Liang Dan, Zhou Hui, Zhang Peng, Chen Yue-Qin, Chen Xiao, Chen Chun-Long, Qu Liang-Hu
Key Laboratory of Gene Engineering of Education Ministry, Biotechnology Research Center, Zhongshan University, Guangzhou 510275, People's Republic of China.
Nucleic Acids Res. 2002 Jul 15;30(14):3262-72. doi: 10.1093/nar/gkf426.
Based on the analysis of structural features and conserved elements, 27 novel snoRNA genes have been identified from rice. All of them belong to the C/D box-containing snoRNA family except for one that belongs to the H/ACA box type. The newly found genes fall into six clusters that comprise at least three snoRNA genes, and in one case as many as nine genes. Interestingly, four of the six clusters are located within the largest intron of a protein coding gene. The majority of intronic snoRNA gene clusters are simply formed by multiple copies of the same species of snoRNA gene that possess the identical functional elements. This implies a possible mechanism of duplication for the origin of repeating snoRNA coding regions in one intron. However, a few intronic snoRNA gene clusters consisting of different snoRNAs species were also observed. Polycistronic precursors from two independently transcribed clusters were demonstrated by RT-PCR and individual snoRNAs processed from the polycistronic precursors were positively determined by reverse transcription assay. Analyses of the intergenic spacers in the clusters showed that, in addition to a very high AT content, the processing signals in rice snoRNA polycistronic transcripts might be different from those of yeast. Our results demonstrate that, in both plants and mammals, numerous snoRNAs can be produced simultaneously from an mRNA precursor of a host gene despite the different arrangements. The intronic snoRNA gene cluster is a novel gene organization, which is so far unique to plants. The conservation of intronic snoRNA gene clusters in plants was further demonstrated by the study of a similar snoRNA gene organization in the first intron of a Hsp70 gene from wild rice and Zizania caduciflora.
基于对结构特征和保守元件的分析,已从水稻中鉴定出27个新的snoRNA基因。除了一个属于H/ACA盒类型外,其余均属于含C/D盒的snoRNA家族。新发现的基因分为六个簇,每个簇至少包含三个snoRNA基因,在一种情况下多达九个基因。有趣的是,六个簇中的四个位于蛋白质编码基因的最大内含子内。大多数内含子snoRNA基因簇是由具有相同功能元件的同一物种snoRNA基因的多个拷贝简单形成的。这暗示了一个内含子中重复snoRNA编码区起源的可能复制机制。然而,也观察到一些由不同snoRNA物种组成的内含子snoRNA基因簇。通过RT-PCR证实了来自两个独立转录簇的多顺反子前体,并通过逆转录测定法确定了从多顺反子前体加工而来的单个snoRNA。对簇中基因间隔区的分析表明,除了非常高的AT含量外,水稻snoRNA多顺反子转录本中的加工信号可能与酵母不同。我们的结果表明,在植物和哺乳动物中,尽管排列方式不同,但许多snoRNA可以从宿主基因的mRNA前体中同时产生。内含子snoRNA基因簇是一种新的基因组织,迄今为止在植物中是独一无二的。通过对野生稻和茭白Hsp70基因第一个内含子中类似snoRNA基因组织的研究,进一步证明了植物中内含子snoRNA基因簇的保守性。