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荸荠淀粉分支酶CwSBEII基因的克隆及其表达分析

赵若男 陈振林 玉万国 许薇 刘英健 宋慕波

赵若男,陈振林,玉万国,等. 荸荠淀粉分支酶CwSBEII基因的克隆及其表达分析 [J]. 福建农业学报,2022,37(12):1546−1553 doi: 10.19303/j.issn.1008-0384.2022.012.005
引用本文: 赵若男,陈振林,玉万国,等. 荸荠淀粉分支酶CwSBEII基因的克隆及其表达分析 [J]. 福建农业学报,2022,37(12):1546−1553 doi: 10.19303/j.issn.1008-0384.2022.012.005
ZHAO R N, CHEN Z L, YU W G, et al. Cloning and Expression of SBEII in Eleocharis tuberosa [J]. Fujian Journal of Agricultural Sciences,2022,37(12):1546−1553 doi: 10.19303/j.issn.1008-0384.2022.012.005
Citation: ZHAO R N, CHEN Z L, YU W G, et al. Cloning and Expression of SBEII in Eleocharis tuberosa [J]. Fujian Journal of Agricultural Sciences,2022,37(12):1546−1553 doi: 10.19303/j.issn.1008-0384.2022.012.005

荸荠淀粉分支酶CwSBEII基因的克隆及其表达分析

doi: 10.19303/j.issn.1008-0384.2022.012.005
基金项目: 国家重点研发计划项目(2018YFD0901003);国家自然科学基金项目(31801607);广西壮族自治区自然科学基金项目(2020GXNSFAA259087、2017GXNSFAA198082);贺州学院博士科研启动基金(HZUBS202106)
详细信息
    作者简介:

    赵若男(1997−),女,硕士研究生,研究方向:果蔬加工与保鲜(E-mail:zhao18278289315@163.com

    通讯作者:

    宋慕波(1986−),男,博士,副研究员,研究方向:果蔬加工与保鲜(E-mail:songmubo1@163.com

  • 中图分类号: S 645.3

Cloning and Expression of SBEII in Eleocharis tuberosa

  • 摘要:   目的  克隆荸荠(Eleocharis tuberosa)淀粉分支酶CwSBEII基因,分析该基因的蛋白功能特性及其在荸荠不同组织以及不同膨大时期的表达模式,为进一步深入研究CwSBEII基因的功能提供理论参考。  方法  采用RT-PCR的方法克隆得到CwSBEII基因的cDNA序列,通过生物信息学分析其蛋白功能特性,利用荧光定量PCR法检测该基因在荸荠球茎中的时空表达特征。  结果  成功克隆得到CwSBEII基因,该基因的开放阅读框(ORF)长度为2547 bp,编码848个氨基酸。CwSBEII蛋白分子量为96100.52 Da;理论等电点(pI)值为5.24,不稳定指数为41.07,GRAVY为−0.473,属于不稳定亲水蛋白。系统进化分析表明,荸荠与禾本科的小麦(Triticum aestivum)、水稻(Oryza sativa)、玉米(Zea mays)的SBEII蛋白聚为一支,亲缘关系最近。荧光定量PCR结果表明,CwSBEII基因在根、叶片、荸荠皮以及荸荠肉中均有表达,但在叶片中的表达量最高。在荸荠球茎膨大初期CwSBEII基因表达出现明显上调。  结论  CwSBEII基因在荸荠中特异性表达,在叶片中的表达量最高,膨大初期表达明显上调,推测该基因在荸荠淀粉合成中发挥着重要作用。
  • 图  1  CwSBEII基因PCR扩增产物

    M:DL5000 DNA Marker;1~2:目的基因片段。

    Figure  1.  Electrophoresis of PCR amplification products of CwSBEII

    M: DL5000 DNA marker; 1–2: target gene fragment.

    图  2  CwSBEII蛋白疏水/亲水性预测

    Figure  2.  Predicted hydrophobicity and hydrophilicity of CwSBEII protein

    图  3  CwSBEII蛋白保守结构域分析

    Figure  3.  Conserved structural domain of CwSBEII protein

    图  4  CwSBEII蛋白二级结构预测

    蓝色(h):α-螺旋;红色(e):延伸链;橙色(c):无规则卷曲;绿色(t):β-折叠。

    Figure  4.  Predicted secondary structure of CwSBEII protein

    Blue (h): α-helix; red (e): extended chain; orange (c): random coils; green (t): β-sheet.

    图  5  CwSBEII蛋白质的三级结构预测

    Figure  5.  Predicted tertiary structure of CwSBEII protein

    图  6  CwSBEII所编码的蛋白质与其他植物蛋白的系统进化树

    Figure  6.  Phylogenetic tree of proteins encoded by CwSBEII and other plant proteins

    图  7  CwSBEII所编码的蛋白质与不同植物SBEII氨基酸序列的多重比对

    #:高度保守的活性位点。

    Figure  7.  Multiplex comparison on amino acid sequences of proteins encoded by CwSBEII and plant SBEIIs

    #: Highly conserved active site.

    图  8  CwSBEII基因在荸荠不同组织中的相对表达

    图中不同小写字母表示5%水平差异显著。图9同。

    Figure  8.  Expressions of CwSBEII in tissues of Chinese water chestnut

    Data with different lowercase letters represent significant difference at 5% level. Same for Fig.9.

    图  9  CwSBEII基因在荸荠膨大时期中的表达变化

    S1~S4分别表示球茎最宽处直径约为10 、20 、35和50 mm。

    Figure  9.  Expressions of CwSBEII during expansion stages of Chinese water chestnut corm

    S1-S4: diameters of widest part of corms being approximately 10, 20, 35, and 50 mm, respectively.

    表  1  荸荠SBEII基因克隆和表达所用引物

    Table  1.   Primer used for cloning and expression analysis of SBEII in Chinese water chestnut

    引物名称
    Primer name
    引物序列(5′-3′)
    Sequence(5′-3′)
    CwSBEII (F)ATGACGTTCGCTCTATCGGGATCGG
    CwSBEII (R)TTACTCCTCACAGAGAGCATAGACA
    Q-PCR CwSBEII (F)CCTCCTGAAGAAGAAAAGTACGTC
    Q-PCR CwSBEII (R)AGCTAGCATAGTAAGAGTGCTCCTG
    18S RNA (F)ATGATTAAGAGGGACAGTCGGGGGC
    18S RNA (R)CTAGGACGGTATCTGATCGTCTTCG
    下载: 导出CSV
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  • 收稿日期:  2022-07-07
  • 修回日期:  2022-10-18
  • 网络出版日期:  2022-12-28
  • 刊出日期:  2022-03-28

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