Cargando…
Bioelectric Signaling Regulates Size in Zebrafish Fins
The scaling relationship between the size of an appendage or organ and that of the body as a whole is tightly regulated during animal development. If a structure grows at a different rate than the rest of the body, this process is termed allometric growth. The zebrafish another longfin (alf) mutant...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3894163/ https://www.ncbi.nlm.nih.gov/pubmed/24453984 http://dx.doi.org/10.1371/journal.pgen.1004080 |
_version_ | 1782299808449429504 |
---|---|
author | Perathoner, Simon Daane, Jacob M. Henrion, Ulrike Seebohm, Guiscard Higdon, Charles W. Johnson, Stephen L. Nüsslein-Volhard, Christiane Harris, Matthew P. |
author_facet | Perathoner, Simon Daane, Jacob M. Henrion, Ulrike Seebohm, Guiscard Higdon, Charles W. Johnson, Stephen L. Nüsslein-Volhard, Christiane Harris, Matthew P. |
author_sort | Perathoner, Simon |
collection | PubMed |
description | The scaling relationship between the size of an appendage or organ and that of the body as a whole is tightly regulated during animal development. If a structure grows at a different rate than the rest of the body, this process is termed allometric growth. The zebrafish another longfin (alf) mutant shows allometric growth resulting in proportionally enlarged fins and barbels. We took advantage of this mutant to study the regulation of size in vertebrates. Here, we show that alf mutants carry gain-of-function mutations in kcnk5b, a gene encoding a two-pore domain potassium (K(+)) channel. Electrophysiological analysis in Xenopus oocytes reveals that these mutations cause an increase in K(+) conductance of the channel and lead to hyperpolarization of the cell. Further, somatic transgenesis experiments indicate that kcnk5b acts locally within the mesenchyme of fins and barbels to specify appendage size. Finally, we show that the channel requires the ability to conduct K(+) ions to increase the size of these structures. Our results provide evidence for a role of bioelectric signaling through K(+) channels in the regulation of allometric scaling and coordination of growth in the zebrafish. |
format | Online Article Text |
id | pubmed-3894163 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-38941632014-01-21 Bioelectric Signaling Regulates Size in Zebrafish Fins Perathoner, Simon Daane, Jacob M. Henrion, Ulrike Seebohm, Guiscard Higdon, Charles W. Johnson, Stephen L. Nüsslein-Volhard, Christiane Harris, Matthew P. PLoS Genet Research Article The scaling relationship between the size of an appendage or organ and that of the body as a whole is tightly regulated during animal development. If a structure grows at a different rate than the rest of the body, this process is termed allometric growth. The zebrafish another longfin (alf) mutant shows allometric growth resulting in proportionally enlarged fins and barbels. We took advantage of this mutant to study the regulation of size in vertebrates. Here, we show that alf mutants carry gain-of-function mutations in kcnk5b, a gene encoding a two-pore domain potassium (K(+)) channel. Electrophysiological analysis in Xenopus oocytes reveals that these mutations cause an increase in K(+) conductance of the channel and lead to hyperpolarization of the cell. Further, somatic transgenesis experiments indicate that kcnk5b acts locally within the mesenchyme of fins and barbels to specify appendage size. Finally, we show that the channel requires the ability to conduct K(+) ions to increase the size of these structures. Our results provide evidence for a role of bioelectric signaling through K(+) channels in the regulation of allometric scaling and coordination of growth in the zebrafish. Public Library of Science 2014-01-16 /pmc/articles/PMC3894163/ /pubmed/24453984 http://dx.doi.org/10.1371/journal.pgen.1004080 Text en © 2014 Perathoner et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Perathoner, Simon Daane, Jacob M. Henrion, Ulrike Seebohm, Guiscard Higdon, Charles W. Johnson, Stephen L. Nüsslein-Volhard, Christiane Harris, Matthew P. Bioelectric Signaling Regulates Size in Zebrafish Fins |
title | Bioelectric Signaling Regulates Size in Zebrafish Fins |
title_full | Bioelectric Signaling Regulates Size in Zebrafish Fins |
title_fullStr | Bioelectric Signaling Regulates Size in Zebrafish Fins |
title_full_unstemmed | Bioelectric Signaling Regulates Size in Zebrafish Fins |
title_short | Bioelectric Signaling Regulates Size in Zebrafish Fins |
title_sort | bioelectric signaling regulates size in zebrafish fins |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3894163/ https://www.ncbi.nlm.nih.gov/pubmed/24453984 http://dx.doi.org/10.1371/journal.pgen.1004080 |
work_keys_str_mv | AT perathonersimon bioelectricsignalingregulatessizeinzebrafishfins AT daanejacobm bioelectricsignalingregulatessizeinzebrafishfins AT henrionulrike bioelectricsignalingregulatessizeinzebrafishfins AT seebohmguiscard bioelectricsignalingregulatessizeinzebrafishfins AT higdoncharlesw bioelectricsignalingregulatessizeinzebrafishfins AT johnsonstephenl bioelectricsignalingregulatessizeinzebrafishfins AT nussleinvolhardchristiane bioelectricsignalingregulatessizeinzebrafishfins AT harrismatthewp bioelectricsignalingregulatessizeinzebrafishfins |