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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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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. |
doi_str_mv | 10.1016/S0006-291X(02)02252-0 |
format | article |
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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.</description><identifier>ISSN: 0006-291X</identifier><identifier>EISSN: 1090-2104</identifier><identifier>DOI: 10.1016/S0006-291X(02)02252-0</identifier><identifier>PMID: 12270141</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>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</subject><ispartof>Biochemical and biophysical research communications, 2002-09, Vol.297 (3), p.632-640</ispartof><rights>2002 Elsevier Science (USA)</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c392t-c77ca645049010c153b1f96bb22cb2c1706b8df0301f873ebe510e88218de7403</citedby><cites>FETCH-LOGICAL-c392t-c77ca645049010c153b1f96bb22cb2c1706b8df0301f873ebe510e88218de7403</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,778,782,27911,27912</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12270141$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wang, De-Shou</creatorcontrib><creatorcontrib>Kobayashi, Tohru</creatorcontrib><creatorcontrib>Senthilkumaran, Balasubramanian</creatorcontrib><creatorcontrib>Sakai, Fumie</creatorcontrib><creatorcontrib>Chery Sudhakumari, Cheni</creatorcontrib><creatorcontrib>Suzuki, Taiga</creatorcontrib><creatorcontrib>Yoshikuni, Michiyasu</creatorcontrib><creatorcontrib>Matsuda, Masaru</creatorcontrib><creatorcontrib>Morohashi, Ken-ichirou</creatorcontrib><creatorcontrib>Nagahama, Yoshitaka</creatorcontrib><title>Molecular cloning of DAX1 and SHP cDNAs and their expression patterns in the Nile tilapia, Oreochromis niloticus</title><title>Biochemical and biophysical research communications</title><addtitle>Biochem Biophys Res Commun</addtitle><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.</description><subject>Actins - genetics</subject><subject>Amino Acid Sequence</subject><subject>Animals</subject><subject>Base Sequence</subject><subject>Cloning, Molecular</subject><subject>DAX-1 Orphan Nuclear Receptor</subject><subject>DAX1</subject><subject>DAX1 gene</subject><subject>DNA Primers</subject><subject>DNA-Binding Proteins - chemistry</subject><subject>DNA-Binding Proteins - genetics</subject><subject>Expressed Sequence Tags</subject><subject>Expression pattern</subject><subject>Freshwater</subject><subject>Gene Expression Regulation</subject><subject>Gonads</subject><subject>Humans</subject><subject>Introns - genetics</subject><subject>Liver</subject><subject>Mammals</subject><subject>Molecular Sequence Data</subject><subject>Nile tilapia</subject><subject>Nuclear receptors</subject><subject>Oreochromis niloticus</subject><subject>Phylogenetic analysis</subject><subject>Phylogeny</subject><subject>Receptors, Cytoplasmic and Nuclear - chemistry</subject><subject>Receptors, Cytoplasmic and Nuclear - genetics</subject><subject>Receptors, Retinoic Acid - chemistry</subject><subject>Receptors, Retinoic Acid - genetics</subject><subject>Recombinant Proteins - chemistry</subject><subject>Repressor Proteins</subject><subject>Sequence Alignment</subject><subject>Sequence Homology, Amino Acid</subject><subject>SHP</subject><subject>SHP gene</subject><subject>Tilapia - genetics</subject><subject>Transcription Factors - chemistry</subject><subject>Transcription Factors - genetics</subject><issn>0006-291X</issn><issn>1090-2104</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><recordid>eNqFkVtLHEEQhRsxxHWTn5DQTxLBMVU99ydZvERh1YARfGt6emq0Q2_3pHtG9N-7N8yjT0VRX1UdzmHsG8IxAhY_7wCgSESNDz9AHIIQuUhgh00QakgEQrbLJu_IHtuP8S8AYlbUn9keClECZjhh_bW3pEerAtfWO-Meue_42ewBuXItv7v8zfXZzSyuu-GJTOD00geK0XjHezUMFFzkxq2G_MZY4oOxqjfqiN8G8vop-IWJ3BnrB6PH-IV96pSN9HVbp-z-4vzP6WUyv_11dTqbJzqtxZDostSqyHLIakDQmKcNdnXRNELoRmgsoWiqtoMUsKvKlBrKEaiqBFYtlRmkU3awudsH_2-kOMilDE3WKkd-jLIUiCXm9YcgVgVABtUSzDegDj7GQJ3sg1mo8CoR5CoTuc5ErgyXIOQ6E7lS8n37YGwW1P7f2oawBE42AC39eDYUZNSGnKbWBNKDbL354MUbkhWamg</recordid><startdate>20020927</startdate><enddate>20020927</enddate><creator>Wang, De-Shou</creator><creator>Kobayashi, Tohru</creator><creator>Senthilkumaran, Balasubramanian</creator><creator>Sakai, Fumie</creator><creator>Chery Sudhakumari, Cheni</creator><creator>Suzuki, Taiga</creator><creator>Yoshikuni, Michiyasu</creator><creator>Matsuda, Masaru</creator><creator>Morohashi, Ken-ichirou</creator><creator>Nagahama, Yoshitaka</creator><general>Elsevier Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>8FD</scope><scope>F1W</scope><scope>FR3</scope><scope>H95</scope><scope>H99</scope><scope>L.F</scope><scope>L.G</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>20020927</creationdate><title>Molecular cloning of DAX1 and SHP cDNAs and their expression patterns in the Nile tilapia, Oreochromis niloticus</title><author>Wang, De-Shou ; Kobayashi, Tohru ; Senthilkumaran, Balasubramanian ; Sakai, Fumie ; Chery Sudhakumari, Cheni ; Suzuki, Taiga ; Yoshikuni, Michiyasu ; Matsuda, Masaru ; Morohashi, Ken-ichirou ; Nagahama, Yoshitaka</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c392t-c77ca645049010c153b1f96bb22cb2c1706b8df0301f873ebe510e88218de7403</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Actins - genetics</topic><topic>Amino Acid Sequence</topic><topic>Animals</topic><topic>Base Sequence</topic><topic>Cloning, Molecular</topic><topic>DAX-1 Orphan Nuclear Receptor</topic><topic>DAX1</topic><topic>DAX1 gene</topic><topic>DNA Primers</topic><topic>DNA-Binding Proteins - chemistry</topic><topic>DNA-Binding Proteins - genetics</topic><topic>Expressed Sequence Tags</topic><topic>Expression pattern</topic><topic>Freshwater</topic><topic>Gene Expression Regulation</topic><topic>Gonads</topic><topic>Humans</topic><topic>Introns - genetics</topic><topic>Liver</topic><topic>Mammals</topic><topic>Molecular Sequence Data</topic><topic>Nile tilapia</topic><topic>Nuclear receptors</topic><topic>Oreochromis niloticus</topic><topic>Phylogenetic analysis</topic><topic>Phylogeny</topic><topic>Receptors, Cytoplasmic and Nuclear - chemistry</topic><topic>Receptors, Cytoplasmic and Nuclear - genetics</topic><topic>Receptors, Retinoic Acid - chemistry</topic><topic>Receptors, Retinoic Acid - genetics</topic><topic>Recombinant Proteins - chemistry</topic><topic>Repressor Proteins</topic><topic>Sequence Alignment</topic><topic>Sequence Homology, Amino Acid</topic><topic>SHP</topic><topic>SHP gene</topic><topic>Tilapia - genetics</topic><topic>Transcription Factors - chemistry</topic><topic>Transcription Factors - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wang, De-Shou</creatorcontrib><creatorcontrib>Kobayashi, Tohru</creatorcontrib><creatorcontrib>Senthilkumaran, Balasubramanian</creatorcontrib><creatorcontrib>Sakai, Fumie</creatorcontrib><creatorcontrib>Chery Sudhakumari, Cheni</creatorcontrib><creatorcontrib>Suzuki, Taiga</creatorcontrib><creatorcontrib>Yoshikuni, Michiyasu</creatorcontrib><creatorcontrib>Matsuda, Masaru</creatorcontrib><creatorcontrib>Morohashi, Ken-ichirou</creatorcontrib><creatorcontrib>Nagahama, Yoshitaka</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Technology Research Database</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>Engineering Research Database</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 1: Biological Sciences & Living Resources</collection><collection>ASFA: Marine Biotechnology Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Marine Biotechnology Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Professional</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Biochemical and biophysical research communications</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wang, De-Shou</au><au>Kobayashi, Tohru</au><au>Senthilkumaran, Balasubramanian</au><au>Sakai, Fumie</au><au>Chery Sudhakumari, Cheni</au><au>Suzuki, Taiga</au><au>Yoshikuni, Michiyasu</au><au>Matsuda, Masaru</au><au>Morohashi, Ken-ichirou</au><au>Nagahama, Yoshitaka</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Molecular cloning of DAX1 and SHP cDNAs and their expression patterns in the Nile tilapia, Oreochromis niloticus</atitle><jtitle>Biochemical and biophysical research communications</jtitle><addtitle>Biochem Biophys Res Commun</addtitle><date>2002-09-27</date><risdate>2002</risdate><volume>297</volume><issue>3</issue><spage>632</spage><epage>640</epage><pages>632-640</pages><issn>0006-291X</issn><eissn>1090-2104</eissn><abstract>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.</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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source | ScienceDirect Freedom Collection 2022-2024 |
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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