Hancock J M, Tautz D, Dover G A
Genetics Department, University of Cambridge, United Kingdom.
Mol Biol Evol. 1988 Jul;5(4):393-414. doi: 10.1093/oxfordjournals.molbev.a040501.
This paper examines the effects of DNA sequence evolution on RNA secondary structures and compensatory mutations. Models of the secondary structures of Drosophila melanogaster 18S ribosomal RNA (rRNA) and of the complex between 2S, 5.8S, and 28S rRNAs have been drawn on the basis of comparative and energetic criteria. The overall AU richness of the D. melanogaster rRNAs allows the resolution of some ambiguities in the structures of both large rRNAs. Comparison of the sequence of expansion segment V2 in D. melanogaster 18S rRNA with the same region in three other Drosophila species and the tsetse fly (Glossina morsitans morsitans) allows us to distinguish between two models for the secondary structure of this region. The secondary structures of the expansion segments of D. melanogaster 28S rRNA conform to a general pattern for all eukaryotes, despite having highly divergent sequences between D. melanogaster and vertebrates. The 70 novel compensatory mutations identified in the 28S rRNA show a strong (70%) bias toward A-U base pairs, suggesting that a process of biased mutation and/or biased fixation of A and T point mutations or AT-rich slippage-generated motifs has occurred during the evolution of D. melanogaster rDNA. This process has not occurred throughout the D. melanogaster genome. The processes by which compensatory pairs of mutations are generated and spread are discussed, and a model is suggested by which a second mutation is more likely to occur in a unit with a first mutation as such a unit begins to spread through the family and concomitantly through the population. Alternatively, mechanisms of proofreading in stem-loop structures at the DNA level, or between RNA and DNA, might be involved. The apparent tolerance of noncompensatory mutations in some stems which are otherwise strongly supported by comparative criteria within D. melanogaster 28S rRNA must be borne in mind when compensatory mutations are used as a criterion in secondary-structure modeling. Noncompensatory mutation may extend to the production of unstable structures where a stem is stabilized by RNA-protein or additional RNA-RNA interactions in the mature ribosome. Of motifs suggested to be involved in rRNA processing, one (CGAAAG) is strongly overrepresented in the 28S rRNA sequence. The data are discussed both in the context of the forces involved with the evolution of multigene families and in the context of molecular coevolution in the rDNA family in particular.
本文研究了DNA序列进化对RNA二级结构和补偿性突变的影响。基于比较和能量标准,绘制了黑腹果蝇18S核糖体RNA(rRNA)以及2S、5.8S和28S rRNA之间复合物的二级结构模型。黑腹果蝇rRNA总体上的AU丰富度有助于解决两种大rRNA结构中的一些模糊问题。将黑腹果蝇18S rRNA中扩展片段V2的序列与其他三种果蝇物种以及采采蝇(Glossina morsitans morsitans)的相同区域进行比较,使我们能够区分该区域二级结构的两种模型。黑腹果蝇28S rRNA扩展片段的二级结构符合所有真核生物的一般模式,尽管黑腹果蝇与脊椎动物之间的序列高度不同。在28S rRNA中鉴定出的70个新的补偿性突变显示出对A-U碱基对有强烈的(70%)偏向性,这表明在黑腹果蝇rDNA进化过程中发生了偏向性突变和/或A和T点突变或富含AT的滑移产生的基序的偏向性固定过程。整个黑腹果蝇基因组中并未发生此过程。本文讨论了补偿性突变对产生和传播的过程,并提出了一个模型,即当一个带有第一个突变的单元开始在家族中传播并随之在群体中传播时,第二个突变更有可能在该单元中发生。或者,可能涉及DNA水平或RNA与DNA之间茎环结构的校对机制。在将补偿性突变用作二级结构建模标准时,必须牢记黑腹果蝇28S rRNA中某些茎段中存在非补偿性突变,而这些茎段在比较标准下得到了有力支持。非补偿性突变可能会延伸至产生不稳定结构,在成熟核糖体中,茎段通过RNA-蛋白质或额外的RNA-RNA相互作用得以稳定。在被认为参与rRNA加工的基序中,一个(CGAAAG)在28S rRNA序列中强烈富集。本文在多基因家族进化所涉及的力量背景下,特别是在rDNA家族分子协同进化的背景下讨论了这些数据。