LncRNA‐IRAR‐mediated regulation of insulin receptor transcripts in Drosophila melanogaster during nutritional stress
The insulin signalling pathway plays a crucial role in regulating the metabolism of sugars, fats and proteins in cells, thereby affecting the growth, metabolism, reproduction and ageing of organisms. However, little is known about the functions of long non‐coding RNAs (lncRNAs) in the regulation of...
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Veröffentlicht in: | Insect molecular biology 2022-06, Vol.31 (3), p.261-272 |
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description | The insulin signalling pathway plays a crucial role in regulating the metabolism of sugars, fats and proteins in cells, thereby affecting the growth, metabolism, reproduction and ageing of organisms. However, little is known about the functions of long non‐coding RNAs (lncRNAs) in the regulation of insulin receptors under stress conditions in insects. In this study, we showed that insulin receptor‐associated lncRNA (IRAR) regulates insulin receptor transcripts in response to nutritional stress in Drosophila melanogaster. Genome editing by CRISPR‐Cas9 showed reduced sensitivity of IRAR mutants to environmental nutritional changes. In contrast, the sensitivity of mutants overexpressing tubulin‐gal4 > IRAR increased under low nutrition. The pupation and eclosion timings in IRAR mutants were significantly delayed with an increase in insulin concentration compared with that in the w1118 group. In addition, the expression pattern of IRAR was almost consistent with that of the four transcripts of the insulin receptor from the embryonic period to the adult period. RNA immunoprecipitation assay showed the direct regulation of insulin receptor transcripts by IRAR to the through FOXO binding under nutritional stress. To our knowledge, this is the first study that describes a model of lncRNA‐mediated development regulation through insulin receptor transcripts.
Insulin receptor transcripts are regulated by IRAR. IRAR causes defects in the sensitivity of nutritional change. Direct regulation of IRAR to the insulin receptor transcripts through FOXO binding under nutritional stress. |
doi_str_mv | 10.1111/imb.12756 |
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Insulin receptor transcripts are regulated by IRAR. IRAR causes defects in the sensitivity of nutritional change. Direct regulation of IRAR to the insulin receptor transcripts through FOXO binding under nutritional stress.</description><identifier>ISSN: 0962-1075</identifier><identifier>EISSN: 1365-2583</identifier><identifier>DOI: 10.1111/imb.12756</identifier><identifier>PMID: 34923706</identifier><language>eng</language><publisher>Chichester, UK: John Wiley & Sons, Ltd</publisher><subject>Aging ; Animals ; CRISPR ; CRISPR‐Cas9 ; Drosophila melanogaster ; Drosophila melanogaster - physiology ; Drosophila Proteins - genetics ; Drosophila Proteins - metabolism ; Eclosion ; Embryos ; Forkhead protein ; Fruit flies ; Genomes ; Immunoprecipitation ; Insects ; Insulin ; Insulin - genetics ; Insulin - metabolism ; insulin receptor ; Insulin receptors ; lncRNA ; Metabolism ; Mutants ; Non-coding RNA ; Nutrient deficiency ; Nutrition ; Pupation ; Receptor, Insulin - genetics ; Receptor, Insulin - metabolism ; Receptors ; RNA, Long Noncoding - genetics ; RNA, Long Noncoding - metabolism ; Sensitivity ; Signal transduction ; starvation ; stress ; Sugar ; Tubulin</subject><ispartof>Insect molecular biology, 2022-06, Vol.31 (3), p.261-272</ispartof><rights>2022 The Royal Entomological Society</rights><rights>2022 The Royal Entomological Society.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3536-c9d02d7f88e0c33ef90632996752b2bceb65516d3df53b9ce62222d32093ecac3</citedby><cites>FETCH-LOGICAL-c3536-c9d02d7f88e0c33ef90632996752b2bceb65516d3df53b9ce62222d32093ecac3</cites><orcidid>0000-0001-8569-3667</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fimb.12756$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fimb.12756$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,778,782,1414,27907,27908,45557,45558</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34923706$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chen, Jie</creatorcontrib><creatorcontrib>Huang, Yuantai</creatorcontrib><creatorcontrib>Qi, Guojun</creatorcontrib><title>LncRNA‐IRAR‐mediated regulation of insulin receptor transcripts in Drosophila melanogaster during nutritional stress</title><title>Insect molecular biology</title><addtitle>Insect Mol Biol</addtitle><description>The insulin signalling pathway plays a crucial role in regulating the metabolism of sugars, fats and proteins in cells, thereby affecting the growth, metabolism, reproduction and ageing of organisms. However, little is known about the functions of long non‐coding RNAs (lncRNAs) in the regulation of insulin receptors under stress conditions in insects. In this study, we showed that insulin receptor‐associated lncRNA (IRAR) regulates insulin receptor transcripts in response to nutritional stress in Drosophila melanogaster. Genome editing by CRISPR‐Cas9 showed reduced sensitivity of IRAR mutants to environmental nutritional changes. In contrast, the sensitivity of mutants overexpressing tubulin‐gal4 > IRAR increased under low nutrition. The pupation and eclosion timings in IRAR mutants were significantly delayed with an increase in insulin concentration compared with that in the w1118 group. In addition, the expression pattern of IRAR was almost consistent with that of the four transcripts of the insulin receptor from the embryonic period to the adult period. RNA immunoprecipitation assay showed the direct regulation of insulin receptor transcripts by IRAR to the through FOXO binding under nutritional stress. To our knowledge, this is the first study that describes a model of lncRNA‐mediated development regulation through insulin receptor transcripts.
Insulin receptor transcripts are regulated by IRAR. IRAR causes defects in the sensitivity of nutritional change. Direct regulation of IRAR to the insulin receptor transcripts through FOXO binding under nutritional stress.</description><subject>Aging</subject><subject>Animals</subject><subject>CRISPR</subject><subject>CRISPR‐Cas9</subject><subject>Drosophila melanogaster</subject><subject>Drosophila melanogaster - physiology</subject><subject>Drosophila Proteins - genetics</subject><subject>Drosophila Proteins - metabolism</subject><subject>Eclosion</subject><subject>Embryos</subject><subject>Forkhead protein</subject><subject>Fruit flies</subject><subject>Genomes</subject><subject>Immunoprecipitation</subject><subject>Insects</subject><subject>Insulin</subject><subject>Insulin - genetics</subject><subject>Insulin - metabolism</subject><subject>insulin receptor</subject><subject>Insulin receptors</subject><subject>lncRNA</subject><subject>Metabolism</subject><subject>Mutants</subject><subject>Non-coding RNA</subject><subject>Nutrient deficiency</subject><subject>Nutrition</subject><subject>Pupation</subject><subject>Receptor, Insulin - genetics</subject><subject>Receptor, Insulin - metabolism</subject><subject>Receptors</subject><subject>RNA, Long Noncoding - genetics</subject><subject>RNA, Long Noncoding - metabolism</subject><subject>Sensitivity</subject><subject>Signal transduction</subject><subject>starvation</subject><subject>stress</subject><subject>Sugar</subject><subject>Tubulin</subject><issn>0962-1075</issn><issn>1365-2583</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kU1u2zAQhYkiQeOkXfQCAYFskoVsigwpcek4fwbcFjDatUBRI4eGJKokhTa7HCFnzElCR24WBTqbAWY-PMy8h9CXlEzTWDPTltOUZlx8QJOUCZ5QnrMDNCFS0CQlGT9Cx95vCSG5FPIjOmKXkrKMiAn6s-r0-tv85el5uZ6vY2uhMipAhR1shkYFYztsa2w6PzSmi1MNfbAOB6c6r53pg49LfO2st_2DaRRuoVGd3SgfwOFqcKbb4G4Izuy0VIN9cOD9J3RYq8bD530_QT9vb34s7pPV97vlYr5KNONMJFpWhFZZnedANGNQSyIYlVJknJa01FAKzlNRsarmrJQaBI1VMUokA600O0Hno27v7K8BfCha4zU08Uawgy-oSClhlyIXET37B93awcWTdxSX0bPoX6QuRkrHl72DuuidaZV7LFJS7OIoYhzFWxyRPd0rDmU09p38638EZiPw2zTw-H-lYvn1apR8Bf1cl3U</recordid><startdate>202206</startdate><enddate>202206</enddate><creator>Chen, Jie</creator><creator>Huang, Yuantai</creator><creator>Qi, Guojun</creator><general>John Wiley & Sons, Ltd</general><general>Blackwell Publishing Ltd</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>7QR</scope><scope>7SS</scope><scope>7TK</scope><scope>7TM</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-8569-3667</orcidid></search><sort><creationdate>202206</creationdate><title>LncRNA‐IRAR‐mediated regulation of insulin receptor transcripts in Drosophila melanogaster during nutritional stress</title><author>Chen, Jie ; Huang, Yuantai ; Qi, Guojun</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3536-c9d02d7f88e0c33ef90632996752b2bceb65516d3df53b9ce62222d32093ecac3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Aging</topic><topic>Animals</topic><topic>CRISPR</topic><topic>CRISPR‐Cas9</topic><topic>Drosophila melanogaster</topic><topic>Drosophila melanogaster - physiology</topic><topic>Drosophila Proteins - genetics</topic><topic>Drosophila Proteins - metabolism</topic><topic>Eclosion</topic><topic>Embryos</topic><topic>Forkhead protein</topic><topic>Fruit flies</topic><topic>Genomes</topic><topic>Immunoprecipitation</topic><topic>Insects</topic><topic>Insulin</topic><topic>Insulin - genetics</topic><topic>Insulin - metabolism</topic><topic>insulin receptor</topic><topic>Insulin receptors</topic><topic>lncRNA</topic><topic>Metabolism</topic><topic>Mutants</topic><topic>Non-coding RNA</topic><topic>Nutrient deficiency</topic><topic>Nutrition</topic><topic>Pupation</topic><topic>Receptor, Insulin - genetics</topic><topic>Receptor, Insulin - metabolism</topic><topic>Receptors</topic><topic>RNA, Long Noncoding - genetics</topic><topic>RNA, Long Noncoding - metabolism</topic><topic>Sensitivity</topic><topic>Signal transduction</topic><topic>starvation</topic><topic>stress</topic><topic>Sugar</topic><topic>Tubulin</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chen, Jie</creatorcontrib><creatorcontrib>Huang, Yuantai</creatorcontrib><creatorcontrib>Qi, Guojun</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Chemoreception Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Insect molecular biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chen, Jie</au><au>Huang, Yuantai</au><au>Qi, Guojun</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>LncRNA‐IRAR‐mediated regulation of insulin receptor transcripts in Drosophila melanogaster during nutritional stress</atitle><jtitle>Insect molecular biology</jtitle><addtitle>Insect Mol Biol</addtitle><date>2022-06</date><risdate>2022</risdate><volume>31</volume><issue>3</issue><spage>261</spage><epage>272</epage><pages>261-272</pages><issn>0962-1075</issn><eissn>1365-2583</eissn><abstract>The insulin signalling pathway plays a crucial role in regulating the metabolism of sugars, fats and proteins in cells, thereby affecting the growth, metabolism, reproduction and ageing of organisms. However, little is known about the functions of long non‐coding RNAs (lncRNAs) in the regulation of insulin receptors under stress conditions in insects. In this study, we showed that insulin receptor‐associated lncRNA (IRAR) regulates insulin receptor transcripts in response to nutritional stress in Drosophila melanogaster. Genome editing by CRISPR‐Cas9 showed reduced sensitivity of IRAR mutants to environmental nutritional changes. In contrast, the sensitivity of mutants overexpressing tubulin‐gal4 > IRAR increased under low nutrition. The pupation and eclosion timings in IRAR mutants were significantly delayed with an increase in insulin concentration compared with that in the w1118 group. In addition, the expression pattern of IRAR was almost consistent with that of the four transcripts of the insulin receptor from the embryonic period to the adult period. RNA immunoprecipitation assay showed the direct regulation of insulin receptor transcripts by IRAR to the through FOXO binding under nutritional stress. To our knowledge, this is the first study that describes a model of lncRNA‐mediated development regulation through insulin receptor transcripts.
Insulin receptor transcripts are regulated by IRAR. IRAR causes defects in the sensitivity of nutritional change. Direct regulation of IRAR to the insulin receptor transcripts through FOXO binding under nutritional stress.</abstract><cop>Chichester, UK</cop><pub>John Wiley & Sons, Ltd</pub><pmid>34923706</pmid><doi>10.1111/imb.12756</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0001-8569-3667</orcidid></addata></record> |
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subjects | Aging Animals CRISPR CRISPR‐Cas9 Drosophila melanogaster Drosophila melanogaster - physiology Drosophila Proteins - genetics Drosophila Proteins - metabolism Eclosion Embryos Forkhead protein Fruit flies Genomes Immunoprecipitation Insects Insulin Insulin - genetics Insulin - metabolism insulin receptor Insulin receptors lncRNA Metabolism Mutants Non-coding RNA Nutrient deficiency Nutrition Pupation Receptor, Insulin - genetics Receptor, Insulin - metabolism Receptors RNA, Long Noncoding - genetics RNA, Long Noncoding - metabolism Sensitivity Signal transduction starvation stress Sugar Tubulin |
title | LncRNA‐IRAR‐mediated regulation of insulin receptor transcripts in Drosophila melanogaster during nutritional stress |
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