用模式生物破译ALS的分子逻辑:“家庭事务”。

SOJ neurology Pub Date : 2017-01-01 Epub Date: 2017-07-19 DOI:10.15226/2374-6858/4/1/00132
Jonathan R Brent, P Hande Ozdinler
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引用次数: 1

摘要

ALS遗传学的最新进展增强了人们的希望,即该疾病发病机制的分子逻辑正在迅速接近。一个新出现的挑战是解剖由ALS基因突变改变的常见和独特的分子途径。啮齿类动物的疾病建模已经产生了许多重要的见解,但随着疾病遗传复杂性的增长,提高速度、成本和遗传可追溯性的额外模型将越来越有必要。果蝇、线虫和斑马鱼等模型对于绘制许多基础生物学过程的分子途径非常重要,但在神经变性研究中却相对不足。在这里,我们强调了用于研究ALS的模型增加多样性的好处和机会。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Deciphering the molecular logic of ALS using model organisms: "A family affair."

Deciphering the molecular logic of ALS using model organisms: "A family affair."

Recent advances in the genetics of ALS have bolstered hope that a molecular logic for the pathogenesis of the disease is fast approaching. An emerging challenge is the dissection of the common and unique molecular pathways altered by ALS gene mutations. Disease modeling in rodents has yielded many important insights, but as the genetic complexity of the disease grows, additional models with improved speed, cost and genetic tractability will be increasingly necessary. Models such as fruitfly, nematode, and zebrafish have been important for diagramming the molecular pathways that underlie many fundamental biological processes, but have been comparatively underutilized in the study of neurodegeneration. Here we highlight the benefits and opportunities for increased diversity in the models used to study ALS.

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