Fine-mapping natural alleles: quantitative complementation to the rescue

被引:31
|
作者
Turner, Thomas L. [1 ]
机构
[1] Univ Calif Santa Barbara, Dept Ecol Evolut & Marine Biol, Santa Barbara, CA 93106 USA
关键词
CRISPR; inversions; QTL mapping; quantitative complementation; GUIDED CAS9 NUCLEASE; DROSOPHILA-MELANOGASTER; TRAIT LOCI; HYBRID INCOMPATIBILITIES; INVERSION POLYMORPHISM; CAENORHABDITIS-ELEGANS; GENETIC INTERACTIONS; ANOPHELES-GAMBIAE; COMPLEX TRAITS; GENOME;
D O I
10.1111/mec.12719
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:2377 / 2382
页数:6
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