Hedgehog signaling mediates adaptive variation in a dynamic functional system in the cichlid feeding apparatus
Adaptive variation in the craniofacial skeleton is a key component of resource specialization and habitat divergence in vertebrates, but the proximate genetic mechanisms that underlie complex patterns of craniofacial variation are largely unknown. Here we demonstrate that the Hedgehog (Hh) signaling...
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Veröffentlicht in: | Proceedings of the National Academy of Sciences - PNAS 2014-06, Vol.111 (23), p.8530-8534 |
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description | Adaptive variation in the craniofacial skeleton is a key component of resource specialization and habitat divergence in vertebrates, but the proximate genetic mechanisms that underlie complex patterns of craniofacial variation are largely unknown. Here we demonstrate that the Hedgehog (Hh) signaling pathway mediates widespread variation across a complex functional system that affects the kinematics of lower jaw depression—the opercular four-bar linkage apparatus—among Lake Malawi cichlids. By using a combined quantitative trait locus mapping and population genetics approach, we show that allelic variation in the Hh receptor, ptch1 , affects the development of distinct bony elements in the head that represent two of three movable links in this functional system. The evolutionarily derived allele is found in species that feed from the water column, and is associated with shifts in anatomy that translate to a four-bar system capable of faster jaw rotation. Alternatively, the ancestral allele is found in species that feed on attached algae, and is associated with the development of a four-bar system that predicts slower jaw movement. Experimental manipulation of the Hh pathway during cichlid development recapitulates functionally salient natural variation in craniofacial geometry. In all, these results significantly extend our understanding of the mechanisms that fine-tune the craniofacial skeletal complex during adaptation to new foraging niches. |
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Craig</creator><creatorcontrib>Hu, Yinan ; Albertson, R. Craig</creatorcontrib><description>Adaptive variation in the craniofacial skeleton is a key component of resource specialization and habitat divergence in vertebrates, but the proximate genetic mechanisms that underlie complex patterns of craniofacial variation are largely unknown. Here we demonstrate that the Hedgehog (Hh) signaling pathway mediates widespread variation across a complex functional system that affects the kinematics of lower jaw depression—the opercular four-bar linkage apparatus—among Lake Malawi cichlids. By using a combined quantitative trait locus mapping and population genetics approach, we show that allelic variation in the Hh receptor, ptch1 , affects the development of distinct bony elements in the head that represent two of three movable links in this functional system. The evolutionarily derived allele is found in species that feed from the water column, and is associated with shifts in anatomy that translate to a four-bar system capable of faster jaw rotation. Alternatively, the ancestral allele is found in species that feed on attached algae, and is associated with the development of a four-bar system that predicts slower jaw movement. Experimental manipulation of the Hh pathway during cichlid development recapitulates functionally salient natural variation in craniofacial geometry. In all, these results significantly extend our understanding of the mechanisms that fine-tune the craniofacial skeletal complex during adaptation to new foraging niches.</description><identifier>ISSN: 0027-8424</identifier><identifier>EISSN: 1091-6490</identifier><identifier>DOI: 10.1073/pnas.1323154111</identifier><identifier>PMID: 24912175</identifier><language>eng</language><publisher>United States: National Academy of Sciences</publisher><subject>Adaptation, Physiological - genetics ; Adaptation, Physiological - physiology ; Algae ; Alleles ; Animals ; Biological Sciences ; Bone Development - genetics ; Bone Development - physiology ; Bones ; Chromosome Mapping ; Cichlidae ; Cichlids - genetics ; Cichlids - growth & development ; Cichlids - physiology ; Evolution ; Feeding Behavior - physiology ; Female ; Fish Proteins - genetics ; Fish Proteins - physiology ; Gene Expression Regulation, Developmental ; Genetic variation ; Genetics ; Genomics ; Geometry ; Hedgehog Proteins - genetics ; Hedgehog Proteins - physiology ; Hyperlinks ; In Situ Hybridization ; Jaw ; Jaw - anatomy & histology ; Jaw - physiology ; Kinematics ; Larva - genetics ; Larva - growth & development ; Larva - physiology ; Larvae ; Larval development ; Male ; Modeling ; Patched Receptors ; Polymorphism, Genetic ; Quantitative Trait Loci - genetics ; Receptors, Cell Surface - genetics ; Receptors, Cell Surface - physiology ; Signal Transduction - genetics ; Signal Transduction - physiology ; Skeletal system ; Skull ; Small mammals</subject><ispartof>Proceedings of the National Academy of Sciences - PNAS, 2014-06, Vol.111 (23), p.8530-8534</ispartof><rights>copyright © 1993–2008 National Academy of Sciences of the United States of America</rights><rights>Copyright National Academy of Sciences Jun 10, 2014</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c590t-4bfacf084a929132dfb2df101d73d372f4d22e477cca48df732d2c978944ba333</citedby><cites>FETCH-LOGICAL-c590t-4bfacf084a929132dfb2df101d73d372f4d22e477cca48df732d2c978944ba333</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://www.pnas.org/content/111/23.cover.gif</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/23776452$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/23776452$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>230,314,727,780,784,803,885,27924,27925,53791,53793,58017,58250</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24912175$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hu, Yinan</creatorcontrib><creatorcontrib>Albertson, R. Craig</creatorcontrib><title>Hedgehog signaling mediates adaptive variation in a dynamic functional system in the cichlid feeding apparatus</title><title>Proceedings of the National Academy of Sciences - PNAS</title><addtitle>Proc Natl Acad Sci U S A</addtitle><description>Adaptive variation in the craniofacial skeleton is a key component of resource specialization and habitat divergence in vertebrates, but the proximate genetic mechanisms that underlie complex patterns of craniofacial variation are largely unknown. Here we demonstrate that the Hedgehog (Hh) signaling pathway mediates widespread variation across a complex functional system that affects the kinematics of lower jaw depression—the opercular four-bar linkage apparatus—among Lake Malawi cichlids. By using a combined quantitative trait locus mapping and population genetics approach, we show that allelic variation in the Hh receptor, ptch1 , affects the development of distinct bony elements in the head that represent two of three movable links in this functional system. The evolutionarily derived allele is found in species that feed from the water column, and is associated with shifts in anatomy that translate to a four-bar system capable of faster jaw rotation. Alternatively, the ancestral allele is found in species that feed on attached algae, and is associated with the development of a four-bar system that predicts slower jaw movement. Experimental manipulation of the Hh pathway during cichlid development recapitulates functionally salient natural variation in craniofacial geometry. In all, these results significantly extend our understanding of the mechanisms that fine-tune the craniofacial skeletal complex during adaptation to new foraging niches.</description><subject>Adaptation, Physiological - genetics</subject><subject>Adaptation, Physiological - physiology</subject><subject>Algae</subject><subject>Alleles</subject><subject>Animals</subject><subject>Biological Sciences</subject><subject>Bone Development - genetics</subject><subject>Bone Development - physiology</subject><subject>Bones</subject><subject>Chromosome Mapping</subject><subject>Cichlidae</subject><subject>Cichlids - genetics</subject><subject>Cichlids - growth & development</subject><subject>Cichlids - physiology</subject><subject>Evolution</subject><subject>Feeding Behavior - physiology</subject><subject>Female</subject><subject>Fish Proteins - genetics</subject><subject>Fish Proteins - physiology</subject><subject>Gene Expression Regulation, Developmental</subject><subject>Genetic variation</subject><subject>Genetics</subject><subject>Genomics</subject><subject>Geometry</subject><subject>Hedgehog Proteins - genetics</subject><subject>Hedgehog Proteins - physiology</subject><subject>Hyperlinks</subject><subject>In Situ Hybridization</subject><subject>Jaw</subject><subject>Jaw - anatomy & histology</subject><subject>Jaw - physiology</subject><subject>Kinematics</subject><subject>Larva - genetics</subject><subject>Larva - growth & development</subject><subject>Larva - physiology</subject><subject>Larvae</subject><subject>Larval development</subject><subject>Male</subject><subject>Modeling</subject><subject>Patched Receptors</subject><subject>Polymorphism, Genetic</subject><subject>Quantitative Trait Loci - genetics</subject><subject>Receptors, Cell Surface - genetics</subject><subject>Receptors, Cell Surface - physiology</subject><subject>Signal Transduction - genetics</subject><subject>Signal Transduction - physiology</subject><subject>Skeletal system</subject><subject>Skull</subject><subject>Small mammals</subject><issn>0027-8424</issn><issn>1091-6490</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkU2P0zAQhiMEYrsLZ06Apb1w6e74K3YuSGgFLNJKHGDP1tRxUlepE-ykUv89Di0tcOJgWZp55pHHb1G8onBDQfHbIWC6oZxxKgWl9EmxoFDRZSkqeFosAJhaasHERXGZ0gYAKqnheXHBREUZVXJRhHtXt27dtyT5NmDnQ0u2rvY4ukSwxmH0O0d2GHPF94H4QJDU-4Bbb0kzBTtXsSNpn0a3ndvj2hHr7brzNWlcVmUjDgNGHKf0onjWYJfcy-N9VTx--vj97n758PXzl7sPD0srKxiXYtWgbUALrFiV16ubVT4UaK14zRVrRM2YE0pZi0LXjcoIs5XSlRAr5JxfFe8P3mFa5XWsC2PEzgzRbzHuTY_e_N0Jfm3afmcElKBAZsG7oyD2PyaXRrP1ybquw-D6KRkqJS2Z1pr_B8plyYFpltHrf9BNP8X8f7-oikupOc3U7YGysU8puub0bgpmjt3MsZtz7HnizZ_rnvjfOWfg7RGYJ086Sg3jRksOmXh9IDZp7OPZwJUqhWRnQ4O9wTb6ZB6_MaAlABWCM8Z_AuNpx0E</recordid><startdate>20140610</startdate><enddate>20140610</enddate><creator>Hu, Yinan</creator><creator>Albertson, R. 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Craig</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Hedgehog signaling mediates adaptive variation in a dynamic functional system in the cichlid feeding apparatus</atitle><jtitle>Proceedings of the National Academy of Sciences - PNAS</jtitle><addtitle>Proc Natl Acad Sci U S A</addtitle><date>2014-06-10</date><risdate>2014</risdate><volume>111</volume><issue>23</issue><spage>8530</spage><epage>8534</epage><pages>8530-8534</pages><issn>0027-8424</issn><eissn>1091-6490</eissn><abstract>Adaptive variation in the craniofacial skeleton is a key component of resource specialization and habitat divergence in vertebrates, but the proximate genetic mechanisms that underlie complex patterns of craniofacial variation are largely unknown. Here we demonstrate that the Hedgehog (Hh) signaling pathway mediates widespread variation across a complex functional system that affects the kinematics of lower jaw depression—the opercular four-bar linkage apparatus—among Lake Malawi cichlids. By using a combined quantitative trait locus mapping and population genetics approach, we show that allelic variation in the Hh receptor, ptch1 , affects the development of distinct bony elements in the head that represent two of three movable links in this functional system. The evolutionarily derived allele is found in species that feed from the water column, and is associated with shifts in anatomy that translate to a four-bar system capable of faster jaw rotation. Alternatively, the ancestral allele is found in species that feed on attached algae, and is associated with the development of a four-bar system that predicts slower jaw movement. Experimental manipulation of the Hh pathway during cichlid development recapitulates functionally salient natural variation in craniofacial geometry. In all, these results significantly extend our understanding of the mechanisms that fine-tune the craniofacial skeletal complex during adaptation to new foraging niches.</abstract><cop>United States</cop><pub>National Academy of Sciences</pub><pmid>24912175</pmid><doi>10.1073/pnas.1323154111</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adaptation, Physiological - genetics Adaptation, Physiological - physiology Algae Alleles Animals Biological Sciences Bone Development - genetics Bone Development - physiology Bones Chromosome Mapping Cichlidae Cichlids - genetics Cichlids - growth & development Cichlids - physiology Evolution Feeding Behavior - physiology Female Fish Proteins - genetics Fish Proteins - physiology Gene Expression Regulation, Developmental Genetic variation Genetics Genomics Geometry Hedgehog Proteins - genetics Hedgehog Proteins - physiology Hyperlinks In Situ Hybridization Jaw Jaw - anatomy & histology Jaw - physiology Kinematics Larva - genetics Larva - growth & development Larva - physiology Larvae Larval development Male Modeling Patched Receptors Polymorphism, Genetic Quantitative Trait Loci - genetics Receptors, Cell Surface - genetics Receptors, Cell Surface - physiology Signal Transduction - genetics Signal Transduction - physiology Skeletal system Skull Small mammals |
title | Hedgehog signaling mediates adaptive variation in a dynamic functional system in the cichlid feeding apparatus |
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