New species form when diverging populations become reproductively isolated. One cause of this isolation is hybrid incompatibility, the sterilit and lethality of interspecific hybrids. This proposal investigates two previously identified genes that interact to cause lethality in hybrids between the fruit fly species Drosophila melanogaster and D. simulans. Sequence analysis of both genes shows that they have evolved under adaptive evolution, a pattern also observed with other hybrid incompatibility genes. Identifying the specific selective forces causing this pattern of molecular evolution will therefore help elucidate the biological causes of speciation. This proposal is based on the recent discovery that these Drosophila hybrid incompatibility genes are required to repress transposable elements, selfish DNAs that can mobilize, reach high copy number, and cause significant damage to eukaryotic genomes. A range of genetic and molecular assays are proposed here to identify how these genes function in repressing transposable elements, including profiling the genome-wide pattern of transposition in mutant lines. Other phenotypic assays will investigate how these genes affect fertility and meiotic performance within their own host species. Attention will then turn to an integrated effort to determine how sequence divergence and adaptive evolution between species has altered specific functions of these genes. Transposable elements are a major cause of spontaneous mutation and DNA damage in eukaryotes including humans. The proposed studies will provide a high resolution view of how transposable element load contributes to host gene evolution and reproductive isolation between species.

Public Health Relevance

The genomes of humans and other animals are littered with parasitic DNAs that can cause havoc when they become unregulated. Many animal genes are dedicated to regulating these parasitic DNAs, and as these genes change they can contribute to the formation of new species. This process can be studied in great detail using experimental genetic approaches in fruit flies.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM074737-11
Application #
8974421
Study Section
Genetic Variation and Evolution Study Section (GVE)
Program Officer
Janes, Daniel E
Project Start
2005-09-01
Project End
2017-11-30
Budget Start
2015-12-01
Budget End
2016-11-30
Support Year
11
Fiscal Year
2016
Total Cost
Indirect Cost
Name
Cornell University
Department
Biochemistry
Type
Schools of Arts and Sciences
DUNS #
872612445
City
Ithaca
State
NY
Country
United States
Zip Code
14850
Wei, Kevin H-C; Lower, Sarah E; Caldas, Ian V et al. (2018) Variable Rates of Simple Satellite Gains across the Drosophila Phylogeny. Mol Biol Evol 35:925-941
Ulmschneider, Martin B; Ulmschneider, Jakob P; Freites, J Alfredo et al. (2017) Transmembrane helices containing a charged arginine are thermodynamically stable. Eur Biophys J 46:627-637
Blum, Jacob A; Bonaccorsi, Silvia; Marzullo, Marta et al. (2017) The Hybrid Incompatibility Genes Lhr and Hmr Are Required for Sister Chromatid Detachment During Anaphase but Not for Centromere Function. Genetics 207:1457-1472
Wei, Kevin H-C; Reddy, Hemakumar M; Rathnam, Chandramouli et al. (2017) A Pooled Sequencing Approach Identifies a Candidate Meiotic Driver in Drosophila. Genetics 206:451-465
Dion-Côté, Anne-Marie; Barbash, Daniel A (2017) Beyond speciation genes: an overview of genome stability in evolution and speciation. Curr Opin Genet Dev 47:17-23
Wei, Kevin H-C; Barbash, Daniel A (2015) Never settling down: frequent changes in sex chromosomes. PLoS Biol 13:e1002077
Gilliland, William D; Colwell, Eileen M; Osiecki, David M et al. (2015) Normal segregation of a foreign-species chromosome during Drosophila female meiosis despite extensive heterochromatin divergence. Genetics 199:73-83
Wei, Kevin H-C; Grenier, Jennifer K; Barbash, Daniel A et al. (2014) Correlated variation and population differentiation in satellite DNA abundance among lines of Drosophila melanogaster. Proc Natl Acad Sci U S A 111:18793-8
Cuykendall, Tawny N; Satyaki, P; Ji, Shuqing et al. (2014) A screen for F1 hybrid male rescue reveals no major-effect hybrid lethality loci in the Drosophila melanogaster autosomal genome. G3 (Bethesda) 4:2451-60
Ferree, Patrick M; Gomez, Karina; Rominger, Peter et al. (2014) Heterochromatin position effects on circularized sex chromosomes cause filicidal embryonic lethality in Drosophila melanogaster. Genetics 196:1001-5

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