Functional Analysis of microRNAs in C. elegans spermatogenesis

NIH RePORTER · NIH · R15 · $450,342 · view on reporter.nih.gov ↗

Abstract

7. PROJECT SUMMARY Small RNAs, including microRNAs, have been shown to play critical roles in the regulation of gene expression in the germ line. However, the specific pathways and targets regulated by individual microRNAs in the process of spermatogenesis remain largely unknown. The identification of direct targets regulated by individual microRNAs remains a central challenge in the field. In this grant, we propose to identify direct targets of germline microRNAs that function in the regulation of spermatogenesis. We are using the model system of C. elegans, which has been instrumental in defining the core principles of individual microRNA regulation of targets in developmental pathways. In prior work, we and others have identified the set of microRNAs that are expressed in C. elegans germ cells and somatic gonad cells. Additionally, we have identified a set of microRNAs that function to regulate sperm formation. However, the pathways and targets that they regulate remain largely uncharacterized. This work will address two central questions: 1) What are the target mRNAs that associate with a germline specific Argonaute protein? 2) How does regulation by microRNAs through the 3’ UTR of target mRNAs act to control spermatogenesis? This work will provide a foundation for future investigation to comprehensively define the microRNA targets that act in the germ line to regulate the process of spermatogenesis.

Key facts

NIH application ID
10580284
Project number
2R15GM126458-02
Recipient
MARQUETTE UNIVERSITY
Principal Investigator
Allison Lynn Abbott
Activity code
R15
Funding institute
NIH
Fiscal year
2022
Award amount
$450,342
Award type
2
Project period
2017-09-21 → 2026-08-31