Jayaraman K, McParland K, Miller P, Ts'o P O
Proc Natl Acad Sci U S A. 1981 Mar;78(3):1537-41. doi: 10.1073/pnas.78.3.1537.
A series of nonionic oligonucleotide analogues, the deoxyribooligonucleoside methylphosphonates, were synthesized. The base sequences of these compounds, d(ApGpGp), d(ApGpGp)(2), and d[(ApGpGp)(2)T], are complementary to the Shine-Dalgarno sequence (-A-C-C-U-C-C-U-) found at the 3' end of bacterial 16S rRNA. These nonionic oligonucleotide analogues were tested for their ability to inhibit the in vitro translation of mRNAs in cell-free systems of Escherichia coli and rabbit reticulocyte. In the E. coli system, both d(ApGpGp)(2) and d[(ApGpGp)(2)T] effectively inhibited MS-2 RNA-directed protein synthesis but they had much less effect on either poly(U)- or poly(A)-directed polypeptide synthesis. In the reticulocyte system, these compounds had no significant effect on the translation of globin mRNA. The observation that d[(ApGpGp)(2)[(3)H]T)] binds to 70S ribosomes (association constant, 2.0 x 10(4) M(-1), 37 degrees C) together with the specificity of the inhibitory action of these compounds on protein synthesis strongly suggests that inhibition of translation is a consequence of analogue binding to Shine-Dalgarno sequence of 16S rRNA. The oligonucleoside methylphosphonates inhibited both protein synthesis (without concurrent inhibition of RNA synthesis) and colony formation by E. coli ML 308-225 (a permeable mutant) whose cell wall contains negligible quantities of lipopolysaccharide but had no effect on wild-type E. coli B. Our preliminary results on the uptake of oligodeoxyribonucleoside methylphosphonates by E. coli B show that these cells are not permeable to oligomers longer than 4 nucleotidyl units. Although oligodeoxyribonucleoside methylphosphonates are taken up by mammalian cells in culture, this series of analogues had negligible inhibitory effects on colony formation by transformed human cells. This study indicates that this class of nonionic oligonucleotide analogues can be used to probe and regulate the function and structure of nucleic acids of defined sequence within living cells.
合成了一系列非离子型寡核苷酸类似物,即脱氧核糖寡核苷甲基膦酸酯。这些化合物d(ApGpGp)、d(ApGpGp)(2)和d[(ApGpGp)(2)T]的碱基序列与细菌16S rRNA 3'端的Shine-Dalgarno序列(-A-C-C-U-C-C-U-)互补。测试了这些非离子型寡核苷酸类似物在大肠杆菌和兔网织红细胞无细胞体系中抑制mRNA体外翻译的能力。在大肠杆菌体系中,d(ApGpGp)(2)和d[(ApGpGp)(2)T]均能有效抑制MS-2 RNA指导的蛋白质合成,但对聚(U)或聚(A)指导的多肽合成影响较小。在网织红细胞体系中,这些化合物对珠蛋白mRNA的翻译无显著影响。d[(ApGpGp)(2)[(3)H]T)]与70S核糖体结合(结合常数,2.0×10(4) M(-1),37℃)以及这些化合物对蛋白质合成抑制作用的特异性这一观察结果强烈表明,翻译抑制是类似物与16S rRNA的Shine-Dalgarno序列结合的结果。寡核苷甲基膦酸酯抑制了蛋白质合成(同时不抑制RNA合成)以及大肠杆菌ML 308-225(一种通透性突变体)的菌落形成,该突变体细胞壁含可忽略不计的脂多糖,但对野生型大肠杆菌B无影响。我们关于大肠杆菌B摄取寡脱氧核糖核苷甲基膦酸酯的初步结果表明,这些细胞对长度超过4个核苷酸单元的寡聚物是不可通透的。尽管寡脱氧核糖核苷甲基膦酸酯可被培养的哺乳动物细胞摄取,但这一系列类似物对转化的人类细胞的菌落形成抑制作用可忽略不计。这项研究表明,这类非离子型寡核苷酸类似物可用于探测和调节活细胞内特定序列核酸的功能和结构。