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秀丽隐杆线虫受精卵的极化通过不同的建立和维持阶段进行。

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

作者信息

Cuenca Adrian A, Schetter Aaron, Aceto Donato, Kemphues Kenneth, Seydoux Geraldine

机构信息

Department of Molecular Biology and Genetics, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205, USA.

出版信息

Development. 2003 Apr;130(7):1255-65. doi: 10.1242/dev.00284.

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.

摘要

秀丽隐杆线虫受精卵沿前后轴的极化依赖于皮质富集(PAR)蛋白和细胞质(MEX - 5/6)蛋白,它们共同作用以响应与精子星体相关的极化信号来定位决定因子(如PIE - 1)。利用延时显微镜和绿色荧光蛋白融合技术,我们分析了野生型和突变型胚胎中PAR - 2、PAR - 6、MEX - 5、MEX - 6和PIE - 1的定位动态。这些研究表明,极化涉及两个在遗传和时间上不同的阶段。在第一阶段(建立),胚胎一端的精子星体将PAR - 3/PAR - 6/PKC3复合物排除在附近的皮质之外,使环状指蛋白PAR - 2在不断扩大的“后部”区域积累。建立阶段的开始涉及非肌肉肌球蛋白NMY - 2和14 - 3 - 3蛋白PAR - 5。激酶PAR - 1以及CCCH指蛋白MEX - 5和MEX - 6在建立阶段也通过反馈环发挥作用,以调节后部区域的生长。第二阶段在原核相遇后开始,此时精子星体开始侵入前部。在这个阶段(维持),PAR - 2通过将PAR - 3/PAR - 6/PKC3复合物排除在后部来维持前后极性。这些发现为PAR蛋白和MEX蛋白如何将短暂的不对称转化为稳定的极化轴提供了一个模型。

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