Jeltsch Albert
Department of Biochemistry, Institute of Biochemistry and Technical Biochemistry, University of Stuttgart, Stuttgart, Germany.
Front Genet. 2018 Jan 26;9:5. doi: 10.3389/fgene.2018.00005. eCollection 2018.
Genome targeting of restriction enzymes and DNA methyltransferases has many important applications including genome and epigenome editing. 15-20 years ago, my group was involved in the development of approaches for programmable genome targeting, aiming to connect enzymes with an oligodeoxynucleotide (ODN), which could form a sequence-specific triple helix at the genomic target site. Importantly, the target site of such enzyme-ODN conjugate could be varied simply by altering the ODN sequence promising great applicative values. However, this approach was facing many problems including the preparation and purification of the enzyme-ODN conjugates, their efficient delivery into cells, slow kinetics of triple helix formation and the requirement of a poly-purine target site sequence. Hence, for several years genome and epigenome editing approaches mainly were based on Zinc fingers and TAL proteins as targeting devices. More recently, CRISPR/Cas systems were discovered, which use a bound RNA for genome targeting that forms an RNA/DNA duplex with one DNA strand of the target site. These systems combine all potential advantages of the once imagined enzyme-ODN conjugates and avoid all main disadvantageous. Consequently, the application of CRISPR/Cas in genome and epigenome editing has exploded in recent years. We can draw two important conclusions from this example of research history. First, evolution still is the better bioengineer than humans and, whenever tested in parallel, natural solutions outcompete engineered ones. Second, CRISPR/Cas system were discovered in pure, curiosity driven, basic research, highlighting that it is basic, bottom-up research paving the way for fundamental innovation.
限制酶和DNA甲基转移酶的基因组靶向具有许多重要应用,包括基因组和表观基因组编辑。15到20年前,我的团队参与了可编程基因组靶向方法的开发,旨在将酶与寡脱氧核苷酸(ODN)连接起来,该寡脱氧核苷酸可在基因组靶位点形成序列特异性三链螺旋。重要的是,这种酶-ODN偶联物的靶位点可以通过改变ODN序列简单地改变,具有很大的应用价值。然而,这种方法面临着许多问题,包括酶-ODN偶联物的制备和纯化、它们有效递送至细胞、三链螺旋形成的动力学缓慢以及对多嘌呤靶位点序列的要求。因此,多年来基因组和表观基因组编辑方法主要基于锌指和TAL蛋白作为靶向装置。最近,发现了CRISPR/Cas系统,该系统使用结合的RNA进行基因组靶向,与靶位点的一条DNA链形成RNA/DNA双链体。这些系统结合了曾经设想的酶-ODN偶联物的所有潜在优势,并避免了所有主要缺点。因此,近年来CRISPR/Cas在基因组和表观基因组编辑中的应用激增。从这个研究历史例子中我们可以得出两个重要结论。第一,进化仍然是比人类更好的生物工程师,并且每当进行并行测试时,自然解决方案胜过工程解决方案。第二,CRISPR/Cas系统是在纯粹的、由好奇心驱动的基础研究中发现的,这突出表明是基础的、自下而上的研究为根本性创新铺平了道路。