Germ cells give rise to eggs and sperm, thus eventually to a whole new organism of the next generation. The formation of germ cells is a critical step in the continuity of life for sexually reproducing organisms like humans. How do germ cells form? It remains the core question of germ cell research. Recently, it was revealed that the development of germ cells rely on a dynamic assembly of ribonucleoproteins (RNPs), germ granules. Me31B protein, a conserved component of germ granules in Drosophila (fruit fly), has been showed to interact with other germ granule proteins and contribute to germ cell formation by regulating the translation of certain germline mRNAs. Our recent study on the Me31B interactome showed that Me31B interacts with four groups of proteins in different types of ribonucleoprotein granules: RNA regulation proteins, glycolytic enzymes, cytoskeleton/motor proteins, and germ plasm components. We hypothesize that Me31B's interaction with these partner proteins as well as Me31B itself play important roles in the regulation of germ granule RNAs, which leads to proper germline development and germ cell formation. Therefore, we propose to investigate the role of Me31B in germ cell development by specifically studying: 1) Me31B Interactome in early Drosophila embryos; 2) The Recruitment Mechanism of Me31B to the Germ Granules; 3) The Mechanism and Function of Me31B-Tud Interaction; 4) The Role of Me31B in Germ Granule RNA Regulation. The proposed study will produce critical information that helps us understand how Me31B works together with its associated proteins and ultimately contributes to germ cell development. Finally, as an essential goal of Academic Research Enhancement Award program, the proposed projects will enhance the education for the undergraduate students at Indiana University Northwest by engaging them in frontline germ cell research.

Public Health Relevance

The proposed research will study the interactome of Me31B in germ granules, the recruitment mechanism, the specific interaction between Me31B and germ granule proteins, and Me31B's role in RNA binding and stability. The findings of the research will provide a better understanding of the role of Me31B in germ cell development at the molecular level. Furthermore, the proposed projects aim to engage undergraduate students in current germ cell research to enhance their education as well as the research environment of Indiana University Northwest.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Academic Research Enhancement Awards (AREA) (R15)
Project #
1R15HD092925-01A1
Application #
9590510
Study Section
Cellular, Molecular and Integrative Reproduction Study Section (CMIR)
Program Officer
Taymans, Susan
Project Start
2018-09-18
Project End
2021-09-17
Budget Start
2018-09-18
Budget End
2021-09-17
Support Year
1
Fiscal Year
2018
Total Cost
Indirect Cost
Name
Indiana University Bloomington
Department
Biology
Type
Schools of Arts and Sciences
DUNS #
006046700
City
Bloomington
State
IN
Country
United States
Zip Code
47401