Characterization of the putative farnesoic acid O-methyltransferase (LvFAMeT) cDNA from white shrimp, Litopenaeus vannamei: Evidence for its role in molting
Methyl farnesoate (MF) is the crustacean homolog of the insect juvenile hormone and is believed to regulate growth and reproduction in crustaceans. Farnesoic acid O-methyltransferase (FAMeT) catalyzes the conversion of farnesoic acid (FA) to MF. Here we report the cloning and characterization of two...
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description | Methyl farnesoate (MF) is the crustacean homolog of the insect juvenile hormone and is believed to regulate growth and reproduction in crustaceans. Farnesoic acid
O-methyltransferase (FAMeT) catalyzes the conversion of farnesoic acid (FA) to MF. Here we report the cloning and characterization of two forms of FAMeTs (i.e. LvFAMeT-S and LvFAMeT-L) from the shrimp
Litopenaeus vannamei. LvFAMeT transcript has a wide tissue distribution pattern in
L. vannamei and is also expressed in nauplius, zoea, mysis, post-larval stages and adults. Unlike FAMeTs reported in other decapods, transcripts of two different sizes were detected in
L. vannamei. We postulate that the wide distribution of LvFAMeT expression may be related to its role in growth and regulation of molting. To study the functions of LvFAMeT in molting, the RNA interference (RNAi) technique was used. Injection of double stranded RNA (dsRNA) for LvFAMeT knocked down the expression of LvFAMeT in shrimp for at least 3 days and the shrimp did not advance to the final stage of molt cycle. Furthermore, the expression of the molt-related genes encoding cathepsin-L and the hemocyanin gene was disturbed. Subsequently, 100% mortality of the shrimp was observed in the LvFAMeT dsRNA-injected shrimp. In contrast, control shrimp completed their molt and proceeded to the next molt cycle. We postulate that, as an important enzyme for the conversion of FA to MF, RNAi injection knocked down the expression of LvFAMeT which could potentially result in a decrease in the production of MF and subsequently, could affect the molting process. The newly identified LvFAMeT may be involved in the control of molting in shrimp. The results of this study demonstrate the potential use of the RNA interference technique to study other putative genes identified in crustaceans. |
doi_str_mv | 10.1016/j.peptides.2007.08.033 |
format | Article |
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O-methyltransferase (FAMeT) catalyzes the conversion of farnesoic acid (FA) to MF. Here we report the cloning and characterization of two forms of FAMeTs (i.e. LvFAMeT-S and LvFAMeT-L) from the shrimp
Litopenaeus vannamei. LvFAMeT transcript has a wide tissue distribution pattern in
L. vannamei and is also expressed in nauplius, zoea, mysis, post-larval stages and adults. Unlike FAMeTs reported in other decapods, transcripts of two different sizes were detected in
L. vannamei. We postulate that the wide distribution of LvFAMeT expression may be related to its role in growth and regulation of molting. To study the functions of LvFAMeT in molting, the RNA interference (RNAi) technique was used. Injection of double stranded RNA (dsRNA) for LvFAMeT knocked down the expression of LvFAMeT in shrimp for at least 3 days and the shrimp did not advance to the final stage of molt cycle. Furthermore, the expression of the molt-related genes encoding cathepsin-L and the hemocyanin gene was disturbed. Subsequently, 100% mortality of the shrimp was observed in the LvFAMeT dsRNA-injected shrimp. In contrast, control shrimp completed their molt and proceeded to the next molt cycle. We postulate that, as an important enzyme for the conversion of FA to MF, RNAi injection knocked down the expression of LvFAMeT which could potentially result in a decrease in the production of MF and subsequently, could affect the molting process. The newly identified LvFAMeT may be involved in the control of molting in shrimp. The results of this study demonstrate the potential use of the RNA interference technique to study other putative genes identified in crustaceans.</description><identifier>ISSN: 0196-9781</identifier><identifier>EISSN: 1873-5169</identifier><identifier>DOI: 10.1016/j.peptides.2007.08.033</identifier><identifier>PMID: 18226425</identifier><identifier>CODEN: PPTDD5</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>Amino Acid Sequence ; Animals ; Base Sequence ; Biological and medical sciences ; Cathepsin L ; Cathepsins - genetics ; Cloning, Molecular ; Cysteine Endopeptidases - genetics ; DNA, Complementary - chemistry ; DNA, Complementary - genetics ; Farnesoic acid ; Female ; Fundamental and applied biological sciences. Psychology ; Gene Expression Regulation, Developmental ; Gene Expression Regulation, Enzymologic ; Hemocyanins - genetics ; In vivo ; Isoenzymes - genetics ; Isoenzymes - metabolism ; Larva - genetics ; Larva - growth & development ; Male ; Methyl farnesoate ; Methyltransferase ; Methyltransferases - genetics ; Methyltransferases - metabolism ; Molecular Sequence Data ; Molting ; Molting - genetics ; Molting - physiology ; Nerve Tissue - metabolism ; Penaeidae - enzymology ; Penaeidae - genetics ; RNA Interference ; Sequence Analysis, DNA ; Shrimp ; Vertebrates: endocrinology</subject><ispartof>Peptides (New York, N.Y. : 1980), 2008-02, Vol.29 (2), p.252-260</ispartof><rights>2007 Elsevier Inc.</rights><rights>2008 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c462t-7bc888eef3fa9209b42d6849dcd82b371fcb10cf7b29fa691f95322b3838d1083</citedby><cites>FETCH-LOGICAL-c462t-7bc888eef3fa9209b42d6849dcd82b371fcb10cf7b29fa691f95322b3838d1083</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0196978107004925$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>309,310,314,776,780,785,786,3537,23909,23910,25118,27901,27902,65306</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=20232023$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18226425$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hui, Jerome Ho Lam</creatorcontrib><creatorcontrib>Tobe, Stephen S.</creatorcontrib><creatorcontrib>Chan, Siu-Ming</creatorcontrib><title>Characterization of the putative farnesoic acid O-methyltransferase (LvFAMeT) cDNA from white shrimp, Litopenaeus vannamei: Evidence for its role in molting</title><title>Peptides (New York, N.Y. : 1980)</title><addtitle>Peptides</addtitle><description>Methyl farnesoate (MF) is the crustacean homolog of the insect juvenile hormone and is believed to regulate growth and reproduction in crustaceans. Farnesoic acid
O-methyltransferase (FAMeT) catalyzes the conversion of farnesoic acid (FA) to MF. Here we report the cloning and characterization of two forms of FAMeTs (i.e. LvFAMeT-S and LvFAMeT-L) from the shrimp
Litopenaeus vannamei. LvFAMeT transcript has a wide tissue distribution pattern in
L. vannamei and is also expressed in nauplius, zoea, mysis, post-larval stages and adults. Unlike FAMeTs reported in other decapods, transcripts of two different sizes were detected in
L. vannamei. We postulate that the wide distribution of LvFAMeT expression may be related to its role in growth and regulation of molting. To study the functions of LvFAMeT in molting, the RNA interference (RNAi) technique was used. Injection of double stranded RNA (dsRNA) for LvFAMeT knocked down the expression of LvFAMeT in shrimp for at least 3 days and the shrimp did not advance to the final stage of molt cycle. Furthermore, the expression of the molt-related genes encoding cathepsin-L and the hemocyanin gene was disturbed. Subsequently, 100% mortality of the shrimp was observed in the LvFAMeT dsRNA-injected shrimp. In contrast, control shrimp completed their molt and proceeded to the next molt cycle. We postulate that, as an important enzyme for the conversion of FA to MF, RNAi injection knocked down the expression of LvFAMeT which could potentially result in a decrease in the production of MF and subsequently, could affect the molting process. The newly identified LvFAMeT may be involved in the control of molting in shrimp. The results of this study demonstrate the potential use of the RNA interference technique to study other putative genes identified in crustaceans.</description><subject>Amino Acid Sequence</subject><subject>Animals</subject><subject>Base Sequence</subject><subject>Biological and medical sciences</subject><subject>Cathepsin L</subject><subject>Cathepsins - genetics</subject><subject>Cloning, Molecular</subject><subject>Cysteine Endopeptidases - genetics</subject><subject>DNA, Complementary - chemistry</subject><subject>DNA, Complementary - genetics</subject><subject>Farnesoic acid</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gene Expression Regulation, Developmental</subject><subject>Gene Expression Regulation, Enzymologic</subject><subject>Hemocyanins - genetics</subject><subject>In vivo</subject><subject>Isoenzymes - genetics</subject><subject>Isoenzymes - metabolism</subject><subject>Larva - genetics</subject><subject>Larva - growth & development</subject><subject>Male</subject><subject>Methyl farnesoate</subject><subject>Methyltransferase</subject><subject>Methyltransferases - genetics</subject><subject>Methyltransferases - metabolism</subject><subject>Molecular Sequence Data</subject><subject>Molting</subject><subject>Molting - genetics</subject><subject>Molting - physiology</subject><subject>Nerve Tissue - metabolism</subject><subject>Penaeidae - enzymology</subject><subject>Penaeidae - genetics</subject><subject>RNA Interference</subject><subject>Sequence Analysis, DNA</subject><subject>Shrimp</subject><subject>Vertebrates: endocrinology</subject><issn>0196-9781</issn><issn>1873-5169</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkdGO1CAUhonRuOPqK2y40WhiK9BOS71yMu6qyejerNeE0oNl0kIFWrM-iw8rzYx66QUhhO9wOP-H0BUlOSW0enPMJ5ii6SDkjJA6JzwnRfEAbSivi2xLq-Yh2hDaVFlTc3qBnoRwJISUZcMfowvKGatKtt2gX_teeqkiePNTRuMsdhrHHvA0x3ReAGvpLQRnFJbKdPg2GyH290P00gYNXgbALw_Lze4z3L3C6v2XHdbejfhHbyLg0HszTq_xwUQ3gZUwB7xIa-UI5i2-XtIAVqUezmMTA_ZuAGwsHt0Qjf32FD3Scgjw7Lxfoq8313f7j9nh9sOn_e6QqbJiMatbxTkH0IWWDSNNW7Ku4mXTqY6ztqipVi0lStcta7SsGqqbbcHSDS94RwkvLtGL07uTd99nCFGMJigYBmnBzUHUhPGq5CtYnUDlXQgetJjSfNLfC0rE6kUcxR8vYvUiCBfJSyq8OneY2xG6f2VnEQl4fgZkUHLQKV1lwl-OEVasK3HvThykPBYDXgRl1gw740FF0Tnzv7_8BokRsb8</recordid><startdate>20080201</startdate><enddate>20080201</enddate><creator>Hui, Jerome Ho Lam</creator><creator>Tobe, Stephen S.</creator><creator>Chan, Siu-Ming</creator><general>Elsevier Inc</general><general>Elsevier Science</general><scope>IQODW</scope><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>7X8</scope></search><sort><creationdate>20080201</creationdate><title>Characterization of the putative farnesoic acid O-methyltransferase (LvFAMeT) cDNA from white shrimp, Litopenaeus vannamei: Evidence for its role in molting</title><author>Hui, Jerome Ho Lam ; Tobe, Stephen S. ; Chan, Siu-Ming</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c462t-7bc888eef3fa9209b42d6849dcd82b371fcb10cf7b29fa691f95322b3838d1083</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Amino Acid Sequence</topic><topic>Animals</topic><topic>Base Sequence</topic><topic>Biological and medical sciences</topic><topic>Cathepsin L</topic><topic>Cathepsins - genetics</topic><topic>Cloning, Molecular</topic><topic>Cysteine Endopeptidases - genetics</topic><topic>DNA, Complementary - chemistry</topic><topic>DNA, Complementary - genetics</topic><topic>Farnesoic acid</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gene Expression Regulation, Developmental</topic><topic>Gene Expression Regulation, Enzymologic</topic><topic>Hemocyanins - genetics</topic><topic>In vivo</topic><topic>Isoenzymes - genetics</topic><topic>Isoenzymes - metabolism</topic><topic>Larva - genetics</topic><topic>Larva - growth & development</topic><topic>Male</topic><topic>Methyl farnesoate</topic><topic>Methyltransferase</topic><topic>Methyltransferases - genetics</topic><topic>Methyltransferases - metabolism</topic><topic>Molecular Sequence Data</topic><topic>Molting</topic><topic>Molting - genetics</topic><topic>Molting - physiology</topic><topic>Nerve Tissue - metabolism</topic><topic>Penaeidae - enzymology</topic><topic>Penaeidae - genetics</topic><topic>RNA Interference</topic><topic>Sequence Analysis, DNA</topic><topic>Shrimp</topic><topic>Vertebrates: endocrinology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hui, Jerome Ho Lam</creatorcontrib><creatorcontrib>Tobe, Stephen S.</creatorcontrib><creatorcontrib>Chan, Siu-Ming</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Peptides (New York, N.Y. : 1980)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hui, Jerome Ho Lam</au><au>Tobe, Stephen S.</au><au>Chan, Siu-Ming</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Characterization of the putative farnesoic acid O-methyltransferase (LvFAMeT) cDNA from white shrimp, Litopenaeus vannamei: Evidence for its role in molting</atitle><jtitle>Peptides (New York, N.Y. : 1980)</jtitle><addtitle>Peptides</addtitle><date>2008-02-01</date><risdate>2008</risdate><volume>29</volume><issue>2</issue><spage>252</spage><epage>260</epage><pages>252-260</pages><issn>0196-9781</issn><eissn>1873-5169</eissn><coden>PPTDD5</coden><abstract>Methyl farnesoate (MF) is the crustacean homolog of the insect juvenile hormone and is believed to regulate growth and reproduction in crustaceans. Farnesoic acid
O-methyltransferase (FAMeT) catalyzes the conversion of farnesoic acid (FA) to MF. Here we report the cloning and characterization of two forms of FAMeTs (i.e. LvFAMeT-S and LvFAMeT-L) from the shrimp
Litopenaeus vannamei. LvFAMeT transcript has a wide tissue distribution pattern in
L. vannamei and is also expressed in nauplius, zoea, mysis, post-larval stages and adults. Unlike FAMeTs reported in other decapods, transcripts of two different sizes were detected in
L. vannamei. We postulate that the wide distribution of LvFAMeT expression may be related to its role in growth and regulation of molting. To study the functions of LvFAMeT in molting, the RNA interference (RNAi) technique was used. Injection of double stranded RNA (dsRNA) for LvFAMeT knocked down the expression of LvFAMeT in shrimp for at least 3 days and the shrimp did not advance to the final stage of molt cycle. Furthermore, the expression of the molt-related genes encoding cathepsin-L and the hemocyanin gene was disturbed. Subsequently, 100% mortality of the shrimp was observed in the LvFAMeT dsRNA-injected shrimp. In contrast, control shrimp completed their molt and proceeded to the next molt cycle. We postulate that, as an important enzyme for the conversion of FA to MF, RNAi injection knocked down the expression of LvFAMeT which could potentially result in a decrease in the production of MF and subsequently, could affect the molting process. The newly identified LvFAMeT may be involved in the control of molting in shrimp. The results of this study demonstrate the potential use of the RNA interference technique to study other putative genes identified in crustaceans.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>18226425</pmid><doi>10.1016/j.peptides.2007.08.033</doi><tpages>9</tpages></addata></record> |
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subjects | Amino Acid Sequence Animals Base Sequence Biological and medical sciences Cathepsin L Cathepsins - genetics Cloning, Molecular Cysteine Endopeptidases - genetics DNA, Complementary - chemistry DNA, Complementary - genetics Farnesoic acid Female Fundamental and applied biological sciences. Psychology Gene Expression Regulation, Developmental Gene Expression Regulation, Enzymologic Hemocyanins - genetics In vivo Isoenzymes - genetics Isoenzymes - metabolism Larva - genetics Larva - growth & development Male Methyl farnesoate Methyltransferase Methyltransferases - genetics Methyltransferases - metabolism Molecular Sequence Data Molting Molting - genetics Molting - physiology Nerve Tissue - metabolism Penaeidae - enzymology Penaeidae - genetics RNA Interference Sequence Analysis, DNA Shrimp Vertebrates: endocrinology |
title | Characterization of the putative farnesoic acid O-methyltransferase (LvFAMeT) cDNA from white shrimp, Litopenaeus vannamei: Evidence for its role in molting |
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