The proposal entitled 'Elucidating the essential role of the evolutionarily conserved IME4 mRNA methyltransferase in metazoan development' is in response to PAR 12-006 Academic Research Enhancement Award (Parent R15). The objective of this project is to elucidate the mechanism by which IME4 affects metazoan development, generating data for rational design to investigate its function in mammalian systems in the context of evolutionary conservation. IME4 (Inducer of Meiosis #4, first identified in budding yeast), is an N6methyltransferase of adenosine residues in messenger RNA without altering the genetic code, i.e., it is a non-editing RNA modification. IME4 is evolutionarily conserved from budding yeast to human beings, yet its biological role remains elusive. Recent publications have mapped the mRNA methylome in mice and human cells showing overlapping categories of this enzyme's putative targets, highlighting its evolutionarily conserved role. However, in vivo whole-organism studies of the biological role of this enzyme are lacking. My previous work in S. cerevisiae showed that this enzyme is key in budding yeast's decision to become a gamete. It appears that IME4's role in yeast is exclusively during meiosis and it is not an essential gene for asexual life. However, in higher organisms where it has been studied, IME4 is an essential gene. In D.melanogaster, our published and preliminary data show it is required for embryo and larval development with important roles later in adult reproduction. Given its high degree of evolutionary conservation, we hypothesize that IME4 is required for essential functions in higher vertebrates, including humans. To test this hypothesis, we will employ biochemical (protein interactions), genetic, and cell biology (microscopy) approaches in D.melanogaster and D. rerio, two evolutionarily distant metazoan species, an invertebrate and a vertebrate respectively, predicting a high degree of functional conservation common to both that will be likely conserved in mammals. Approaches and techniques will provide excellent venues to train students in developing critical thinking skills and gain first-hand experience in the design and technology involved in biological experimentation. This project will generate important data that will impact the field of RNA modifications in developmental biology.

Public Health Relevance

The proposed research entitled 'Elucidating the essential role of the evolutionarily conserved IME4 mRNA methyltransferase in metazoan development' is in response to PAR 12-006 Academic Research Enhancement Award (Parent R15). The objective of this project is to elucidate the mechanism by which IME4, an evolutionarily conserved enzyme that modifies gene transcripts, affects animal development, thus generating data that will facilitate its investigation in higher vertebrates, including humans. To accomplish this goal, the proposed study employs biochemical (protein interactions), genetic (gene ablation effects), and cell biology (microscopic observations) approaches to analyze IME4 in both fruit flies (D.melanogaster ) and zebrafish (D. rerio), two evolutionarily distant species. The specific aims will yield a comprehensive functional characterization of this enzyme in the context of whole organisms, and data generated will be interpreted in the context of each model organism individually and in comparison, to highlight the species-specific versus the evolutionarily conserved roles of IME4. Anticipated results from this project will generate important information that will impact the field of RNA modifications in developmental biology. The experimental approaches used will provide training opportunities to undergraduate and graduate students in molecular biology research techniques not available to them at Clarkson University, an institution that is not a major recipient of NIH support.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Academic Research Enhancement Awards (AREA) (R15)
Project #
1R15GM113180-01
Application #
8812310
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Bender, Michael T
Project Start
2015-07-01
Project End
2018-06-30
Budget Start
2015-07-01
Budget End
2018-06-30
Support Year
1
Fiscal Year
2015
Total Cost
Indirect Cost
Name
Clarkson University
Department
Biology
Type
Schools of Arts and Sciences
DUNS #
041590993
City
Potsdam
State
NY
Country
United States
Zip Code
13699