The long-term goal of the proposed work is to gain a better understanding of how gene expression is regulated during mammalian cell development. This proposal focuses on the study of mRNA, which can be regulated in many ways to provide multiple layers of gene expression control. In order for cells to progress through different stages of development, its mRNAs must undergo extensive stage-specific changes. Defects in mRNA regulation are the direct cause of many human diseases, thus a better understanding of how mRNAs are regulated is essential. Our plan is to isolate mouse cells that are in specific stages of development and perform comprehensive analyses to identify changes in mRNA regulation, understand the functional significance of these changes, and determine how these changes are controlled at the molecular level. To do so, we have developed a new approach to purify male mouse germ cells in each of the major stages of gametogenesis (the process by which sperm are generated). Combining this new cell isolation strategy with powerful genetic, biochemical, deep sequencing, and bioinformatic tools, we will be able to perform comprehensive, global analyses of multiple layers of mRNA-based gene control in wild type mice as well as mice lacking an essential protein necessary for proper RNA regulation. In doing so, we will gain important insights into mechanisms and functions of mRNA regulation in different stages of cell development in unprecedented molecular and cellular detail. As a result, this study will lead to an improved understanding of how gene expression is controlled through mRNA regulation during cell development, and has the potential to provide important new insights into human reproductive biology and the molecular mechanisms controlling fertility.

Public Health Relevance

Key to understanding how different cells develop is an improved understanding of how their genes are regulated. This study will investigate how genes are regulated during the development of male germ cells - the cells that develop into sperm. The information obtained in this study will improve our understanding of the fundamentals of how genes are controlled and also provide insights into human reproductive biology that have the potential to impact therapeutic strategies to assist reproduction as well as male contraception.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM107331-02
Application #
8728294
Study Section
Molecular Genetics A Study Section (MGA)
Program Officer
Bender, Michael T
Project Start
2013-09-01
Project End
2018-08-31
Budget Start
2014-09-01
Budget End
2015-08-31
Support Year
2
Fiscal Year
2014
Total Cost
Indirect Cost
Name
Case Western Reserve University
Department
Biochemistry
Type
Schools of Medicine
DUNS #
City
Cleveland
State
OH
Country
United States
Zip Code
44106
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Zagore, Leah L; Sweet, Thomas J; Hannigan, Molly M et al. (2018) DAZL Regulates Germ Cell Survival through a Network of PolyA-Proximal mRNA Interactions. Cell Rep 25:1225-1240.e6
Hannigan, Molly M; Zagore, Leah L; Licatalosi, Donny D (2017) Ptbp2 Controls an Alternative Splicing Network Required for Cell Communication during Spermatogenesis. Cell Rep 19:2598-2612
Licatalosi, Donny D (2016) Roles of RNA-binding Proteins and Post-transcriptional Regulation in Driving Male Germ Cell Development in the Mouse. Adv Exp Med Biol 907:123-51
Zagore, Leah L; Grabinski, Sarah E; Sweet, Thomas J et al. (2015) RNA Binding Protein Ptbp2 Is Essential for Male Germ Cell Development. Mol Cell Biol 35:4030-42
Sweet, Thomas J; Licatalosi, Donny D (2014) 3' end formation and regulation of eukaryotic mRNAs. Methods Mol Biol 1125:3-12