AUTHOR=Karageorgiou Charikleia , Tarrío Rosa , Rodríguez-Trelles Francisco 

TITLE=The Cyclically Seasonal Drosophila subobscura Inversion O7 Originated From Fragile Genomic Sites and Relocated Immunity and Metabolic Genes

JOURNAL=Frontiers in Genetics

VOLUME=11

YEAR=2020

URL=https://www.frontiersin.org/journals/genetics/articles/10.3389/fgene.2020.565836

DOI=10.3389/fgene.2020.565836

ISSN=1664-8021

ABSTRACT=<p>Chromosome inversions are important contributors to standing genetic variation in <italic>Drosophila subobscura</italic>. Presently, the species is experiencing a rapid replacement of high-latitude by low-latitude inversions associated with global warming. Yet not all low-latitude inversions are correlated with the ongoing warming trend. This is particularly unexpected in the case of O<sub>7</sub> because it shows a regular seasonal cycle that peaks in summer and rose with a heatwave. The inconsistent behavior of O<sub>7</sub> across components of the ambient temperature suggests that is causally more complex than simply due to temperature alone. In order to understand the dynamics of O<sub>7</sub>, high-quality genomic data are needed to determine both the breakpoints and the genetic content. To fill this gap, here we generated a PacBio long read-based chromosome-scale genome assembly, from a highly homozygous line made isogenic for an O<underline><sub>3</sub><sub>+</sub><sub>4</sub></underline><sub>+</sub><sub>7</sub> chromosome. Then we isolated the complete continuous sequence of O<sub>7</sub> by conserved synteny analysis with the available reference genome. Main findings include the following: (i) the assembled O<sub>7</sub> inversion stretches 9.936 Mb, containing &gt; 1,000 annotated genes; (ii) O<sub>7</sub> had a complex origin, involving multiple breaks associated with non-B DNA-forming motifs, formation of a microinversion, and ectopic repair in <italic>trans</italic> with the two homologous chromosomes; (iii) the O<sub>7</sub> breakpoints carry a pre-inversion record of fragility, including a sequence insertion, and transposition with later inverted duplication of an <italic>Attacin</italic> immunity gene; and (iv) the O<sub>7</sub> inversion relocated the major insulin signaling <italic>forkhead box subgroup O</italic> (<italic>foxo</italic>) gene in tight linkage with its antagonistic regulatory partner <italic>serine/threonine–protein kinase B</italic> (<italic>Akt1</italic>) and disrupted concerted evolution of the two inverted <italic>Attacin</italic> duplicates, reattaching them to dFOXO metabolic enhancers. Our findings suggest that O<sub>7</sub> exerts antagonistic pleiotropic effects on reproduction and immunity, setting a framework to understand its relationship with climate change. Furthermore, they are relevant for fragility in genome rearrangement evolution and for current views on the contribution of breakage versus repair in shaping inversion-breakpoint junctions.</p>