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Physiol. Genomics 17: 245-252, 2004. First published February 3, 2004; doi:10.1152/physiolgenomics.00186.2003
1094-8341/04 $5.00
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Received 3 November 2003; accepted in final form 29 January 2004.
Physiological Genomics 17:245-252 (2004)
1094-8341/04 $5.00 © 2004 American Physiological Society

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A comprehensive nonredundant expressed sequence tag collection for the developing Rattus norvegicus heart

Jennifer J.S. Laffin 1, Todd E. Scheetz 2, Maria de Fatima Bonaldo 1, Rebecca S. Reiter 3, Shereen Chang 1, Mari Eyestone 1, Hakeem Abdulkawy 2, Bartley Brown 2, Chad Roberts 2, Dylan Tack 2, Tamara Kucaba 1, Jim Jung-Ching Lin 3, Val C. Sheffield 1, Thomas L. Casavant 2 and M. Bento Soares 1,4

1 Department of Pediatrics and Interdepartmental-Genetics Graduate Program, The University of Iowa, Iowa City, Iowa 52242
2 Department of Engineering, The University of Iowa, Iowa City, Iowa 52242
3 Department of Biological Sciences, The University of Iowa, Iowa City, Iowa 52242
4 Departments of Biochemistry, Physiology, and Biophysics, and Orthopaedics, The University of Iowa, Iowa City, Iowa 52242

Congenital heart defects affect ~1,000,000 people in the United States, with 40,000 new births contributing to that number every year. A large percentage of these defects can be attributed to septal defects. We assembled a nonredundant collection of over 12,000 expressed sequence tags (ESTs) from a total of 30,000 ESTs, with the ultimate goal of identifying spatially and/or temporally regulated genes during heart septation. These ESTs were compiled from nonnormalized, normalized, and serially subtracted cDNA libraries derived from two sets of tissue samples. The first includes microdissected rat hearts from embryonic (E) days E13, E15, and E16.5–E18.5 and adult heart. The second includes hearts from embryonic days E17, E19, and E21 and postnatal (P) days P1, P12, P74, and P200. Over 6,000 novel ESTs were identified in the libraries derived from these two sets of tissues, all of which have been contributed to the NCBI rat UniGene collection. It is anticipated that such EST and cDNA clone resources will prove invaluable to gene expression studies aimed at the understanding of the molecular mechanisms underlying heart septation defects.

cDNA library; gene expression; cardiovascular development




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