bioRxivPlant Biology
microRNA-triggered transposon small RNAs mediate genome dosage response
F. Borges, J.-S. Parent, F. van Ex, P. Wolff, G. Martinez, C. Kohler, R. A. Martienssen
Abstract
Chromosome dosage plays a significant role in reproductive isolation and speciation in both plants and animals, but underlying mechanisms are largely obscure1. Transposable elements can promote hybridity through maternal small RNA2, and have been postulated to regulate dosage response via neighboring imprinted genes3,4. Here, we show that a highly conserved microRNA in plants, miR845, targets the tRNAMet primer-binding site (PBS) of LTR-retrotransposons in Arabidopsis pollen, and triggers the accumulation of 21 to 22-nucleotide small RNA in a dose dependent fashion via RNA polymerase IV. We show that these epigenetically activated small-interfering RNAs (easiRNAs) mediate hybridization barriers between diploid seed parents and tetraploid pollen parents (\"the triploid block\"), and that natural variation for miR845 may account for \"endosperm balance\" allowing formation of triploid seeds. Targeting the PBS with small RNA is a common mechanism for transposon control in mammals and plants, and provides a uniquely sensitive means to monitor chromosome dosage and imprinting in the developing seed.
- organism: Arabidopsis
- assay: ChIP-seq
- assay: spatial transcriptomics
- research focus: chromatin & epigenetic regulation
- research focus: cell type annotation
- research focus: gene regulatory network inference
- approach: experimental assay
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