The Mina and Everard Goodman Faculty of Life Sciences, Bar-Ilan University, Ramat-Gan 52900, Israel.
BMC Genomics. 2010 Nov 4;11:615. doi: 10.1186/1471-2164-11-615.
Recent studies have provided extensive evidence for multitudes of non-coding RNA (ncRNA) transcripts in a wide range of eukaryotic genomes. ncRNAs are emerging as key players in multiple layers of cellular regulation. With the availability of many whole genome sequences, comparative analysis has become a powerful tool to identify ncRNA molecules. In this study, we performed a systematic genome-wide in silico screen to search for novel small ncRNAs in the genome of Trypanosoma brucei using techniques of comparative genomics.
In this study, we identified by comparative genomics, and validated by experimental analysis several novel ncRNAs that are conserved across multiple trypanosomatid genomes. When tested on known ncRNAs, our procedure was capable of finding almost half of the known repertoire through homology over six genomes, and about two-thirds of the known sequences were found in at least four genomes. After filtering, 72 conserved unannotated sequences in at least four genomes were found, 29 of which, ranging in size from 30 to 392 nts, were conserved in all six genomes. Fifty of the 72 candidates in the final set were chosen for experimental validation. Eighteen of the 50 (36%) were shown to be expressed, and for 11 of them a distinct expression product was detected, suggesting that they are short ncRNAs. Using functional experimental assays, five of the candidates were shown to be novel H/ACA and C/D snoRNAs; these included three sequences that appear as singletons in the genome, unlike previously identified snoRNA molecules that are found in clusters. The other candidates appear to be novel ncRNA molecules, and their function is, as yet, unknown.
Using comparative genomic techniques, we predicted 72 sequences as ncRNA candidates in T. brucei. The expression of 50 candidates was tested in laboratory experiments. This resulted in the discovery of 11 novel short ncRNAs in procyclic stage T. brucei, which have homologues in the other trypansomatids. A few of these molecules are snoRNAs, but most of them are novel ncRNA molecules. Based on this study, our analysis suggests that the total number of ncRNAs in trypanosomatids is in the range of several hundred.
最近的研究为广泛的真核生物基因组中的大量非编码 RNA(ncRNA)转录本提供了广泛的证据。ncRNA 正在成为细胞调节多个层次的关键参与者。随着许多全基因组序列的可用性,比较分析已成为识别 ncRNA 分子的强大工具。在这项研究中,我们使用比较基因组学技术在布氏锥虫基因组中进行了系统的全基因组计算机筛选,以寻找新的小 ncRNA。
在这项研究中,我们通过比较基因组学鉴定并通过实验分析验证了几种在多个锥虫生物基因组中保守的新型 ncRNA。在已知的 ncRNA 上进行测试时,我们的程序通过六个基因组上的同源性几乎可以找到已知曲目的一半,并且至少在四个基因组中发现了三分之二的已知序列。经过过滤,在至少四个基因组中发现了 72 个保守的未注释序列,其中 29 个大小在 30 到 392 个核苷酸之间,在所有六个基因组中都保守。最终集合中的 72 个候选者中有 50 个被选中进行实验验证。其中 18 个(36%)被证明可表达,其中 11 个检测到独特的表达产物,表明它们是短 ncRNA。使用功能实验测定法,其中五个候选者被证明是新型 H/ACA 和 C/D snoRNA;其中三个序列在基因组中作为单一样本出现,与先前鉴定的 snoRNA 分子不同,这些 snoRNA 分子存在于簇中。其他候选者似乎是新型 ncRNA 分子,其功能尚不清楚。
使用比较基因组技术,我们预测了 72 个序列作为 T. brucei 的 ncRNA 候选者。在实验室实验中测试了 50 个候选者的表达。这导致在布氏锥虫的前鞭毛体阶段发现了 11 个新型短 ncRNA,这些 ncRNA 在其他锥虫生物中具有同源物。这些分子中的一些是 snoRNA,但大多数是新型 ncRNA 分子。基于这项研究,我们的分析表明,锥虫生物中的 ncRNA 总数在几百个左右。