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Spatiotemporal control of gene expression boundaries using a feedforward loop
Author(s) -
Reeves Gregory,
Bandodkar Prasad,
Al Asafen Hadel
Publication year - 2020
Publication title -
the faseb journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.709
H-Index - 277
eISSN - 1530-6860
pISSN - 0892-6638
DOI - 10.1096/fasebj.2020.34.s1.00347
Subject(s) - morphogen , feed forward , dorsum , transcription factor , biological system , multiplicative function , computer science , biology , physics , computational biology , gene , mathematics , genetics , anatomy , engineering , mathematical analysis , control engineering
A feed forward loop (FFL) is commonly observed in several biological networks. The FFL network motif has been mostly been studied with respect to variation of the input signal in time, with only a few studies of FFL activity in a spatially distributed system such as morphogen‐mediated tissue patterning. However, most morphogen gradients also evolve in time. We studied the spatiotemporal behavior of a coherent FFL in two contexts: (1) a generic, oscillating morphogen gradient and (2) the dorsal‐ventral patterning of the early Drosophila embryo by a gradient of the NF‐κB homolog Dorsal with its early target Twist. In both models, we found features in the dynamics of the intermediate node – phase difference and noise filtering – that were largely independent of the parameterization of the models, and thus were functions of the structure of the FFL itself. In the Dorsal gradient model, we also found that the dynamics of Dorsal require maternal pioneering factor Zelda for proper target gene expression. Support or Funding Information During this work, GTR and PB were partially supported by NIH grant (number R21HD092830), and GTR and HA were partially supported by NSF CAREER award (number CBET‐1254344).A . Schematic figure depicting the generic morphogen gradient model. The inset shows the variation of the concentration of the primary transcription factor A in space and time. B . Schematic figure depicting the Dl/Twi/Zld model. The inset shows the variation of the concentration of the primary transcription factor Dl in space and time. The peaks in the Dl gradient amplitude in time correspond to nuclear cycles 11–14.