Burton R S, Metz E C, Flowers J M, Willett C S
Marine Biology Research Division 0202, Scripps Institution of Oceanography, University of California, San Diego, La Jolla, CA 92093-0202, USA.
Gene. 2005 Jan 3;344:105-13. doi: 10.1016/j.gene.2004.09.001.
Eukaryotic nuclear ribosomal DNA (rDNA) is typically arranged as a series of tandem repeats coding for 18S, 5.8S, and 28S ribosomal RNAs. Transcription of rDNA repeats is initiated in the intergenic spacer (IGS) region upstream of the 18S gene. The IGS region itself typically consists of a set of subrepeats that function as transcriptional enhancers. Two important evolutionary forces have been proposed to act on the IGS region: first, selection may favor changes in the number of subrepeats that adaptively adjust rates of rDNA transcription, and second, coevolution of IGS sequence with RNA polymerase I transcription factors may lead to species specificity of the rDNA transcription machinery. To investigate the potential role of these forces on population differentiation and hybrid breakdown in the intertidal copepod Tigriopus californicus, we have characterized the rDNA of five T. californicus populations from the Pacific Coast of North America and one sample of T. brevicornicus from Scotland. Major findings are as follows: (1) the structural genes for 18S and 28S are highly conserved across T. californicus populations, in contrast to other nuclear and mitochondrial DNA (mtDNA) genes previously studied in these populations. (2) There is extensive differentiation among populations in the IGS region; in the extreme, no homology is observed across the IGS sequences (>2 kb) from the two Tigriopus species. (3) None of the Tigriopus IGS sequences have the subrepeat structure common to other eukaryotic IGS regions. (4) Segregation of rDNA in laboratory crosses indicates that rDNA is located on at least two separate chromosomes in T. californicus. These data suggest that although IGS length polymorphism does not appear to play the adaptive role hypothesized in some other eukaryotic systems, sequence divergence in the rDNA promoter region within the IGS could lead to population specificity of transcription in hybrids.
真核细胞核核糖体DNA(rDNA)通常排列成一系列串联重复序列,编码18S、5.8S和28S核糖体RNA。rDNA重复序列的转录起始于18S基因上游的基因间隔区(IGS)。IGS区域本身通常由一组作为转录增强子的亚重复序列组成。已提出两种重要的进化力量作用于IGS区域:第一,选择可能有利于亚重复序列数量的变化,从而适应性地调节rDNA转录速率;第二,IGS序列与RNA聚合酶I转录因子的共同进化可能导致rDNA转录机制的物种特异性。为了研究这些力量对潮间带桡足类加州虎斑猛水蚤种群分化和杂种衰败的潜在作用,我们对来自北美太平洋海岸的五个加州虎斑猛水蚤种群的rDNA以及来自苏格兰的一个短角虎斑猛水蚤样本进行了特征分析。主要发现如下:(1)与之前在这些种群中研究的其他核DNA和线粒体DNA(mtDNA)基因不同,18S和28S的结构基因在加州虎斑猛水蚤种群中高度保守。(2)IGS区域在种群间存在广泛分化;在极端情况下,两个虎斑猛水蚤物种的IGS序列(>2 kb)之间未观察到同源性。(3)虎斑猛水蚤的IGS序列均不具有其他真核IGS区域常见的亚重复结构。(4)实验室杂交中rDNA的分离表明,rDNA位于加州虎斑猛水蚤的至少两条不同染色体上。这些数据表明,尽管IGS长度多态性似乎并未发挥在其他一些真核系统中假设的适应性作用,但IGS内rDNA启动子区域的序列差异可能导致杂种中转录的种群特异性。