| Literature DB >> 33793935 |
Parth Patel1, Sandra M Mathioni2, Reza Hammond1, Alex E Harkess2, Atul Kakrana1, Siwaret Arikit3, Ayush Dusia4, Blake C Meyers1,2,5.
Abstract
In monocots other than maize (Zea mays) and rice (Oryza sativa), the repertoire and diversity of microRNAs (miRNAs) and the populations of phased, secondary, small interfering RNAs (phasiRNAs) are poorly characterized. To remedy this, we sequenced small RNAs (sRNA) from vegetative and dissected inflorescence tissue in 28 phylogenetically diverse monocots and from several early-diverging angiosperm lineages, as well as publicly available data from 10 additional monocot species. We annotated miRNAs, small interfering RNAs (siRNAs) and phasiRNAs across the monocot phylogeny, identifying miRNAs apparently lost or gained in the grasses relative to other monocot families, as well as a number of transfer RNA fragments misannotated as miRNAs. Using our miRNA database cleaned of these misannotations, we identified conservation at the 8th, 9th, 19th, and 3'-end positions that we hypothesize are signatures of selection for processing, targeting, or Argonaute sorting. We show that 21-nucleotide (nt) reproductive phasiRNAs are far more numerous in grass genomes than other monocots. Based on sequenced monocot genomes and transcriptomes, DICER-LIKE5, important to 24-nt phasiRNA biogenesis, likely originated via gene duplication before the diversification of the grasses. This curated database of phylogenetically diverse monocot miRNAs, siRNAs, and phasiRNAs represents a large collection of data that should facilitate continued exploration of sRNA diversification in flowering plants. © American Society of Plant Biologists 2021. All rights reserved. For permissions, please email: journals.permissions@oup.com.Entities:
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Year: 2021 PMID: 33793935 PMCID: PMC8133688 DOI: 10.1093/plphys/kiab001
Source DB: PubMed Journal: Plant Physiol ISSN: 0032-0889 Impact factor: 8.340