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Vol. 10, Issue 12, 1915-1927, December 2000
LETTER
Identification, Characterization, and Mapping of Expressed Sequence Tags from an Embryonic Zebrafish Heart cDNA Library
Christopher
Ton,1
David M.
Hwang,1
Adam A.
Dempsey,1
Hong-Chang
Tang,1
Jennifer
Yoon,1
Mindy
Lim,1
John D.
Mably,2
Mark C.
Fishman,2 and
Choong-Chin
Liew1,3,4
1 Department of Laboratory Medicine and Pathobiology,
University of Toronto, Toronto, Ontario M5G 1L5, Canada;
2 Cardiovascular Research Center, Massachusetts General
Hospital, Charlestown, Massachusetts 02129, USA and Department of
Medicine, Harvard Medical School, Boston, Massachusetts 02115, USA;
3 The Cardiovascular Genomic Unit, Brigham and Women's
Hospital, Harvard Medical School, Boston, Massachusetts 02115, USA
The generation of expressed sequence tags (ESTs) has proven to be a
rapid and economical approach by which to identify and characterize
expressed genes. We generated 5102 ESTs from a 3-d-old embryonic
zebrafish heart cDNA library. Of these, 57.6% matched to known genes,
14.2% matched only to other ESTs, and 27.8% showed no match to any
ESTs or known genes. Clustering of all ESTs identified 359 unique
clusters comprising 1771 ESTs, whereas the remaining 3331 ESTs did not
cluster. This estimates the number of unique genes identified in the
data set to be approximately 3690. A total of 1242 unique known genes
were used to analyze the gene expression patterns in the zebrafish
embryonic heart. These were categorized into seven categories on the
basis of gene function. The largest class of genes represented those
involved in gene/protein expression (25.9% of known transcripts). This
class was followed by genes involved in metabolism (18.7%), cell
structure/motility (16.4%), cell signaling and communication (9.6%),
cell/organism defense (7.1%), and cell division (4.4%). Unclassified
genes constituted the remaining 17.91%. Radiation hybrid mapping was
performed for 102 ESTs and comparison of map positions between
zebrafish and human identified new synteny groups. Continued
comparative analysis will be useful in defining the boundaries of
conserved chromosome segments between zebrafish and humans, which will
facilitate the transfer of genetic information between the two
organisms and improve our understanding of vertebrate evolution.
[The sequence data described in this paper have
been submitted to the GenBank data library under accession nos.
BE693120-BE693210 and BE704450.]
4
Corresponding author.
10:1915-1927 ©2000 by Cold Spring Harbor Laboratory Press ISSN 1088-9051/00 $5.00

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