Optogenetic investigation of BMP target gene expression diversity

被引:24
作者
Rogers, Katherine W. [1 ]
ElGamacy, Mohammad [1 ,2 ,3 ]
Jordan, Benjamin M. [4 ]
Mueller, Patrick [1 ,2 ]
机构
[1] Max Planck Gesell, Friedrich Miescher Lab, Syst Biol Dev Grp, Tubingen, Germany
[2] Eberhard Karls Univ Tubingen, Translat Oncol Div, Modeling Tumorigenesis Grp, Tubingen, Germany
[3] Heliopolis Biotechnol Ltd, London, England
[4] Harvard Univ, Dept Organism & Evolutionary Biol, Cambridge, MA 02138 USA
来源
ELIFE | 2020年 / 9卷
基金
欧洲研究理事会;
关键词
DORSOVENTRAL PATTERN-FORMATION; TGF-BETA; DIFFERENTIAL EXPRESSION; HOMEOBOX GENE; POSITIONAL INFORMATION; ACTIVITY GRADIENT; ZEBRAFISH EMBRYO; NODAL SIGNALS; FGF; ECTODERM;
D O I
10.7554/eLife.58641
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Signaling molecules activate distinct patterns of gene expression to coordinate embryogenesis, but how spatiotemporal expression diversity is generated is an open question. In zebrafish, a BMP signaling gradient patterns the dorsal-ventral axis. We systematically identified target genes responding to BMP and found that they have diverse spatiotemporal expression patterns. Transcriptional responses to optogenetically delivered high- and low-amplitude BMP signaling pulses indicate that spatiotemporal expression is not fully defined by different BMP signaling activation thresholds. Additionally, we observed negligible correlations between spatiotemporal expression and transcription kinetics for the majority of analyzed genes in response to BMP signaling pulses. In contrast, spatial differences between BMP target genes largely collapsed when FGF and Nodal signaling were inhibited. Our results suggest that, similar to other patterning systems, combinatorial signaling is likely to be a major driver of spatial diversity in BMP-dependent gene expression in zebrafish.
引用
收藏
页码:1 / 44
页数:44
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