Department of Biology, McMaster University, Hamilton, ON L8S 4K1, Canada.
Division of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA 91125, USA.
G3 (Bethesda). 2022 Jul 6;12(7). doi: 10.1093/g3journal/jkac101.
The nematode Caenorhabditis briggsae is routinely used in comparative and evolutionary studies involving its well-known cousin Caenorhabditis elegans. The C. briggsae genome sequence has accelerated research by facilitating the generation of new resources, tools, and functional studies of genes. While substantial progress has been made in predicting genes and start sites, experimental evidence is still lacking in many cases. Here, we report an improved annotation of the C. briggsae genome using the trans-spliced exon coupled RNA end determination technique. In addition to identifying the 5' ends of expressed genes, we have discovered operons and paralogs. In summary, our analysis yielded 10,243 unique 5' end sequence tags with matches in the C. briggsae genome. Of these, 6,395 were found to represent 4,252 unique genes along with 362 paralogs and 52 previously unknown exons. These genes included 14 that are exclusively trans-spliced in C. briggsae when compared with C. elegans orthologs. A major contribution of this study is the identification of 492 high confidence operons, of which two-thirds are fully supported by tags. In addition, 2 SL1-type operons were discovered. Interestingly, comparisons with C. elegans showed that only 40% of operons are conserved. Of the remaining operons, 73 are novel, including 12 that entirely lack orthologs in C. elegans. Further analysis revealed that 4 of the 12 novel operons are conserved in Caenorhabditis nigoni. Altogether, the work described here has significantly advanced our understanding of the C. briggsae system and serves as a rich resource to aid biological studies involving this species.
秀丽隐杆线虫(Caenorhabditis elegans)是一种常用的模式生物,在涉及比较和进化研究中被广泛应用。秀丽隐杆线虫的近亲秀丽新杆线虫(Caenorhabditis briggsae)也常被用于此类研究。秀丽新杆线虫的基因组序列为新资源的生成、工具的开发以及基因功能研究提供了便利,从而加速了相关研究。虽然在预测基因和启动子方面已经取得了相当大的进展,但在许多情况下仍然缺乏实验证据。在这里,我们报告了一种使用转剪接外显子偶联 RNA 末端确定技术改进秀丽新杆线虫基因组注释的方法。除了确定表达基因的 5' 端之外,我们还发现了操纵子和旁系同源基因。总之,我们的分析产生了 10243 个独特的 5' 端序列标签,这些标签在秀丽新杆线虫基因组中都有匹配。其中,有 6395 个被发现代表 4252 个独特的基因,包括 362 个旁系同源基因和 52 个未知的外显子。这些基因包括 14 个在秀丽新杆线虫中与秀丽隐杆线虫的同源基因相比是特异性转剪接的基因。本研究的一个主要贡献是鉴定了 492 个高置信度的操纵子,其中三分之二的操纵子都得到了标签的充分支持。此外,还发现了两个 SL1 型操纵子。有趣的是,与秀丽隐杆线虫的比较表明,只有 40%的操纵子是保守的。在剩下的操纵子中,有 73 个是新的,其中包括 12 个在秀丽隐杆线虫中完全没有同源基因的操纵子。进一步的分析表明,这 12 个新的操纵子中有 4 个在尼氏小杆线虫(Caenorhabditis nigoni)中是保守的。总的来说,这里描述的工作极大地提高了我们对秀丽新杆线虫系统的理解,为涉及该物种的生物学研究提供了丰富的资源。