Temperature and insulin signaling regulate body size in Hydra by the Wnt and TGF-beta pathways

被引:29
作者
Mortzfeld, Benedikt M. [1 ,3 ]
Taubenheim, Jan [1 ,4 ]
Klimovich, Alexander, V [1 ]
Fraune, Sebastian [1 ,4 ]
Rosenstiel, Philip [2 ]
Bosch, Thomas C. G. [1 ]
机构
[1] Christian Albrechts Univ Kiel, Zool Inst, Botan Garten 1-9, D-24118 Kiel, Germany
[2] Christian Albrechts Univ Kiel, Univ Hosp Schleswig Holstein, Inst Clin Mol Biol, Rosalind Franklin Str 12, D-24105 Kiel, Germany
[3] Univ Massachusetts, Dept Bioengn, 285 Old Westport Rd, Dartmouth, MA 02747 USA
[4] Heinrich Heine Univ Dusseldorf, Inst Zool & Organism Interact, Univ Str 1, D-40225 Dusseldorf, Germany
关键词
RNA-SEQ READS; C-ELEGANS; GROWTH; MECHANISMS; EXPRESSION; ALIGNMENT; PATTERN; GENOME; FOXO; GENERATION;
D O I
10.1038/s41467-019-11136-6
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
How multicellular organisms assess and control their size is a fundamental question in biology, yet the molecular and genetic mechanisms that control organ or organism size remain largely unsolved. The freshwater polyp Hydra demonstrates a high capacity to adapt its body size to different temperatures. Here we identify the molecular mechanisms controlling this phenotypic plasticity and show that temperature-induced cell number changes are controlled by Wnt- and TGF-beta signaling. Further we show that insulin-like peptide receptor (INSR) and forkhead box protein O (FoxO) are important genetic drivers of size determination controlling the same developmental regulators. Thus, environmental and genetic factors directly affect developmental mechanisms in which cell number is the strongest determinant of body size. These findings identify the basic mechanisms as to how size is regulated on an organismic level and how phenotypic plasticity is integrated into conserved developmental pathways in an evolutionary informative model organism.
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页数:13
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