Genetic control of developmental timing

NIH RePORTER · NIH · R35 · $820,328 · view on reporter.nih.gov ↗

Abstract

Project Summary/Abstract Animal development involves the precise control of cell division, cellular quiescence, cell fate specification, differentiation, and morphogenesis. All these processes are controlled by cell signaling and genetic regulatory mechanisms whose components and interactions have been shaped by evolution for maximum fitness. We study genetic regulatory networks in C. elegans that are responsible for orchestrating temporal patterns of developmental events during larval development, with an eye on uncovering principles and mechanisms that ensure robust coordination of developmental progression throughout the animal. We will expand on our previous studies of the roles of microRNA pathways in developmental robustness to investigate mechanisms coupling microRNA biogenesis to developmental progression under conditions of stress. We will continue to explore the roles of microRNAs and other factors in coordinating transcriptional and post-transcriptional regulatory mechanisms for robust temporal control of development, particularly in the context of deeply conserved microRNAs and microRNA target motifs. We will investigate the relationship of the periodic components of worm development -- particularly molting and larval diapause – to the progressive advancement of stage identify and cell fate progression, with the aim of testing hypotheses for how cell divisions and cell fate transitions are coordinated on the organism level.

Key facts

NIH application ID
10147889
Project number
5R35GM131741-03
Recipient
UNIV OF MASSACHUSETTS MED SCH WORCESTER
Principal Investigator
Victor Ambros
Activity code
R35
Funding institute
NIH
Fiscal year
2021
Award amount
$820,328
Award type
5
Project period
2019-05-01 → 2024-04-30