Abstract
Reproductive isolation and speciation are driven by the convergence of environmental and genetic variation. The integration of these variation sources is thought to occur through epigenetic marks including DNA methylation. Proteins containing a methyl-CpG-binding domain (MBD) bind methylated DNA and interpret epigenetic marks, providing a dynamic yet evolutionarily adapted cellular output. Here, we report the Drosophila MBD-containing proteins, dMBD-R2 and dMBD2/3, contribute to reproductive isolation and survival behavioral strategies. Drosophila melanogaster males with a reduction in dMBD-R2 specifically in octopamine (OA) neurons exhibit courtship toward divergent interspecies D. virilis and D. yakuba females and a decrease in conspecific mating success. Conspecific male-male courtship is increased between dMBD-R2-deficient males while aggression is reduced. These changes in adaptive behavior are separable as males with a hypermethylated OA neuronal genome exhibited a decrease in aggression without altering male-male courtship. These results suggest Drosophila MBD-containing proteins are required within the OA neural circuitry to inhibit interspecies and conspecific male-male courtship and indicate that the genetically hard-wired neural mechanisms enforcing behavioral reproductive isolation include the interpretation of the epigenome.
| Original language | English |
|---|---|
| Article number | 5420 |
| Journal | Scientific Reports |
| Volume | 7 |
| Issue number | 1 |
| DOIs | |
| State | Published - Dec 1 2017 |
Funding
The authors thank Frank Lyko for kindly providing the UAS-Dnmt3a line and the Bloomington Stock Center for Drosophila stocks. We thank Jessica Bailey for work on initial experiments and the University of Montana Molecular Histology and Fluorescence Imaging Core and Lou Herrit for technical expertise. The nc82 antibody was developed by Eric Buchner obtained from the Developmental Studies Hybridoma Bank developed under the auspices of the NICHD and maintained by the Department of Biology, University of Iowa (Iowa City, IA). The National Institutes of Health Center of Biomedical Research Excellence grant P20RR015583 and the University of Montana Research Grant Program to SJC supported this work.
| Funders | Funder number |
|---|---|
| P20RR015583 | |
| University of Iowa | |
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