The long-term goal of this proposal is to understand the molecular mechanisms of Rib nucleoprotein (RNP) granules. RNP granules are found in a diversity of cells and are typically involved in RNA metabolism. In germ cells of many metazoans, specialized RNP granules, known as germ granules, are required for cell differentiation into functional gametes. The Caenorhabditis elegans germ granule, the P-granule, is required for germline maintenance. P-granule assembly requires the Caenorhabditis sp. specific scaffold proteins, PGL-1 and PGL-3, and the highly conserved Vasa-related DEAD-box helicases, GLH-1 and GLH-4. Vasa helicases are found in all metazoans and are necessary for fertility in mammals. This proposal uses the P-granule as a model to study the assembly and function of germ granules. I will study the mechanistic roles of the PGL and GLH proteins in RNA processing and granule formation, and investigate the molecular function of P-granules. Along the way, I will learn new methods in RNA sequencing, C. elegans genome editing, and single molecule microscopy, enabling me to analyze and test my structural models in vitro and in vivo. The R00 phase will continue using these methods to probe the biological function of P-granules related to assembly dynamics and RNA metabolism. The basic mechanisms of P-granules will undoubtedly provide insight into the function of germ granules in tissue development and a greater overall understanding how RNP granules function in cell biology.

Public Health Relevance

Germ cells have specialized assemblies of protein and RNA complexes, termed germ granules, necessary for gamete development. One central player in germ granules is Vasa, a conserved protein required for fertility in mammals. Understanding the function of germ granules and Vasa in worms will give us a greater fundamental insight into their roles in human germ cell development.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Career Transition Award (K99)
Project #
1K99HD081208-01A1
Application #
8889395
Study Section
Pediatrics Subcommittee (CHHD)
Program Officer
Ravindranath, Neelakanta
Project Start
2015-03-01
Project End
2017-02-28
Budget Start
2015-03-01
Budget End
2016-02-29
Support Year
1
Fiscal Year
2015
Total Cost
$101,199
Indirect Cost
$7,496
Name
University of Wisconsin Madison
Department
Biochemistry
Type
Schools of Earth Sciences/Natur
DUNS #
161202122
City
Madison
State
WI
Country
United States
Zip Code
53715
Aoki, Scott T; Porter, Douglas F; Prasad, Aman et al. (2018) An RNA-Binding Multimer Specifies Nematode Sperm Fate. Cell Rep 23:3769-3775
Noble, Daniel C; Aoki, Scott T; Ortiz, Marco A et al. (2016) Genomic Analyses of Sperm Fate Regulator Targets Reveal a Common Set of Oogenic mRNAs in Caenorhabditis elegans. Genetics 202:221-34
Aoki, Scott T; Kershner, Aaron M; Bingman, Craig A et al. (2016) PGL germ granule assembly protein is a base-specific, single-stranded RNase. Proc Natl Acad Sci U S A 113:1279-84