A long noncoding RNA at the cortex locus controls adaptive coloration in butterflies
Evolutionary variation in the wing pigmentation of butterflies and moths offers striking examples of adaptation by crypsis and mimicry. The locus has been independently mapped as the locus controlling color polymorphisms in 15 lepidopteran species, suggesting that it acts as a genomic hotspot for th...
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creator | Livraghi, Luca Hanly, Joseph J Evans, Elizabeth Wright, Charlotte J Loh, Ling S Mazo-Vargas, Anyi Kamrava, Kiana Carter, Alexander van der Heijden, Eva S M Reed, Robert D Papa, Riccardo Jiggins, Chris D Martin, Arnaud |
description | Evolutionary variation in the wing pigmentation of butterflies and moths offers striking examples of adaptation by crypsis and mimicry. The
locus has been independently mapped as the locus controlling color polymorphisms in 15 lepidopteran species, suggesting that it acts as a genomic hotspot for the diversification of wing patterns, but functional validation through protein-coding knockouts has proven difficult to obtain. Our study unveils the role of a long noncoding RNA (lncRNA) which we name
, transcribed from the
locus, in modulating color patterning in butterflies. Strikingly,
expression prefigures most melanic patterns during pupal development, suggesting an early developmental role in specifying scale identity. To test this, we generated CRISPR mosaic knock-outs in five nymphalid butterfly species and show that
mutagenesis yields transformations of dark pigmented scales into white or light-colored scales. Genotyping of
germline mutants associates these phenotypes to small on-target deletions at the conserved first exon of
. In contrast,
germline mutant butterflies with confirmed null alleles lack any wing phenotype and exclude a color patterning role for this adjacent gene. Overall, these results show that a lncRNA gene acts as a master switch of color pattern specification and played key roles in the adaptive diversification of wing patterns in butterflies. |
doi_str_mv | 10.1073/pnas.2403326121 |
format | Article |
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locus has been independently mapped as the locus controlling color polymorphisms in 15 lepidopteran species, suggesting that it acts as a genomic hotspot for the diversification of wing patterns, but functional validation through protein-coding knockouts has proven difficult to obtain. Our study unveils the role of a long noncoding RNA (lncRNA) which we name
, transcribed from the
locus, in modulating color patterning in butterflies. Strikingly,
expression prefigures most melanic patterns during pupal development, suggesting an early developmental role in specifying scale identity. To test this, we generated CRISPR mosaic knock-outs in five nymphalid butterfly species and show that
mutagenesis yields transformations of dark pigmented scales into white or light-colored scales. Genotyping of
germline mutants associates these phenotypes to small on-target deletions at the conserved first exon of
. In contrast,
germline mutant butterflies with confirmed null alleles lack any wing phenotype and exclude a color patterning role for this adjacent gene. Overall, these results show that a lncRNA gene acts as a master switch of color pattern specification and played key roles in the adaptive diversification of wing patterns in butterflies.</description><identifier>ISSN: 0027-8424</identifier><identifier>ISSN: 1091-6490</identifier><identifier>EISSN: 1091-6490</identifier><identifier>DOI: 10.1073/pnas.2403326121</identifier><identifier>PMID: 39213180</identifier><language>eng</language><publisher>United States: National Academy of Sciences</publisher><subject>Adaptation, Physiological - genetics ; Animals ; Butterflies & moths ; Butterflies - genetics ; Color ; Cortex ; CRISPR ; Crypsis ; Dark adaptation ; Genotyping ; Mimicry ; Mutagenesis ; Mutants ; Non-coding RNA ; Pattern formation ; Patterning ; Phenotype ; Phenotypes ; Pigmentation ; Pigmentation - genetics ; Ribonucleic acid ; RNA ; RNA, Long Noncoding - genetics ; Wings ; Wings, Animal - anatomy & histology ; Wings, Animal - growth & development</subject><ispartof>Proceedings of the National Academy of Sciences - PNAS, 2024-09, Vol.121 (36), p.e2403326121</ispartof><rights>Copyright National Academy of Sciences Sep 3, 2024</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c209t-1582efb32bfd361a6b1ebc3c52fe18091a11954220f46de9e6605176fe96fdb3</cites><orcidid>0000-0002-6065-6728 ; 0000-0002-5980-2249 ; 0000-0002-9459-9776 ; 0009-0008-1894-0873 ; 0000-0003-0981-7984 ; 0000-0002-7809-062X ; 0000-0002-2597-7550 ; 0000-0001-9644-2871 ; 0000-0002-7986-9993 ; 0009-0004-6459-7958</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39213180$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Livraghi, Luca</creatorcontrib><creatorcontrib>Hanly, Joseph J</creatorcontrib><creatorcontrib>Evans, Elizabeth</creatorcontrib><creatorcontrib>Wright, Charlotte J</creatorcontrib><creatorcontrib>Loh, Ling S</creatorcontrib><creatorcontrib>Mazo-Vargas, Anyi</creatorcontrib><creatorcontrib>Kamrava, Kiana</creatorcontrib><creatorcontrib>Carter, Alexander</creatorcontrib><creatorcontrib>van der Heijden, Eva S M</creatorcontrib><creatorcontrib>Reed, Robert D</creatorcontrib><creatorcontrib>Papa, Riccardo</creatorcontrib><creatorcontrib>Jiggins, Chris D</creatorcontrib><creatorcontrib>Martin, Arnaud</creatorcontrib><title>A long noncoding RNA at the cortex locus controls adaptive coloration in butterflies</title><title>Proceedings of the National Academy of Sciences - PNAS</title><addtitle>Proc Natl Acad Sci U S A</addtitle><description>Evolutionary variation in the wing pigmentation of butterflies and moths offers striking examples of adaptation by crypsis and mimicry. The
locus has been independently mapped as the locus controlling color polymorphisms in 15 lepidopteran species, suggesting that it acts as a genomic hotspot for the diversification of wing patterns, but functional validation through protein-coding knockouts has proven difficult to obtain. Our study unveils the role of a long noncoding RNA (lncRNA) which we name
, transcribed from the
locus, in modulating color patterning in butterflies. Strikingly,
expression prefigures most melanic patterns during pupal development, suggesting an early developmental role in specifying scale identity. To test this, we generated CRISPR mosaic knock-outs in five nymphalid butterfly species and show that
mutagenesis yields transformations of dark pigmented scales into white or light-colored scales. Genotyping of
germline mutants associates these phenotypes to small on-target deletions at the conserved first exon of
. In contrast,
germline mutant butterflies with confirmed null alleles lack any wing phenotype and exclude a color patterning role for this adjacent gene. Overall, these results show that a lncRNA gene acts as a master switch of color pattern specification and played key roles in the adaptive diversification of wing patterns in butterflies.</description><subject>Adaptation, Physiological - genetics</subject><subject>Animals</subject><subject>Butterflies & moths</subject><subject>Butterflies - genetics</subject><subject>Color</subject><subject>Cortex</subject><subject>CRISPR</subject><subject>Crypsis</subject><subject>Dark adaptation</subject><subject>Genotyping</subject><subject>Mimicry</subject><subject>Mutagenesis</subject><subject>Mutants</subject><subject>Non-coding RNA</subject><subject>Pattern formation</subject><subject>Patterning</subject><subject>Phenotype</subject><subject>Phenotypes</subject><subject>Pigmentation</subject><subject>Pigmentation - genetics</subject><subject>Ribonucleic acid</subject><subject>RNA</subject><subject>RNA, Long Noncoding - genetics</subject><subject>Wings</subject><subject>Wings, Animal - anatomy & histology</subject><subject>Wings, Animal - growth & development</subject><issn>0027-8424</issn><issn>1091-6490</issn><issn>1091-6490</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkN9LwzAQx4Mobk6ffZOCL750u0varHkcw18wFGTvJW0T7eiSmqSi_70Zmwo-3R33uePLh5BLhCnCnM16I_2UZsAY5UjxiIwRBKY8E3BMxgB0nhYZzUbkzPsNAIi8gFMyYoIiwwLGZL1IOmteE2NNbZs2di9Pi0SGJLyppLYuqM8I1IOPgwnOdj6RjexD-7Fbd9bJ0FqTtCaphhCU012r_Dk50bLz6uJQJ2R9d7tePqSr5_vH5WKV1hRESDEvqNIVo5VuGEfJK1RVzeqcahXDCZSIIs8oBZ3xRgnFOeQ451oJrpuKTcjN_m3v7PugfCi3ra9V10mj7OBLBkIUwHgOEb3-h27s4EwMVzIEmkd7kEVqtqdqZ713Spe9a7fSfZUI5c53ufNd_vmOF1eHv0O1Vc0v_yOYfQOnV3sP</recordid><startdate>20240903</startdate><enddate>20240903</enddate><creator>Livraghi, Luca</creator><creator>Hanly, Joseph J</creator><creator>Evans, Elizabeth</creator><creator>Wright, Charlotte J</creator><creator>Loh, Ling S</creator><creator>Mazo-Vargas, Anyi</creator><creator>Kamrava, Kiana</creator><creator>Carter, Alexander</creator><creator>van der Heijden, Eva S M</creator><creator>Reed, Robert D</creator><creator>Papa, Riccardo</creator><creator>Jiggins, Chris D</creator><creator>Martin, Arnaud</creator><general>National Academy of Sciences</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>7QG</scope><scope>7QL</scope><scope>7QP</scope><scope>7QR</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TK</scope><scope>7TM</scope><scope>7TO</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-6065-6728</orcidid><orcidid>https://orcid.org/0000-0002-5980-2249</orcidid><orcidid>https://orcid.org/0000-0002-9459-9776</orcidid><orcidid>https://orcid.org/0009-0008-1894-0873</orcidid><orcidid>https://orcid.org/0000-0003-0981-7984</orcidid><orcidid>https://orcid.org/0000-0002-7809-062X</orcidid><orcidid>https://orcid.org/0000-0002-2597-7550</orcidid><orcidid>https://orcid.org/0000-0001-9644-2871</orcidid><orcidid>https://orcid.org/0000-0002-7986-9993</orcidid><orcidid>https://orcid.org/0009-0004-6459-7958</orcidid></search><sort><creationdate>20240903</creationdate><title>A long noncoding RNA at the cortex locus controls adaptive coloration in butterflies</title><author>Livraghi, Luca ; Hanly, Joseph J ; Evans, Elizabeth ; Wright, Charlotte J ; Loh, Ling S ; Mazo-Vargas, Anyi ; Kamrava, Kiana ; Carter, Alexander ; van der Heijden, Eva S M ; Reed, Robert D ; Papa, Riccardo ; Jiggins, Chris D ; Martin, Arnaud</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c209t-1582efb32bfd361a6b1ebc3c52fe18091a11954220f46de9e6605176fe96fdb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Adaptation, Physiological - genetics</topic><topic>Animals</topic><topic>Butterflies & moths</topic><topic>Butterflies - genetics</topic><topic>Color</topic><topic>Cortex</topic><topic>CRISPR</topic><topic>Crypsis</topic><topic>Dark adaptation</topic><topic>Genotyping</topic><topic>Mimicry</topic><topic>Mutagenesis</topic><topic>Mutants</topic><topic>Non-coding RNA</topic><topic>Pattern formation</topic><topic>Patterning</topic><topic>Phenotype</topic><topic>Phenotypes</topic><topic>Pigmentation</topic><topic>Pigmentation - genetics</topic><topic>Ribonucleic acid</topic><topic>RNA</topic><topic>RNA, Long Noncoding - genetics</topic><topic>Wings</topic><topic>Wings, Animal - anatomy & histology</topic><topic>Wings, Animal - growth & development</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Livraghi, Luca</creatorcontrib><creatorcontrib>Hanly, Joseph J</creatorcontrib><creatorcontrib>Evans, Elizabeth</creatorcontrib><creatorcontrib>Wright, Charlotte J</creatorcontrib><creatorcontrib>Loh, Ling S</creatorcontrib><creatorcontrib>Mazo-Vargas, Anyi</creatorcontrib><creatorcontrib>Kamrava, Kiana</creatorcontrib><creatorcontrib>Carter, Alexander</creatorcontrib><creatorcontrib>van der Heijden, Eva S M</creatorcontrib><creatorcontrib>Reed, Robert D</creatorcontrib><creatorcontrib>Papa, Riccardo</creatorcontrib><creatorcontrib>Jiggins, Chris D</creatorcontrib><creatorcontrib>Martin, Arnaud</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Proceedings of the National Academy of Sciences - PNAS</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Livraghi, Luca</au><au>Hanly, Joseph J</au><au>Evans, Elizabeth</au><au>Wright, Charlotte J</au><au>Loh, Ling S</au><au>Mazo-Vargas, Anyi</au><au>Kamrava, Kiana</au><au>Carter, Alexander</au><au>van der Heijden, Eva S M</au><au>Reed, Robert D</au><au>Papa, Riccardo</au><au>Jiggins, Chris D</au><au>Martin, Arnaud</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A long noncoding RNA at the cortex locus controls adaptive coloration in butterflies</atitle><jtitle>Proceedings of the National Academy of Sciences - PNAS</jtitle><addtitle>Proc Natl Acad Sci U S A</addtitle><date>2024-09-03</date><risdate>2024</risdate><volume>121</volume><issue>36</issue><spage>e2403326121</spage><pages>e2403326121-</pages><issn>0027-8424</issn><issn>1091-6490</issn><eissn>1091-6490</eissn><abstract>Evolutionary variation in the wing pigmentation of butterflies and moths offers striking examples of adaptation by crypsis and mimicry. The
locus has been independently mapped as the locus controlling color polymorphisms in 15 lepidopteran species, suggesting that it acts as a genomic hotspot for the diversification of wing patterns, but functional validation through protein-coding knockouts has proven difficult to obtain. Our study unveils the role of a long noncoding RNA (lncRNA) which we name
, transcribed from the
locus, in modulating color patterning in butterflies. Strikingly,
expression prefigures most melanic patterns during pupal development, suggesting an early developmental role in specifying scale identity. To test this, we generated CRISPR mosaic knock-outs in five nymphalid butterfly species and show that
mutagenesis yields transformations of dark pigmented scales into white or light-colored scales. Genotyping of
germline mutants associates these phenotypes to small on-target deletions at the conserved first exon of
. In contrast,
germline mutant butterflies with confirmed null alleles lack any wing phenotype and exclude a color patterning role for this adjacent gene. Overall, these results show that a lncRNA gene acts as a master switch of color pattern specification and played key roles in the adaptive diversification of wing patterns in butterflies.</abstract><cop>United States</cop><pub>National Academy of Sciences</pub><pmid>39213180</pmid><doi>10.1073/pnas.2403326121</doi><orcidid>https://orcid.org/0000-0002-6065-6728</orcidid><orcidid>https://orcid.org/0000-0002-5980-2249</orcidid><orcidid>https://orcid.org/0000-0002-9459-9776</orcidid><orcidid>https://orcid.org/0009-0008-1894-0873</orcidid><orcidid>https://orcid.org/0000-0003-0981-7984</orcidid><orcidid>https://orcid.org/0000-0002-7809-062X</orcidid><orcidid>https://orcid.org/0000-0002-2597-7550</orcidid><orcidid>https://orcid.org/0000-0001-9644-2871</orcidid><orcidid>https://orcid.org/0000-0002-7986-9993</orcidid><orcidid>https://orcid.org/0009-0004-6459-7958</orcidid></addata></record> |
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subjects | Adaptation, Physiological - genetics Animals Butterflies & moths Butterflies - genetics Color Cortex CRISPR Crypsis Dark adaptation Genotyping Mimicry Mutagenesis Mutants Non-coding RNA Pattern formation Patterning Phenotype Phenotypes Pigmentation Pigmentation - genetics Ribonucleic acid RNA RNA, Long Noncoding - genetics Wings Wings, Animal - anatomy & histology Wings, Animal - growth & development |
title | A long noncoding RNA at the cortex locus controls adaptive coloration in butterflies |
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