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Molecular cloning of DAX1 and SHP cDNAs and their expression patterns in the Nile tilapia, Oreochromis niloticus
Piscine DAX1 and SHP cDNAs with an open reading frame encoding 296 and 258 amino acid residues, respectively, as well as SHP partial gene fragment, were cloned from Nile tilapia. Phylogenetic analyses of DAX1s, SHPs, and homologous EST fragments indicate that DAX1 and SHP are conserved in gene struc...
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Published in: | Biochemical and biophysical research communications 2002-09, Vol.297 (3), p.632-640 |
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Main Authors: | , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Piscine
DAX1 and
SHP cDNAs with an open reading frame encoding 296 and 258 amino acid residues, respectively, as well as
SHP partial gene fragment, were cloned from Nile tilapia. Phylogenetic analyses of
DAX1s,
SHPs, and homologous EST fragments indicate that
DAX1 and
SHP are conserved in gene structure and are present throughout vertebrates. A single band of ∼1.4
kb for
DAX1 and of ∼1.2
kb for
SHP was detected in the Northern blot analysis. Tissue distribution analysis by RT-PCR showed that fish
DAX1 and
SHP mRNAs are widely expressed in adult tissues, with the most abundant expression in gonads and liver, respectively.
DAX1 and
SHP were also detected in gonads of both sexes at 5–90 days after hatching (dah). However, the expression of
DAX1 is weak at 5 and 10
dah and then significantly up-regulated between 10 and 15
dah, whereas the expression of
SHP is moderate and consistent during the ontogeny. |
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ISSN: | 0006-291X 1090-2104 |
DOI: | 10.1016/S0006-291X(02)02252-0 |