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2. The First Afiliated Hospital, Xinjiang Medical University, Urumqi 830011, China;
3. College of Basic Medicine, Xinjiang Medical University, Urumqi 830011, China, fund=null, authors=SHENG Lei1 , MA Li2 , XIERZHATIJIANG Sulaiman3 , ABUDULA Abulizi1 , ABUDUKADEER Abida2 , authorsList=SHENG Lei, MA Li, XIERZHATIJIANG Sulaiman, ABUDULA Abulizi, ABUDUKADEER Abida), CN=ArticleExt(id=1242131810583392867, articleId=1242131807735460432, tenantId=1146029695717560320, journalId=1146031591421210625, language=CN, title=宫颈癌中CALCA 基因甲基化与HPV16-E7致癌蛋白表达的依存关系, columnId=1146540929516700224, journalTitle=科技导报, columnName=研究论文, runingTitle=null, highlight=null, articleAbstract=选择HPV16 阳性宫颈癌细胞和RNAi 技术,研究CALCA 基因甲基化与HPV16-E7 致癌蛋白表达的依存关系。构建慢病毒siRNA 重组表达载体,建立稳定表达HPV 16-E 7-siRNA 的RNAi 细胞模型。以SiHa 细胞和RNAi 细胞模型的基因组DNA 为对象,选择CALCA 基因启动子区富含CpG 岛屿的目标片段,使用亚硫酸氢盐测序法(bisulfite sequencing PCR,BSP)筛查分析,研究RNAi 抑制HPV16-E 7 表达后,CALCA 基因甲基化状态的可逆性程度。选出CALCA 基因启动子区富含CpG 位点的目标片段,其大小为365 bp,含有19 个CpG 岛屿,发现其中13 个CpG 位点的胞嘧啶在SiHa 细胞基因组DNA 中发生了甲基化(13/19),而在表达HPV 16-E 7-siRNA 的RNAi 细胞模型中,所有CpG 位点的甲基化已发生逆转(0/19 位点)。本研究从细胞水平证明了宫颈癌细胞内的CALCA 基因启动子高甲基化对HPV16-E7 致癌蛋白表达有依赖性,为进一步研究E7 蛋白的作用及致癌机制奠定了重要的物质基础。, correspAuthors=null, authorNote=盛磊,博士研究生,研究方向为宫颈癌预警和发病机制,电子信箱:shenglei950505@163.com, correspAuthorsNote=阿比达·阿不都卡德尔,副主任医师,研究方向为妇科肿瘤,电子信箱:abida0724@126.com, copyrightStatement=null, copyrightOwner=null, extLink=null, articleAbsUrl=null, sourceXml=null, magXml=null, pdfUrl=null, pdf=eC1BH3GEPxMJq/c2mSCz5g==, pdfFileSize=2789211, pdfExtLink=null, richHtmlUrl=null, mobilePdfUrl=null, reviewReport=null, pdfFirstPage=null, abstractGraph=null, abstractGraphContent=null, abstractVideo=null, citation=null, cebUrl=null, magXmlContent=null, mapNumber=null, authorCompany=1. 新疆医科大学新疆地方病分子生物学实验室, 乌鲁木齐 830011;
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科技导报
| 研究论文 2014, 32(10): 63-67
宫颈癌中
CALCA 基因甲基化与HPV16-E7致癌蛋白表达的依存关系
全屏
盛磊1 , 马丽2 , 希尔扎提江·苏来曼3 , 阿布力孜·阿布杜拉1 , 阿比达·阿不都卡德尔2
作者信息
1. 新疆医科大学新疆地方病分子生物学实验室, 乌鲁木齐 830011;
2. 新疆医科大学第一附属医院, 乌鲁木齐 830011;
3. 新疆医科大学基础医学院, 乌鲁木齐 830011
通讯作者:
阿比达·阿不都卡德尔,副主任医师,研究方向为妇科肿瘤,电子信箱:abida0724@126.com
Association of CALCA Gene Methylation and HPV16-E7 Oncoprotein Expression in Cervical Cancer
Affiliations
出版时间: 2014-04-08
doi: 10.3981/j.issn.1000-7857.2014.10.011
文章导航
选择HPV16 阳性宫颈癌细胞和RNAi 技术,研究CALCA 基因甲基化与HPV16-E7 致癌蛋白表达的依存关系。构建慢病毒siRNA 重组表达载体,建立稳定表达HPV 16-E 7-siRNA 的RNAi 细胞模型。以SiHa 细胞和RNAi 细胞模型的基因组DNA 为对象,选择CALCA 基因启动子区富含CpG 岛屿的目标片段,使用亚硫酸氢盐测序法(bisulfite sequencing PCR,BSP)筛查分析,研究RNAi 抑制HPV16-E 7 表达后,CALCA 基因甲基化状态的可逆性程度。选出CALCA 基因启动子区富含CpG 位点的目标片段,其大小为365 bp,含有19 个CpG 岛屿,发现其中13 个CpG 位点的胞嘧啶在SiHa 细胞基因组DNA 中发生了甲基化(13/19),而在表达HPV 16-E 7-siRNA 的RNAi 细胞模型中,所有CpG 位点的甲基化已发生逆转(0/19 位点)。本研究从细胞水平证明了宫颈癌细胞内的CALCA 基因启动子高甲基化对HPV16-E7 致癌蛋白表达有依赖性,为进一步研究E7 蛋白的作用及致癌机制奠定了重要的物质基础。
降钙素相关肽基因
/
宫颈癌
/
RNA 干扰
/
HPV16
/
E7 基因
The dependence of the CALCA gene promoter hypermethylation on the HPV16-E7 oncoprotein expression is investigated by the RNAi technique and using the HPV16-positive SiHa cervical carcinoma cells as the target cells. A recombinant lentiviral siRNA expression vector is constructed, and an RNAi cell model stably expressing the HPV 16-E 7-siRNA is established. After the extraction of the genomic DNA from the SiHa cells and the RNAi cell model, the reversibility of the CALCA gene promoter hypermethylation induced by the RNAi inhibition of the HPV16-E7 oncogene expression is analyzed by the PCR amplification, the subsequent cloning and the sequencing of a CpG-rich target fragment in the CALCA gene promoter. A 365 bp CpG-rich sequence selected in the CALCA promoter region is found as the target fragment containing 19 CpG islands, among which the cytosine of 13 CpG sites is methylated in the genomic DNA of the SiHa cells (13/19 CpG sites), whereas all methylations are fully reversed in the RNAi cell model expressing the HPV 16-E 7-siRNA (0/19 CpG sites). It is shown that the CALCA gene promoter hypermethylation is directly dependent on the HPV16-E7 oncoprotein expression in the cervical carcinoma cells, and the foundation for the role study and the carcinogenic mechanism of the E7 protein is established.
CALCA
/
cervical cancer
/
RNAi
/
HPV16
/
E7 gene
盛磊, 马丽, 希尔扎提江·苏来曼, 阿布力孜·阿布杜拉, 阿比达·阿不都卡德尔.
宫颈癌中CALCA 基因甲基化与HPV16-E7致癌蛋白表达的依存关系.
科技导报,
2014
, 32
(10)
: 63
-67
.
DOI: 10.3981/j.issn.1000-7857.2014.10.011
SHENG Lei, MA Li, XIERZHATIJIANG Sulaiman, ABUDULA Abulizi, ABUDUKADEER Abida.
Association of CALCA Gene Methylation and HPV16-E7 Oncoprotein Expression in Cervical Cancer[J].
Science & Technology Review ,
2014
, 32
(10)
: 63
-67
.
DOI: 10.3981/j.issn.1000-7857.2014.10.011
2014年第32卷第10期
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文章信息
doi: 10.3981/j.issn.1000-7857.2014.10.011
接收时间:2013-10-10
首发时间:2014-04-19
出版时间:2014-04-08
收稿日期:2013-10-10
修回日期:2013-12-25
通讯作者:
阿比达·阿不都卡德尔,副主任医师,研究方向为妇科肿瘤,电子信箱:abida0724@126.com
https://castjournals.cast.org.cn/joweb/kjdb/CN/10.3981/j.issn.1000-7857.2014.10.011
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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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