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Dynamic changes of small RNAs in rice spikelet development reveal specialized reproductive phasiRNA pathways

Dissection of the genetic pathways and mechanisms by which anther development occurs in grasses is crucial for both a basic understanding of plant development and for examining traits of agronomic importance such as male sterility. In rice, MULTIPLE SPOROCYTES1 (MSP1), a leucine-rich-repeat receptor...

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Autores principales: Fei, Qili, Yang, Li, Liang, Wanqi, Zhang, Dabing, Meyers, Blake C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5100018/
https://www.ncbi.nlm.nih.gov/pubmed/27702997
http://dx.doi.org/10.1093/jxb/erw361
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author Fei, Qili
Yang, Li
Liang, Wanqi
Zhang, Dabing
Meyers, Blake C.
author_facet Fei, Qili
Yang, Li
Liang, Wanqi
Zhang, Dabing
Meyers, Blake C.
author_sort Fei, Qili
collection PubMed
description Dissection of the genetic pathways and mechanisms by which anther development occurs in grasses is crucial for both a basic understanding of plant development and for examining traits of agronomic importance such as male sterility. In rice, MULTIPLE SPOROCYTES1 (MSP1), a leucine-rich-repeat receptor kinase, plays an important role in anther development by limiting the number of sporocytes. OsTDL1a (a TPD1-like gene in rice) encodes a small protein that acts as a cofactor of MSP1 in the same regulatory pathway. In this study, we analyzed small RNA and mRNA changes in different stages of spikelets from wild-type rice, and from msp1 and ostdl1a mutants. Analysis of the small RNA data identified miRNAs demonstrating differential abundances. miR2275 was depleted in the two rice mutants; this miRNA is specifically enriched in anthers and functions to trigger the production of 24-nt phased secondary siRNAs (phasiRNAs) from PHAS loci. We observed that the 24-nt phasiRNAs as well as their precursor PHAS mRNAs were also depleted in the two mutants. An analysis of co-expression identified three Argonaute-encoding genes (OsAGO1d, OsAGO2b, and OsAGO18) that accumulate transcripts coordinately with phasiRNAs, suggesting a functional relationship. By mRNA in situ analysis, we demonstrated a strong correlation between the spatiotemporal pattern of these OsAGO transcripts and phasiRNA accumulations.
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spelling pubmed-51000182016-11-10 Dynamic changes of small RNAs in rice spikelet development reveal specialized reproductive phasiRNA pathways Fei, Qili Yang, Li Liang, Wanqi Zhang, Dabing Meyers, Blake C. J Exp Bot Research Paper Dissection of the genetic pathways and mechanisms by which anther development occurs in grasses is crucial for both a basic understanding of plant development and for examining traits of agronomic importance such as male sterility. In rice, MULTIPLE SPOROCYTES1 (MSP1), a leucine-rich-repeat receptor kinase, plays an important role in anther development by limiting the number of sporocytes. OsTDL1a (a TPD1-like gene in rice) encodes a small protein that acts as a cofactor of MSP1 in the same regulatory pathway. In this study, we analyzed small RNA and mRNA changes in different stages of spikelets from wild-type rice, and from msp1 and ostdl1a mutants. Analysis of the small RNA data identified miRNAs demonstrating differential abundances. miR2275 was depleted in the two rice mutants; this miRNA is specifically enriched in anthers and functions to trigger the production of 24-nt phased secondary siRNAs (phasiRNAs) from PHAS loci. We observed that the 24-nt phasiRNAs as well as their precursor PHAS mRNAs were also depleted in the two mutants. An analysis of co-expression identified three Argonaute-encoding genes (OsAGO1d, OsAGO2b, and OsAGO18) that accumulate transcripts coordinately with phasiRNAs, suggesting a functional relationship. By mRNA in situ analysis, we demonstrated a strong correlation between the spatiotemporal pattern of these OsAGO transcripts and phasiRNA accumulations. Oxford University Press 2016-11 2016-10-04 /pmc/articles/PMC5100018/ /pubmed/27702997 http://dx.doi.org/10.1093/jxb/erw361 Text en © The Author 2016. Published by Oxford University Press on behalf of the Society for Experimental Biology. http://creativecommons.org/licenses/by/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Paper
Fei, Qili
Yang, Li
Liang, Wanqi
Zhang, Dabing
Meyers, Blake C.
Dynamic changes of small RNAs in rice spikelet development reveal specialized reproductive phasiRNA pathways
title Dynamic changes of small RNAs in rice spikelet development reveal specialized reproductive phasiRNA pathways
title_full Dynamic changes of small RNAs in rice spikelet development reveal specialized reproductive phasiRNA pathways
title_fullStr Dynamic changes of small RNAs in rice spikelet development reveal specialized reproductive phasiRNA pathways
title_full_unstemmed Dynamic changes of small RNAs in rice spikelet development reveal specialized reproductive phasiRNA pathways
title_short Dynamic changes of small RNAs in rice spikelet development reveal specialized reproductive phasiRNA pathways
title_sort dynamic changes of small rnas in rice spikelet development reveal specialized reproductive phasirna pathways
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5100018/
https://www.ncbi.nlm.nih.gov/pubmed/27702997
http://dx.doi.org/10.1093/jxb/erw361
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