Columbia University Medical Center, Howard Hughes Medical Institute, New York, New York 10032, USA.
Genetics. 2010 Feb;184(2):317-9. doi: 10.1534/genetics.109.112938.
Much of our understanding of how organisms develop and function is derived from the extraordinarily powerful, classic approach of screening for mutant organisms in which a specific biological process is disrupted. Reaping the fruits of such forward genetic screens in metazoan model systems like Drosophila, Caenorhabditis elegans, or zebrafish traditionally involves time-consuming positional cloning strategies that result in the identification of the mutant locus. Whole genome sequencing (WGS) has begun to provide an effective alternative to this approach through direct pinpointing of the molecular lesion in a mutated strain isolated from a genetic screen. Apart from significantly altering the pace and costs of genetic analysis, WGS also provides new perspectives on solving genetic problems that are difficult to tackle with conventional approaches, such as identifying the molecular basis of multigenic and complex traits.
我们对生物发育和功能的理解在很大程度上来自于通过筛选特定生物过程被破坏的突变生物体的这种强大的经典方法。在多细胞模式生物系统中,如果蝇、秀丽隐杆线虫或斑马鱼中,收获正向遗传筛选的成果传统上涉及耗时的定位克隆策略,从而确定突变基因座。全基因组测序(WGS)已开始通过直接确定从遗传筛选中分离出的突变株中的分子病变,为这种方法提供了有效的替代方法。除了显著改变遗传分析的速度和成本外,WGS 还为解决传统方法难以解决的遗传问题提供了新的视角,例如确定多基因和复杂性状的分子基础。