Hybrid incompatibility caused by an epiallele

Todd Blevins, Jing Wang, Frédéric Pontvianne , Craig Pikaard
Publication Date
April 2017
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Hybrid incompatibility resulting from deleterious gene combinations is thought to be an important step toward reproductive isolation and speciation. Here, we demonstrate involvement of a silent epiallele in hybrid incompatibility. In Arabidopsis thaliana accession Cvi-0, one of the two copies of a duplicated histidine biosynthesis gene, HISN6A, is mutated, making HISN6B essential. In contrast, in accession Col-0, HISN6A is essential because HISN6B is not expressed. Owing to these differences, Cvi-0 × Col-0 hybrid progeny that are homozygous for both Cvi-0 HISN6A and Col-0 HISN6B do not survive. We show that HISN6B of Col-0 is not a defective pseudogene, but a stably silenced epiallele. Mutating HISTONE DEACETYLASE 6 (HDA6), or the cytosine methyltransferase genes MET1 or CMT3, erases HISN6B's silent locus identity, reanimating the gene to circumvent hisn6a lethality and hybrid incompatibility. These results show that HISN6-dependent hybrid lethality is a revertible epigenetic phenomenon and provide additional evidence that epigenetic variation has the potential to limit gene flow between diverging populations of a species.


Todd Blevins, Jing Wang, Frédéric Pontvianne and Craig S. Pikaard (2017). Hybrid incompatibility caused by an epiallele. Proc. Natl. Acad. Sci. 114:3702-3707

            **This paper was highlighted in a perspectives article:  Bente, H. and O. Mittelsten-Scheid (2017). Epigenetic contribution to diversification. Proc.  Natl. Acad. Sci. 114:3558-3560