Characterization of phosphorus-regulated miR399 and miR827 and their isomirs in barley under phosphorus-sufficient and phosphorus-deficient conditions

被引:91
作者
Hackenberg, Michael [1 ]
Shi, Bu-Jun [2 ]
Gustafson, Perry [3 ]
Langridge, Peter [2 ]
机构
[1] Univ Granada, Dept Genet, Computat Genom & Bioinformat Grp, E-18071 Granada, Spain
[2] Univ Adelaide, Australian Ctr Plant Funct Genom, Urrbrae, SA 5064, Australia
[3] Univ Missouri, USDA ARS, Columbia, MO 65211 USA
基金
澳大利亚研究理事会;
关键词
Barley; Phosphorus; miR399; miR827; Isomir; Antisense; Targets; Differential expression; SMALL RNAS; PHOSPHATE TRANSPORTERS; KINETIC-PROPERTIES; MATURE MICRORNAS; SIRNA BIOGENESIS; IDENTIFICATION; ARABIDOPSIS; GENE; TRANSCRIPTION; HOMEOSTASIS;
D O I
10.1186/1471-2229-13-214
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Background: miR399 and miR827 are both involved in conserved phosphorus (P) deficiency signalling pathways. miR399 targets the PHO2 gene encoding E2 enzyme that negatively regulates phosphate uptake and root-to-shoot allocation, while miR827 targets SPX-domain-containing genes that negatively regulate other P-responsive genes. However, the response of miR399 and miR827 to P conditions in barley has not been investigated. Results: In this study, we investigated the expression profiles of miR399 and miR827 in barley (Hordeum vulagre L.) under P-deficient and P-sufficient conditions. We identified 10 members of the miR399 family and one miR827 gene in barley, all of which were significantly up-regulated under deficient P. In addition, we found many isomirs of the miR399 family and miR827, most of which were also significantly up-regulated under deficient P. Several isomirs of miR399 members were found to be able to cleave their predicted targets in vivo. Surprisingly, a few small RNAs (sRNAs) derived from the single-stranded loops of the hairpin structures of MIR399b and MIR399e-1 were also found to be able to cleave their predicted targets in vivo. Many antisense sRNAs of miR399 and a few for miR827 were also detected, but they did not seem to be regulated by P. Intriguingly, the lowest expressed member, hvu-miR399k, had four-fold more antisense sRNAs than sense sRNAs, and furthermore under P sufficiency, the antisense sRNAs are more frequent than the sense sRNAs. We identified a potential regulatory network among miR399, its target HvPHO2 and target mimics HvIPS1 and HvIPS2 in barley under P-deficient and P-sufficient conditions. Conclusions: Our data provide an important insight into the mechanistic regulation and function of miR399, miR827 and their isomirs in barley under different P conditions.
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页数:17
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