银屑病5q15易感区域功能性变异搜寻及生物学作用网络构建
批准号:
31671307
项目类别:
面上项目
资助金额:
60.0 万元
负责人:
程晖
依托单位:
学科分类:
表型、行为与疾病的遗传学基础
结题年份:
2020
批准年份:
2016
项目状态:
已结题
项目参与者:
盛宇俊、高金平、郑晓冬、陈刚、朱正伟、闻雷雷、朱才红、郭慧敏
中文摘要
银屑病易复发、难根治,严重影响患者身心健康。申请人从事银屑病发病机制研究十年,在青年基金资助下,从基因分型、基因表达、通路分析等多角度证实LNPEP可能参与MHC I类分子抗原提呈或NF-κB信号通路影响疾病发生。收集20对患者皮损/非皮损组织及20例对照组织开展全基因组表达谱预实验,发现LNPEP在组织中表达与银屑病显著相关(P=3×10-15)。本课题基于前期疾病全基因组基因分型、全外显子测序及组织基因表达谱数据库万余例数据,拟以千人基因组数据为参考,采用Impute2软件,对LNPEP所在5q15区域行基因填补(Imputation),筛选关键基因;开展基因测序搜寻功能性致病变异;并在大样本人群中验证(5000- 5000),建立基因间生物学交互作用网络,从基因共表达研究功能学角度加以验证,并构建多基因风险预测模型,力求将基础理论成果应用于转化医学,为疾病诊断治疗靶标筛查提供突破口。
英文摘要
Psoriasis is a common relapsing and remitting skin disease, which severely affected physical and mental health of patients. The applicant has been working on the research of the pathogenesis of psoriasis for 10 years. Under the support of Young Scientist's Fund, we identified that the LNPEP gene may be involved in MHC class I molecules antigen presenting or the NF-κB signaling pathway for psoriasis by several different ways, such as gene genotyping, gene expression, path analysis and so on. Then we collected 20 pairs of lesions and non-lesions in each patient and 20 skin tissues of the controls to perform the whole genome expression analysis, and found that the expression of LNPEP in skins was significantly associated with psoriasis(P=3×10-15). Based on three databases of genome-wide genotyping, exome sequencing and whole genome expression profiling, with more than ten thousand data information, This study plans to take 1000 Genomes data for reference, carry out imputation in 5q15 that LNPEP was located for the key susceptibility genes using IMPUTE2 software, search for the functional variants by conducting gene sequencing with replication in a large number of samples (5000 cases and 5000 controls), establish gene-gene biological interaction network verified by gene co-expression analysis, and then build the genetic risk prediction model, which will help to apply basic theory achievement to translational medicine, and also will be a valuable breakthrough of the target identification for the disease diagnosis and treatment in the future.
银屑病易复发、难根治,严重影响患者身心健康。课题组基于前期对银屑病全基因组基因分型、全外显子组、靶向测序和验证数据联合分析的基础上,在5q15区域开展功能性致病变异搜寻研究,发现本课题研究区域(5q15)等区域内25个基因的外显子插入缺失(InDels),解释了大约1.29%的银屑病遗传度;探寻到5q15区域的ERAP1基因上6个SNPs和几种单倍型与汉族人银屑病相关,提示是ERAP1银屑病的关键易感基因,单倍型分析提示几种特殊单倍型有预测疾病的功能;揭示了5q15区域ERAP1和HLA及MIR548AZ和TYK2的交互作用在银屑病发病中重要作用,构建了基因间生物学交互作用网络,提示免疫系统和抗原加工途径在银屑病发病机制中发挥重要作用。同时课题组还对5q15周围区域与银屑病相关的易感变异展开搜寻,发现ADRA1B基因变异不仅与中国人群银屑病有关,还与中重度银屑病及银屑病发病年龄早的临床亚型相关,为完善生物学作用网络构建提供了更多的遗传信息,开展5q15区域相关的基因型与表型相关性研究,DNA甲基化与银屑病发病相关性研究,力求将基础理论成果应用于转化医学,为银屑病药物靶点研发、疾病预防与诊疗提供新的视角,同时进一步推进了银屑病遗传学研究和精准医学研究进程。
期刊论文列表
专著列表
科研奖励列表
会议论文列表
专利列表
登录
查看更多内容
Correlation analysis of the HLA-DPB1*05:01 and BTNL2 genes within the histocompatibility complex region with a clinical phenotype of psoriasis vulgaris in the Chinese Han population
MHC区HLA-DPB105:01基因和BTNL2基因与中国汉族人群寻常型银屑病临床表型的相关性分析
DOI:
10.1002/jgm.2961
发表时间:
2017-09-01
期刊:
JOURNAL OF GENE MEDICINE
影响因子:
3.5
作者:
[Guo, Huimin, Huang, Yong, Zhang, Xuejun]
通讯作者:
Zhang, Xuejun
Genetic Study on Small Insertions and Deletions in Psoriasis Reveals a Role in Complex Human Diseases
银屑病中小插入和缺失的遗传学研究揭示了其在复杂人类疾病中的作用
DOI:
10.1016/j.jid.2019.03.1157
发表时间:
2019
期刊:
Journal of Investigative Dermatology
影响因子:
6.5
作者:
[Zhen Qi, Yang Zhenjun, Wang Wenjun, Li Bao, Bai Mingzhou, Wu Jing, Ge Huiyao, Dong Zirui, Shen Juan, Tang Huayang, Sun Silong, Qiu Ying, Xu Jinjin, Qu Xiaoxiao, Wang Ying, Yi Meihui, Hu Huaqing, Xu Yuanhong, Cheng Hui, Liang Bo, Gao Jinping, Shao Haojing, Jian Zhengwen, Gao Qia]
通讯作者:
Gao Qia
Fine mapping and subphenotyping implicates ADRA1B gene variants in psoriasis susceptibility in a Chinese population
精细定位和亚表型分析表明 ADRA1B 基因变异与中国人群银屑病易感性有关
DOI:
10.2217/epi-2018-0131
发表时间:
2019-03-01
期刊:
EPIGENOMICS
影响因子:
3.8
作者:
[Fan, Xing, Wang, Hongyan, Schork, Nicholas J.]
通讯作者:
Schork, Nicholas J.
DNA methylation profile of psoriatic skins from different body locations
身体不同部位银屑病皮肤的 DNA 甲基化谱
DOI:
10.2217/epi-2018-0225
发表时间:
2019
期刊:
Epigenomics
影响因子:
3.8
作者:
[Mingshun Wu, Xueying Li, Chaowen Zhang, Chuanliang Zhang, Danfeng Qian, Jie Ma, Minglong Cai, Lili Tang, Hui Cheng, Changbing Shen, Gang Chen, Xiaodong Zheng, Xuejun Zhang, Fusheng Zhou]
通讯作者:
Fusheng Zhou
LNPEP基因与汉族人银屑病发病机制相关性研究
-
批准号:31200939
-
项目类别:青年科学基金项目
-
资助金额:25.0万元
-
批准年份:2012
-
负责人:程晖
-
依托单位:
国内基金
海外基金