Covalent post-translational modifications (PTMs) of histone proteins are widely believed to facilitate epigenetic inheritance of gene expression information from one cell generation to the next. However, this premise has not been directly tested in animals, limiting our understanding of the contribution of PTMs to complex molecular or developmental processes that underlie human disease. To interrogate this relationship, we have developed a genetic strategy in Drosophila melanogaster for replacement of the endogenous histone gene cluster with an engineered multigene array of the five core histone subunits with specific mutations in modifiable residues. Methylation of lysine 36 in the histone H3 subunit (H3K36) is a transcription-linked PTM that has well- characterized roles in suppression of cryptic initiation and regulation of alternative splicing, making it an attractive choice for study using our system.
We aim to use H3K36 mutant models to evaluate the contribution of H3K36 methylation to proper proliferation and development. Additionally, we aim to directly test the molecular requirement for H3K36 methylation in proper regulation of global gene expression and alternative splicing, and to correlate molecular role with observed cellular and developmental phenotypes. These studies will be the first to directly test the interplay between molecular mechanisms in which H3K36 methylation takes a part and cellular and developmental processes that are relevant to disease.

Public Health Relevance

Covalent modifications to histone proteins are thought to regulate gene expression for the purposes of development, cell proliferation and cell fate through epigenetic inheritance of information not encoded in DNA, but the effects of eliminating histone modifications have never been unambiguously tested in a model organism that is highly relevant to human disease. To remedy this, we have built a genetic system in the Drosophila melanogaster model organism that is optimized to test the epigenetic contributions of histone proteins and their modifications to gene expression and disease phenotypes. We propose to use our system to study how epigenetic inheritance of specific histone modifications affects complex processes in metazoans, including development, proliferation/differentiation decisions and alternative splicing, and to use that information to improve insights into disease mechanisms in which histone modifications play a role.

Agency
National Institute of Health (NIH)
Type
Predoctoral Individual National Research Service Award (F31)
Project #
1F31CA177088-01A1
Application #
8649283
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Korczak, Jeannette F
Project Start
Project End
Budget Start
Budget End
Support Year
1
Fiscal Year
2014
Total Cost
Indirect Cost
Name
University of North Carolina Chapel Hill
Department
Genetics
Type
Schools of Medicine
DUNS #
City
Chapel Hill
State
NC
Country
United States
Zip Code
27599