The Black Family Stem Cell Institute, Icahn School of Medicine at Mount Sinai, New York, New York 10029, USA.
Department of Developmental and Regenerative Biology, Icahn School of Medicine at Mount Sinai, 1425 Madison Avenue, 13-20E, New York, New York 10029, USA.
Nat Commun. 2016 May 27;7:11742. doi: 10.1038/ncomms11742.
Loss-of-function studies are fundamental for dissecting gene function. Yet, methods to rapidly and effectively perturb genes in mammalian cells, and particularly in stem cells, are scarce. Here we present a system for simultaneous conditional regulation of two different proteins in the same mammalian cell. This system harnesses the plant auxin and jasmonate hormone-induced degradation pathways, and is deliverable with only two lentiviral vectors. It combines RNAi-mediated silencing of two endogenous proteins with the expression of two exogenous proteins whose degradation is induced by external ligands in a rapid, reversible, titratable and independent manner. By engineering molecular tuners for NANOG, CHK1, p53 and NOTCH1 in mammalian stem cells, we have validated the applicability of the system and demonstrated its potential to unravel complex biological processes.
失活功能研究对于剖析基因功能至关重要。然而,在哺乳动物细胞中,特别是在干细胞中,快速有效地干扰基因的方法却很少。在这里,我们提出了一种在同一哺乳动物细胞中同时对两种不同蛋白质进行条件调控的系统。该系统利用植物生长素和茉莉酸激素诱导的降解途径,仅用两个慢病毒载体即可实现。它将两种内源性蛋白质的 RNAi 介导沉默与两种外源性蛋白质的表达相结合,这两种外源性蛋白质的降解可通过外部配体快速、可逆、可滴定和独立地诱导。通过在哺乳动物干细胞中对 NANOG、CHK1、p53 和 NOTCH1 进行分子调谐器的工程设计,我们验证了该系统的适用性,并证明了其在揭示复杂生物学过程中的潜力。