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. 2020 Oct 27;21(21):7974. doi: 10.3390/ijms21217974

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© 2020 by the authors.

Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).

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Expression analysis of miRNAs and their target genes. miRNAs and their respective target genes expressing under R. solani infection were quantitatively analyzed through RT-qPCR. Data represented after internal reference genes U6 (for miRNAs) and OsActin1 (for target genes) normalization. The error bars represent the standard error of three biological replicates. X-axis: samples and Y-axis: fold change expression in the fungal-infected sample in comparison to the control. Bars represent miRNAs, while lines represent target genes expression.

Expression analysis of miRNAs and their target genes. miRNAs and their respective target genes expressing under R. solani infection were quantitatively analyzed through RT-qPCR. Data represented after internal reference genes U6 (for miRNAs) and OsActin1 (for target genes) normalization. The error bars represent the standard error of three biological replicates. X-axis: samples and Y-axis: fold change expression in the fungal-infected sample in comparison to the control. Bars represent miRNAs, while lines represent target genes expression.