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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
Main Authors: Wang, De-Shou, Kobayashi, Tohru, Senthilkumaran, Balasubramanian, Sakai, Fumie, Chery Sudhakumari, Cheni, Suzuki, Taiga, Yoshikuni, Michiyasu, Matsuda, Masaru, Morohashi, Ken-ichirou, Nagahama, Yoshitaka
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cited_by cdi_FETCH-LOGICAL-c392t-c77ca645049010c153b1f96bb22cb2c1706b8df0301f873ebe510e88218de7403
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container_title Biochemical and biophysical research communications
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creator Wang, De-Shou
Kobayashi, Tohru
Senthilkumaran, Balasubramanian
Sakai, Fumie
Chery Sudhakumari, Cheni
Suzuki, Taiga
Yoshikuni, Michiyasu
Matsuda, Masaru
Morohashi, Ken-ichirou
Nagahama, Yoshitaka
description 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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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.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>12270141</pmid><doi>10.1016/S0006-291X(02)02252-0</doi><tpages>9</tpages></addata></record>
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ispartof Biochemical and biophysical research communications, 2002-09, Vol.297 (3), p.632-640
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subjects Actins - genetics
Amino Acid Sequence
Animals
Base Sequence
Cloning, Molecular
DAX-1 Orphan Nuclear Receptor
DAX1
DAX1 gene
DNA Primers
DNA-Binding Proteins - chemistry
DNA-Binding Proteins - genetics
Expressed Sequence Tags
Expression pattern
Freshwater
Gene Expression Regulation
Gonads
Humans
Introns - genetics
Liver
Mammals
Molecular Sequence Data
Nile tilapia
Nuclear receptors
Oreochromis niloticus
Phylogenetic analysis
Phylogeny
Receptors, Cytoplasmic and Nuclear - chemistry
Receptors, Cytoplasmic and Nuclear - genetics
Receptors, Retinoic Acid - chemistry
Receptors, Retinoic Acid - genetics
Recombinant Proteins - chemistry
Repressor Proteins
Sequence Alignment
Sequence Homology, Amino Acid
SHP
SHP gene
Tilapia - genetics
Transcription Factors - chemistry
Transcription Factors - genetics
title Molecular cloning of DAX1 and SHP cDNAs and their expression patterns in the Nile tilapia, Oreochromis niloticus
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