Genome annotation of Caenorhabditis briggsae by TEC-RED identifies new exons, paralogs, and conserved and novel operons

Author:

Jhaveri Nikita1,van den Berg Wouter1ORCID,Hwang Byung Joon2,Muller Hans-Michael2,Sternberg Paul W2ORCID,Gupta Bhagwati P1ORCID

Affiliation:

1. Department of Biology, McMaster University , Hamilton, ON L8S 4K1, Canada

2. Division of Biology and Biological Engineering, California Institute of Technology , Pasadena, CA 91125, USA

Abstract

Abstract 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.

Funder

BPG

Natural Sciences and Engineering Research Council of Canada

Howard Hughes Medical Institute

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology

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