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

被引:226
作者
Cuenca, AA [1 ]
Schetter, A
Aceto, D
Kemphues, K
Seydoux, G
机构
[1] Johns Hopkins Univ, Sch Med, Dept Mol Biol & Genet, Baltimore, MD 21205 USA
[2] Cornell Univ, Dept Mol Biol & Genet, Ithaca, NY 14853 USA
来源
DEVELOPMENT | 2003年 / 130卷 / 07期
关键词
polarity; embryo; par genes; C; elegans;
D O I
10.1242/dev.00284
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
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.
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页码:1255 / 1265
页数:11
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