Moonbase
← Back to Awards
F31NIH · EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENTNIH

Using genetics and optogenetics to dissect how Rho signaling is coordinated at distinct subcellular domains to drive epithelial tissue morphogenesis

Countryman, Andrew Dylan (Contact)·COLUMBIA UNIV NEW YORK MORNINGSIDE, NY·2025–2027·ACTIVE
Donate

INSTITUTION

COLUMBIA UNIV NEW YORK MORNINGSIDE, NY

PRINCIPAL INVESTIGATOR

Countryman, Andrew Dylan (Contact)

FUNDING

$50K

YEAR

2025

MOONBASE SCORE

Still being scored

LOADING MOONBASE SCORE

Abstract

Project Summary/Abstract During embryonic development, cellular cytoskeletal machinery produces mechanical forces to deform epithelial tissue sheets into complex structures. Although the gene and protein regulatory networks that direct development have been the focus of many studies, much less is known about how these patterned molecular programs generate cell and tissue-scale forces to physically sculpt developing tissues and organs. Convergent extension is a widely conserved morphogenetic process employed extensively across animal development, and its failure is associated with common congenital anomalies in humans. However, the nature of the subcellular forces directing tissue convergent extension remain poorly understood. Here, I propose using the Drosophila melanogaster embryo as a model for dissecting the interplay of the actomyosin-generated subcellular forces that direct cell intercalations during convergent extension. In Aim 1, I seek to quantify and correlate actomyosin dynamics at cell apices, junctions, and lateral domains during both germband extension, in which contractility at these domains cooperatively drives cell rearrangements, and ventral furrow formation, in which contractility at these domains drives both in-plane cell rearrangements and out-of-plane tissue bending. Then, using genetic mutants that disrupt actomyosin patterning in the early embryo, I plan to study how defects in coordination between apical, junctional, and lateral actomyosin contribute to perturbed developmental phenotypes. In Aim 2, I propose using optogenetic control of Rho signaling to specifically and simultaneously manipulate actomyosin at cell junctions, apices, and lateral domains in order to build a bottom-up understanding of how actomyosin coordination across different subcellular domains enacts distinct cell and tissue-scale morphogenetic processes. I will use insight gained from endogenous germband extension and ventral furrow formation processes to manipulate the frequency, duration, magnitude, and coordination of these distinct subcellular contractile optogenetic inputs, and measure the resulting cell and tissue deformations. These studies will elucidate the biochemical and mechanical nature of epithelial remodeling during convergent extension, contributing to our understanding of healthy and perturbed developmental processes.

F31EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENTSpecial Emphasis Panel[ZRG1 F05-E (20)]aboutunderstandingcoordinationmechanicalextensionremodelinglateralmorphogeneticdisruptdevelopingenactssummarysfdgeneticorderduringcomplexresultingformationsignaling

Are you the primary organization running this research?

The two tools below are built for the principal investigator & host institution behind this project.