Norga Koenraad K, Gurganus Marjorie C, Dilda Christy L, Yamamoto Akihiko, Lyman Richard F, Patel Prajal H, Rubin Gerald M, Hoskins Roger A, Mackay Trudy F, Bellen Hugo J
Howard Hughes Medical Institute, Department of Molecular and Human Genetics, Baylor College of Medicine, One Baylor Plaza, Room T630, Houston, TX 77030, USA.
Curr Biol. 2003 Aug 19;13(16):1388-96. doi: 10.1016/s0960-9822(03)00546-3.
The identification of the function of all genes that contribute to specific biological processes and complex traits is one of the major challenges in the postgenomic era. One approach is to employ forward genetic screens in genetically tractable model organisms. In Drosophila melanogaster, P element-mediated insertional mutagenesis is a versatile tool for the dissection of molecular pathways, and there is an ongoing effort to tag every gene with a P element insertion. However, the vast majority of P element insertion lines are viable and fertile as homozygotes and do not exhibit obvious phenotypic defects, perhaps because of the tendency for P elements to insert 5' of transcription units. Quantitative genetic analysis of subtle effects of P element mutations that have been induced in an isogenic background may be a highly efficient method for functional genome annotation.
Here, we have tested the efficacy of this strategy by assessing the extent to which screening for quantitative effects of P elements on sensory bristle number can identify genes affecting neural development. We find that such quantitative screens uncover an unusually large number of genes that are known to function in neural development, as well as genes with yet uncharacterized effects on neural development, and novel loci.
Our findings establish the use of quantitative trait analysis for functional genome annotation through forward genetics. Similar analyses of quantitative effects of P element insertions will facilitate our understanding of the genes affecting many other complex traits in Drosophila.
确定所有参与特定生物学过程和复杂性状的基因的功能是后基因组时代的主要挑战之一。一种方法是在遗传上易于处理的模式生物中进行正向遗传筛选。在黑腹果蝇中,P 元素介导的插入诱变是剖析分子途径的一种通用工具,目前正在努力用 P 元素插入标记每个基因。然而,绝大多数 P 元素插入系作为纯合子是可行且可育的,并且没有表现出明显的表型缺陷,这可能是因为 P 元素倾向于插入转录单位的 5'端。对在同基因背景下诱导的 P 元素突变的细微效应进行数量遗传分析可能是功能基因组注释的一种高效方法。
在这里,我们通过评估筛选 P 元素对感觉刚毛数量的定量效应能够鉴定影响神经发育的基因的程度,测试了该策略的有效性。我们发现,这种定量筛选揭示了大量已知在神经发育中起作用的基因,以及对神经发育有尚未表征效应的基因和新位点。
我们的研究结果确立了通过正向遗传学利用数量性状分析进行功能基因组注释的方法。对 P 元素插入的定量效应进行类似分析将有助于我们理解影响果蝇许多其他复杂性状的基因。