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Expressed Sequence Tags (ESTs)

Volume 533 of the series Methods in Molecular Biology pp 153-187

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Large-Scale Sequencing and Analytical Processing of ESTs

  • Makedonka MitrevaAffiliated withGenome Sequencing Center, Department of Genetics, Washington University School of Medicine
  • , Elaine R. MardisAffiliated withGenome Sequencing Center, Department of Genetics, Washington University School of Medicine

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Abstract

Expressed sequence tags (ESTs) have proven to be one of the most rapid and cost-effective routes to gene discovery for eukaryotic genomes. Furthermore, their multipurpose uses, such as in probe design for microarrays, determining alternative splicing, verifying open reading frames, and confirming exon/intron and gene boundaries, to name a few, further justify their inclusion in many genomic characterization projects. Hence, there has been a constant increase in the number of ESTs deposited into the dbEST division of GenBank. This trend also correlates to ever-improving molecular techniques for obtaining biological material, performing RNA extraction, and constructing cDNA libraries, and predominantly to ever-evolving sequencing chemistry and instrumentation, as well as to decreased sequencing costs. This chapter describes large-scale sequencing of ESTs on two distinct platforms: the ABI 3730xl and the 454 Life Sciences GS20 sequencers, and the corresponding processes of sequence extraction, processing, and submissions to public databases. While the conventional 3730xl sequencing process is described, starting with the plating of an already-existing cDNA library, the section on 454 GS20 pyrosequencing also includes a method for generating full-length cDNA sequences. With appropriate bioinformatics tools, each of these platforms either used independently or coupled together provide a powerful combination for comprehensive exploration of an organism’s transcriptome.

Key words

Expressed sequence tags EST sequencing cDNA capillary sequencing ABI 3730xl pyrosequencing GS20