Abstract

BackgroundIn plants, microRNAs (miRNAs) regulate gene expression mainly at the post-transcriptional level. Previous studies have demonstrated that miRNA-mediated gene silencing pathways play vital roles in plant development. Here, we used a high-throughput sequencing approach to characterize the miRNAs and their targeted transcripts in the leaf, flower and fruit of sweet orange.ResultsA total of 183 known miRNAs and 38 novel miRNAs were identified. An in-house script was used to identify all potential secondary siRNAs derived from miRNA-targeted transcripts using sRNA and degradome sequencing data. Genome mapping revealed that these miRNAs were evenly distributed across the genome with several small clusters, and 69 pre-miRNAs were co-localized with simple sequence repeats (SSRs). Noticeably, the loop size of pre-miR396c was influenced by the repeat number of CUU unit. The expression pattern of miRNAs among different tissues and developmental stages were further investigated by both qRT-PCR and RNA gel blotting. Interestingly, Csi-miR164 was highly expressed in fruit ripening stage, and was validated to target a NAC transcription factor. This study depicts a global picture of miRNAs and their target genes in the genome of sweet orange, and focused on the comparison among leaf, flower and fruit tissues.ConclusionsThis study provides a global view of miRNAs and their target genes in different tissue of sweet orange, and focused on the identification of miRNA involved in the regulation of fruit ripening. The results of this study lay a foundation for unraveling key regulators of orange fruit development and ripening on post-transcriptional level.Electronic supplementary materialThe online version of this article (doi:10.1186/1471-2164-15-695) contains supplementary material, which is available to authorized users.

Highlights

  • In plants, microRNAs regulate gene expression mainly at the post-transcriptional level

  • The duplex is separated by helicase and the mature Micro RNA (miRNA) is incorporated into an ARGONAUTE 1 (AGO1) protein to

  • The miRNA is incorporated into AGO1 which guides 5’ cleavage of the target, and RNA-dependent RNA polymerase 6 (RDR6) synthesizes a double-stranded RNA fragment that is subsequently cut into secondary siRNAs

Read more

Summary

Introduction

MicroRNAs (miRNAs) regulate gene expression mainly at the post-transcriptional level. The duplex is separated by helicase and the mature miRNA is incorporated into an ARGONAUTE 1 (AGO1) protein to Typically, miRNA-guided cleavage represses target gene expression; a group of 22 nt miRNAs trigger secondary siRNA biogenesis in plants [5]. DCL2 generates 22 nt miRNAs by processing perfect duplexes comprising a 22 nt miRNA and a 22 nt miRNA* The latter type of 22 nt miRNA may trigger secondary siRNA biogenesis. During this process, the miRNA is incorporated into AGO1 which guides 5’ cleavage of the target, and RNA-dependent RNA polymerase 6 (RDR6) synthesizes a double-stranded RNA fragment that is subsequently cut into secondary siRNAs. With the exception of the 24 nt secondary siRNAs (triggered by miR2775), most secondary siRNAs are 21 nt in length [5,6]. All of the secondary siRNAs described above may incorporate into AGOs and function as miRNAs [6,7]

Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call