Department of Chemistry, Wesleyan University, Middletown, CT 06459, USA.
J Mol Biol. 2010 Apr 2;397(3):677-88. doi: 10.1016/j.jmb.2010.01.068. Epub 2010 Feb 2.
Intrinsic transcription termination sites generally contain a tract of adenines in the DNA template that yields a tract of uracils at the 3' end of the nascent RNA. To understand how this base sequence contributes to termination of transcription, we have investigated two nucleic acid structures. The first is the RNA-DNA hybrid that contains the uracil tract 5'-rUUUUUAU-3' from the tR2 intrinsic terminator of bacteriophage lambda. The second is the homologous DNA-DNA duplex that contains the adenine tract 5'-dATAAAAA-3'. This duplex is present at the tR2 site when the DNA is not transcribed. The opening and the stability of each rU-dA/dT-dA base pair in the two structures are characterized by imino proton exchange and nuclear magnetic resonance spectroscopy. The results reveal concerted opening of the central rU-dA base pairs in the RNA-DNA hybrid. Furthermore, the stability profile of the adenine tract in the RNA-DNA hybrid is very different from that of the tract in the template DNA-DNA duplex. In the RNA-DNA hybrid, the stabilities of rU-dA base pairs range from 4.3 to 6.5 kcal/mol (at 10 degrees C). The sites of lowest stability are identified at the central positions of the tract. In the template DNA-DNA duplex, the dT-dA base pairs are more stable than the corresponding rU-dA base pairs in the hybrid by 0.9 to 4.6 kcal/mol and, in contrast to the RNA-DNA hybrid, the central base pairs have the highest stability. These results suggest that the central rU-dA/dT-dA base pairs in the adenine tract make the largest energetic contributions to transcription termination by promoting both the dissociation of the RNA transcript and the closing of the transcription bubble. The results also suggest that the high stability of dT-dA base pairs in the DNA provides a signal for the pausing of RNA polymerase at the termination site.
内在转录终止位点通常在 DNA 模板中包含一段腺嘌呤,在新生 RNA 的 3'端产生一段尿嘧啶。为了了解这个碱基序列如何促进转录终止,我们研究了两种核酸结构。第一种是包含噬菌体 λ tR2 内在终止子中尿嘧啶序列 5'-rUUUUUAU-3'的 RNA-DNA 杂交体。第二种是含有腺嘌呤序列 5'-dATAAAAA-3'的同源 DNA-DNA 双链体。当 DNA 不转录时,该双链体存在于 tR2 位点。通过亚氨基质子交换和核磁共振波谱法,对两种结构中每个 rU-dA/dT-dA 碱基对的开口和稳定性进行了表征。结果表明,RNA-DNA 杂交体中的中心 rU-dA 碱基对协同打开。此外,RNA-DNA 杂交体中腺嘌呤序列的稳定性特征与模板 DNA-DNA 双链体中的序列非常不同。在 RNA-DNA 杂交体中,rU-dA 碱基对的稳定性范围为 4.3 至 6.5 kcal/mol(在 10°C 时)。稳定性最低的位点位于序列的中心位置。在模板 DNA-DNA 双链体中,dT-dA 碱基对比杂交体中的相应 rU-dA 碱基对稳定 0.9 至 4.6 kcal/mol,与 RNA-DNA 杂交体相反,中心碱基对具有最高的稳定性。这些结果表明,腺嘌呤序列中的中心 rU-dA/dT-dA 碱基对通过促进 RNA 转录本的解离和转录泡的闭合,对转录终止做出最大的能量贡献。结果还表明,DNA 中 dT-dA 碱基对的高稳定性为 RNA 聚合酶在终止位点的暂停提供了信号。