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Dang Ren-Mei, Zheng Wen-Jie, Ding Ning, Wen Shan-Shan. Cloning and stress expression analysis of the TaHDA19 gene in Triticum aestivum[J]. Plant Science Journal, 2019, 37(4): 495-502. DOI: 10.11913/PSJ.2095-0837.2019.40495
Citation: Dang Ren-Mei, Zheng Wen-Jie, Ding Ning, Wen Shan-Shan. Cloning and stress expression analysis of the TaHDA19 gene in Triticum aestivum[J]. Plant Science Journal, 2019, 37(4): 495-502. DOI: 10.11913/PSJ.2095-0837.2019.40495

Cloning and stress expression analysis of the TaHDA19 gene in Triticum aestivum

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This work was supported by a grant from the ‘Tang Zhongying’ Breeding Research Institute of Northwest A & F University.

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  • Received Date: December 26, 2018
  • Revised Date: January 20, 2019
  • Available Online: October 31, 2022
  • Published Date: August 27, 2019
  • A RPD3/HDA1 histone deacetylase gene TaHDA19 was amplified from the Triticum aestivum variety ‘Kenong 199’ by gene cloning techniques and analyzed by bioinformatics. Results showed that gene's open reading frame (ORF) was 1560 bp in length and encoded 519 amino acids. The amino acid sequence contained the typical domain Hist-deacety1. Promoter analysis showed that the gene contained a variety of response elements, such as light response elements I-box and G-box, hormone response element ABRE, and low temperature response element LTR. The gene expression pattern of ‘Kenong 199’ in different tissues and under different stress conditions was analyzed. Results showed that the gene was expressed in roots, stems, leaves, and young spikes, with the highest expression found in leaves. In addition, the gene expression levels were different under ABA, NaCl, and PEG treatment for 0, 1, 3, 6, 12, and 24 h. The gene was up-regulated in the 12 growth stages after heat-stress treatment at 35℃ and 42℃ for 1 h compared with the control.
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