Omi Kazuya, Tokunaga Katsushi, Hohjoh Hirohiko
Department of Human Genetics, Graduate School of Medicine, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-0033, Japan.
FEBS Lett. 2004 Jan 30;558(1-3):89-95. doi: 10.1016/S0014-5793(04)00017-1.
The effect of RNA interference (RNAi) induced by synthetic small interfering RNAs (siRNAs) on proliferating mammalian cells appears to last for approximately 3-7 days after its induction. Here we show that the RNAi activity induced by a synthetic 21-nucleotide siRNA duplex in postmitotic neurons, mouse primary hippocampal neurons and neurons that differentiated from mouse embryonal carcinoma P19 cells persists for at least 3 weeks, suggesting long-lasting RNAi activity in mammalian neurons. In addition, we also show that an apoptotic (or antiviral) pathway triggered by long dsRNAs is generated during neuronal differentiation of P19 cells, by which the sequence-specific RNAi activity involving long dsRNA appears to be masked.
合成的小干扰RNA(siRNA)诱导的RNA干扰(RNAi)对增殖的哺乳动物细胞的影响在诱导后似乎持续约3至7天。在此我们表明,合成的21核苷酸siRNA双链体在有丝分裂后神经元、小鼠原代海马神经元以及从小鼠胚胎癌P19细胞分化而来的神经元中诱导的RNAi活性持续至少3周,这表明哺乳动物神经元中存在持久的RNAi活性。此外,我们还表明,在P19细胞的神经元分化过程中会产生由长双链RNA触发的凋亡(或抗病毒)途径,通过该途径,涉及长双链RNA的序列特异性RNAi活性似乎被掩盖。