McTaggart Seanna J, Crease Teresa J
Department of Zoology, University of Guelph, Guelph, Ontario, Canada.
Mol Biol Evol. 2005 May;22(5):1309-19. doi: 10.1093/molbev/msi119. Epub 2005 Mar 2.
The high rate of sequence divergence in nuclear ribosomal RNA (rRNA) expansion segments offers a unique opportunity to study the importance of natural selection in their evolution. To this end, we polymerase chain reaction amplified and cloned a 589-nt fragment of the 18S rRNA gene containing expansion segments 43/e1 and 43/e4 from six individual Daphnia obtusa from four populations. We screened 2,588 clones using single-stranded conformation polymorphism analysis and identified 103 unique haplotype sequences. We detected two pairs of indel sites in segment 43/e4 that complement each other when the secondary structure of the linear sequence is formed. Seven of the 12 observed combinations of length variants at these four sites (haplotypes) are shared between individuals from different populations, which may suggest that some of the length variation was present in their common ancestor. Haplotypes with uncompensated indels were only observed at low frequencies, while compensated indel haplotypes were found at a wide range of frequencies, supporting the hypothesis that the energetic stability of expansion segments is a trait under natural selection. In addition, there was strong linkage disequilibrium between the four complementary indel sites, particularly those that pair with one another in the secondary structure. Despite selection against unpaired bulges at these four indel sites, some nucleotides that form unpaired bulges are highly conserved in segment 43/e4, indicating that they are under a different selective constraint, possibly due to their role in higher level structural interactions.
核糖体RNA(rRNA)扩展片段中的高序列分歧率为研究自然选择在其进化中的重要性提供了独特的机会。为此,我们通过聚合酶链反应扩增并克隆了来自四个种群的六只钝额溞个体的18S rRNA基因的一个589 nt片段,该片段包含扩展片段43/e1和43/e4。我们使用单链构象多态性分析筛选了2588个克隆,并鉴定出103个独特的单倍型序列。我们在片段43/e4中检测到两对插入/缺失位点,当形成线性序列的二级结构时,它们相互互补。在这四个位点(单倍型)观察到的12种长度变体组合中的七种在来自不同种群的个体之间共享,这可能表明一些长度变异存在于它们的共同祖先中。具有未补偿插入/缺失的单倍型仅在低频下观察到,而补偿插入/缺失单倍型在广泛的频率范围内被发现,这支持了扩展片段的能量稳定性是自然选择下的一个特征的假设。此外,这四个互补插入/缺失位点之间存在很强的连锁不平衡,特别是那些在二级结构中相互配对的位点。尽管在这四个插入/缺失位点选择不利于未配对的凸起,但一些形成未配对凸起的核苷酸在片段43/e4中高度保守,这表明它们受到不同的选择约束,可能是由于它们在更高层次结构相互作用中的作用。