Chalcone synthase genes from milk thistle (Silybum marianum): isolation and expression analysis
Silymarin is a flavonoid compound derived from milk thistle ( Silybum marianum ) seeds which has several pharmacological applications. Chalcone synthase (CHS) is a key enzyme in the biosynthesis of flavonoids; thereby, the identification of CHS encoding genes in milk thistle plant can be of great im...
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Veröffentlicht in: | Journal of genetics 2015-12, Vol.94 (4), p.611-617 |
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creator | SANJARI, SEPIDEH SHOBBAR, ZAHRA SADAT EBRAHIMI, MOHSEN HASANLOO, TAHEREH SADAT-NOORI, SEYED-AHMAD TIRNAZ, SOODEH |
description | Silymarin is a flavonoid compound derived from milk thistle (
Silybum marianum
) seeds which has several pharmacological applications. Chalcone synthase (CHS) is a key enzyme in the biosynthesis of flavonoids; thereby, the identification of
CHS
encoding genes in milk thistle plant can be of great importance. In the current research, fragments of
CHS
genes were amplified using degenerate primers based on the conserved parts of Asteraceae
CHS
genes, and then cloned and sequenced. Analysis of the resultant nucleotide and deduced amino acid sequences led to the identification of two different members of
CHS
gene family,
SmCHS1
and
SmCHS2
. Third member, full-length cDNA (
SmCHS3
) was isolated by rapid amplification of cDNA ends (RACE), whose open reading frame contained 1239 bp including exon 1 (190 bp) and exon 2 (1049 bp), encoding 63 and 349 amino acids, respectively.
In silico
analysis of SmCHS3 sequence contains all the conserved CHS sites and shares high homology with CHS proteins from other plants. Real-time PCR analysis indicated that
SmCHS1
and
SmCHS3
had the highest transcript level in petals in the early flowering stage and in the stem of five upper leaves, followed by five upper leaves in the mid-flowering stage which are most probably involved in anthocyanin and silymarin biosynthesis. |
doi_str_mv | 10.1007/s12041-015-0560-7 |
format | Article |
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Silybum marianum
) seeds which has several pharmacological applications. Chalcone synthase (CHS) is a key enzyme in the biosynthesis of flavonoids; thereby, the identification of
CHS
encoding genes in milk thistle plant can be of great importance. In the current research, fragments of
CHS
genes were amplified using degenerate primers based on the conserved parts of Asteraceae
CHS
genes, and then cloned and sequenced. Analysis of the resultant nucleotide and deduced amino acid sequences led to the identification of two different members of
CHS
gene family,
SmCHS1
and
SmCHS2
. Third member, full-length cDNA (
SmCHS3
) was isolated by rapid amplification of cDNA ends (RACE), whose open reading frame contained 1239 bp including exon 1 (190 bp) and exon 2 (1049 bp), encoding 63 and 349 amino acids, respectively.
In silico
analysis of SmCHS3 sequence contains all the conserved CHS sites and shares high homology with CHS proteins from other plants. Real-time PCR analysis indicated that
SmCHS1
and
SmCHS3
had the highest transcript level in petals in the early flowering stage and in the stem of five upper leaves, followed by five upper leaves in the mid-flowering stage which are most probably involved in anthocyanin and silymarin biosynthesis.</description><identifier>ISSN: 0022-1333</identifier><identifier>EISSN: 0973-7731</identifier><identifier>DOI: 10.1007/s12041-015-0560-7</identifier><identifier>PMID: 26690515</identifier><language>eng</language><publisher>New Delhi: Springer India</publisher><subject>Acyltransferases - genetics ; Amino Acid Sequence ; Amino acids ; Animal Genetics and Genomics ; Asteraceae ; Biomedical and Life Sciences ; Dairy industry ; Enzymes ; Evolutionary Biology ; Flowers & plants ; Flowers - genetics ; Gene expression ; Gene Expression Regulation, Plant - genetics ; Genes ; Genes, Plant - genetics ; Genetics ; Isoflavones ; Life Sciences ; Microbial Genetics and Genomics ; Milk ; Molecular Sequence Data ; Plant Genetics and Genomics ; Plant Leaves - genetics ; Polymerase chain reaction ; Research Article ; Silybum marianum ; Silybum marianum - genetics</subject><ispartof>Journal of genetics, 2015-12, Vol.94 (4), p.611-617</ispartof><rights>Indian Academy of Sciences 2015</rights><rights>COPYRIGHT 2015 Springer</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c542t-f672261143ddccbdc33a0db5d1d9f3d9a017a4fa9198b999eaf06a6c909a3203</citedby><cites>FETCH-LOGICAL-c542t-f672261143ddccbdc33a0db5d1d9f3d9a017a4fa9198b999eaf06a6c909a3203</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s12041-015-0560-7$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s12041-015-0560-7$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26690515$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>SANJARI, SEPIDEH</creatorcontrib><creatorcontrib>SHOBBAR, ZAHRA SADAT</creatorcontrib><creatorcontrib>EBRAHIMI, MOHSEN</creatorcontrib><creatorcontrib>HASANLOO, TAHEREH</creatorcontrib><creatorcontrib>SADAT-NOORI, SEYED-AHMAD</creatorcontrib><creatorcontrib>TIRNAZ, SOODEH</creatorcontrib><title>Chalcone synthase genes from milk thistle (Silybum marianum): isolation and expression analysis</title><title>Journal of genetics</title><addtitle>J Genet</addtitle><addtitle>J Genet</addtitle><description>Silymarin is a flavonoid compound derived from milk thistle (
Silybum marianum
) seeds which has several pharmacological applications. Chalcone synthase (CHS) is a key enzyme in the biosynthesis of flavonoids; thereby, the identification of
CHS
encoding genes in milk thistle plant can be of great importance. In the current research, fragments of
CHS
genes were amplified using degenerate primers based on the conserved parts of Asteraceae
CHS
genes, and then cloned and sequenced. Analysis of the resultant nucleotide and deduced amino acid sequences led to the identification of two different members of
CHS
gene family,
SmCHS1
and
SmCHS2
. Third member, full-length cDNA (
SmCHS3
) was isolated by rapid amplification of cDNA ends (RACE), whose open reading frame contained 1239 bp including exon 1 (190 bp) and exon 2 (1049 bp), encoding 63 and 349 amino acids, respectively.
In silico
analysis of SmCHS3 sequence contains all the conserved CHS sites and shares high homology with CHS proteins from other plants. Real-time PCR analysis indicated that
SmCHS1
and
SmCHS3
had the highest transcript level in petals in the early flowering stage and in the stem of five upper leaves, followed by five upper leaves in the mid-flowering stage which are most probably involved in anthocyanin and silymarin biosynthesis.</description><subject>Acyltransferases - genetics</subject><subject>Amino Acid Sequence</subject><subject>Amino acids</subject><subject>Animal Genetics and Genomics</subject><subject>Asteraceae</subject><subject>Biomedical and Life Sciences</subject><subject>Dairy industry</subject><subject>Enzymes</subject><subject>Evolutionary Biology</subject><subject>Flowers & plants</subject><subject>Flowers - genetics</subject><subject>Gene expression</subject><subject>Gene Expression Regulation, Plant - genetics</subject><subject>Genes</subject><subject>Genes, Plant - genetics</subject><subject>Genetics</subject><subject>Isoflavones</subject><subject>Life Sciences</subject><subject>Microbial Genetics and Genomics</subject><subject>Milk</subject><subject>Molecular Sequence Data</subject><subject>Plant Genetics and Genomics</subject><subject>Plant Leaves - genetics</subject><subject>Polymerase chain reaction</subject><subject>Research Article</subject><subject>Silybum marianum</subject><subject>Silybum marianum - genetics</subject><issn>0022-1333</issn><issn>0973-7731</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNqNkctu1TAQhiNERS_wAGxQJDbtIsWXxI7ZVUfcpEos6N6axPY5Lk588CQS5-1xmoIKaiXkxXjG3z-a8V8Urym5pITId0gZqWlFaFORRpBKPitOiJK8kpLT5_lOGKso5_y4OEW8XVJJ2IvimAmhSEObk0JvdhD6ONoSD-O0A7Tl1o4WS5fiUA4-fC-nnccp2PL8mw-Hbs5VSB7Gebh4X3qMASYfxxJGU9qf-2QR1xTCAT2-LI4cBLSv7uNZcfPxw83mc3X99dOXzdV11Tc1myonJGOC0pob0_ed6TkHYrrGUKMcNwoIlVA7UFS1nVLKgiMCRK-IAs4IPyvO17b7FH_MFic9eOxtCDDaOKOmUrSNrHkr_gNtaN0qzllG3_6D3sY55c3uqLrO08gH1BaC1X50cUrQL031laSyZawRMlOXj1D5GDv4xQDnc_0vAV0FfYqIyTq9Tz5__UFTohf79Wq_zvbrxX69aN7cDzx3gzV_FL_9zgBbAcxP49amBxs92fUXduu4iQ</recordid><startdate>20151201</startdate><enddate>20151201</enddate><creator>SANJARI, SEPIDEH</creator><creator>SHOBBAR, ZAHRA SADAT</creator><creator>EBRAHIMI, MOHSEN</creator><creator>HASANLOO, TAHEREH</creator><creator>SADAT-NOORI, SEYED-AHMAD</creator><creator>TIRNAZ, SOODEH</creator><general>Springer India</general><general>Springer</general><general>Springer Nature B.V</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>3V.</scope><scope>7SS</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>M7P</scope><scope>MBDVC</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>20151201</creationdate><title>Chalcone synthase genes from milk thistle (Silybum marianum): isolation and expression analysis</title><author>SANJARI, SEPIDEH ; SHOBBAR, ZAHRA SADAT ; EBRAHIMI, MOHSEN ; HASANLOO, TAHEREH ; SADAT-NOORI, SEYED-AHMAD ; TIRNAZ, SOODEH</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c542t-f672261143ddccbdc33a0db5d1d9f3d9a017a4fa9198b999eaf06a6c909a3203</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Acyltransferases - genetics</topic><topic>Amino Acid Sequence</topic><topic>Amino acids</topic><topic>Animal Genetics and Genomics</topic><topic>Asteraceae</topic><topic>Biomedical and Life Sciences</topic><topic>Dairy industry</topic><topic>Enzymes</topic><topic>Evolutionary Biology</topic><topic>Flowers & plants</topic><topic>Flowers - genetics</topic><topic>Gene expression</topic><topic>Gene Expression Regulation, Plant - genetics</topic><topic>Genes</topic><topic>Genes, Plant - genetics</topic><topic>Genetics</topic><topic>Isoflavones</topic><topic>Life Sciences</topic><topic>Microbial Genetics and Genomics</topic><topic>Milk</topic><topic>Molecular Sequence Data</topic><topic>Plant Genetics and Genomics</topic><topic>Plant Leaves - genetics</topic><topic>Polymerase chain reaction</topic><topic>Research Article</topic><topic>Silybum marianum</topic><topic>Silybum marianum - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>SANJARI, SEPIDEH</creatorcontrib><creatorcontrib>SHOBBAR, ZAHRA SADAT</creatorcontrib><creatorcontrib>EBRAHIMI, MOHSEN</creatorcontrib><creatorcontrib>HASANLOO, TAHEREH</creatorcontrib><creatorcontrib>SADAT-NOORI, SEYED-AHMAD</creatorcontrib><creatorcontrib>TIRNAZ, SOODEH</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Biological Science Database</collection><collection>Research Library (Corporate)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of genetics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>SANJARI, SEPIDEH</au><au>SHOBBAR, ZAHRA SADAT</au><au>EBRAHIMI, MOHSEN</au><au>HASANLOO, TAHEREH</au><au>SADAT-NOORI, SEYED-AHMAD</au><au>TIRNAZ, SOODEH</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Chalcone synthase genes from milk thistle (Silybum marianum): isolation and expression analysis</atitle><jtitle>Journal of genetics</jtitle><stitle>J Genet</stitle><addtitle>J Genet</addtitle><date>2015-12-01</date><risdate>2015</risdate><volume>94</volume><issue>4</issue><spage>611</spage><epage>617</epage><pages>611-617</pages><issn>0022-1333</issn><eissn>0973-7731</eissn><abstract>Silymarin is a flavonoid compound derived from milk thistle (
Silybum marianum
) seeds which has several pharmacological applications. Chalcone synthase (CHS) is a key enzyme in the biosynthesis of flavonoids; thereby, the identification of
CHS
encoding genes in milk thistle plant can be of great importance. In the current research, fragments of
CHS
genes were amplified using degenerate primers based on the conserved parts of Asteraceae
CHS
genes, and then cloned and sequenced. Analysis of the resultant nucleotide and deduced amino acid sequences led to the identification of two different members of
CHS
gene family,
SmCHS1
and
SmCHS2
. Third member, full-length cDNA (
SmCHS3
) was isolated by rapid amplification of cDNA ends (RACE), whose open reading frame contained 1239 bp including exon 1 (190 bp) and exon 2 (1049 bp), encoding 63 and 349 amino acids, respectively.
In silico
analysis of SmCHS3 sequence contains all the conserved CHS sites and shares high homology with CHS proteins from other plants. Real-time PCR analysis indicated that
SmCHS1
and
SmCHS3
had the highest transcript level in petals in the early flowering stage and in the stem of five upper leaves, followed by five upper leaves in the mid-flowering stage which are most probably involved in anthocyanin and silymarin biosynthesis.</abstract><cop>New Delhi</cop><pub>Springer India</pub><pmid>26690515</pmid><doi>10.1007/s12041-015-0560-7</doi><tpages>7</tpages></addata></record> |
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source | MEDLINE; Indian Academy of Sciences; Springer Nature - Complete Springer Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals |
subjects | Acyltransferases - genetics Amino Acid Sequence Amino acids Animal Genetics and Genomics Asteraceae Biomedical and Life Sciences Dairy industry Enzymes Evolutionary Biology Flowers & plants Flowers - genetics Gene expression Gene Expression Regulation, Plant - genetics Genes Genes, Plant - genetics Genetics Isoflavones Life Sciences Microbial Genetics and Genomics Milk Molecular Sequence Data Plant Genetics and Genomics Plant Leaves - genetics Polymerase chain reaction Research Article Silybum marianum Silybum marianum - genetics |
title | Chalcone synthase genes from milk thistle (Silybum marianum): isolation and expression analysis |
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