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神经元内的结构区室:微丝异构体mRNA和蛋白质的发育调控组织

Structural compartments within neurons: developmentally regulated organization of microfilament isoform mRNA and protein.

作者信息

Hannan A J, Gunning P, Jeffrey P L, Weinberger R P

机构信息

Developmental Neurobiology Unit, Children's Medical Research Institute, Westmead, NSW, Australia.

出版信息

Mol Cell Neurosci. 1998 Aug;11(5-6):289-304. doi: 10.1006/mcne.1998.0693.

Abstract

The microfilament system is thought to be a crucial cytoskeletal component regulating development and mature function of neurons. The intracellular distribution of the microfilament isoform components, actin and tropomyosin (Tm), in neurons primarily in vivo, has been investigated at both the mRNA and the protein level using isoform specific riboprobes and antibodies. Our in vivo and in vitro studies have identified at least six neuronal compartments based on microfilament isoform mRNA localization: the developing soma, the mature soma, growth cone, developing axon hillock/proximal axon, mature somatodendritic and mature axonal pole soma. Protein localization patterns revealed that the isoforms were frequently distributed over a wider area than their respective mRNAs, suggesting that isoform specific patterns of mRNA targeting may influence, but do not absolutely determine, microfilament isoform location. Tm4 and Tm5 showed identical mRNA targeting in the developing neuron but distinct protein localization patterns. We suggest that in this instance mRNA location may best be viewed as a regulated site of synthesis and assembly, rather than a regulator of protein localization per se. In addition, Tm5 and beta-actin mRNA and protein locations were developmentally regulated, suggesting the possibility that environmental signals modulate targeting of specific mRNAs and their proteins. Thus, developmentally regulated mRNA localization and positional translation may act in concert with protein transport to regulate neuronal microfilament composition and consequently neuronal structure.

摘要

微丝系统被认为是调节神经元发育和成熟功能的关键细胞骨架成分。利用亚型特异性核糖探针和抗体,在mRNA和蛋白质水平上研究了主要在体内神经元中微丝亚型成分肌动蛋白和原肌球蛋白(Tm)的细胞内分布。我们的体内和体外研究基于微丝亚型mRNA定位确定了至少六个神经元区室:发育中的胞体、成熟的胞体、生长锥、发育中的轴丘/近端轴突、成熟的体树突和成熟的轴突极体胞体。蛋白质定位模式显示,这些亚型的分布区域通常比各自的mRNA更广泛,这表明mRNA靶向的亚型特异性模式可能会影响但并非绝对决定微丝亚型的位置。Tm4和Tm5在发育中的神经元中显示出相同的mRNA靶向,但蛋白质定位模式不同。我们认为,在这种情况下,mRNA的位置最好被视为合成和组装的调控位点,而不是蛋白质定位本身的调节因子。此外,Tm5和β-肌动蛋白的mRNA和蛋白质位置受到发育调控,这表明环境信号可能调节特定mRNA及其蛋白质的靶向。因此,发育调控的mRNA定位和定位翻译可能与蛋白质运输协同作用,以调节神经元微丝组成,进而调节神经元结构。

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