Literature DB >> 34533872

Relaxed selection on male mitochondrial genes in DUI bivalves eases the need for mitonuclear coevolution.

Gerald P Maeda1, Mariangela Iannello2, Hunter J McConie1, Fabrizio Ghiselli2, Justin C Havird1.   

Abstract

Mitonuclear coevolution is an important prerequisite for efficient energy production in eukaryotes. However, many bivalve taxa experience doubly uniparental inheritance (DUI) and have sex-specific mitochondrial (mt) genomes, providing a challenge for mitonuclear coevolution. We examined possible mechanisms to reconcile mitonuclear coevolution with DUI. No nuclear-encoded, sex-specific OXPHOS paralogs were found in the DUI clam Ruditapes philippinarum, refuting OXPHOS paralogy as a solution in this species. It is also unlikely that mt changes causing disruption of nuclear interactions are strongly selected against because sex-specific mt-residues or those under positive selection in M mt genes were not depleted for contacting nuclear-encoded residues. However, M genomes showed consistently higher dN /dS ratios compared to putatively ancestral F genomes in all mt OXPHOS genes and across all DUI species. Further analyses indicated that this was consistently due to relaxed, not positive selection on M vs. F mt OXPHOS genes. Similarly, selection was relaxed on the F genome of DUI species compared to species with strict maternal inheritance. Coupled with recent physiological and molecular evolution studies, we suggest that relaxed selection on M mt function limits the need to maintain mitonuclear interactions in M genomes compared to F genomes. We discuss our findings with regard to OXPHOS function and the origin of DUI.
© 2021 European Society for Evolutionary Biology.

Entities:  

Keywords:  ORFans; cytonuclear coevolution; cytonuclear interactions; mitochondrial respiration; mt-miRNAs; nuclear compensation; smithRNAs

Mesh:

Substances:

Year:  2021        PMID: 34533872      PMCID: PMC9090438          DOI: 10.1111/jeb.13931

Source DB:  PubMed          Journal:  J Evol Biol        ISSN: 1010-061X            Impact factor:   2.516


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