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System Analysis of MIRNAs in Maize Internode Elongation.


ABSTRACT: MicroRNAs (miRNAs), the post-transcriptional gene regulators, are known to play an important role in plant development. The identification of differentially expressed miRNAs could better help us understand the post-transcriptional regulation that occurs during maize internode elongation. Accordingly, we compared the expression of MIRNAs between fixed internode and elongation internode samples and classified six differentially expressed MIRNAs as internode elongation-responsive miRNAs including zma-MIR160c, zma-MIR164b, zma-MIR164c, zma-MIR168a, zma-MIR396f, and zma-MIR398b, which target mRNAs supported by transcriptome sequencing. Functional enrichment analysis for predictive target genes showed that these miRNAs were involved in the development of internode elongation by regulating the genes respond to hormone signaling. To further reveal how miRNA affects internode elongation by affecting target genes, the miRNA-mRNA-PPI (protein and protein interaction) network was constructed to summarize the interaction of miRNAs and these target genes. Our results indicate that miRNAs regulate internode elongation in maize by targeting genes related to cell expansion, cell wall synthesis, transcription, and regulatory factors.

SUBMITTER: Peng C 

PROVIDER: S-EPMC6769733 | biostudies-literature | 2019 Aug

REPOSITORIES: biostudies-literature

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System Analysis of <i>MIRNAs</i> in Maize Internode Elongation.

Peng Chuanxi C   Wang Xing X   Feng Tianyu T   He Rui R   Zhang Mingcai M   Li Zhaohu Z   Zhou Yuyi Y   Duan Liusheng L  

Biomolecules 20190827 9


MicroRNAs (miRNAs), the post-transcriptional gene regulators, are known to play an important role in plant development. The identification of differentially expressed miRNAs could better help us understand the post-transcriptional regulation that occurs during maize internode elongation. Accordingly, we compared the expression of <i>MIRNAs</i> between fixed internode and elongation internode samples and classified six differentially expressed <i>MIRNAs</i> as internode elongation-responsive miRN  ...[more]

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