MicroRNA Omics Analysis of Camellia sinesis Pollen Tubes in Response to Low-Temperature and Nitric Oxide

Biomolecules. 2021 Jun 23;11(7):930. doi: 10.3390/biom11070930.

Abstract

Nitric oxide (NO) as a momentous signal molecule participates in plant reproductive development and responds to various abiotic stresses. Here, the inhibitory effects of the NO-dominated signal network on the pollen tube growth of Camellia sinensis under low temperature (LT) were studied by microRNA (miRNA) omics analysis. The results showed that 77 and 71 differentially expressed miRNAs (DEMs) were induced by LT and NO treatment, respectively. Gene ontology (GO) analysis showed that DEM target genes related to microtubules and actin were enriched uniquely under LT treatment, while DEM target genes related to redox process were enriched uniquely under NO treatment. In addition, the target genes of miRNA co-regulated by LT and NO are only located on the cell membrane and cell wall, and most of them are enriched in metal ion binding and/or transport and cell wall organization. Furthermore, DEM and its target genes related to metal ion binding/transport, redox process, actin, cell wall organization and carbohydrate metabolism were identified and quantified by functional analysis and qRT-PCR. In conclusion, miRNA omics analysis provides a complex signal network regulated by NO-mediated miRNA, which changes cell structure and component distribution by adjusting Ca2+ gradient, thus affecting the polar growth of the C. sinensis pollen tube tip under LT.

Keywords: Camellia sinensis; low-temperature; microRNA; nitric oxide; pollen tube growth.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Camellia sinensis / genetics*
  • Camellia sinensis / metabolism
  • Cold Temperature*
  • Gene Regulatory Networks / drug effects
  • Gene Regulatory Networks / physiology
  • MicroRNAs / genetics*
  • MicroRNAs / metabolism
  • Nitric Oxide / pharmacology*
  • Pollen Tube / drug effects
  • Pollen Tube / genetics*
  • Pollen Tube / metabolism
  • Sequence Analysis, RNA / methods*

Substances

  • MicroRNAs
  • Nitric Oxide