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精细定位天然等位基因:定量互补拯救。

Fine-mapping natural alleles: quantitative complementation to the rescue.

机构信息

Department of Ecology, Evolution, and Marine Biology, University of California, Santa Barbara, Noble Hall, Room 2128, Santa Barbara, CA, 93106-9620, USA.

出版信息

Mol Ecol. 2014 May;23(10):2377-82. doi: 10.1111/mec.12719. Epub 2014 Apr 16.

Abstract

Mapping the genes responsible for natural variation and divergence is a challenging task. Many studies have mapped genes to genomic regions or generated lists of candidates, but few studies have implicated specific genes with a high standard of evidence. I propose that combining recent advances in genomic engineering with a modified version of the quantitative complementation test will help turn candidate genes into causal genes. By creating loss-of-function mutations in natural strains, and using these mutations to quantitatively fail-to-complement natural alleles, fine mapping should be greatly facilitated. As an example, I propose that the CRISPR/Cas9 system could be combined with the FLP/FRT system to fine-map genes in the numerous systems where inversions have frustrated these efforts.

摘要

绘制负责自然变异和分化的基因图谱是一项具有挑战性的任务。许多研究已经将基因映射到基因组区域或生成候选基因列表,但很少有研究用高标准的证据表明特定基因的作用。我提出,将基因组工程的最新进展与改良的定量互补测试相结合,将有助于候选基因转化为因果基因。通过在自然品系中创建功能丧失突变,并使用这些突变对自然等位基因进行定量互补失败,精细映射应该会得到极大的促进。例如,我建议将 CRISPR/Cas9 系统与 FLP/FRT 系统相结合,以对众多因倒位而使这些努力受挫的系统中的基因进行精细映射。

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