Schrader Tina A, Schrader Michael
College of Life and Environmental Sciences, Biosciences, University of Exeter, Geoffrey Pope Building, Stocker Road, Exeter, EX4 4QD, Devon, UK.
Methods Mol Biol. 2017;1595:69-79. doi: 10.1007/978-1-4939-6937-1_8.
RNAi technologies are a valuable tool in the identification and investigation of proteins that are involved in peroxisome biogenesis and function. Small interfering RNA (siRNA) has developed into the most commonly used RNAi tool for the induction of transient, short-term silencing of protein coding genes. Although siRNA can induce gene knockdown in a variety of mammalian cell lines, their utility is limited by efficient uptake of synthetic oligonucleotides into the cells. Here, we describe different transfection methods that have been successfully used by us to silence peroxisomal genes in a variety of cell lines, including primary human skin fibroblasts, which are usually difficult to transfect.
RNA干扰技术是鉴定和研究参与过氧化物酶体生物发生和功能的蛋白质的宝贵工具。小干扰RNA(siRNA)已发展成为诱导蛋白质编码基因瞬时、短期沉默最常用的RNA干扰工具。尽管siRNA可在多种哺乳动物细胞系中诱导基因敲低,但其效用受限于合成寡核苷酸有效摄取进入细胞。在此,我们描述了我们已成功用于在多种细胞系中沉默过氧化物酶体基因的不同转染方法,包括通常难以转染的原代人皮肤成纤维细胞。