Cargando…
Fate plasticity and reprogramming in genetically distinct populations of Danio leucophores
Understanding genetic and cellular bases of adult form remains a fundamental goal at the intersection of developmental and evolutionary biology. The skin pigment cells of vertebrates, derived from embryonic neural crest, are a useful system for elucidating mechanisms of fate specification, pattern f...
Autores principales: | , , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Academy of Sciences
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6575160/ https://www.ncbi.nlm.nih.gov/pubmed/31138706 http://dx.doi.org/10.1073/pnas.1901021116 |
_version_ | 1783427805349937152 |
---|---|
author | Lewis, Victor M. Saunders, Lauren M. Larson, Tracy A. Bain, Emily J. Sturiale, Samantha L. Gur, Dvir Chowdhury, Sarwat Flynn, Jessica D. Allen, Michael C. Deheyn, Dimitri D. Lee, Jennifer C. Simon, Julian A. Lippincott-Schwartz, Jennifer Raible, David W. Parichy, David M. |
author_facet | Lewis, Victor M. Saunders, Lauren M. Larson, Tracy A. Bain, Emily J. Sturiale, Samantha L. Gur, Dvir Chowdhury, Sarwat Flynn, Jessica D. Allen, Michael C. Deheyn, Dimitri D. Lee, Jennifer C. Simon, Julian A. Lippincott-Schwartz, Jennifer Raible, David W. Parichy, David M. |
author_sort | Lewis, Victor M. |
collection | PubMed |
description | Understanding genetic and cellular bases of adult form remains a fundamental goal at the intersection of developmental and evolutionary biology. The skin pigment cells of vertebrates, derived from embryonic neural crest, are a useful system for elucidating mechanisms of fate specification, pattern formation, and how particular phenotypes impact organismal behavior and ecology. In a survey of Danio fishes, including the zebrafish Danio rerio, we identified two populations of white pigment cells—leucophores—one of which arises by transdifferentiation of adult melanophores and another of which develops from a yellow–orange xanthophore or xanthophore-like progenitor. Single-cell transcriptomic, mutational, chemical, and ultrastructural analyses of zebrafish leucophores revealed cell-type–specific chemical compositions, organelle configurations, and genetic requirements. At the organismal level, we identified distinct physiological responses of leucophores during environmental background matching, and we showed that leucophore complement influences behavior. Together, our studies reveal independently arisen pigment cell types and mechanisms of fate acquisition in zebrafish and illustrate how concerted analyses across hierarchical levels can provide insights into phenotypes and their evolution. |
format | Online Article Text |
id | pubmed-6575160 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | National Academy of Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-65751602019-06-21 Fate plasticity and reprogramming in genetically distinct populations of Danio leucophores Lewis, Victor M. Saunders, Lauren M. Larson, Tracy A. Bain, Emily J. Sturiale, Samantha L. Gur, Dvir Chowdhury, Sarwat Flynn, Jessica D. Allen, Michael C. Deheyn, Dimitri D. Lee, Jennifer C. Simon, Julian A. Lippincott-Schwartz, Jennifer Raible, David W. Parichy, David M. Proc Natl Acad Sci U S A Biological Sciences Understanding genetic and cellular bases of adult form remains a fundamental goal at the intersection of developmental and evolutionary biology. The skin pigment cells of vertebrates, derived from embryonic neural crest, are a useful system for elucidating mechanisms of fate specification, pattern formation, and how particular phenotypes impact organismal behavior and ecology. In a survey of Danio fishes, including the zebrafish Danio rerio, we identified two populations of white pigment cells—leucophores—one of which arises by transdifferentiation of adult melanophores and another of which develops from a yellow–orange xanthophore or xanthophore-like progenitor. Single-cell transcriptomic, mutational, chemical, and ultrastructural analyses of zebrafish leucophores revealed cell-type–specific chemical compositions, organelle configurations, and genetic requirements. At the organismal level, we identified distinct physiological responses of leucophores during environmental background matching, and we showed that leucophore complement influences behavior. Together, our studies reveal independently arisen pigment cell types and mechanisms of fate acquisition in zebrafish and illustrate how concerted analyses across hierarchical levels can provide insights into phenotypes and their evolution. National Academy of Sciences 2019-06-11 2019-05-28 /pmc/articles/PMC6575160/ /pubmed/31138706 http://dx.doi.org/10.1073/pnas.1901021116 Text en Copyright © 2019 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/ https://creativecommons.org/licenses/by-nc-nd/4.0/This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Biological Sciences Lewis, Victor M. Saunders, Lauren M. Larson, Tracy A. Bain, Emily J. Sturiale, Samantha L. Gur, Dvir Chowdhury, Sarwat Flynn, Jessica D. Allen, Michael C. Deheyn, Dimitri D. Lee, Jennifer C. Simon, Julian A. Lippincott-Schwartz, Jennifer Raible, David W. Parichy, David M. Fate plasticity and reprogramming in genetically distinct populations of Danio leucophores |
title | Fate plasticity and reprogramming in genetically distinct populations of Danio leucophores |
title_full | Fate plasticity and reprogramming in genetically distinct populations of Danio leucophores |
title_fullStr | Fate plasticity and reprogramming in genetically distinct populations of Danio leucophores |
title_full_unstemmed | Fate plasticity and reprogramming in genetically distinct populations of Danio leucophores |
title_short | Fate plasticity and reprogramming in genetically distinct populations of Danio leucophores |
title_sort | fate plasticity and reprogramming in genetically distinct populations of danio leucophores |
topic | Biological Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6575160/ https://www.ncbi.nlm.nih.gov/pubmed/31138706 http://dx.doi.org/10.1073/pnas.1901021116 |
work_keys_str_mv | AT lewisvictorm fateplasticityandreprogrammingingeneticallydistinctpopulationsofdanioleucophores AT saunderslaurenm fateplasticityandreprogrammingingeneticallydistinctpopulationsofdanioleucophores AT larsontracya fateplasticityandreprogrammingingeneticallydistinctpopulationsofdanioleucophores AT bainemilyj fateplasticityandreprogrammingingeneticallydistinctpopulationsofdanioleucophores AT sturialesamanthal fateplasticityandreprogrammingingeneticallydistinctpopulationsofdanioleucophores AT gurdvir fateplasticityandreprogrammingingeneticallydistinctpopulationsofdanioleucophores AT chowdhurysarwat fateplasticityandreprogrammingingeneticallydistinctpopulationsofdanioleucophores AT flynnjessicad fateplasticityandreprogrammingingeneticallydistinctpopulationsofdanioleucophores AT allenmichaelc fateplasticityandreprogrammingingeneticallydistinctpopulationsofdanioleucophores AT deheyndimitrid fateplasticityandreprogrammingingeneticallydistinctpopulationsofdanioleucophores AT leejenniferc fateplasticityandreprogrammingingeneticallydistinctpopulationsofdanioleucophores AT simonjuliana fateplasticityandreprogrammingingeneticallydistinctpopulationsofdanioleucophores AT lippincottschwartzjennifer fateplasticityandreprogrammingingeneticallydistinctpopulationsofdanioleucophores AT raibledavidw fateplasticityandreprogrammingingeneticallydistinctpopulationsofdanioleucophores AT parichydavidm fateplasticityandreprogrammingingeneticallydistinctpopulationsofdanioleucophores |