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Merondun, J.

Publications and source records attributed to Merondun, J..

2 recordsLinked to original sources

The contribution of epigenetic variation to evolution in crows

Chromatin modifications provide a substrate for epigenetic variation with evolutionary potential. To quantify the contribution of this layer of variation to evolution we leveraged genome and methylome sequencing data from an incipient avian species: all-black carrion crows, grey-coated hooded crows and their hybrids. Combining controlled experimentation under common garden conditions and sampling of natural genetic variation across the hybrid zone we show that 5mC methylation variation was almost exclusively explained by genome properties and ontogenetic program of the organism. Evidence for an environmental contribution was minor, and all methylation variation of potential importance to speciation clustered in intergenic space within a genomic region of elevated genetic differentiation encoding the diagnostic color-contrast between taxa. We conclude that methylation variation may aid in phenotypic translation of genetic polymorphism, but provides little scope for an autonomous contribution to evolution in this system.

evolutionary biology↗

Epigenetic mechanisms of partial dosage compensation in an avian, female heterogametic system

The evolution of genetic sex determination is often accompanied by degradation of one of the proto sex chromosomes. Male heterogametic systems have evolved convergent, epigenetic mechanisms restoring the resulting imbalance in gene dosage between diploid autosomes (AA) and the hemizygous sex chromosome (X). Female heterogametic systems (AAf ZWf, AAm ZZm) tend to only show partial dosage compensation (0.5 < Zf:AAf < 1) and dosage balance (0.5<Zf:ZZm<1). The underlying mechanism remains largely elusive. Here, we quantified gene expression for a total of 15 male and female Eurasian crows (Corvus (corone) spp.) raised under common garden conditions. In addition, we characterized aspects of the regulatory landscape quantifying genome-wide ATAC-seq and 5mC methylation profiles. Partial dosage compensation was explained by female upregulation of Z-linked genes accompanied by increased chromatin accessibility on the female Z chromosome. 5mC methylation was strongly reduced in open chromatin-regions and GC islands and showed chromosome-, but no sex-specific variation. With the exception of the pseudo-autosomal region (PAR), female upregulation of gene expression was evenly spread across the Z chromosome without evidence for regional epigenetic regulation, as has for example been suggested for the male hypermethylated region (MHM) in chicken. Our results support the hypothesis that partial dosage compensation in female heterogametic systems is subject to chromosome-wide, epigenetic control mediated by differential chromatin accessibility between the sexes.

genomics↗