Maintenance ofthe adult male germline is essential for reproduction. Still a poorly understood process, germline stem cell self-renewal appears to be influenced by epigenetic chromatin modifications and subsequent nuclear organization. This proposal is designed to increase our understanding of these epigenetic regulatory processes. We hypothesize that histone modification and associated nuclear protein composition, including transcriptional repressor complexes and chromatin remodeling factors, are important determinants in whether stem cells self-renew or differentiate. Using mouse spermatogonia as a model, we will address the regulation of stem cell self-renewal in two specific aims.
The first aim will examine the role of Polycomb group proteins on gene silencing in self-renewing spermatogonia. To achieve this aim, two distinct spermatogonial populations will be separated by fluorescence-activated cell sorting (FACS) and analyzed by transcriptional profiling. Potential Polycomb group binding sites will then be identified by chromatin immunoprecipitation. Loss-of-function effects will be examined by one of two methods: generation of conditional knockout mice or RNAi knockdown and transplantation of cultured spermatogonial stem cells into recipient testes.
The second aim will examine the role of nuclear matrix proteins in the maintenance of selfrenewing spermatogonia. Proteomic profiling will be performed after fractionating nuclear matrix proteins from FACS-sorted germ cells and identifying their composition by liquid chromatography-mass spectrometry. Generation of conditional knockout mice or RNAi and transplantation experiments will then be performed to assess the functional importance of matrix-associated proteins. The proposed research for this award is designed to encompass both the mentored phase (K99) and the independent phase (ROO), with a transition period built into the plan to successfully bridge the two phases. This project is now poised to enter the ROO phase, extending the progress made during the K99 phase and achieving the major aspects of both specific aims.

Public Health Relevance

This research will greatly contribute to the emerging field of regenerative medicine. Recent reports of pluripotent embryonic stem cell-like colonies emanating from cultured male germline stem cells warrant further study into the epigenetic control of stem cells in the testis. Deficiencies in histone modifications have also been linked to infertility, while altered nuclear matrix proteins have been implicated in cancer.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Research Transition Award (R00)
Project #
5R00HD055330-05
Application #
8197721
Study Section
Special Emphasis Panel (NSS)
Program Officer
Moss, Stuart B
Project Start
2010-01-01
Project End
2013-12-31
Budget Start
2012-01-01
Budget End
2013-12-31
Support Year
5
Fiscal Year
2012
Total Cost
$246,512
Indirect Cost
$78,817
Name
Children's Memorial Hospital (Chicago)
Department
Type
DUNS #
074438755
City
Chicago
State
IL
Country
United States
Zip Code
60611
Huszar, Jessica M; Payne, Christopher J (2014) MIR146A inhibits JMJD3 expression and osteogenic differentiation in human mesenchymal stem cells. FEBS Lett 588:1850-6
Gallagher, Shannon J; Kofman, Amber E; Huszar, Jessica M et al. (2013) Distinct requirements for Sin3a in perinatal male gonocytes and differentiating spermatogonia. Dev Biol 373:83-94
Kofman, Amber E; Huszar, Jessica M; Payne, Christopher J (2013) Transcriptional analysis of histone deacetylase family members reveal similarities between differentiating and aging spermatogonial stem cells. Stem Cell Rev 9:59-64
Kofman, Amber E; McGraw, Margeaux R; Payne, Christopher J (2012) Rapamycin increases oxidative stress response gene expression in adult stem cells. Aging (Albany NY) 4:279-89
Payne, Christopher J; Gallagher, Shannon J; Foreman, Oded et al. (2010) Sin3a is required by sertoli cells to establish a niche for undifferentiated spermatogonia, germ cell tumors, and spermatid elongation. Stem Cells 28:1424-34