The germline produces gametes that transmit parental epigenetic and genetic information to offspring. The maintenance of germline and the development of functional gametes require Piwi, an ancient member of the Argonaute family, and Piwi-interacting small RNAs (piRNA). Compared to other types of small RNAs (e.g., microRNAs and siRNAs), piRNA biogenesis remains mysterious largely owing to their exclusive expression in the germline and sequence diversity between organisms. Over the past decade, significant progress has been made toward elucidating the function of the piRNA pathway as a defense mechanism against transposable elements. Yet organisms including worms and mice express thousands of piRNAs that do not correspond to transposon sequences, suggesting that piRNAs may have alternative functions. My preliminary findings suggest that C. elegans piRNAs regulate endogenous gene expression and influence developmental processes. The goal of this proposal is to address fundamental questions regarding the piRNA pathway: How is piRNA expression controlled at the transcription level? How are piRNA precursors processed into mature piRNAs? Do piRNAs regulate the expression of germline genes? And how do they influence cellular and developmental processes? During the K99 phase of this award, I will: (1) define the transcription program of piRNA producing loci and chromatin factors associated with piRNA genes; (2) characterize a cap structure on piRNA precursors and study its role in piRNA expression; (3) established a cell free system to characterize enzymatic activity of Piwi and piRNA-processing enzymes. During the R00 phase of the award, I will: (1) continue the in vitro biochemical studies; (2) determine how piRNAs regulate developmental processes such as dosage compensation; (3) investigate potential auto-regulation of Piwi expression. Taken together, the proposed research will provide a framework for studying piRNA biogenesis in C. elegans and in other species. It will greatly advance our understanding of mechanism and functions of piRNAs in germline maintenance and gametogenesis. Ultimately the work will provide new tools and therapies that will improve human fertility and health.

Public Health Relevance

piRNAs are germline-specific small RNAs required for gametogenesis and germline immortality. The proposed studies will elucidate the mechanisms of piRNA biogenesis and provide insights into fundamental mechanisms by which piRNAs control germline development and function. Ultimately, the work will provide new tools and treatments that will improve human fertility and health.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Career Transition Award (K99)
Project #
1K99GM124460-01
Application #
9371628
Study Section
Special Emphasis Panel (ZGM1)
Program Officer
Zuk, Dorit
Project Start
2017-07-01
Project End
2019-06-30
Budget Start
2017-07-01
Budget End
2018-06-30
Support Year
1
Fiscal Year
2017
Total Cost
Indirect Cost
Name
University of Massachusetts Medical School Worcester
Department
Genetics
Type
Schools of Medicine
DUNS #
603847393
City
Worcester
State
MA
Country
United States
Zip Code
01655
Tang, Wen; Seth, Meetu; Tu, Shikui et al. (2018) A Sex Chromosome piRNA Promotes Robust Dosage Compensation and Sex Determination in C. elegans. Dev Cell 44:762-770.e3
Seth, Meetu; Shirayama, Masaki; Tang, Wen et al. (2018) The Coding Regions of Germline mRNAs Confer Sensitivity to Argonaute Regulation in C. elegans. Cell Rep 22:2254-2264
Shen, En-Zhi; Chen, Hao; Ozturk, Ahmet R et al. (2018) Identification of piRNA Binding Sites Reveals the Argonaute Regulatory Landscape of the C. elegans Germline. Cell 172:937-951.e18