Shimatani Zenpei, Nishizawa-Yokoi Ayako, Endo Masaki, Toki Seiichi, Terada Rie
Laboratory of Plant Molecular Genetics, Graduate School of Biological Sciences, Nara Institute of Science and Technology Ikoma, Japan.
Plant Genome Engineering Research Unit, Agrogenomics Research Center, National Institute of Agrobiological Sciences Tsukuba, Japan.
Front Plant Sci. 2015 Jan 5;5:748. doi: 10.3389/fpls.2014.00748. eCollection 2014.
Gene targeting (GT) refers to the designed modification of genomic sequence(s) through homologous recombination (HR). GT is a powerful tool both for the study of gene function and for molecular breeding. However, in transformation of higher plants, non-homologous end joining (NHEJ) occurs overwhelmingly in somatic cells, masking HR-mediated GT. Positive-negative selection (PNS) is an approach for finding HR-mediated GT events because it can eliminate NHEJ effectively by expression of a negative-selection marker gene. In rice-a major crop worldwide-reproducible PNS-mediated GT of endogenous genes has now been successfully achieved. The procedure is based on strong PNS using diphtheria toxin A-fragment as a negative marker, and has succeeded in the directed modification of several endogenous rice genes in various ways. In addition to gene knock-outs and knock-ins, a nucleotide substitution in a target gene was also achieved recently. This review presents a summary of the development of the rice PNS system, highlighting its advantages. Different types of gene modification and gene editing aimed at developing new plant breeding technology based on PNS are discussed.
基因打靶(GT)是指通过同源重组(HR)对基因组序列进行的设计修饰。基因打靶对于基因功能研究和分子育种而言都是一种强大的工具。然而,在高等植物转化过程中,非同源末端连接(NHEJ)在体细胞中占主导地位,掩盖了HR介导的基因打靶。正负筛选(PNS)是一种寻找HR介导的基因打靶事件的方法,因为它可以通过表达负筛选标记基因有效消除NHEJ。在全球主要作物水稻中,现已成功实现了可重复的PNS介导的内源基因基因打靶。该方法基于使用白喉毒素A片段作为负标记的强PNS,并已成功以多种方式对多个水稻内源基因进行了定向修饰。除了基因敲除和敲入外,最近还实现了靶基因中的核苷酸替换。本文综述了水稻PNS系统的发展概况,突出了其优势。还讨论了旨在基于PNS开发新植物育种技术的不同类型的基因修饰和基因编辑。