Adaptive evolution of an essential telomere protein restricts telomeric retrotransposons.

Abstract

Essential, conserved cellular processes depend not only on essential, strictly conserved proteins but also on essential proteins that evolve rapidly. To probe this poorly understood paradox, we exploited the rapidly evolving <i>Drosophila</i> telomere-binding protein, <i>cav</i>/HOAP, which protects chromosomes from lethal end-to-end fusions. We replaced the <i>D. melanogaster</i> HOAP with a highly diverged version from its close relative, <i>D. yakuba</i>. The <i>D</i>. <i>yakuba</i> HOAP ('HOAP[yak]') localizes to <i>D. melanogaster</i> telomeres and protects <i>D. melanogaster</i> chromosomes from fusions. However, HOAP[yak] fails to rescue a previously uncharacterized HOAP function: silencing of the specialized telomeric retrotransposons that, instead of telomerase, maintain chromosome length in <i>Drosophila.</i> Whole genome sequencing and cytogenetics of experimentally evolved populations revealed that HOAP[yak] triggers telomeric retrotransposon proliferation, resulting in aberrantly long telomeres. This evolution-generated, separation-of-function allele resolves the paradoxical observation that a fast-evolving essential gene directs an essential, strictly conserved function: telomeric retrotransposon containment, not end-protection, requires evolutionary innovation at HOAP.