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神经丝蛋白-L基因无义突变导致鹌鹑神经丝蛋白缺乏。

Neurofilament deficiency in quail caused by nonsense mutation in neurofilament-L gene.

作者信息

Ohara O, Gahara Y, Miyake T, Teraoka H, Kitamura T

机构信息

Shionogi Research Laboratories, Shionogi & Co., Ltd., Osaka, Japan.

出版信息

J Cell Biol. 1993 Apr;121(2):387-95. doi: 10.1083/jcb.121.2.387.

Abstract

The existence of a neurofilament-deficient mutant of Japanese quail was recently documented (Yamasaki, H., C. Itakura, and M. Mizutani. 1991. Acta Neuropathol. 82:427-434), but the genetic events leading to the neurofilament deficiency have yet to be determined. Our molecular biological analyses revealed that the expression of neurofilament-L (NF-L) gene was specifically repressed in neurons of this mutant. To search for mutation(s) responsible for the shutdown of this gene expression, we cloned and sequenced the NF-L genes in the wild-type and mutant quails. It is eventually found that the NF-L gene in the mutant includes a nonsense mutation at the deduced amino acid residue 114, indicating that the mutant is incapable of producing even a trace amount of polymerization-competent NF-L protein at any situation. The identification of this nonsense mutation provides us with a solid basis on which molecular mechanisms underlying the alteration in the neuronal cytoskeletal architecture in the mutant should be interpreted.

摘要

最近有文献记载了日本鹌鹑存在神经丝缺陷突变体(Yamasaki, H., C. Itakura, and M. Mizutani. 1991. Acta Neuropathol. 82:427 - 434),但导致神经丝缺陷的遗传事件尚未确定。我们的分子生物学分析表明,神经丝-L(NF-L)基因的表达在该突变体的神经元中被特异性抑制。为了寻找导致该基因表达关闭的突变,我们克隆并测序了野生型和突变型鹌鹑的NF-L基因。最终发现,突变体中的NF-L基因在推导的氨基酸残基114处存在无义突变,这表明该突变体在任何情况下都无法产生哪怕微量的具有聚合能力的NF-L蛋白。这种无义突变的鉴定为我们解释突变体中神经元细胞骨架结构改变的分子机制提供了坚实的基础。

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