The proper development of eggs and sperm is required for most animal reproduction. As such, primordial germ cell specification, the setting aside of the cells that give rise to eggs and sperm, is a crucial time in animal development for future reproductive success. In mice and humans, intercellular signals are required to induce germ cell differentiation during development, whereas flies and worms use a distinct, maternally-acquired mechanism to determine their germ cells. The long-term goal of this project is to understand the precise inductive signaling and molecular mechanisms that restrict the germ-cell inducing signals and to determine how these mechanisms contribute to the proper differentiation of the germ cell fate. Nodal signaling is required in both mice and sea stars to se up the developmental axes that restrict the potential to become germ cells. We hypothesize that Nodal signaling restricts the population of cells that can become germ cells. We will rigorously test this hypothesis by perturbing Nodal signaling and determining the precise molecular mechanisms that contribute to the negative accumulation of mRNAs for germ cell specification. In addition, we will define the morphogenetic cellular phenotypes required for the establishment of a germ cell specification niche and determine how Nodal signaling inhibits cells from taking on these morphogenetic cellular traits. These results will be complementary, and integrated into, models of mammalian germ cell induction, but the purpose of this research is to use an organism tractable for cellular and biochemical approaches. Insights into the precise molecular mechanisms that regulate the differentiation of the germ cell fate are crucial to identify novel genes involved in: the genetic basis of infertility, the induction of life-threatening teratomas, ad the proliferative abilities of cancers with upregulated germ-cell associated genes.

Public Health Relevance

Eggs and sperm are the only cells in the human body that retain the natural potential to give rise to the next generation. The proper development of primordial germ cells, the cells that give rise to eggs and sperm, is crucial for reproduction and when misregulated likely leads to sterility, the formation of life-threatening teratomas, and the proliferation of certain cancers. This project will elucidate novel signaling and molecular targets required for the proper development of germ cells.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Predoctoral Individual National Research Service Award (F31)
Project #
5F31GM112479-02
Application #
8911175
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Brown, Patrick
Project Start
2014-09-01
Project End
2017-08-31
Budget Start
2015-09-01
Budget End
2016-08-31
Support Year
2
Fiscal Year
2015
Total Cost
Indirect Cost
Name
Brown University
Department
Biochemistry
Type
Schools of Medicine
DUNS #
001785542
City
Providence
State
RI
Country
United States
Zip Code
Fresques, Tara M; Wessel, Gary M (2018) Nodal induces sequential restriction of germ cell factors during primordial germ cell specification. Development 145:
Fresques, Tara; Swartz, Steven Zachary; Juliano, Celina et al. (2016) The diversity of nanos expression in echinoderm embryos supports different mechanisms in germ cell specification. Evol Dev 18:267-78