High-Throughput Gene Discovery in the Rat
- Todd E. Scheetz1,6,12,
- Jennifer J. Laffin8,
- Brian Berger8,
- Sara Holte8,
- Susan A. Baumes8,
- Robert Brown II8,
- Shereen Chang8,
- Justin Coco8,
- Jim Conklin8,
- Keith Crouch8,
- Micca Donohue8,
- Greg Doonan8,
- Chris Estes8,
- Mari Eyestone8,
- Katrina Fishler8,
- Jack Gardiner8,
- Lankai Guo8,
- Brad Johnson8,
- Catherine Keppel8,
- Rikki Kreger8,
- Mark Lebeck8,
- Rudy Marcelino8,
- Vladan Miljkovich8,
- Mindee Perdue8,
- Ling Qui8,
- Joshua Rehmann8,
- Rebecca S. Reiter3,
- Bridgette Rhoads8,
- Kelly Schaefer8,
- Christina Smith8,
- Ivana Sunjevaric8,
- Kurtis Trout8,
- Ning Wu8,
- Clayton L. Birkett5,
- Jared Bischof5,
- Barry Gackle5,
- Allen Gavin5,
- A. Jason Grundstad5,
- Brian Mokrzycki5,
- Chris Moressi5,
- Brian O'Leary5,
- Kevin Pedretti5,
- Chad Roberts5,
- Natalie L. Robinson5,
- Michael Smith5,
- Dylan Tack5,
- Nishank Trivedi5,
- Tamara Kucaba8,
- Tom Freeman11,
- Jim J.-C. Lin3,
- Maria F. Bonaldo8,
- Thomas L. Casavant1,4,5,
- Val C. Sheffield8,10, and
- M. Bento Soares8,2,7,9
- 1 Center for Bioinformatics and Computational Biology, The University of Iowa, Iowa City, Iowa 52242, USA
- 2 Department of Biochemistry, The University of Iowa, Iowa City, Iowa 52242, USA
- 3 Department of Biological Sciences, The University of Iowa, Iowa City, Iowa 52242, USA
- 4 Department of Biomedical Engineering, The University of Iowa, Iowa City, Iowa 52242, USA
- 5 Departments of Electrical and Computer Engineering, The University of Iowa, Iowa City, Iowa 52242, USA
- 6 Department of Ophthalmology, The University of Iowa, Iowa City, Iowa 52242, USA
- 7 Department of Orthopaedics, The University of Iowa, Iowa City, Iowa 52242, USA
- 8 Department of Pediatrics, The University of Iowa, Iowa City, Iowa 52242, USA
- 9 Departments of Physiology and Biophysics, The University of Iowa, Iowa City, Iowa 52242, USA
- 10 Howard Hughes Medical Institute, The University of Iowa, Iowa City, Iowa 52242, USA
- 11 The Sanger Center, Hinxton, Cambridge CB10 1SB, UK
Abstract
The rat is an important animal model for human diseases and is widely used in physiology. In this article we present a new strategy for gene discovery based on the production of ESTs from serially subtracted and normalized cDNA libraries, and we describe its application for the development of a comprehensive nonredundant collection of rat ESTs. Our new strategy appears to yield substantially more EST clusters per ESTs sequenced than do previous approaches that did not use serial subtraction. However, multiple rounds of library subtraction resulted in high frequencies of otherwise rare internally primed cDNAs, defining the limits of this powerful approach. To date, we have generated >200,000 3′ ESTs from >100 cDNA libraries representing a wide range of tissues and developmental stages of the laboratory rat. Most importantly, we have contributed to ∼50,000 rat UniGene clusters. We have identified, arrayed, and derived 5′ ESTs from >30,000 unique rat cDNA clones. Complete information, including radiation hybrid mapping data, is also maintained locally at http://genome.uiowa.edu/clcg.html. All of the sequences described in this article have been submitted to the dbEST division of the NCBI.
Footnotes
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[The following individuals kindly provided reagents, samples, or unpublished information as indicated in the paper: S. Brown, F. Lamb, H. Lan, J.B. Lian, the McArdle Laboratory of Cancer Research, J. Morcuende, A. Novakovich, G.S. Stein, J. Stevens, B. Strausberg, and P. Wackym.]
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Article and publication are at http://www.genome.org/cgi/doi/10.1101/gr.1414204.
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↵12 Corresponding author. E-MAIL tscheetz{at}eng.uiowa.edu; FAX (319) 338-0944.
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- Accepted November 17, 2003.
- Received April 9, 2003.
- Cold Spring Harbor Laboratory Press











