Yamamoto Takashi
Department of Mathematical and Life Sciences, Graduate School of Science, Hiroshima University, Japan.
Clin Calcium. 2017;27(11):1638-1644.
Programmable site-specific nuclease mediated-genome editing is an emerging biotechnology for precise manipulation of target genes. In genome editing, gene-knockout as well as gene-knockin are possible in various organisms and cultured cells. CRISPR-Cas9, which was developed in 2012, is a convenient and efficient programmable site-specific nuclease and the use spreads around the world rapidly. For this, it is important for the progress of life science research to introduce the genome editing technology.
可编程位点特异性核酸酶介导的基因组编辑是一种用于精确操纵靶基因的新兴生物技术。在基因组编辑中,基因敲除以及基因敲入在各种生物体和培养细胞中都是可行的。2012年开发的CRISPR-Cas9是一种方便且高效的可编程位点特异性核酸酶,其应用迅速在全球范围内传播。为此,引入基因组编辑技术对生命科学研究的进展至关重要。