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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Journal Experts 2023
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.
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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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