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tenantId=1146029695717560320, journalId=1279045329999892481, language=CN, title=绵羊不同组织细胞中Marco基因启动子甲基化与转录表达水平的关联性分析, columnId=1282278062347764011, journalTitle=中国畜牧杂志, columnName=遗传育种, runingTitle=null, highlight=null, articleAbstract=本研究旨在揭示绵羊胶原样结构巨噬细胞受体(Macrophage Receptor with Collagenous Structure,Marco)组织特异性表达的机制,探讨Marco表达水平与其启动子甲基化的相关性。通过检测肺组织、肺泡巨噬细胞及脾脏细胞中Marco mRNA表达量,利用亚硫酸氢盐测序法(BSP)测定Marco启动子甲基化水平,进一步测定Marco启动子活性,分析DNA甲基化酶处理对Marco启动子活性的影响。结果显示,脾脏组织中Marco mRNA表达量最高,肺脏次之,肺泡巨噬细胞表达量极低;甲基化测定结果显示,Marco启动子甲基化水平在肺泡巨噬细胞最高(96.4%),肺脏处于中等(60.7%),脾脏最低(55.4%)。荧光素酶活性检测表明,Marco启动子具有较高的活性,且启动子区域甲基化抑制Marco启动子活性;初步证实Marco启动子甲基化水平与其在组织中的限制表达存在密切联系。本研究为后续深入探究Marco基因的转录调控机理提供了重要参考依据。, authors=薛嘉熹1 , 王钢2 , 顾兰英1 , 张秦川1 , 赵广新1 , 孙延鸣1 , 贺笋2 , 张彦兵1 , authorsList=薛嘉熹, 王钢, 顾兰英, 张秦川, 赵广新, 孙延鸣, 贺笋, 张彦兵, authorCompany=1.石河子大学动物科技学院; 2.天康制药股份有限公司, correspAuthors=贺笋, authorNote=薛嘉熹(2001-),男,甘肃金昌人,本科生,研究方向为动物医学,E-mail:19190249702@163.com; 王钢(1986-),男,湖南人,硕士,兽医师,主要从事临床兽医学研究,E-mail:wanggang@tecon-bio.com;, 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pdfUrlCn=https://castjournals.cast.org.cn/joweb/zgxmzz/CN/PDF/10.19556/j.0258-7033.20250205-04, pdfUrlEn=https://castjournals.cast.org.cn/joweb/zgxmzz/EN/PDF/10.19556/j.0258-7033.20250205-04, aliStartDate=null, aliEndDate=null, collectionFlag=false, citedCount=null, citedUrl=null, previewStatus=0, delFlag=0, hasFullText=0, orderTime=1765987200000, fullTextJson=null, articleText=null, reference=[1]郭旺,彭光众,黄宏奥,等.鸡marco稳转巨噬细胞系的构建与鉴定[J].畜牧兽医学报, 2024, 55(11):5310-5316. [2]Gough P J, Gordon S. The role of scavenger receptors in the innate immune system[J]. Microbes Infect, 2000, 2(3):305-311. [3]Krieger M, Herz J. Structures and functions of multiligand lipoprotein receptors:macrophage scavenger receptors and LDL receptor-related protein(LRP)[J]. Annu Rev Biochem,1994, 63:601-637. [4]陈佳阔,曹鑫艳,魏立翔,等.绵羊清道夫受体MARCO基因启动子克隆及生物信息学分析[J].动物医学进展, 2022,43(12):56-60. [5]Kraal G, van der Laan L J, Elomaa O, et al. The macrophage receptor MARCO[J]. Microbes Infect, 2000, 2(3):313-316. [6]相笑. PRRSV感染下调猪肺泡巨噬细胞清道夫受体A表达的机制研究[D].北京:中国农业科学院, 2018. [7]Jiang Y, Xie M, Chen W, et al. The sheep genome illuminates biology of the rumen and lipid metabolism[J]. Science, 2014,344(6188):1168-1173. [8]张晶,刘瑞,米浩源. DNA甲基化在法医个体年龄推断中的研究进展[J].生命科学, 2025, 37(4):1-15. [9]Bird A. DNA methylation patterns and epigenetic memory[J].Genes Dev, 2002, 16(1):6-21. [10]Lucibelli F, Valoroso M C, Aceto S. 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中国畜牧杂志
|遗传育种
2026
, 62
(2) :
206
-210
绵羊不同组织细胞中Marco基因启动子甲基化与转录表达水平的关联性分析
全屏
薛嘉熹1 , 王钢2 , 顾兰英1 , 张秦川1 , 赵广新1 , 孙延鸣1 , 贺笋2 , 张彦兵1
作者信息
1.石河子大学动物科技学院; 2.天康制药股份有限公司
通讯作者:
贺笋
作者简介:
薛嘉熹(2001-),男,甘肃金昌人,本科生,研究方向为动物医学,E-mail:19190249702@163.com; 王钢(1986-),男,湖南人,硕士,兽医师,主要从事临床兽医学研究,E-mail:wanggang@tecon-bio.com;
Affiliations
出版时间: 2025-12-18
doi: 10.19556/j.0258-7033.20250205-04
文章导航
本研究旨在揭示绵羊胶原样结构巨噬细胞受体(Macrophage Receptor with Collagenous Structure,Marco)组织特异性表达的机制,探讨Marco表达水平与其启动子甲基化的相关性。通过检测肺组织、肺泡巨噬细胞及脾脏细胞中Marco mRNA表达量,利用亚硫酸氢盐测序法(BSP)测定Marco启动子甲基化水平,进一步测定Marco启动子活性,分析DNA甲基化酶处理对Marco启动子活性的影响。结果显示,脾脏组织中Marco mRNA表达量最高,肺脏次之,肺泡巨噬细胞表达量极低;甲基化测定结果显示,Marco启动子甲基化水平在肺泡巨噬细胞最高(96.4%),肺脏处于中等(60.7%),脾脏最低(55.4%)。荧光素酶活性检测表明,Marco启动子具有较高的活性,且启动子区域甲基化抑制Marco启动子活性;初步证实Marco启动子甲基化水平与其在组织中的限制表达存在密切联系。本研究为后续深入探究Marco基因的转录调控机理提供了重要参考依据。
DNA甲基化
/
胶原样结构巨噬细胞受体
/
启动子
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肺泡巨噬细胞
薛嘉熹, 王钢, 顾兰英, 张秦川, 赵广新, 孙延鸣, 贺笋, 张彦兵.
绵羊不同组织细胞中Marco基因启动子甲基化与转录表达水平的关联性分析.
中国畜牧杂志,
2026
, 62
(2)
: 206
-210
.
DOI: 10.19556/j.0258-7033.20250205-04
国家自然科学基金项目(32360901);兵团指导性科技计划项目(2023ZD042);新疆维吾尔自治区两区项目(2023LQ03003);新疆维吾尔自治区科学基金项目(2022D01B197);石河子大学高层次人才科研启动项目(RCZK202043);
参考文献
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2026年第62卷第2期
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doi: 10.19556/j.0258-7033.20250205-04
首发时间:2026-07-01
出版时间:2025-12-18
https://castjournals.cast.org.cn/joweb/zgxmzz/CN/10.19556/j.0258-7033.20250205-04
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2种不同金属材料的力学参数
科 Family 属数 Number of genus 种数 Number of species 占总种数比例 Percentage of total species (%) 属 Genus 种数 Number of species 占总种数比例 Percentage of total species (%) 鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78 小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39 多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39 红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87 小菇属 Mycena 11 5.26 光柄菇属 Pluteus 5 2.39 红菇属 Russula 17 8.13 栓菌属 Trametes 5 2.39
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