Sox5 functions as a fate switch in medaka pigment cell development.

Mechanisms generating diverse cell types from multipotent progenitors are crucial for normal development. Neural crest cells (NCCs) are multipotent stem cells that give rise to numerous cell-types, including pigment cells. Medaka has four types of NCC-derived pigment cells (xanthophores, leucophores...

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Main Authors: Yusuke Nagao, Takao Suzuki, Atsushi Shimizu, Tetsuaki Kimura, Ryoko Seki, Tomoko Adachi, Chikako Inoue, Yoshihiro Omae, Yasuhiro Kamei, Ikuyo Hara, Yoshihito Taniguchi, Kiyoshi Naruse, Yuko Wakamatsu, Robert N Kelsh, Masahiko Hibi, Hisashi Hashimoto
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2014-04-01
Series:PLoS Genetics
Online Access:http://europepmc.org/articles/PMC3974636?pdf=render
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author Yusuke Nagao
Takao Suzuki
Atsushi Shimizu
Tetsuaki Kimura
Ryoko Seki
Tomoko Adachi
Chikako Inoue
Yoshihiro Omae
Yasuhiro Kamei
Ikuyo Hara
Yoshihito Taniguchi
Kiyoshi Naruse
Yuko Wakamatsu
Robert N Kelsh
Masahiko Hibi
Hisashi Hashimoto
author_facet Yusuke Nagao
Takao Suzuki
Atsushi Shimizu
Tetsuaki Kimura
Ryoko Seki
Tomoko Adachi
Chikako Inoue
Yoshihiro Omae
Yasuhiro Kamei
Ikuyo Hara
Yoshihito Taniguchi
Kiyoshi Naruse
Yuko Wakamatsu
Robert N Kelsh
Masahiko Hibi
Hisashi Hashimoto
author_sort Yusuke Nagao
collection DOAJ
description Mechanisms generating diverse cell types from multipotent progenitors are crucial for normal development. Neural crest cells (NCCs) are multipotent stem cells that give rise to numerous cell-types, including pigment cells. Medaka has four types of NCC-derived pigment cells (xanthophores, leucophores, melanophores and iridophores), making medaka pigment cell development an excellent model for studying the mechanisms controlling specification of distinct cell types from a multipotent progenitor. Medaka many leucophores-3 (ml-3) mutant embryos exhibit a unique phenotype characterized by excessive formation of leucophores and absence of xanthophores. We show that ml-3 encodes sox5, which is expressed in premigratory NCCs and differentiating xanthophores. Cell transplantation studies reveal a cell-autonomous role of sox5 in the xanthophore lineage. pax7a is expressed in NCCs and required for both xanthophore and leucophore lineages; we demonstrate that Sox5 functions downstream of Pax7a. We propose a model in which multipotent NCCs first give rise to pax7a-positive partially fate-restricted intermediate progenitors for xanthophores and leucophores; some of these progenitors then express sox5, and as a result of Sox5 action develop into xanthophores. Our results provide the first demonstration that Sox5 can function as a molecular switch driving specification of a specific cell-fate (xanthophore) from a partially-restricted, but still multipotent, progenitor (the shared xanthophore-leucophore progenitor).
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spelling doaj.art-4bd71a774b4c4aeebec4d9423f1e9db32022-12-21T17:43:51ZengPublic Library of Science (PLoS)PLoS Genetics1553-73901553-74042014-04-01104e100424610.1371/journal.pgen.1004246Sox5 functions as a fate switch in medaka pigment cell development.Yusuke NagaoTakao SuzukiAtsushi ShimizuTetsuaki KimuraRyoko SekiTomoko AdachiChikako InoueYoshihiro OmaeYasuhiro KameiIkuyo HaraYoshihito TaniguchiKiyoshi NaruseYuko WakamatsuRobert N KelshMasahiko HibiHisashi HashimotoMechanisms generating diverse cell types from multipotent progenitors are crucial for normal development. Neural crest cells (NCCs) are multipotent stem cells that give rise to numerous cell-types, including pigment cells. Medaka has four types of NCC-derived pigment cells (xanthophores, leucophores, melanophores and iridophores), making medaka pigment cell development an excellent model for studying the mechanisms controlling specification of distinct cell types from a multipotent progenitor. Medaka many leucophores-3 (ml-3) mutant embryos exhibit a unique phenotype characterized by excessive formation of leucophores and absence of xanthophores. We show that ml-3 encodes sox5, which is expressed in premigratory NCCs and differentiating xanthophores. Cell transplantation studies reveal a cell-autonomous role of sox5 in the xanthophore lineage. pax7a is expressed in NCCs and required for both xanthophore and leucophore lineages; we demonstrate that Sox5 functions downstream of Pax7a. We propose a model in which multipotent NCCs first give rise to pax7a-positive partially fate-restricted intermediate progenitors for xanthophores and leucophores; some of these progenitors then express sox5, and as a result of Sox5 action develop into xanthophores. Our results provide the first demonstration that Sox5 can function as a molecular switch driving specification of a specific cell-fate (xanthophore) from a partially-restricted, but still multipotent, progenitor (the shared xanthophore-leucophore progenitor).http://europepmc.org/articles/PMC3974636?pdf=render
spellingShingle Yusuke Nagao
Takao Suzuki
Atsushi Shimizu
Tetsuaki Kimura
Ryoko Seki
Tomoko Adachi
Chikako Inoue
Yoshihiro Omae
Yasuhiro Kamei
Ikuyo Hara
Yoshihito Taniguchi
Kiyoshi Naruse
Yuko Wakamatsu
Robert N Kelsh
Masahiko Hibi
Hisashi Hashimoto
Sox5 functions as a fate switch in medaka pigment cell development.
PLoS Genetics
title Sox5 functions as a fate switch in medaka pigment cell development.
title_full Sox5 functions as a fate switch in medaka pigment cell development.
title_fullStr Sox5 functions as a fate switch in medaka pigment cell development.
title_full_unstemmed Sox5 functions as a fate switch in medaka pigment cell development.
title_short Sox5 functions as a fate switch in medaka pigment cell development.
title_sort sox5 functions as a fate switch in medaka pigment cell development
url http://europepmc.org/articles/PMC3974636?pdf=render
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