Transposable element and host silencing activity in gigantic genomes
0301 basic medicine
Piwi-interacting RNA
QH301-705.5
Genome Evolution and Polyploidy in Plants
TE silencing
TE diversity
Plant Science
Gene
TE expression
Transposable element
Agricultural and Biological Sciences
Cell and Developmental Biology
Clustered Regularly Interspaced Short Palindromic Repeats and CRISPR-associated proteins
03 medical and health sciences
RNA interference
Biochemistry, Genetics and Molecular Biology
Genetics
Regulation of gene expression
Biology (General)
RNA Sequencing Data Analysis
Molecular Biology
Biology
Genome
piRNA pathway
Transposable Elements
Life Sciences
Gene silencing
Functional genomics
Genomics
salamander
genome size evolution
FOS: Biological sciences
RNA
DOI:
10.3389/fcell.2023.1124374
Publication Date:
2023-02-24T06:46:21Z
AUTHORS (10)
ABSTRACT
Transposable elements (TEs) and the silencing machinery of their hosts are engaged in a germline arms-race dynamic that shapes TE accumulation and, therefore, genome size. In animal species with extremely large genomes (>10 Gb), TE accumulation has been pushed to the extreme, prompting the question of whether TE silencing also deviates from typical conditions. To address this question, we characterize TE silencing via two pathways—the piRNA pathway and KRAB-ZFP transcriptional repression—in the male and female gonads of Ranodon sibiricus, a salamander species with a ∼21 Gb genome. We quantify 1) genomic TE diversity, 2) TE expression, and 3) small RNA expression and find a significant relationship between the expression of piRNAs and TEs they target for silencing in both ovaries and testes. We also quantified TE silencing pathway gene expression in R. sibiricus and 14 other vertebrates with genome sizes ranging from 1 to 130 Gb and find no association between pathway expression and genome size. Taken together, our results reveal that the gigantic R. sibiricus genome includes at least 19 putatively active TE superfamilies, all of which are targeted by the piRNA pathway in proportion to their expression levels, suggesting comprehensive piRNA-mediated silencing. Testes have higher TE expression than ovaries, suggesting that they may contribute more to the species’ high genomic TE load. We posit that apparently conflicting interpretations of TE silencing and genomic gigantism in the literature, as well as the absence of a correlation between TE silencing pathway gene expression and genome size, can be reconciled by considering whether the TE community or the host is currently “on the attack” in the arms race dynamic.
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CITATIONS (10)
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