• 中文核心期刊
  • CSCD来源期刊
  • 中国科技核心期刊
  • CA、CABI、ZR收录期刊

碱胁迫下樱桃砧木生理生化响应与转录组特征分析

Physiological and Biochemical Responses and Transcriptome Characteristics of Cherry Rootstock under Alkaline Stress

  • 摘要:
    目的 为选择适应盐碱地区樱桃砧木提供理论依据。
    方法 以6种樱桃砧木‘吉塞拉6号’(G6)、‘吉塞拉17号’(G17)、‘马哈利’(M)、‘兰丁’(L)、‘克雷姆斯克5号’(K5)和‘鲁S-SST-PPA-012-2009’(Y1)为试验对象,探讨不同pH(7.0、7.5、8.0、8.5、9.0和9.5)处理2和4周后上述砧木植株生长(株高和茎粗)和生理生化(叶片相对电导率、叶片叶绿素、丙二醛,脯氨酸,可溶性糖,SOD和CAT活性)的影响,同时对筛选出来的耐碱和不耐碱砧木进行转录组分析。
    结果 6种砧木在pH值为7.0~8.0下均能正常生长,但随着pH值升高,如pH值9.5,所有砧木株高与茎粗增长量均受到抑制。通过对碱胁迫后叶片相对电导率、叶片叶绿素、丙二醛,脯氨酸,可溶性糖,超氧化物歧化酶(superoxide dismutase, SOD)活性和过氧化氢酶(catalase, CAT)活性分析发现,M、K5和Y1砧木表现出较好的耐受潜力;而G6、G17和L砧木的耐受性相对较弱。通过转录组分析,M和L砧木经pH 7.0(CK)、pH 8.5和pH 9.5处理2和4周后,发现M砧木筛选出13个差异表达基因,L砧木筛选出7个差异表达基因。经KEGG富集分析发现,经pH 9.5处理的M砧木与对照组的差异表达基因富集在次生代谢物的生物合成途径和植物激素信号转导通路,而L砧木的差异表达基因主要参与代谢途径以及次生代谢物的生物合成。
    结论 上述结果初步阐明了次生代谢物参与调控了不同樱桃砧木的耐碱性,且在沿海高碱地区M、K5和Y1砧木具有较高的应用潜力。

     

    Abstract:
    Objective Physiological and biochemical properties and transcriptome characteristics of cherry rootstock in response to alkaline stress were studied.
    Method Rootstocks of 6 cherry varieties, including Gisela 6 (G6), Gisela 17 (G17), Mahaleb (M), Landing (L), Krymsk 5 (K5), and Lu S-SST-PPA-012-2009 (Y1), were grown in pots at pH 7.0 (CK), 7.5, 8.0, 8.5, 9.0 or 9.5. Plant height and stem diameter as growth indicators as well as relative conductivity, contents of chlorophyll, malondialdehyde, proline, and soluble sugar, and activities of SOD and CAT in the leaves were measured 2 and 4 weeks after the treatments. Transcriptomes of representative alkaline-tolerant and susceptible rootstocks were analyzed.
    Result All 6 rootstocks grew normally in the pots of pHs between 7.0 and 8.0. But at high alkalinity, e.g., pH 9.5, the growth was suppressed showing reduced plant height and stem diameter. And the leaf relative conductivity and contents of chlorophyll, malondialdehyde, proline, and soluble sugar and the activities of SOD and CAT in G6, G17, and L became lower than those in M, K5, and Y1, indicating differentiated tolerance of the two groups to the risen pH in soil. The treatments of pH 7.0, 8.5, and 9.5 induced transcriptome changes in the genes with 13 differentially expressed genes (DEGs) in M and 7 DEGs in L. The KEGG analysis indicated that the DEGs in the pH 9.5-treated alkaline-resistant M rootstock were enriched in the secondary metabolite biosynthesis and plant hormone signal transduction pathways, while those in the pH 9.5-treated L were largely related to the metabolic and secondary metabolite biosynthesis pathways.
    Conclusion Preliminarily, the results obtained by this study suggested that the secondary metabolites played a major role in regulating alkaline tolerance of cherry rootstocks. The tolerant M, K5, and Y1 would be more appropriate than the other three cultivars for application in coastal areas with soil of high pHs.

     

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