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Transition from natal downs to juvenile feathers: conserved regulatory switches in Neoaves
The transition from natal downs for heat conservation to juvenile feathers for simple flight is a remarkable environmental adaptation process in avian evolution. However, the underlying epigenetic mechanism for this primary feather transition is mostly unknown. Here we conducted time-ordered gene co...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Journal Experts
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10602114/ https://www.ncbi.nlm.nih.gov/pubmed/37886492 http://dx.doi.org/10.21203/rs.3.rs-3382427/v1 |
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author | Li, Wen-Hsiung Chuong, Cheng Ming Chen, Chih-Kuan Wu, Ping Jiang, Ting-Xin Harn, Hans I-Chen Liu, Tzu-Yu Yu, Zhou Lu, Jiayi Chang, Yao-Ming Yue, Zhicao Lin, Jinnjy Vu, Trieu-Duc Huang, Tao-Yu Ng, Chen Siang |
author_facet | Li, Wen-Hsiung Chuong, Cheng Ming Chen, Chih-Kuan Wu, Ping Jiang, Ting-Xin Harn, Hans I-Chen Liu, Tzu-Yu Yu, Zhou Lu, Jiayi Chang, Yao-Ming Yue, Zhicao Lin, Jinnjy Vu, Trieu-Duc Huang, Tao-Yu Ng, Chen Siang |
author_sort | Li, Wen-Hsiung |
collection | PubMed |
description | The transition from natal downs for heat conservation to juvenile feathers for simple flight is a remarkable environmental adaptation process in avian evolution. However, the underlying epigenetic mechanism for this primary feather transition is mostly unknown. Here we conducted time-ordered gene co-expression network construction, epigenetic analysis, and functional perturbations in developing feather follicles to elucidate four downy-juvenile feather transition events. We discovered that LEF1 works as a key hub of Wnt signaling to build rachis and converts radial downy to bilateral symmetry. Extracellular matrix reorganization leads to peripheral pulp formation, which mediates epithelial -mesenchymal interactions for branching morphogenesis. ACTA2 compartments dermal papilla stem cells for feather cycling. Novel usage of scale keratins strengthens feather sheath with SOX14 as the epigenetic regulator. We found this primary feather transition largely conserved in chicken (precocious) and zebra finch (altricial) and discussed the possibility that this evolutionary adaptation process started in feathered dinosaurs. |
format | Online Article Text |
id | pubmed-10602114 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Journal Experts |
record_format | MEDLINE/PubMed |
spelling | pubmed-106021142023-10-27 Transition from natal downs to juvenile feathers: conserved regulatory switches in Neoaves Li, Wen-Hsiung Chuong, Cheng Ming Chen, Chih-Kuan Wu, Ping Jiang, Ting-Xin Harn, Hans I-Chen Liu, Tzu-Yu Yu, Zhou Lu, Jiayi Chang, Yao-Ming Yue, Zhicao Lin, Jinnjy Vu, Trieu-Duc Huang, Tao-Yu Ng, Chen Siang Res Sq Article The transition from natal downs for heat conservation to juvenile feathers for simple flight is a remarkable environmental adaptation process in avian evolution. However, the underlying epigenetic mechanism for this primary feather transition is mostly unknown. Here we conducted time-ordered gene co-expression network construction, epigenetic analysis, and functional perturbations in developing feather follicles to elucidate four downy-juvenile feather transition events. We discovered that LEF1 works as a key hub of Wnt signaling to build rachis and converts radial downy to bilateral symmetry. Extracellular matrix reorganization leads to peripheral pulp formation, which mediates epithelial -mesenchymal interactions for branching morphogenesis. ACTA2 compartments dermal papilla stem cells for feather cycling. Novel usage of scale keratins strengthens feather sheath with SOX14 as the epigenetic regulator. We found this primary feather transition largely conserved in chicken (precocious) and zebra finch (altricial) and discussed the possibility that this evolutionary adaptation process started in feathered dinosaurs. American Journal Experts 2023-10-03 /pmc/articles/PMC10602114/ /pubmed/37886492 http://dx.doi.org/10.21203/rs.3.rs-3382427/v1 Text en https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format, so long as attribution is given to the creator. The license allows for commercial use. |
spellingShingle | Article Li, Wen-Hsiung Chuong, Cheng Ming Chen, Chih-Kuan Wu, Ping Jiang, Ting-Xin Harn, Hans I-Chen Liu, Tzu-Yu Yu, Zhou Lu, Jiayi Chang, Yao-Ming Yue, Zhicao Lin, Jinnjy Vu, Trieu-Duc Huang, Tao-Yu Ng, Chen Siang Transition from natal downs to juvenile feathers: conserved regulatory switches in Neoaves |
title | Transition from natal downs to juvenile feathers: conserved regulatory switches in Neoaves |
title_full | Transition from natal downs to juvenile feathers: conserved regulatory switches in Neoaves |
title_fullStr | Transition from natal downs to juvenile feathers: conserved regulatory switches in Neoaves |
title_full_unstemmed | Transition from natal downs to juvenile feathers: conserved regulatory switches in Neoaves |
title_short | Transition from natal downs to juvenile feathers: conserved regulatory switches in Neoaves |
title_sort | transition from natal downs to juvenile feathers: conserved regulatory switches in neoaves |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10602114/ https://www.ncbi.nlm.nih.gov/pubmed/37886492 http://dx.doi.org/10.21203/rs.3.rs-3382427/v1 |
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