Quantitative in vitro and in vivo analyses of oscillatory processes in early zebrafish embryos

NIH RePORTER · NIH · R35 · $336,822 · view on reporter.nih.gov ↗

Abstract

Project Summary Our broad research goal is to develop a comprehensive understanding of stochastic cellular and developmental processes, during which form and pattern emerge from the simple beginnings of a fertilized egg. In specific, we pursue questions of how clocks are designed and coordinate to produce collective behaviors with spatiotemporal accuracy during embryo development. Our research emphasizes on both the development of novel methods and applications to relevant questions. One research goal is to develop an interdisciplinary platform that enables computational search and experimental reconstitution and manipulation of biological oscillators, to determine the recurring clock network topologies and functions. The other is to understand how a pattern is formed with high spatiotemporal accuracy during zebrafish somitogenesis, through the interactions of multiple clocks, including a mitotic clock to “tell” a cell when to proliferate and a segmentation clock to “tell” when a somite is to form. The two research directions are interrelated. Theoretical modeling, microfluidics, and advanced imaging tools at the single molecule and single cell levels will facilitate the investigation of these phenomena.

Key facts

NIH application ID
9937748
Project number
5R35GM119688-05
Recipient
UNIVERSITY OF MICHIGAN AT ANN ARBOR
Principal Investigator
Qiong Yang
Activity code
R35
Funding institute
NIH
Fiscal year
2020
Award amount
$336,822
Award type
5
Project period
2016-08-19 → 2022-05-31