Nussinov R
Laboratory of Mathematical Biology, NCI, NIH, Bethesda, MD 20892.
Comput Appl Biosci. 1991 Jul;7(3):295-9. doi: 10.1093/bioinformatics/7.3.295.
DNA and RNA molecules contain signals which are recognized by regulatory proteins or enzymes either directly, through their nucleotide sequences or indirectly, through induced structural changes on their neighboring sequences. To date, most signal searches have been focused on specific recurrences of nucleotide sequences. Much less attention has been directed towards the structure, flexibility and hydrogen-bonding patterns that recognition elements may possess. Here we review the various methods involved in such searches. In particular, however, we also address the searches for potential properties. In this regard it is of interest to inspect the asymmetry in the distributions of complementary oligomers near biological features. Upstream of transcription initiation the frequencies of G-rich oligomers are particularly high (Nussinov, 1987a; 1990). The frequencies of C-rich oligomers are lower. A-tracts are also very frequent in these regions. This may correlate with the recent finding that guanine, but not cytosine, tracts enhance A-tract directed bends (Milton et al., 1990). Presumably A-tracts near G-tracts on the same strand may induce a structural change in the G-tracts which may enhance the bend. G-tracts may have the potential for participating in a DNA bend due to their compression of the major groove. Thus, proteins may not always be necessary to induce DNA conformational changes. This example illustrates the importance of studies of the properties of DNA oligomers in regulatory regions, and of algorithms for their detection.
DNA和RNA分子含有一些信号,这些信号可被调节蛋白或酶直接通过其核苷酸序列识别,或间接通过其相邻序列的诱导结构变化来识别。迄今为止,大多数信号搜索都集中在核苷酸序列的特定重复上。而对于识别元件可能具有的结构、灵活性和氢键模式则关注较少。在此,我们综述了此类搜索所涉及的各种方法。然而,特别地,我们也探讨了对潜在特性的搜索。在这方面,考察生物特征附近互补寡聚物分布的不对称性是很有意义的。在转录起始上游,富含G的寡聚物频率特别高(努西诺夫,1987a;1990)。富含C的寡聚物频率较低。A序列在这些区域也非常频繁。这可能与最近的发现相关,即鸟嘌呤序列而非胞嘧啶序列会增强A序列导向的弯曲(米尔顿等人,1990)。据推测,同一条链上靠近G序列的A序列可能会诱导G序列发生结构变化,从而增强弯曲。由于G序列对大沟的压缩,它们可能具有参与DNA弯曲的潜力。因此,诱导DNA构象变化不一定总是需要蛋白质。这个例子说明了研究调控区域DNA寡聚物特性以及其检测算法的重要性。