4.3 Article

Genome-wide identification of microRNAs involved in the somatic embryogenesis of Eucalyptus

期刊

G3-GENES GENOMES GENETICS
卷 11, 期 4, 页码 -

出版社

OXFORD UNIV PRESS INC
DOI: 10.1093/g3journal/jkab070

关键词

Eucalyptus; miRNA; vegetative propagation; somatic embryogenesis; dedifferentiation; callus

资金

  1. Guangxi Science and Technology Program [GuiKeAD18281086]
  2. Guangxi Forestry Science and Technology Project [2016[11], 2014[033]]
  3. National Natural Science Foundation of China [31400522]
  4. Department of Human Resources and Social Security of Guangxi Zhuang Autonomous Region [GuiCaiSheHan2018112]

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This study analyzed the miRNA profiles of differentiated and dedifferentiated tissues of two Eucalyptus species, identifying miRNAs involved in somatic embryogenesis. The findings provide a valuable resource for future research and enhance our understanding of miRNA regulation during Eucalyptus somatic embryogenesis.
MicroRNAs (miRNAs) are small noncoding RNAs (18-24 nt) and function in many biological processes in plants. Although Eucalyptus trees are widely planted across the world, our understanding of the miRNA regulation in the somatic embryogenesis (SE) of Eucalyptus is still poor. Here we reported, for the first time, the miRNA profiles of differentiated and dedifferentiated tissues of two Eucalyptus species and identified miRNAs involved in SE of Eucalyptus. Stem and tissue culture-induced callus were obtained from the subculture seedlings of E. camaldulensis and E. grandis x urophylla and were used as differentiated and dedifferentiated samples, respectively. Small RNA sequencing generated 304.2 million clean reads for the Eucalyptus samples (n=3) and identified 888 miRNA precursors (197 known and 691 novel) for Eucalyptus. These miRNAs were mainly distributed in chromosomes Chr03, Chr05, and Chr08 and can produce 46 miRNA clusters. Then, we identified 327 and 343 differentially expressed miRNAs (DEmiRs) in the dedifferentiation process of E. camaldulensis and E. grandis x urophylla, respectively. DEmiRs shared by the two Eucalyptus species might be involved in the development of embryonic callus, such as MIR156, MIR159, MIR160, MIR164, MIR166, MIR169, MIR171, MIR399, and MIR482. Notably, we identified 81 upregulated and 67 downregulated miRNAs specific to E. camaldulensis, which might be associated with the high embryogenic potential. Target prediction and functional analysis showed that they might be involved in longevity regulating and plant hormone signal transduction pathways. Further, using the gene expression profiles, we observed the negative regulation of miRNA-target pairs, such as MIR160 similar to ARF18, MIR396 similar to GRF6, MIR166 similar to ATHB15/HD-ZIP, and MIR156/MIR157 similar to SPL1. Interestingly, transcription factors such as WRKY, MYB, GAMYB, TCP4, and PIL1 were found to be regulated by the DEmiRs. The genes encoding PIL1 and RPS21C, regulated by upregulated miRNAs (e.g., egd-N-miR63-5p, egd-N-miR63-5p, and MIR169,) were downregulated exclusively in the dedifferentiation of E. camaldulensis. This is the first time to study the miRNA regulation in the dedifferentiation process of Eucalyptus and it will provide a valuable resource for future studies. More importantly, it will improve our understanding of miRNA regulation during the somatic embryogenesis of Eucalyptus and benefit the Eucalyptus breeding program.

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