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Home > Archive>Volume 21, Issue 3, 2020 >734-742. DOI:10.13430/j.cnki.jpgr.20190731001 Online First
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Homologous Cloning and Expression Analysis of Apple Lipoxygenase Gene MdLOX1a
DOI:
10.13430/j.cnki.jpgr.20190731001
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  • YUE Xuan-xuan

    YUE Xuan-xuan

    College of Horticulture Science and Engineering, Shandong Agricultural University / State Key Laboratory of Crop Biology
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  • WANG Qing-peng

    WANG Qing-peng

    College of Horticulture Science and Engineering, Shandong Agricultural University / State Key Laboratory of Crop Biology
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  • FANG Hong-cheng

    FANG Hong-cheng

    College of Horticulture Science and Engineering, Shandong Agricultural University / State Key Laboratory of Crop Biology
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  • HU Jia-fei

    HU Jia-fei

    College of Horticulture Science and Engineering, Shandong Agricultural University / State Key Laboratory of Crop Biology
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  • SU Meng-yu

    SU Meng-yu

    College of Horticulture Science and Engineering, Shandong Agricultural University / State Key Laboratory of Crop Biology
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  • ZHANG Zong-ying

    ZHANG Zong-ying

    College of Horticulture Science and Engineering, Shandong Agricultural University / State Key Laboratory of Crop Biology
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  • WANG Nan

    WANG Nan

    College of Horticulture Science and Engineering, Shandong Agricultural University / State Key Laboratory of Crop Biology
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  • CHEN Xue-sen

    CHEN Xue-sen

    College of Horticulture Science and Engineering, Shandong Agricultural University / State Key Laboratory of Crop Biology
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Affiliation:

College of Horticulture Science and Engineering, Shandong Agricultural University / State Key Laboratory of Crop Biology

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Fund Project:

the National Natural Science Foundation of China (31730080,31701892); the National Key Research and Development Project (2016YFC0501505)

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    Abstract:

    Lipoxygenase is a key enzyme involved in the pathway of fatty acid metabolism, and plays an important role in the growth and development of plants, responses to environmental stresses and the synthesis of aroma components. In this study, the red callus from the leaves of 'Zihong 3' was used for PCR amplification of the MdLOX1a gene and its partial promoter sequence. Sequencing analysis revealed that MdLOX1a has an open reading frame of 2592 bp encoding for 863 deduced amino acids, with a predicted protein molecular weight of 97.69 KDa and the isoelectric point of 5.14. The MdLOX1a gene was found to be localized on chromosome 9 of the apple genome, consisting of 8 exons and 7 introns. Phylogenetic tree analysis with amino acid sequence indicated that MdLOX1a and Pb9S-LOX5 were assigned within the same branch. In addition, we obtained the MdLOX1a promoter sequence with a length of 1058 bp, which contained several cis-acting elements in response to various stresses. Subcellular localization revealed that MdLOX1a was localized on both the cell membrane and the nucleus. The tissue disparity analysis showed that the expression level of MdLOX1a gene was abundant in the pericarp, followed by flower and pulp. The expression of MdLOX1a gene gradually increased with fruit ripening, and its transcription has been induced under continuous light treatment. The expression of MdLOX1a gene was significantly reduced after low temperature (16 ℃) and exogenous ABA treatment at different concentrations. The overexpression of MdLOX1a showed that the transgenic lines showed the induction of the aromatic components in relative to the control lines, suggesting that MdLOX1a might associate with the synthesis of aroma components.

    Key words:apple; MdLOX1a; expression analysis; subcellular localization; functional verification
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History
  • Received:July 31,2019
  • Revised:March 17,2020
  • Adopted:October 09,2019
  • Online: May 18,2020
  • Published:
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