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Matthias Platzer

Publications and source records attributed to Matthias Platzer.

2 recordsLinked to original sources

Convergent evolution of genes controlling mitonuclear balance in annual fishes

Complexes of the respiratory chain are formed in a complex process where nuclearly-and mitochondrially-encoded components are assembled and inserted into the inner mitochondrial membrane. The coordination of this process is named mitonuclear balance and experimental manipulations of mitonuclear balance can increase longevity of laboratory species.\n\nHere, we investigated the pattern of positive selection in annual (i.e. short-lived)and non-annual (i.e. long-lived) African killifishes to identify a genomic substrate for evolution of annual life history (and reduced lifespan).\n\nWe identified genes under positive selection in all mitonuclear balance: mitochondrial (mt) DNA replication, transcription from mt promoters, processing and stabilization of mt RNAs, mt translation, assembly of respiratory chain complexes and electron transport chain. Signs of convergent evolution are observed in four out of five steps. This strongly indicates that these genes are preferential genetic targets for the evolution of short lifespan and annual life cycle

Evolutionary Biology

MicroRNAs provide the first evidence of genetic link between diapause and aging in vertebrates

Diapause and aging are controlled by overlapping genetic mechanisms in C.elegans and these include microRNAs (miRNAs). Here, we investigated miRNA regulation in embryos of annual killifish that naturally undergo diapause to overcome desiccation of their habitats. We compared miRNA expression in diapausing and non-diapausing embryos in three independent lineages of killifish. We identified 13 miRNAs with similar regulation in all three lineages. One of these is miR-430, which is known as key regulator of early embryonic development in fish. We further tested whether this regulation overlaps with the aging-dependent regulation of miRNAs in one annual species: Nothobranchius furzeri. We found that miR-101a and miR-18a are regulated in the same direction during diapause and aging. These results provide the first evidence that overlapping genetic networks control diapause and aging in vertebrates and suggest that diapause mimics aging to some extent.

Genomics