Gene Regulatory Network of Dorsolateral Prefrontal Cortex: a Master Regulator Analysis of Major Psychiatric Disorders

2019 ◽  
Vol 57 (3) ◽  
pp. 1305-1316
Author(s):  
Giovana Bristot ◽  
Marco Antônio De Bastiani ◽  
Bianca Pfaffenseller ◽  
Flávio Kapczinski ◽  
Márcia Kauer-Sant’Anna
2019 ◽  
Vol 85 (10) ◽  
pp. S354
Author(s):  
Bianca Pfaffenseller ◽  
Giovana Bristot ◽  
Marco Antônio De Bastiani ◽  
Flávio Kapczinski ◽  
Márcia Kauer-Sant’Anna

Author(s):  
Wendy M. Reeves ◽  
Kotaro Shimai ◽  
Konner M. Winkley ◽  
Michael T. Veeman

AbstractThe notochord is a defining feature of the chordates. The transcription factor Brachyury (Bra) is a key regulator of notochord fate but here we show that it is not a unitary master regulator in the model chordate Ciona. Ectopic Bra expression only partially reprograms other cell types to a notochord-like transcriptional profile and a subset of notochord-enriched genes are unaffected by CRISPR Bra disruption. We identify Foxa.a and Mnx as potential co-regulators and find that combinatorial cocktails are more effective at reprograming other cell types than Bra alone. We reassess the network relationships between Bra, Foxa.a and other components of the notochord gene regulatory network and find that Foxa.a expression in the notochord is regulated by vegetal FGF signaling. It is a direct activator of Bra expression and has a binding motif that is significantly enriched in the regulatory regions of notochord-enriched genes. These and other results indicate that Bra and Foxa.a act together in a regulatory network dominated by positive feed-forward interactions, with neither being a classically-defined master regulator.


Development ◽  
2021 ◽  
pp. dev.195230
Author(s):  
Wendy M. Reeves ◽  
Kotaro Shimai ◽  
Konner M. Winkley ◽  
Michael T. Veeman

The notochord is a defining feature of the chordates. The transcription factor Brachyury (Bra) is a key regulator of notochord fate but here we show that it is not a unitary master regulator in the model chordate Ciona. Ectopic Bra expression only partially reprograms other cell types to a notochord-like transcriptional profile and a subset of notochord-enriched genes are unaffected by CRISPR Bra disruption. We identify Foxa.a and Mnx as potential co-regulators and find that combinatorial cocktails are more effective at reprograming other cell types than Bra alone. We reassess the network relationships between Bra, Foxa.a, and other components of the notochord gene regulatory network and find that Foxa.a expression in the notochord is regulated by vegetal FGF signaling. It is a direct activator of Bra expression and has a binding motif that is significantly enriched in the regulatory regions of notochord-enriched genes. These and other results indicate that Bra and Foxa.a act together in a regulatory network dominated by positive feed-forward interactions, with neither being a classically-defined master regulator.


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