Baylis Howard A, Vázquez-Manrique Rafael P
Department of Zoology, University of Cambridge, Cambridge, U.K.
ScientificWorldJournal. 2011 Jul 7;11:1394-410. doi: 10.1100/tsw.2011.126.
Caenorhabditis elegans has a complete annotated genome sequence that is augmented by increasing quantities of data from high-throughput postgenomic analyses. This has led to an increasing need to identify the biological functions of specific genes using reverse genetics, i.e., moving from gene to phenotype. Fundamental to this aim is the ability to alter the structure of particular genes by means that are not accessible to classical genetic strategies. Thus, one dream of C. elegans researchers is to establish a toolkit for the controlled manipulation of any loci within the genome. Although C. elegans is amenable to a wide variety of genetic and molecular manipulations, controlled manipulation of endogenous genes by, for example, gene targeting has proved elusive until relatively recently. In this review, we describe and discuss the different methods available for the inactivation and modification of endogenous loci with a focus on strategies that permit some measure of control in this process. We describe methods that use random mutagenesis to isolate mutations in specific genes. We then focus on techniques that allow controlled manipulation of the genome: gene modification by transposon mobilisation, gene knock-out mediated by zinc-finger nucleases, and gene targeting by biolistic transformation.
秀丽隐杆线虫拥有完整的注释基因组序列,高通量后基因组分析产生的数据量不断增加,进一步丰富了该序列。这使得利用反向遗传学(即从基因到表型)来确定特定基因的生物学功能的需求日益增长。实现这一目标的基础是能够通过经典遗传策略无法实现的方法改变特定基因的结构。因此,秀丽隐杆线虫研究人员的一个梦想是建立一套用于可控操纵基因组内任何位点的工具包。尽管秀丽隐杆线虫适用于多种遗传和分子操作,但直到最近,通过例如基因靶向对内源基因进行可控操纵仍难以实现。在这篇综述中,我们描述并讨论了用于使内源位点失活和修饰的不同方法,重点关注在此过程中允许一定程度控制的策略。我们描述了使用随机诱变来分离特定基因中突变的方法。然后我们重点介绍允许对基因组进行可控操纵的技术:通过转座子动员进行基因修饰、由锌指核酸酶介导的基因敲除以及通过生物弹道转化进行基因靶向。