The evolutionally-conserved function of group B1 Sox family members confers the unique role of Sox2 in mouse ES cells

被引:27
作者
Niwa, Hitoshi [1 ,2 ]
Nakamura, Akira [3 ]
Urata, Makoto [4 ]
Shirae-Kurabayashi, Maki [5 ]
Kuraku, Shigehiro [6 ]
Russell, Steven [7 ]
Ohtsuka, Satoshi [1 ,8 ]
机构
[1] RIKEN, Ctr Dev Biol, Lab Pluripotent Stem Cell Studies, Chuo Ku, Kobe, Hyogo 6500047, Japan
[2] Kumamoto Univ, Inst Mol Embryol & Genet, Dept Pluripotent Stem Cell Biol, Chuo Ku, 2-2-1 Honjo, Kumamoto 8600811, Japan
[3] Kumamoto Univ, Inst Mol Embryol & Genet, Dept Germline Dev, Chuo Ku, 2-2-1 Honjo, Kumamoto 8600811, Japan
[4] Kanazawa Univ, Inst Nat & Environm Technol, Noto Marine Lab, Ogi 34-11, Hohsu, Ishikawa 9270553, Japan
[5] Nagoya Univ, Grad Sch Sci, Sugashima Marine Biol Lab, Sugashima Cho 429 63, Toba C, Mie 5170004, Japan
[6] RIKEN, Ctr Life Sci Technol, Phyloinformat Unit, Chuo Ku, 2-2-3 Minatojima Minamimachi, Kobe, Hyogo 6500047, Japan
[7] Univ Cambridge, Dept Genet, Downing St, Cambridge CB2 3EH, England
[8] Kanazawa Med Univ, Med Res Inst, Dept Life Sci, Kaho Ku, 1-1 Daigaku, Uchinada, Ishikawa 9200293, Japan
来源
BMC EVOLUTIONARY BIOLOGY | 2016年 / 16卷
基金
英国生物技术与生命科学研究理事会;
关键词
Pluripotent stem cells; Sox2; Evolution; Co-option; PRIMITIVE ENDODERM DIFFERENTIATION; EMBRYONIC STEM-CELLS; SELF-RENEWAL; PLURIPOTENCY; EXPRESSION; GENES; POU5F1; IDENTIFICATION; ENHANCERS; PROTEINS;
D O I
10.1186/s12862-016-0755-4
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: In mouse ES cells, the function of Sox2 is essential for the maintenance of pluripotency. Since the Sox-family of transcription factors are well conserved in the animal kingdom, addressing the evolutionary origin of Sox2 function in pluripotent stem cells is intriguing from the perspective of understanding the origin of pluripotency. Results: Here we approach this question using a functional complementation assay in inducible Sox2-null ES cells. Assaying mouse Sox proteins from different Groups, we found that only Group B1 and Group G proteins were able to support pluripotency. Interestingly, invertebrate homologs of mammalian Group B1 Sox proteins were able to replace the pluripotency-associated function of mouse Sox2. Moreover, the mouse ES cells rescued by the Drosophila SoxNeuro protein are able to contribute to chimeric embryos. Conclusions: These data indicate that the function of mouse Sox2 supporting pluripotency is based on an evolutionally conserved activity of the Group B1 Sox family. Since pluripotent stem cell population in developmental process could be regarded as the evolutional novelty in vertebrates, it could be regarded as a co-optional use of their evolutionally conserved function.
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页数:12
相关论文
共 36 条
[1]   Context-Dependent Wiring of Sox2 Regulatory Networks for Self-Renewal of Embryonic and Trophoblast Stem Cells [J].
Adachi, Kenjiro ;
Nikaido, Itoshi ;
Ohta, Hiroshi ;
Ohtsuka, Satoshi ;
Ura, Hiroki ;
Kadota, Mitsutaka ;
Wakayama, Teruhiko ;
Ueda, Hiroki R. ;
Niwa, Hitoshi .
MOLECULAR CELL, 2013, 52 (03) :380-392
[2]   Phylogeny of the SOX family of developmental transcription factors based on sequence and structural indicators [J].
Bowles, J ;
Schepers, G ;
Koopman, P .
DEVELOPMENTAL BIOLOGY, 2000, 227 (02) :239-255
[3]   Morphological evidence that the molecularly determined Ciona intestinalis type A and type B are different species: Ciona robusta and Ciona intestinalis [J].
Brunetti, Riccardo ;
Gissi, Carmela ;
Pennati, Roberta ;
Caicci, Federico ;
Gasparini, Fabio ;
Manni, Lucia .
JOURNAL OF ZOOLOGICAL SYSTEMATICS AND EVOLUTIONARY RESEARCH, 2015, 53 (03) :186-193
[4]   LIF/STAT3 controls ES cell self-renewal and pluripotency by a Myc-dependent mechanism [J].
Cartwright, P ;
McLean, C ;
Sheppard, A ;
Rivett, D ;
Jones, K ;
Dalton, S .
DEVELOPMENT, 2005, 132 (05) :885-896
[5]   Replacement of mouse Sox10 by the Drosophila ortholog Sox100B provides evidence for co-option of SoxE proteins into vertebrate-specific gene-regulatory networks through altered expression [J].
Cossais, Francois ;
Sock, Elisabeth ;
Hornig, Julia ;
Schreiner, Silke ;
Kellerer, Susanne ;
Boesl, Michael R. ;
Russell, Steven ;
Wegner, Michael .
DEVELOPMENTAL BIOLOGY, 2010, 341 (01) :267-281
[6]   On the origin of POU5F1 [J].
Frankenberg, Stephen ;
Renfree, Marilyn B. .
BMC BIOLOGY, 2013, 11
[7]   The evolution of class V POU domain transcription factors in vertebrates and their characterisation in a marsupial [J].
Frankenberg, Stephen ;
Pask, Andrew ;
Renfree, Marilyn B. .
DEVELOPMENTAL BIOLOGY, 2010, 337 (01) :162-170
[8]   The master control gene for morphogenesis and evolution of the eye [J].
Gehring, WJ .
GENES TO CELLS, 1996, 1 (01) :11-15
[9]   Klf4 reverts developmentally programmed restriction of ground state pluripotency [J].
Guo, Ge ;
Yang, Jian ;
Nichols, Jennifer ;
Hall, John Simon ;
Eyres, Isobel ;
Mansfield, William ;
Smith, Austin .
DEVELOPMENT, 2009, 136 (07) :1063-1069
[10]   Molecular Signatures of the Three Stem Cell Lineages in Hydra and the Emergence of Stem Cell Function at the Base of Multicellularity [J].
Hemmrich, Georg ;
Khalturin, Konstantin ;
Boehm, Anna-Marei ;
Puchert, Malte ;
Anton-Erxleben, Friederike ;
Wittlieb, Joerg ;
Klostermeier, Ulrich C. ;
Rosenstiel, Philip ;
Oberg, Hans-Heinrich ;
Domazet-Loso, Tomislav ;
Sugimoto, Toshimi ;
Niwa, Hitoshi ;
Bosch, Thomas C. G. .
MOLECULAR BIOLOGY AND EVOLUTION, 2012, 29 (11) :3267-3280