The phenomenon of de novo gene birth may underlie what makes each species unique, yet it remains poorly understood. We have recently found evidence that regions of the genome thought to be junk DNA can be translated, providing an evolutionary reservoir of ?proto-genes? that promote de novo gene birth. This proposal aims at characterizing the mechanisms and dynamics of proto-gene evolution by investigating three complementary angles: 1) How do proto-genes promote adaptation? To answer this question, we will overexpress proto-genes and assorted control sequences in yeast and dissect their impact on cellular fitness across multiple environmental conditions. 2) Is the proto-gene model universal? To answer this question, we will perform a computational reconstruction of the natural history of de novo gene birth in mammals, insects, malaria and fungi though the design and implementation of novel dating algorithms. This will enable us to evaluate which features that characterize these distinct lineages, such as genome size for example, influence the frequency of proto-gene evolution. 2) How do genomic sequences exit the non-genic state? It is unclear whether a proto-gene is more likely to emerge from a non-genic sequence following mutations emulating a novel promoter structure, or an open reading frame. To assess the feasibility of these competing mechanisms, we will construct yeast mutants where a gene has been synthetically killed by destroying either is open reading frame or its promoter. We will then evolve these mutants under a variety of selective pressures and observe if one mechanism is more successful than the other.

Public Health Relevance

This project investigates the mechanisms through which novel proteins evolve in nature. This research is expected to lead to a better understanding of how species get to look and behave so differently from each other. It should also prove relevant to public health issues involving adaptation processes, such as the arms race between hosts and virulent pathogens or the rapid evolution of cancer cells.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Transition Award (R00)
Project #
4R00GM108865-03
Application #
9460085
Study Section
Special Emphasis Panel (NSS)
Program Officer
Janes, Daniel E
Project Start
2014-05-01
Project End
2020-02-29
Budget Start
2017-04-15
Budget End
2018-02-28
Support Year
3
Fiscal Year
2017
Total Cost
$249,000
Indirect Cost
$88,355
Name
University of Pittsburgh
Department
Biology
Type
Schools of Medicine
DUNS #
004514360
City
Pittsburgh
State
PA
Country
United States
Zip Code
15213
Ernst, Peter B; Carvunis, Anne-Ruxandra (2018) Of mice, men and immunity: a case for evolutionary systems biology. Nat Immunol 19:421-425
Domazet-Lošo, Tomislav; Carvunis, Anne-Ruxandra; Albà, M Mar et al. (2017) No Evidence for Phylostratigraphic Bias Impacting Inferences on Patterns of Gene Emergence and Evolution. Mol Biol Evol 34:843-856
Carvunis, Anne-Ruxandra; Wang, Tina; Skola, Dylan et al. (2015) Evidence for a common evolutionary rate in metazoan transcriptional networks. Elife 4: