Urnov Fyodor D, Rebar Edward J, Reik Andreas, Pandolfi Pier Paolo
Sangamo Biosciences, Pt. Richmond Technology Center, CA 94804, USA.
EMBO Rep. 2002 Jul;3(7):610-5. doi: 10.1093/embo-reports/kvf140.
Despite its central importance in gene regulation, chromatin in mammalian cells remains relatively poorly understood-a predicament due to the paucity of robust genetic tools in mammals, the complexity of the chromatin remodeling machinery, and the dynamic properties of chromatin in vivo. Here we review recent developments in understanding endogenous mammalian gene regulation via the use of designed transcription factors (TFs). These include mutated forms of naturally occurring TFs that exhibit dominant-negative activity, and designed proteins with novel, predetermined DNA-binding specificities. Systematic targeting of designed TFs to particular promoters is helping to illuminate the complex rules that chromatin imposes on TF access and action in vivo. We evaluate the potential applications of these proteins as probes of mammalian chromatin-based regulatory pathways and their potential for the therapy of human disease, highlighting leukemia in particular.
尽管染色质在基因调控中至关重要,但哺乳动物细胞中的染色质仍相对难以理解——这一困境源于哺乳动物中强大的遗传工具匮乏、染色质重塑机制的复杂性以及体内染色质的动态特性。在此,我们回顾了通过使用设计转录因子(TFs)来理解内源性哺乳动物基因调控的最新进展。这些包括具有显性负性活性的天然TFs的突变形式,以及具有新颖、预定DNA结合特异性的设计蛋白。将设计TFs系统地靶向特定启动子有助于阐明染色质在体内对TF进入和作用所施加的复杂规则。我们评估了这些蛋白作为哺乳动物基于染色质的调控途径探针的潜在应用及其治疗人类疾病(特别是白血病)的潜力。