Genome-wide assembly and analysis of alternative transcripts in mouse

  1. Alexei A. Sharov,
  2. Dawood B. Dudekula, and
  3. Minoru S.H. Ko1
  1. Developmental Genomics and Aging Section, Laboratory of Genetics, National Institute on Aging, National Institutes of Health, Baltimore, Maryland 21224, USA

Abstract

To build a mouse gene index with the most comprehensive coverage of alternative transcription/splicing (ATS), we developed an algorithm and a fully automated computational pipeline for transcript assembly from expressed sequences aligned to the genome. We identified 191,946 genomic loci, which included 27,497 protein-coding genes and 11,906 additional gene candidates (e.g., nonprotein-coding, but multiexon). Comparison of the resulting gene index with TIGR, UniGene, DoTS, and ESTGenes databases revealed that it had a greater number of transcripts, a greater average number of exons and introns with proper splicing sites per gene, and longer ORFs. The 27,497 protein-coding genes had 77,138 transcripts, i.e., 2.8 transcripts per gene on average. Close examination of transcripts led to a combinatorial table of 23 types of ATS units, only nine of which were previously described, i.e., 14 types of alternative splicing, seven types of alternative starts, and two types of alternative termination. The 47%, 18%, and 14% of 20,323 multiexon protein-coding genes with proper splice sites had alternative splicings, alternative starts, and alternative terminations, respectively. The gene index with the comprehensive ATS will provide a useful platform for analyzing the nature and mechanism of ATS, as well as for designing the accurate exon-based DNA microarrays.

Footnotes

  • [Supplemental material is available online at www.genome.org and http://lgsun.grc.nia.nih.gov/geneindex4/. The sequence data from this study have been submitted to GenBank under accession nos. CK329321–CK334090; CF891695–CF906652; CF906741–CF916750; CK334091–CK347104; CK387035–CK393993; CN660032–CN690720; CN690721–CN725493.]

  • Article and publication are at http://www.genome.org/cgi/doi/10.1101/gr.3269805. Freely available online through the Genome Research Immediate Open Access option.

  • 1 Corresponding author. E-mail kom{at}mail.nih.gov; fax (410) 558-8331.

    • Accepted February 23, 2005.
    • Received September 20, 2004.
| Table of Contents
OPEN ACCESS ARTICLE

Preprint Server