BMC Plant Biology (Mar 2021)

Transcriptome and metabolome profiling provide insights into molecular mechanism of pseudostem elongation in banana

  • Guiming Deng,
  • Fangcheng Bi,
  • Jing Liu,
  • Weidi He,
  • Chunyu Li,
  • Tao Dong,
  • Qiaosong Yang,
  • Huijun Gao,
  • Tongxin Dou,
  • Xiaohong Zhong,
  • Miao Peng,
  • Ganjun Yi,
  • Chunhua Hu,
  • Ou Sheng

DOI
https://doi.org/10.1186/s12870-021-02899-6
Journal volume & issue
Vol. 21, no. 1
pp. 1 – 14

Abstract

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Abstract Background Banana plant height is an important trait for horticultural practices and semi-dwarf cultivars show better resistance to damages by wind and rain. However, the molecular mechanisms controlling the pseudostem height remain poorly understood. Herein, we studied the molecular changes in the pseudostem of a semi-dwarf banana mutant Aifen No. 1 (Musa spp. Pisang Awak sub-group ABB) as compared to its wild-type dwarf cultivar using a combined transcriptome and metabolome approach. Results A total of 127 differentially expressed genes and 48 differentially accumulated metabolites were detected between the mutant and its wild type. Metabolites belonging to amino acid and its derivatives, flavonoids, lignans, coumarins, organic acids, and phenolic acids were up-regulated in the mutant. The transcriptome analysis showed the differential regulation of genes related to the gibberellin pathway, auxin transport, cell elongation, and cell wall modification. Based on the regulation of gibberellin and associated pathway-related genes, we discussed the involvement of gibberellins in pseudostem elongation in the mutant banana. Genes and metabolites associated with cell wall were explored and their involvement in cell extension is discussed. Conclusions The results suggest that gibberellins and associated pathways are possibly developing the observed semi-dwarf pseudostem phenotype together with cell elongation and cell wall modification. The findings increase the understanding of the mechanisms underlying banana stem height and provide new clues for further dissection of specific gene functions.

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