Eccles Institute of Human Genetics, School of Medicine, University of Utah, Salt Lake City, Utah, 84112.
School of Biological Sciences, University of Utah, Salt Lake City, Utah, 84112.
Genetics. 2020 Aug;215(4):923-930. doi: 10.1534/genetics.120.303394. Epub 2020 Jun 25.
Site-specific recombinases are widely used tools for analysis of genetics, development, and cell biology, and many schemes have been devised to alter gene expression by recombinase-mediated DNA rearrangements. Because the and target sites for the commonly used FLP and Cre recombinases are asymmetrical, and must pair in the same direction to recombine, construct design must take into account orientation of the target sites. Both direct and inverted configurations have been used. However, the outcome of recombination between target sites on sister chromatids is frequently overlooked. This is especially consequential with inverted target sites, where exchange between oppositely oriented target sites on sisters will produce dicentric and acentric chromosomes. By using constructs that have inverted target sites in and in mice, we show here that dicentric chromosomes are produced in the presence of recombinase, and that the frequency of this event is quite high. The negative effects on cell viability and behavior can be significant, and should be considered when using such constructs.
位点特异性重组酶广泛用于遗传学、发育和细胞生物学的分析,已经设计了许多方案通过重组酶介导的 DNA 重排来改变基因表达。由于常用的 FLP 和 Cre 重组酶的 和 靶位点是不对称的,并且必须以相同的方向配对才能重组,因此构建设计必须考虑靶位点的方向。直接和倒置配置都已被使用。然而,姐妹染色单体上靶位点之间的重组的结果经常被忽视。在倒置靶位点中尤其如此,因为姐妹染色单体上相反定向的靶位点之间的交换将产生双中心和无着丝粒染色体。通过使用在 和 小鼠中具有倒置靶位点的构建体,我们在这里表明,在存在重组酶的情况下会产生双中心染色体,并且该事件的频率相当高。对细胞活力和行为的负面影响可能是显著的,在使用此类构建体时应予以考虑。