A novel computational approach to the silencing of Sugarcane Bacilliform Guadeloupe A Virus determines potential host-derived MicroRNAs in sugarcane (Saccharum officinarum L.)

Institute of Tropical Bioscience and Biotechnology, Chinese Academy of Tropical Agricultural Sciences, Haikou, Hainan, China
Haikou Experimental Station, Chinese Academy of Tropical Agricultural Sciences, Haikou, Hainan, China
Department of Plant Breeding and Genetics, University College of Agriculture and Environmental Sciences, The Islamia University of Bahawalpur, Baghdad-Ul-Jadeed Campus, Bahawalpur, South Punjab, Pakistan
Zhanjiang Experimental Station, Chinese Academy of Tropical Agricultural Sciences, Zhanjiang, Guandong, China
DOI
10.7287/peerj.preprints.27842v1
Subject Areas
Biotechnology, Computational Biology, Virology
Keywords
Computational algorithms, R language, miRNA, Saccharum officinarum, Sugarcane Bacilliform Guadeloupe A Virus, Target prediction
Copyright
© 2019 Ashraf et al.
Licence
This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ Preprints) and either DOI or URL of the article must be cited.
Cite this article
Ashraf F, Ashraf MA, Hu X, Zhang S. 2019. A novel computational approach to the silencing of Sugarcane Bacilliform Guadeloupe A Virus determines potential host-derived MicroRNAs in sugarcane (Saccharum officinarum L.) PeerJ Preprints 7:e27842v1

Abstract

Sugarcane Bacilliform Guadeloupe A Virus (SCBGAV, genus Badnavirus, family Caulimoviridae) is an emerging, deleterious pathogen of sugarcane which presents a substantial barrier to producing high sugarcane earnings. The circular, double-stranded (ds) DNA genome of SCBGAV (7.4 Kb) is composed of three open reading frames (ORF) that replicate by a reverse transcriptase. In the current study, we used miRNA target prediction algorithms to identify and comprehensively analyze the genome-wide sugarcane (Saccharum officinarum L.)-encoded microRNA (miRNA) targets against the SCBGAV. A total of 28 potential mature target miRNAs were retrieved from the miRBase database and were further analyzed for hybridization to the SCBGAV genome. Multiple computational approaches—including miRNA-target seed pairing, multiple target positions, minimum free energy, target site accessibility, maximum complementarity, pattern recognition and minimum folding energy for attachments— were considered by all algorithms. Only 4 sugarcane miRNAs are selected for SCBGAV silencing. Among those 4, sof-miR396 was identified as the top effective candidate, capable of targeting the vital ORF3 which encodes polyprotein of the SCBGAV genome. miRanda, RNA22 and RNAhybrid algorithms predicted hybridization of sof-miR396 at common locus position 3394. A Circos plot was created to study the network visualization of sugarcane-encoded miRNAs with SCBGAV genes determines detailed evidence for any ideal targets of SCBGAV ORFs by precise miRNAs. The present study concludes a comprehensive report towards the creation of SCBGAV-resistant sugarcane through the expression analysis of the identified miRNAs.

Author Comment

This is a submission to PeerJ for review.

Supplemental Information

Computational prediction of Sugarcane-encoded MicroRNAs in the Genome of SCBGAV

Computational prediction of Sugarcane-encoded MicroRNAs in the Genome of SCBGAV using all algorithms.

DOI: 10.7287/peerj.preprints.27842v1/supp-1

SCBGAV Gene position table.1

Sugarcane-encoded miRNA target sites locus position in each gene of SCBGAV.

DOI: 10.7287/peerj.preprints.27842v1/supp-2

Identification of Common miRNAs

Consensus Sugarcane-encoded miRNA were selected by all algorithms.

DOI: 10.7287/peerj.preprints.27842v1/supp-3

Sugarcane-encoded miRNAs in the SCBGAV genome

Sugarcane-encoded miRNAs with SCBGAV genomic positions predicted by all algorithms.

DOI: 10.7287/peerj.preprints.27842v1/supp-4