Patel Sejal, Rana Jagruti, Roy Jyoti, Huang Haidong
Department of Chemistry and Environmental Science, New Jersey Institute of Technology, 323 Martin L, King Blvd, Newark, NJ, 07102, USA.
Chem Cent J. 2012 Jan 13;6:3. doi: 10.1186/1752-153X-6-3.
Chemical agents that cleave HIV genome can be potentially used for anti-HIV therapy. In this report, the cleavage of the upper stem-loop region of HIV-1 TAR RNA was studied in a variety of buffers containing organic catalysts. trans-(±)-Cyclohexane-1,2-diamine was found to cleave the RNA with the highest activity (31%, 37°C, 18 h). Cleavage of the RNA in trans-(±)-cyclohexane-1,2-diamine buffer was also studied when the RNA was hybridized with complementary DNAs. A pyrene-modified C3 spacer was incorporated to the DNA strand to facilitate the formation of a RNA bulge loop in the RNA/DNA duplex. In contrast, unmodified DNAs cannot efficiently generate RNA bulge loops, regardless of the DNA sequences. The results showed that the pyrene-stablized RNA bulge loops were efficiently and site-specifically cleaved by trans-(±)-cyclohexane-1,2-diamine.
能够切割HIV基因组的化学试剂有潜力用于抗HIV治疗。在本报告中,我们研究了在含有有机催化剂的多种缓冲液中HIV-1 TAR RNA上茎环区域的切割情况。发现反式-(±)-环己烷-1,2-二胺切割RNA的活性最高(31%,37°C,18小时)。当RNA与互补DNA杂交时,我们也研究了在反式-(±)-环己烷-1,2-二胺缓冲液中RNA的切割情况。将芘修饰的C3间隔基掺入DNA链中,以促进RNA/DNA双链体中RNA凸起环的形成。相比之下,无论DNA序列如何,未修饰的DNA都不能有效地产生RNA凸起环。结果表明,芘稳定的RNA凸起环能被反式-(±)-环己烷-1,2-二胺有效且位点特异性地切割。