-1 in wild-type and mutant embryos. These studies reveal that polarization involves two genetically and temporally distinct phases. During the first phase (establishment), the sperm asters at one end of the embryo exclude the PAR-3/PAR-6/PKC3 complex from the nearby cortex, allowing the ring finger protein PAR-2 to accumulate in an expanding 'posterior' domain. Onset of the establishment phase involves the non-muscle myosin NMY-2 and the 14-3-3 protein PAR-5. The kinase PAR-1 and the CCCH finger proteins MEX-5 and MEX-6 also function during the establishment phase in a feedback loop to regulate growth of the posterior domain. The second phase begins after pronuclear meeting, when the sperm asters begin to invade the anterior. During this phase (maintenance), PAR-2 maintains anterior-posterior polarity by excluding the PAR-3/PAR-6/PKC3 complex from the posterior. These findings provide a model for how PAR and MEX proteins convert a transient asymmetry into a stably polarized axis.

MeSH Terms
14-3-3 Proteins Animals Caenorhabditis elegans/embryology Caenorhabditis elegans Proteins/genetics,metabolism Green Fluorescent Proteins Helminth Proteins/genetics,metabolism Luminescent Proteins/genetics,metabolism Mutation Nuclear Proteins/genetics,metabolism Proteins/genetics,metabolism Receptor, PAR-2 Receptors, Thrombin/genetics,metabolism Recombinant Fusion Proteins/genetics,metabolism Tyrosine 3-Monooxygenase/genetics,metabolism Zygote/physiology
Chemicals
14-3-3 Proteins Caenorhabditis elegans Proteins Helminth Proteins Luminescent Proteins MEX-5 protein, C elegans MEX-6 protein, C elegans Nuclear Proteins Proteins Receptor, PAR-2 Receptors, Thrombin Recombinant Fusion Proteins par-5 protein, C elegans par-6 protein, C elegans pie-1 protein, C elegans Green Fluorescent Proteins Tyrosine 3-Monooxygenase
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Cuenca Adrian A
Department of Molecular Biology and Genetics, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205, USA.
Schetter Aaron
Aceto Donato
Kemphues Kenneth
Seydoux Geraldine
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Article Info
Journal
Development (Cambridge, England)
Abbr.
Development
ISSN
0950-1991
Published
2003-04-00
Pages
1255-65
Language
English
Region
England
NLM ID
8701744
PMCID
PMC1761648
Subset
IM
Grants
NIGMS NIH HHS · R01 GM064537 · United States
NIGMS NIH HHS · R01GM64537 · United States
NICHD NIH HHS · R01HD27689 · United States
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