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Optogenetic Control of Nodal Signaling Reveals a Temporal Pattern of Nodal Signaling Regulating Cell Fate Specification during Gastrulation
被引:81
|作者:
Sako, Keisuke
[1
]
Pradhan, Saurabh J.
[2
]
Barone, Vanessa
[1
]
Ingles-Prieto, Alvaro
[3
]
Mueller, Patrick
[4
]
Ruprecht, Verena
[1
]
Capek, Daniel
[1
]
Galande, Sanjeev
[2
]
Janovjak, Harald
[3
]
Heisenberg, Carl-Philipp
[1
]
机构:
[1] IST Austria, Dev Biol Lab, A-3400 Klosterneuburg, Austria
[2] Indian Inst Sci Educ & Res, Pune 411008, Maharashtra, India
[3] IST Austria, Lab Synthet Physiol, A-3400 Klosterneuburg, Austria
[4] Max Planck Gesell, Friedrich Miescher Lab, D-72076 Tubingen, Germany
来源:
关键词:
ONE-EYED PINHEAD;
ENDODERM FORMATION;
MORPHOGEN GRADIENTS;
AXIS FORMATION;
NO TAIL;
ZEBRAFISH;
MESODERM;
CYCLOPS;
GENE;
ACTIVATION;
D O I:
10.1016/j.celrep.2016.06.036
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
During metazoan development, the temporal pattern of morphogen signaling is critical for organizing cell fates in space and time. Yet, tools for temporally controlling morphogen signaling within the embryo are still scarce. Here, we developed a photoactivatable Nodal receptor to determine how the temporal pattern of Nodal signaling affects cell fate specification during zebrafish gastrulation. By using this receptor to manipulate the duration of Nodal signaling in vivo by light, we show that extended Nodal signaling within the organizer promotes prechordal plate specification and suppresses endoderm differentiation. Endoderm differentiation is suppressed by extended Nodal signaling inducing expression of the transcriptional repressor goosecoid (gsc) in prechordal plate progenitors, which in turn restrains Nodal signaling from upregulating the endoderm differentiation gene sox17 within these cells. Thus, optogenetic manipulation of Nodal signaling identifies a critical role of Nodal signaling duration for organizer cell fate specification during gastrulation.
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页码:866 / 877
页数:12
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