Zemann Anja, op de Bekke Anja, Kiefmann Martin, Brosius Jürgen, Schmitz Jürgen
Institute of Experimental Pathology (ZMBE), University of Münster, D-48149 Münster, Germany.
Nucleic Acids Res. 2006 May 19;34(9):2676-85. doi: 10.1093/nar/gkl359. Print 2006.
In contrast to mRNAs, which are templates for translating proteins, non-protein coding (npc) RNAs (also known as 'non-coding' RNA, ncRNA), exhibit various functions in different compartments and developmental stages of the cell. Small nucleolar RNAs (snoRNAs), one of the largest classes of npcRNAs, guide post-transcriptional modifications of other RNAs that are crucial for appropriate RNA folding as well as for RNA-RNA and RNA-protein interactions. Although snoRNA genes comprise a significant fraction of the eutherian genome, identifying and characterizing large numbers of them is not sufficiently accessible by classical computer searches alone. Furthermore, most previous investigations of snoRNAs yielded only limited indications of their evolution. Using data obtained by a combination of high-throughput cDNA library screening and computational search strategies based on a modified DNAMAN program, we characterized 151 npcRNAs, and in particular 121 snoRNAs, from Caenorhabditis elegans and extensively compared them with those in the related, Caenorhabditis briggsae. Detailed comparisons of paralog snoRNAs in the two nematodes revealed, in addition to trans-duplication, a novel, cis-duplication distribution strategy with insertions near to the original loci. Some snoRNAs coevolved with their modification target sites, demonstrating the close interaction of complementary regions. Some target sites modified by snoRNAs were changed, added or lost, documenting a high degree of evolutionary plasticity of npcRNAs.
与作为蛋白质翻译模板的信使核糖核酸(mRNA)不同,非蛋白质编码(npc)RNA(也称为“非编码”RNA,ncRNA)在细胞的不同区室和发育阶段发挥着多种功能。小核仁RNA(snoRNA)是最大类别的npcRNA之一,它指导其他RNA的转录后修饰,这些修饰对于RNA的正确折叠以及RNA-RNA和RNA-蛋白质相互作用至关重要。尽管snoRNA基因在真兽类基因组中占很大比例,但仅通过传统的计算机搜索还不足以识别和表征大量的snoRNA。此外,以前对snoRNA的大多数研究仅给出了其进化的有限线索。我们结合高通量cDNA文库筛选和基于改良DNAMAN程序的计算搜索策略获得的数据,对秀丽隐杆线虫的151种npcRNA进行了表征,特别是121种snoRNA,并将它们与相关的briggsae秀丽隐杆线虫中的npcRNA进行了广泛比较。对这两种线虫中旁系同源snoRNA的详细比较表明,除了转座复制外,还存在一种新的顺式复制分布策略,即在原始基因座附近插入。一些snoRNA与其修饰靶位点共同进化,表明互补区域之间存在密切相互作用。一些被snoRNA修饰的靶位点发生了改变、增加或丢失,这证明了npcRNA具有高度的进化可塑性。