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对果蝇缺失突变进行胚胎表型和孤儿受体配体的系统筛选。

Systematic screening of Drosophila deficiency mutations for embryonic phenotypes and orphan receptor ligands.

机构信息

Division of Biology, California Institute of Technology, Pasadena, California, United States of America.

出版信息

PLoS One. 2010 Aug 19;5(8):e12288. doi: 10.1371/journal.pone.0012288.

Abstract

This paper defines a collection of Drosophila deletion mutations (deficiencies) that can be systematically screened for embryonic phenotypes, orphan receptor ligands, and genes affecting protein localization. It reports the results of deficiency screens we have conducted that have revealed new axon guidance phenotypes in the central nervous system and neuromuscular system and permitted a quantitative assessment of the number of potential genes involved in regulating guidance of specific motor axon branches. Deficiency "kits" that cover the genome with a minimum number of lines have been established to facilitate gene mapping. These kits cannot be systematically analyzed for phenotypes, however, since embryos homozygous for many deficiencies in these kits fail to develop due to the loss of key gene products encoded within the deficiency. To create new kits that can be screened for phenotype, we have examined the development of the nervous system in embryos homozygous for more than 700 distinct deficiency mutations. A kit of approximately 400 deficiency lines for which homozygotes have a recognizable nervous system and intact body walls encompasses >80% of the genome. Here we show examples of screens of this kit for orphan receptor ligands and neuronal antigen expression. It can also be used to find genes involved in expression, patterning, and subcellular localization of any protein that can be visualized by antibody staining. A subset kit of 233 deficiency lines, for which homozygotes develop relatively normally to late stage 16, covers approximately 50% of the genome. We have screened it for axon guidance phenotypes, and we present examples of new phenotypes we have identified. The subset kit can be used to screen for phenotypes affecting all embryonic organs. In the future, these deficiency kits will allow Drosophila researchers to rapidly and efficiently execute genome-wide anatomical screens that require examination of individual embryos at high magnification.

摘要

本文定义了一组果蝇缺失突变(缺陷),可对其进行系统筛选,以获得胚胎表型、孤儿受体配体和影响蛋白质定位的基因。本文报告了我们进行的缺陷筛选结果,这些结果揭示了中枢神经系统和神经肌肉系统中的新轴突导向表型,并对涉及调节特定运动轴突分支导向的潜在基因数量进行了定量评估。已经建立了覆盖基因组的最小缺陷线数的“缺陷试剂盒”,以促进基因定位。然而,这些试剂盒不能系统地进行表型分析,因为这些试剂盒中许多缺陷的纯合子胚胎由于缺陷内编码的关键基因产物的丢失而无法发育。为了创建可用于筛选表型的新试剂盒,我们检查了超过 700 个不同缺陷纯合子胚胎的神经系统发育情况。大约 400 条缺陷线的试剂盒,其纯合子具有可识别的神经系统和完整的体壁,涵盖了 >80%的基因组。本文展示了该试剂盒筛选孤儿受体配体和神经元抗原表达的示例。它还可用于发现任何可通过抗体染色可视化的蛋白质的表达、模式形成和亚细胞定位所涉及的基因。一个由 233 条缺陷线组成的子集试剂盒,其纯合子发育到晚期 16 期相对正常,覆盖了大约 50%的基因组。我们已经对其进行了轴突导向表型筛选,并展示了我们发现的一些新表型。该子集试剂盒可用于筛选影响所有胚胎器官的表型。将来,这些缺陷试剂盒将使果蝇研究人员能够快速有效地执行需要在高倍放大下检查单个胚胎的全基因组解剖筛选。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/35b4/2924397/235a5d7718c7/pone.0012288.g001.jpg

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