4.7 Article

Genome-wide identification and characterization of the MdBZR1 gene family in apple and their roles in improvement of drought tolerance

Journal

SCIENTIA HORTICULTURAE
Volume 288, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.scienta.2021.110359

Keywords

Apple; MdBZR1-6; Genome-wide analysis; Gene expression; Transcription factors; Drought tolerance

Categories

Funding

  1. National Key Research and Development Program [2017YFC1502805]
  2. Fruit Innovation Team Project of Shandong Modern Agricultural Industrial Technology System [SDAIT-06-01]
  3. Major scientific and technological innovation projects in Shandong Province [2018CXGC0209]
  4. National key research and development plan [2018YFD1000104]
  5. Provincial Natural Science Foundation of Shandong [ZR2018MC023]
  6. National Natural Science Foundation of China [31872041]
  7. Funding for major agricultural application technology innovation projects in Shandong Province
  8. Shandong Province Agricultural Good Seed Project grant [2020LZGC007, 2020LZGC00702]

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Through bioinformatic analyses, 11 members of the MdBZR1 gene family were identified in apple, and the characteristics of these genes were further studied, including gene structures, protein sequences, conserved motifs, and cis-elements in promotor regions. The study also showed that overexpression of MdBZR1-6 improved drought tolerance in transgenic apple callus.
The brassinazole-resistant (BZR) transcription factors (TFs) are key components in the brassinosteroid signaling pathway that play pivotal roles in plant growth and development. However, the functions of BZR TFs in apple during stress is poorly understood. In the present study, by searching the apple genome database, we identified 11 members of the apple BZR1 gene family. We performed bioinformatic analyses on these sequences, and predicted the gene structures, protein sequences, conserved protein motifs, and cis-elements in the promotor regions. We further characterized the apple MdBZR1-6 gene by determining its subcellular location in the cell membrane and used qRT-PCR assays to examine its expression pattern in five tissues and in apple seedlings exposed to simulated drought and low-temperature stress. Our results showed that MdBZR proteins are highly conserved in plant species. In addition, we showed that the overexpression of MdBZR1-6 significantly improved the tolerance of transgenic apple callus to simulated drought stress. The results of our study establish a foundation for the further analysis of the function of MdBZR1 proteins in apple, and provide candidate genes for the potential improvement of drought tolerance in apple.

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