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A bird-like genome from a frog: Mechanisms of genome size reduction in the ornate burrowing frog, . | LitMetric

A bird-like genome from a frog: Mechanisms of genome size reduction in the ornate burrowing frog, .

Proc Natl Acad Sci U S A

Institute for Applied Ecology, Faculty of Science and Technology, University of Canberra, Canberra, ACT, Australia 2617

Published: March 2021

AI Article Synopsis

Article Abstract

The diversity of genome sizes across the tree of life is of key interest in evolutionary biology. Various correlates of variation in genome size, such as accumulation of transposable elements (TEs) or rate of DNA gain and loss, are well known, but the underlying molecular mechanisms driving or constraining genome size are poorly understood. Here, we study one of the smallest genomes among frogs characterized thus far, that of the ornate burrowing frog () from Australia, and compare it to other published frog and vertebrate genomes to examine the forces driving reduction in genome size. At ∼1.06 gigabases (Gb), the genome is like that of birds, revealing four major mechanisms underlying TE dynamics: reduced abundance of all major classes of TEs; increased net deletion bias in TEs; drastic reduction in intron lengths; and expansion via gene duplication of the repertoire of TE-suppressing Piwi genes, accompanied by increased expression of Piwi-interacting RNA (piRNA)-based TE-silencing pathway genes in germline cells. Transcriptomes from multiple tissues in both sexes corroborate these results and provide insight into sex-differentiation pathways in Genome skimming of two closely related frog species ( and ) confirms a reduction in TEs as a major driver of genome reduction in and supports a macroevolutionary scenario of small genome size in frogs driven by convergence in life history, especially rapid tadpole development and tadpole diet. The genome offers a model for future comparative studies on mechanisms of genome size reduction in amphibians and vertebrates generally.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7980411PMC
http://dx.doi.org/10.1073/pnas.2011649118DOI Listing

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