Sex pheromone in the moth Heliothis virescens is produced as a mixture of two pools: de novo and via precursor storage in glycerolipids
Most species of moths use a female-produced volatile sex pheromone, typically produced via de novo fatty acid synthesis in a specialized gland, for communication among mates. While de novo biosynthesis of pheromone (DNP) is rapid, suggesting transient precursor acids, substantial amounts of pheromon...
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description | Most species of moths use a female-produced volatile sex pheromone, typically produced via de novo fatty acid synthesis in a specialized gland, for communication among mates. While de novo biosynthesis of pheromone (DNP) is rapid, suggesting transient precursor acids, substantial amounts of pheromone precursor (and other) acids are stored, predominantly in triacylglycerols in the pheromone gland. Whether these stored acids are converted to pheromone later or not has been the subject of some debate. Using a tracer/tracee approach, in which we fed female Heliothis virescens U-13C-glucose, we were able to distinguish two pools of pheromone, in which precursors were temporally separated (after and before feeding on labeled glucose): DNP synthesized from a mixed tracer/tracee acetyl CoA pool after feeding, and pheromone made from precursor acids primarily synthesized before feeding, which we call recycled precursor fat pheromone (RPP). DNP titer varied from high (during scotophase) to low (photophase) and with presence/absence of pheromone biosynthesis activating neuropeptide (PBAN), in accord with native pheromone titer previously observed. By contrast, RPP was constant throughout the photoperiod and did not change with PBAN presence/absence. The amount of RPP (6.3–10.3 ng/female) was typically much lower than that of DNP, especially during the scotophase (peak DNP, 105 ng/female). We propose an integral role for stored fats in pheromone biosynthesis, in which they are hydrolyzed and re-esterified throughout the photoperiod, with a small proportion of liberated precursor acyl CoAs being converted to pheromone. During the sexually active period, release of PBAN results in increased flux of glucose (from trehalose) and hydrolyzed acids entering the mitochondria, producing acetyl CoA precursor for de novo fat and pheromone biosynthesis.
[Display omitted]
•Tracer-tracee method demonstrates two routes for pheromone biosynthesis in moth Heliothis virescens.•De novo-produced pheromone (DNP) varies during the photophase, while recycled precursor fat pheromone (RPP) does not.•DNP is PBAN dependent, while RPP production is not.•RPP production is essential for gland function, but contributes little to pheromonal communication. |
doi_str_mv | 10.1016/j.ibmb.2017.06.004 |
format | Article |
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[Display omitted]
•Tracer-tracee method demonstrates two routes for pheromone biosynthesis in moth Heliothis virescens.•De novo-produced pheromone (DNP) varies during the photophase, while recycled precursor fat pheromone (RPP) does not.•DNP is PBAN dependent, while RPP production is not.•RPP production is essential for gland function, but contributes little to pheromonal communication.</description><identifier>ISSN: 0965-1748</identifier><identifier>EISSN: 1879-0240</identifier><identifier>DOI: 10.1016/j.ibmb.2017.06.004</identifier><identifier>PMID: 28619669</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>acetyl coenzyme A ; Age Factors ; Animal biology ; Animals ; Biochemistry ; Biochemistry, Molecular Biology ; biosynthesis ; Chemical communication ; fatty acids ; Female ; females ; glucose ; Glucose - metabolism ; Heliothis virescens ; hydrolysis ; Invertebrate Zoology ; Lepidoptera ; Life Sciences ; Mass isotopomer distribution analysis ; mitochondria ; moths ; Moths - metabolism ; Neuropeptides - metabolism ; Noctuidae ; pheromone biosynthesis activating neuropeptide ; Photoperiod ; photophase ; scotophase ; Sex Attractants - biosynthesis ; sex pheromones ; Stable isotope ; Tracer/tracee ; trehalose ; Trehalose - metabolism ; triacylglycerols ; Triglycerides - metabolism</subject><ispartof>Insect biochemistry and molecular biology, 2017-08, Vol.87, p.26-34</ispartof><rights>2017 Elsevier Ltd</rights><rights>Copyright © 2017 Elsevier Ltd. All rights reserved.</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c467t-b05c1492b01aa48986b400e869e62fc9cf6ac76b68d44dcc6e7b8329741f8fc73</citedby><cites>FETCH-LOGICAL-c467t-b05c1492b01aa48986b400e869e62fc9cf6ac76b68d44dcc6e7b8329741f8fc73</cites><orcidid>0000-0003-1666-295X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0965174817300802$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,776,780,881,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28619669$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.science/hal-02573190$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Foster, Stephen P.</creatorcontrib><creatorcontrib>Anderson, Karin G.</creatorcontrib><creatorcontrib>Casas, Jérôme</creatorcontrib><title>Sex pheromone in the moth Heliothis virescens is produced as a mixture of two pools: de novo and via precursor storage in glycerolipids</title><title>Insect biochemistry and molecular biology</title><addtitle>Insect Biochem Mol Biol</addtitle><description>Most species of moths use a female-produced volatile sex pheromone, typically produced via de novo fatty acid synthesis in a specialized gland, for communication among mates. While de novo biosynthesis of pheromone (DNP) is rapid, suggesting transient precursor acids, substantial amounts of pheromone precursor (and other) acids are stored, predominantly in triacylglycerols in the pheromone gland. Whether these stored acids are converted to pheromone later or not has been the subject of some debate. Using a tracer/tracee approach, in which we fed female Heliothis virescens U-13C-glucose, we were able to distinguish two pools of pheromone, in which precursors were temporally separated (after and before feeding on labeled glucose): DNP synthesized from a mixed tracer/tracee acetyl CoA pool after feeding, and pheromone made from precursor acids primarily synthesized before feeding, which we call recycled precursor fat pheromone (RPP). DNP titer varied from high (during scotophase) to low (photophase) and with presence/absence of pheromone biosynthesis activating neuropeptide (PBAN), in accord with native pheromone titer previously observed. By contrast, RPP was constant throughout the photoperiod and did not change with PBAN presence/absence. The amount of RPP (6.3–10.3 ng/female) was typically much lower than that of DNP, especially during the scotophase (peak DNP, 105 ng/female). We propose an integral role for stored fats in pheromone biosynthesis, in which they are hydrolyzed and re-esterified throughout the photoperiod, with a small proportion of liberated precursor acyl CoAs being converted to pheromone. During the sexually active period, release of PBAN results in increased flux of glucose (from trehalose) and hydrolyzed acids entering the mitochondria, producing acetyl CoA precursor for de novo fat and pheromone biosynthesis.
[Display omitted]
•Tracer-tracee method demonstrates two routes for pheromone biosynthesis in moth Heliothis virescens.•De novo-produced pheromone (DNP) varies during the photophase, while recycled precursor fat pheromone (RPP) does not.•DNP is PBAN dependent, while RPP production is not.•RPP production is essential for gland function, but contributes little to pheromonal communication.</description><subject>acetyl coenzyme A</subject><subject>Age Factors</subject><subject>Animal biology</subject><subject>Animals</subject><subject>Biochemistry</subject><subject>Biochemistry, Molecular Biology</subject><subject>biosynthesis</subject><subject>Chemical communication</subject><subject>fatty acids</subject><subject>Female</subject><subject>females</subject><subject>glucose</subject><subject>Glucose - metabolism</subject><subject>Heliothis virescens</subject><subject>hydrolysis</subject><subject>Invertebrate Zoology</subject><subject>Lepidoptera</subject><subject>Life Sciences</subject><subject>Mass isotopomer distribution analysis</subject><subject>mitochondria</subject><subject>moths</subject><subject>Moths - metabolism</subject><subject>Neuropeptides - metabolism</subject><subject>Noctuidae</subject><subject>pheromone biosynthesis activating neuropeptide</subject><subject>Photoperiod</subject><subject>photophase</subject><subject>scotophase</subject><subject>Sex Attractants - biosynthesis</subject><subject>sex pheromones</subject><subject>Stable isotope</subject><subject>Tracer/tracee</subject><subject>trehalose</subject><subject>Trehalose - metabolism</subject><subject>triacylglycerols</subject><subject>Triglycerides - metabolism</subject><issn>0965-1748</issn><issn>1879-0240</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkc9u1DAQhy0EokvhBTggH-GQMM46_oO4VBWwSCv1UDhbjjPpepXEwU6W9gl4bbxs6bE9jWx9vxl7PkLeMigZMPFxX_pmaMoKmCxBlAD8GVkxJXUBFYfnZAVa1AWTXJ2RVyntIRO8li_JWaUE00LoFflzjbd02mEMQxiR-pHOO6RDmHd0g73P1Sd68BGTwzHRfJhiaBeHLbWJWjr423mJSENH59-BTiH06RNtkY7hEKgd2xy2OYNuiSlEmuYQ7c2_QTf9nctzez_5Nr0mLzrbJ3xzX8_Jz69fflxuiu3Vt--XF9vCcSHnooHaMa6rBpi1XGklGg6ASmgUVee064R1UjRCtZy3zgmUjVpXWnLWqc7J9Tn5cOq7s72Zoh9svDPBerO52JrjHVS1XDMNB5bZ9yc2f_nXgmk2g89r6Hs7YliSqfJC65oLqJ9EmWYg9ZopldHqhLoYUorYPTyDgTl6NXtz9GqOXg0Ik63l0Lv7_kszYPsQ-S8yA59PAOblHTxGk5zHMXvK7txs2uAf6_8Xy4K0gQ</recordid><startdate>20170801</startdate><enddate>20170801</enddate><creator>Foster, Stephen P.</creator><creator>Anderson, Karin G.</creator><creator>Casas, Jérôme</creator><general>Elsevier Ltd</general><general>Elsevier</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>7X8</scope><scope>7S9</scope><scope>L.6</scope><scope>1XC</scope><scope>VOOES</scope><orcidid>https://orcid.org/0000-0003-1666-295X</orcidid></search><sort><creationdate>20170801</creationdate><title>Sex pheromone in the moth Heliothis virescens is produced as a mixture of two pools: de novo and via precursor storage in glycerolipids</title><author>Foster, Stephen P. ; Anderson, Karin G. ; Casas, Jérôme</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c467t-b05c1492b01aa48986b400e869e62fc9cf6ac76b68d44dcc6e7b8329741f8fc73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>acetyl coenzyme A</topic><topic>Age Factors</topic><topic>Animal biology</topic><topic>Animals</topic><topic>Biochemistry</topic><topic>Biochemistry, Molecular Biology</topic><topic>biosynthesis</topic><topic>Chemical communication</topic><topic>fatty acids</topic><topic>Female</topic><topic>females</topic><topic>glucose</topic><topic>Glucose - metabolism</topic><topic>Heliothis virescens</topic><topic>hydrolysis</topic><topic>Invertebrate Zoology</topic><topic>Lepidoptera</topic><topic>Life Sciences</topic><topic>Mass isotopomer distribution analysis</topic><topic>mitochondria</topic><topic>moths</topic><topic>Moths - metabolism</topic><topic>Neuropeptides - metabolism</topic><topic>Noctuidae</topic><topic>pheromone biosynthesis activating neuropeptide</topic><topic>Photoperiod</topic><topic>photophase</topic><topic>scotophase</topic><topic>Sex Attractants - biosynthesis</topic><topic>sex pheromones</topic><topic>Stable isotope</topic><topic>Tracer/tracee</topic><topic>trehalose</topic><topic>Trehalose - metabolism</topic><topic>triacylglycerols</topic><topic>Triglycerides - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Foster, Stephen P.</creatorcontrib><creatorcontrib>Anderson, Karin G.</creatorcontrib><creatorcontrib>Casas, Jérôme</creatorcontrib><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><collection>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><collection>Hyper Article en Ligne (HAL) (Open Access)</collection><jtitle>Insect biochemistry and molecular biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Foster, Stephen P.</au><au>Anderson, Karin G.</au><au>Casas, Jérôme</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Sex pheromone in the moth Heliothis virescens is produced as a mixture of two pools: de novo and via precursor storage in glycerolipids</atitle><jtitle>Insect biochemistry and molecular biology</jtitle><addtitle>Insect Biochem Mol Biol</addtitle><date>2017-08-01</date><risdate>2017</risdate><volume>87</volume><spage>26</spage><epage>34</epage><pages>26-34</pages><issn>0965-1748</issn><eissn>1879-0240</eissn><abstract>Most species of moths use a female-produced volatile sex pheromone, typically produced via de novo fatty acid synthesis in a specialized gland, for communication among mates. While de novo biosynthesis of pheromone (DNP) is rapid, suggesting transient precursor acids, substantial amounts of pheromone precursor (and other) acids are stored, predominantly in triacylglycerols in the pheromone gland. Whether these stored acids are converted to pheromone later or not has been the subject of some debate. Using a tracer/tracee approach, in which we fed female Heliothis virescens U-13C-glucose, we were able to distinguish two pools of pheromone, in which precursors were temporally separated (after and before feeding on labeled glucose): DNP synthesized from a mixed tracer/tracee acetyl CoA pool after feeding, and pheromone made from precursor acids primarily synthesized before feeding, which we call recycled precursor fat pheromone (RPP). DNP titer varied from high (during scotophase) to low (photophase) and with presence/absence of pheromone biosynthesis activating neuropeptide (PBAN), in accord with native pheromone titer previously observed. By contrast, RPP was constant throughout the photoperiod and did not change with PBAN presence/absence. The amount of RPP (6.3–10.3 ng/female) was typically much lower than that of DNP, especially during the scotophase (peak DNP, 105 ng/female). We propose an integral role for stored fats in pheromone biosynthesis, in which they are hydrolyzed and re-esterified throughout the photoperiod, with a small proportion of liberated precursor acyl CoAs being converted to pheromone. During the sexually active period, release of PBAN results in increased flux of glucose (from trehalose) and hydrolyzed acids entering the mitochondria, producing acetyl CoA precursor for de novo fat and pheromone biosynthesis.
[Display omitted]
•Tracer-tracee method demonstrates two routes for pheromone biosynthesis in moth Heliothis virescens.•De novo-produced pheromone (DNP) varies during the photophase, while recycled precursor fat pheromone (RPP) does not.•DNP is PBAN dependent, while RPP production is not.•RPP production is essential for gland function, but contributes little to pheromonal communication.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>28619669</pmid><doi>10.1016/j.ibmb.2017.06.004</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0003-1666-295X</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | acetyl coenzyme A Age Factors Animal biology Animals Biochemistry Biochemistry, Molecular Biology biosynthesis Chemical communication fatty acids Female females glucose Glucose - metabolism Heliothis virescens hydrolysis Invertebrate Zoology Lepidoptera Life Sciences Mass isotopomer distribution analysis mitochondria moths Moths - metabolism Neuropeptides - metabolism Noctuidae pheromone biosynthesis activating neuropeptide Photoperiod photophase scotophase Sex Attractants - biosynthesis sex pheromones Stable isotope Tracer/tracee trehalose Trehalose - metabolism triacylglycerols Triglycerides - metabolism |
title | Sex pheromone in the moth Heliothis virescens is produced as a mixture of two pools: de novo and via precursor storage in glycerolipids |
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