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在使用RNAi超敏秀丽隐杆线虫菌株nre-1(hd20) lin-15b(hd126)进行的大规模RNA干扰筛选中鉴定出的轴突导向基因。

Axon guidance genes identified in a large-scale RNAi screen using the RNAi-hypersensitive Caenorhabditis elegans strain nre-1(hd20) lin-15b(hd126).

作者信息

Schmitz Caroline, Kinge Parag, Hutter Harald

机构信息

Max Planck Institute for Medical Research, Jahnstrasse 29, 69120 Heidelberg, Germany.

出版信息

Proc Natl Acad Sci U S A. 2007 Jan 16;104(3):834-9. doi: 10.1073/pnas.0510527104. Epub 2007 Jan 9.

Abstract

The navigation of axons toward their targets is a highly dynamic and precisely regulated process during nervous system development. The molecular basis of this navigation process is only partly understood. In Caenorhabditis elegans, we isolated the RNAi-hypersensitive strain nre-1(hd20) lin-15b(hd126), which allows us to phenocopy axon guidance defects of known genes by feeding RNAi. We used this mutant strain to systematically screen 4,577 genes on chromosomes I and III for axon guidance phenotypes. We identified 93 genes whose down-regulation led to penetrant ventral cord fasciculation defects or motoneuron commissure outgrowth defects. These genes encode various classes of proteins, ranging from secreted or putative cell surface proteins to transcription factors controlling gene expression. A majority of the genes is evolutionary conserved and previously uncharacterized. In addition, we found axon guidance functions for known genes like pry-1, a component of the Wnt-signaling pathway, and ced-1, a receptor required for the engulfment of neurons undergoing apoptosis during development. Our screen provides insights into molecular pathways operating during the generation of neuronal circuits and provides a basis for a more detailed analysis of gene networks regulating axon navigation.

摘要

在神经系统发育过程中,轴突向其靶标的导航是一个高度动态且精确调控的过程。目前仅部分了解这一导航过程的分子基础。在秀丽隐杆线虫中,我们分离出了RNAi超敏菌株nre-1(hd20) lin-15b(hd126),通过喂食RNAi,我们能够模拟已知基因的轴突导向缺陷。我们利用该突变菌株系统地筛选了I号和III号染色体上的4577个基因,以寻找轴突导向表型。我们鉴定出93个基因,其下调会导致明显的腹侧索束状化缺陷或运动神经元连合生长缺陷。这些基因编码各类蛋白质,从分泌型或假定的细胞表面蛋白到控制基因表达的转录因子。大多数基因在进化上是保守的,且此前未被表征。此外,我们还发现了已知基因的轴突导向功能,如Wnt信号通路的一个组成部分pry-1,以及发育过程中吞噬凋亡神经元所需的受体ced-1。我们的筛选为神经元回路生成过程中运作的分子途径提供了见解,并为更详细分析调节轴突导航的基因网络奠定了基础。

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