Fibroblast growth factor signalling controls nervous system patterning and pigment cell formation in Ciona intestinalis

被引:45
作者
Racioppi, Claudia [1 ]
Kamal, Ashwani K. [1 ]
Razy-Krajka, Florian [2 ]
Gambardella, Gennaro [3 ]
Zanetti, Laura [1 ]
di Bernardo, Diego [3 ]
Sanges, Remo [4 ]
Christiaen, Lionel A. [2 ]
Ristoratore, Filomena [1 ]
机构
[1] Stn Zool Anton Dorhn, Cellular & Dev Biol Lab, I-80121 Naples, Italy
[2] NYU, Dept Biol, Ctr Dev Genet, New York, NY 10003 USA
[3] Telethon Inst Genet & Med TIGEM, I-80131 Naples, Italy
[4] Stn Zool Anton Dorhn, Anim Physiol & Evolut Lab, I-80121 Naples, Italy
关键词
DEVELOPMENTAL BIOLOGY; TRANSCRIPTION FACTORS; PROTEIN TRAFFICKING; ASCIDIAN EMBRYOS; LARVA; GENE; IDENTIFICATION; CHORDATE; NETWORK; RAB32;
D O I
10.1038/ncomms5830
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
During the development of the central nervous system (CNS), combinations of transcription factors and signalling molecules orchestrate patterning, specification and differentiation of neural cell types. In vertebrates, three types of melanin-containing pigment cells, exert a variety of functional roles including visual perception. Here we analysed the mechanisms underlying pigment cell specification within the CNS of a simple chordate, the ascidian Ciona intestinalis. Ciona tadpole larvae exhibit a basic chordate body plan characterized by a small number of neural cells. We employed lineage-specific transcription profiling to characterize the expression of genes downstream of fibroblast growth factor signalling, which govern pigment cell formation. We demonstrate that FGF signalling sequentially imposes a pigment cell identity at the expense of anterior neural fates. We identify FGF-dependent and pigment cell-specific factors, including the small GTPase, Rab32/38 and demonstrated its requirement for the pigmentation of larval sensory organs.
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页数:17
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