Izsvák Z, Ivics Z, Plasterk R H
Division of Molecular Biology Centre for Biomedical Genetics, The Netherlands Cancer Institute, Amsterdam, The Netherlands.
J Mol Biol. 2000 Sep 8;302(1):93-102. doi: 10.1006/jmbi.2000.4047.
Sleeping Beauty (SB), a member of the Tc1/mariner superfamily of transposable elements, is the only active DNA-based transposon system of vertebrate origin that is available for experimental manipulation. We have been using the SB element as a research tool to investigate some of the cis and trans-requirements of element mobilization, and mechanisms that regulate transposition in vertebrate species. In contrast to mariner transposons, which are regulated by overexpression inhibition, the frequency of SB transposition was found to be roughly proportional to the amount of transposase present in cells. Unlike Tc1 and mariner elements, SB contains two binding sites within each of its terminal inverted repeats, and we found that the presence of both of these sites is a strict requirement for mobilization. In addition to the size of the transposon itself, the length as well as sequence of the DNA outside the transposon have significant effects on transposition. As a general rule, the closer the transposon ends are, the more efficient transposition is from a donor molecule. We have found that SB can transform a wide range of vertebrate cells from fish to human. However, the efficiency and precision of transposition varied significantly among cell lines, suggesting potential involvement of host factors in SB transposition. A positive-negative selection assay was devised to enrich populations of cells harboring inserted transposons in their chromosomes. Using this assay, of the order of 10,000 independent transposon insertions can be generated in human cells in a single transfection experiment. Sleeping Beauty can be a powerful alternative to other vectors that are currently used for the production of transgenic animals and for human gene therapy.
睡美人(SB)是转座元件Tc1/水手超家族的成员,是唯一可用于实验操作的、起源于脊椎动物的基于DNA的活性转座子系统。我们一直将SB元件用作研究工具,以探究元件转座的一些顺式和反式要求,以及脊椎动物物种中转座调控的机制。与受过表达抑制调控的水手转座子不同,发现SB转座的频率大致与细胞中转座酶的量成正比。与Tc1和水手元件不同,SB在其每个末端反向重复序列内都包含两个结合位点,并且我们发现这两个位点的存在是转座的严格要求。除了转座子本身的大小外,转座子外部DNA的长度和序列对转座也有显著影响。一般来说,转座子末端越靠近,从供体分子进行转座的效率就越高。我们发现SB可以转化从鱼类到人类的多种脊椎动物细胞。然而,转座的效率和精确性在不同细胞系中差异很大,这表明宿主因子可能参与了SB转座。设计了一种正负选择测定法,以富集染色体中含有插入转座子的细胞群体。使用这种测定法,在一次转染实验中可以在人类细胞中产生约10000个独立的转座子插入。睡美人可以成为目前用于生产转基因动物和人类基因治疗的其他载体的有力替代品。