张明, 杨帅, 曹艳飞, 卢晓文, 焦钰. 2023: 马氏珠母贝组蛋白乙酰化修饰相关基因的分子进化及功能分析. 南方农业学报, 54(2): 575-585. DOI: 10.3969/j.issn.2095-1191.2023.02.026
引用本文: 张明, 杨帅, 曹艳飞, 卢晓文, 焦钰. 2023: 马氏珠母贝组蛋白乙酰化修饰相关基因的分子进化及功能分析. 南方农业学报, 54(2): 575-585. DOI: 10.3969/j.issn.2095-1191.2023.02.026
ZHANG Ming, YANG Shuai, CAO Yan-fei, LU Xiao-wen, JIAO Yu. 2023: Molecular evolution and functional analysis of histone acetylation modification related genes in Pinctada fucata martensii. Journal of Southern Agriculture, 54(2): 575-585. DOI: 10.3969/j.issn.2095-1191.2023.02.026
Citation: ZHANG Ming, YANG Shuai, CAO Yan-fei, LU Xiao-wen, JIAO Yu. 2023: Molecular evolution and functional analysis of histone acetylation modification related genes in Pinctada fucata martensii. Journal of Southern Agriculture, 54(2): 575-585. DOI: 10.3969/j.issn.2095-1191.2023.02.026

马氏珠母贝组蛋白乙酰化修饰相关基因的分子进化及功能分析

Molecular evolution and functional analysis of histone acetylation modification related genes in Pinctada fucata martensii

  • 摘要: 【目的】分析组蛋白乙酰化修饰相关基因的分子进化及其在马氏珠母贝(Pinctada fucata martensii)植核后的表达变化,明确组蛋白乙酰化修饰在植核免疫中的作用,为合理控制植核免疫反应提供理论依据。【方法】通过生物信息学分析方法对马氏珠母贝、长牡蛎、斑马鱼及人类等9个物种的组蛋白乙酰转移酶(HAT)和组蛋白去乙酰化酶(HDAC)进行全基因组鉴定,并分析其分子进化历程,同时通过已有的转录组数据分析马氏珠母贝HATHDAC基因在植核后的表达变化,采用组蛋白H3/H4总乙酰化定量分析试剂盒检测马氏珠母贝植核后血细胞组蛋白H3/H4乙酰化水平。【结果】HATHDAC基因家族在9个物种基因组中的数目差异不明显,其原始共同祖先(MRCA)共包含8个HAT基因家族的9个基因及19个HDAC基因家族的22个基因。马氏珠母贝基因组含有2个HAT家族(GNAT和MYST)的8个基因(2个GNAT类基因,6个MYST类基因); HAT基因家族成员中含有18个保守氨基酸序列,且所有MYST类基因均含有MOZ_SAS结构域,GNAT类基因则含有Hat1_N或Acetyltransf_1结构域,即具有较高的保守性。马氏珠母贝基因组含有13个HDAC家族的18个基因,包含3个I类、3个II类、10个Ⅲ类和2个IV类。其中,HDAC Ⅲ类基因家族包含3个保守氨基酸序列,HDAC I/II/IV类基因家族包含21个保守氨基酸序列,但分布位置和序列组成差异明显,说明该家族成员结构具有多样性。马氏珠母贝、长牡蛎和人类中HDAC Ⅲ类基因均包含1~2个SIR2结构域,HDAC I/II/IV类基因包含1个或多个Hist-deacety1结构域。在马氏珠母贝血细胞转录组中可检测到所有的HDACHAT基因,HDAC基因在植核后的表达呈动态变化,而多数HAT基因表达未发生变化;植核后6、12和24 h马氏珠母贝血细胞组蛋白H3和H4的乙酰化修饰水平显著上升(P<0.05),至植核后48 h组蛋白H3仍保持较高乙酰化水平,而组蛋白H4乙酰化水平恢复正常。【结论】组蛋白乙酰化修饰相关基因的基因组拷贝数、结构域组成及保守氨基酸序列等在不同物种间具有保守性,且组蛋白乙酰化修饰参与调控马氏珠母贝的植核免疫。

     

    Abstract: 【Objective】To analyze molecular evolution of histone acetylation modification related genes and expression changes of the genes in Pinctada fucata martensii after nucleus transplantation,and to make clear the function of histone acetylation modification on nucleus transplantation immunity,so as to provide theoretical and technical guidance for appropriate control of immune response to nucleus transplantation.【Method】 Whole genome identification of histone acetylase(HAT)and histone deacetylase(HDAC)related genes in 9 species including P. fucata martensii,Crassostrea gigas,Danio rerio and Homo sapiens was operated through bioinformatics methods,and molecular evolution of the genes was analyzed. Based on transcriptomes data already obtained,expression change of HAT and HDAC genes in P. fucata martensii after nucleus transplantation,and hemocyte histone H3/H4 acetylation level was determined using histone H3/ H4 total acetylation quantitative analysis kit.【Result】The numbers of HAT and HDAC gene families in the genomes of 9 species varied inobviously,and the most recent common ancestor(MRCA)included 9 genes from 8 HAT gene families and 22 genes from 19 HDAC gene families. P. fucata martensii genome contained 8 genes(2 GNAT-like genes and 6 MYST-like genes)from 2 HAT families(GNAT and MYST);HAT gene family members contained 18 conserved amino acid sequences,and all existing MYST-like genes contained MOZ_SAS domain and GNAT-like genes contained Hat1_N or Acetyltransf_1 domains,indicating that the sequences were highly conserved. P. fucata martensii genome contained 18 genes from 13 HDAC gene families,including 3 genes in Class I,3 in Class II,10 in Class III and 2 in Class IV. HDAC Class III gene family contained 3 conserved amino acid sequences,and HDAC Class I/II/ IV gene families contained 21 conserved amino acid sequences,but they were distributed in different positions and had different sequence composition, indicating that the structure of the family members was diverse. HDAC Class III genes in P. fucata martensii,C. agigas, and H. sapiens contained from 1 to 2 SIR2 domains,and HDAC Class I/II/IV genes contained one or more Hist-deacety1 domains. Hemocytes transcriptome of P. fucata martensii contained all of the detected HDAC and HAT genes,and expression of HDAC genes changed dynamically after nucleus transplantation,but most expression of HAT genes did not change;acetylation modification level of histone H3 and histone H4 increased significantly at 6,12 and 24 h after nucleus transplantation in P. fucata martensiiP<0.05),and at 48 h,the acetylation level of histone H3 was still high,while the acetylation level of histone H4 returned to normal.【Conclusion】Genome copy number,domain composition and conserved amino acid sequence of histone acetylation related genes are conserved in different species,and histone acetylation modification is involved in regulation of immune response to nucleus transplantation in P. fucata martensii.

     

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