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组蛋白甲基化与去乙酰化对蛇足石杉内生真菌盘长孢状刺盘孢合成石杉碱甲的影响
引用本文:沈鹏原,康信聪,胡莉琴,张家银,刘东波.组蛋白甲基化与去乙酰化对蛇足石杉内生真菌盘长孢状刺盘孢合成石杉碱甲的影响[J].菌物学报,2019,38(2):242-253.
作者姓名:沈鹏原  康信聪  胡莉琴  张家银  刘东波
作者单位:湖南农业大学园艺园林学院 湖南长沙410128;国家中医药管理局亚健康干预技术实验室 湖南长沙410128;湖南农业大学园艺园林学院 湖南长沙410128;国家中医药管理局亚健康干预技术实验室 湖南长沙410128;湖南省作物种质创新与资源利用重点实验室 湖南长沙410128;湖南省植物功能成分利用协同创新中心 湖南长沙410128
基金项目:国家自然科学基金(81773850);国家自然科学基金;湖南省科技重大专项(2017SK1020)
摘    要:以蛇足石杉Huperzia serrata内生真菌盘长孢状刺盘孢Cg01菌株为研究对象,利用PEG介导的同源重组转化体系,对Cg01组蛋白甲基化酶基因(histone methyltransferases,HMT)CgClr4和组蛋白去乙酰化酶基因(histone deacetylase,HDAC)CgClr3CgSir2进行基因敲除与回补,并通过实时荧光定量PCR(RT-qPCR)检测了回补株中对应基因表达量以及高效液相色谱HPLC检测突变体菌株中石杉碱甲huperzine A(HupA)产量。结果显示3个基因敲除突变体菌株ΔCgClr4、ΔCgClr3、ΔCgSir2的HupA产量分别为255μg/L、270μg/L、244μg/L,与野生型菌株相比分别下降了21.3%、16.6%、24.7%。在基因回补突变体菌株ΔCgClr4/CgClr4、ΔCgClr3/CgClr3、ΔCgSir2/CgSir2中,相应回补基因表达均与野生型无显著性差异,其HupA产量分别为351.9μg/L、334.7μg/L、331μg/L,回补菌株的HupA产量回复到野生型水平。结果表明这3个基因均具有调控内生真菌盘长孢状刺盘孢Cg01合成HupA的作用,为研究蛇足石杉内生真菌中石杉碱甲的合成调控机制提供了理论基础和新的思路。

关 键 词:组蛋白  基因敲除  基因回补  石杉碱甲  生物合成
收稿时间:2018-09-12

Effects of histone methylation and deacetylation on the biosynthesis of huperzine A in the endophytic fungus Colletotrichum gloeosporioides
Authors:SHEN Peng-Yuan  KANG Xin-Cong  HU Li-Qin  ZHANG Jia-Yin  LIU Dong-Bo
Institution:①Horticulture and Landscape College, Hunan Agricultural University, Changsha, Hunan 410128, China②State Key Laboratory of Subhealth Intervention Technology, Changsha, Hunan 410128, China③Hunan Provincial Key Laboratory of Crop Germplasm Innovation and Utilization, Hunan Agricultural University, Changsha, Hunan 410128, China④Hunan Co-Innovation Center for Utilization of Botanical Functional Ingredients, Changsha, Hunan 410128, China
Abstract:A histone methyltransferases (HMT) gene CgClr4 and two histone deacetylase (HDAC) gene, CgClr3 and CgSir2, were knocked out and then complemented in the endophytic fungus Colletotrichum gloeosporioides strain Cg01 in Huperzia serrata by the PEG-mediated genetic transformation system. The expression of the corresponding genes in the complemented strains were detected by RT-qPCR and huperzine A (HupA) production in the mutant strains were analyzed by high performance liquid chromatography (HPLC). It was found that the HupA production of the 3 gene knockout mutant strains ΔCgClr4, ΔCgClr3 and ΔCgSir2 were 255μg/L, 270μg/L and 244μg/L respectively, decreased by 21.3%, 16.6% and 24.7% as compared with wild type (WT). There is no significant difference between the gene expression of the corresponding gene in the complemented strains ΔCgClr4/CgClr4, ΔCgClr3/CgClr3 and ΔCgSir2/CgSir2 and that in the wild type strain, with the HupA production to be 351.9μg/L, 334.7μg/L and 331μg/L, respectively. The HupA production of complemented strains was restored to that of the wild type strain. The results showed that these three genes had the function of regulating the biosynthesis of HupA, which provided a theoretical basis and a new insight for studying the synthetic mechanism of HupA in endophytic fungi of Huperzia serrata.
Keywords:histone  gene knockout  gene rescue  huperzine A  biosynthesis  
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