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小鼠胞内氯离子通道5基因启动子核心功能区域鉴定及转录调控分析
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作者 巨婷婷 吕文涛 +5 位作者 于渤洋 刘洋 姜美华 许玲 赵泽平 尹靖东 《中国农业大学学报》 CAS CSCD 北大核心 2012年第5期137-143,共7页
为研究胞内氯离子通道5基因(Chloride intracellular channel 5,CLIC5)广泛参与调节细胞内的各项生理活动与生化反应,并探讨该基因自身的表达调控机制,以小鼠基因组序列为模板,利用PCR技术扩增小鼠CLIC5基因5′上游调控序列,将其插入荧... 为研究胞内氯离子通道5基因(Chloride intracellular channel 5,CLIC5)广泛参与调节细胞内的各项生理活动与生化反应,并探讨该基因自身的表达调控机制,以小鼠基因组序列为模板,利用PCR技术扩增小鼠CLIC5基因5′上游调控序列,将其插入荧光素酶报告基因表达载体(pGL3-Basic)中,同时采用5′侧翼区缺失的方法构建了7个缺失不同DNA片段的荧光素酶表达载体。重组质粒与海肾荧光素酶载体(phRL-TK)共同瞬时转染HEK-293细胞,经双荧光素酶报告基因活性分析后,确定CLIC5基因的核心启动子区。利用生物信息学方法预测其中转录因子结合位点及启动子区甲基化状况。结果表明,CLIC5基因启动子缺乏TATA盒,但含有典型的GC盒及其他潜在转录因子结合位点;双荧光素酶报告基因活性分析表明,CLIC5基因-329~+1、-624~+1、-917~+1和-2 230~+1区域的启动子活性较高,其中-624~+1区域的启动子活性最强。进一步分析表明,启动子区-624~-329存在负性调控元件,预测存在转录因子结合位点RXR heterodimer binding sites与GC-Box factorsSp1/GC,-420~-283范围内存在CpG岛位点。 展开更多
关键词 clic5 表达调控 启动子 转录因子 CPG岛
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荣昌猪和3种瘦肉型猪胞内氯离子通道5基因多态性的分布
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作者 张海燕 王强 +1 位作者 尼健君 尹靖东 《中国畜牧杂志》 CAS 北大核心 2010年第11期22-24,共3页
采用微卫星技术对159头荣昌猪、52头长白猪、247头大白猪和46头杜洛克猪4个品种的胞内氯离子通道5基因(CLIC5)多态性进行调查分析。结果表明:CLIC5有3个等位基因(A、B和C),4个猪种的CLIC5基因都存在多态性,但不同猪群中,CLIC5等位基因... 采用微卫星技术对159头荣昌猪、52头长白猪、247头大白猪和46头杜洛克猪4个品种的胞内氯离子通道5基因(CLIC5)多态性进行调查分析。结果表明:CLIC5有3个等位基因(A、B和C),4个猪种的CLIC5基因都存在多态性,但不同猪群中,CLIC5等位基因的频率差异较大,其中荣昌猪A型等位基因频率较高,而引进猪种中C型等位基因频率较高。4种猪群中,共有6种基因型(AA、AB、BB、AC、BC和CC),大白猪各基因型频率为0.01、0.04、0.05、0.09、0.20和0.61,长白猪为0、0.10、0.06、0.09、0.27和0.48,杜洛克猪为0、0.09、0.11、0.13、0.32和0.35,荣昌猪为0.31、0.43、0.20、0.04、0.01和0.01。所有的基因型在不同猪种中均符合哈迪-温伯格平衡。 展开更多
关键词 clic5基因 基因多态性 微卫星
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Early dynamic transcriptomic changes during preoperative radiotherapy in patients with rectal cancer: A feasibility study 被引量:3
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作者 Stephane Supiot Wilfried Gouraud +7 位作者 Loc Campion Pascal Jezéquel Bruno Buecher Josiane Charrier Marie-Francoise Heymann Marc-Andre Mahé Emmanuel Rio Michel Chérel 《World Journal of Gastroenterology》 SCIE CAS 2013年第21期3249-3254,共6页
AIM: To develop novel biomarkers of rectal radiotherapy, we measured gene expression profiles on biopsies taken before and during preoperative radiotherapy. METHODS: Six patients presenting with a locally advanced rec... AIM: To develop novel biomarkers of rectal radiotherapy, we measured gene expression profiles on biopsies taken before and during preoperative radiotherapy. METHODS: Six patients presenting with a locally advanced rectal cancer (T>T2, N0/Nx, M0) eligible for preoperative radiotherapy (45 Gy in 25 fractions) were selected in a pilot study. Six tumor and 3 normal tissues biopsies were taken before and during radiotherapy,after a dose of 7.2 Gy at a median time of 1 h following irradiation (0:27-2:12). Tumor or normal tissue purity was assessed by a pathologist prior to RNA extraction. Mean RNA content was 23 μg/biopsy (14-37) before radiotherapy and 22.7 μg/biopsy (12-35) during radiotherapy. After RNA amplification, biopsies were analysed with 54K HG-U133A Plus 2.0 Affymetrix expression micro-arrays. Data were normalized according to MAS5 algorithm. A gene expression ratio was calculated as: (gene expression during radiotherapy-gene expression before radiotherapy)/gene expression before radiotherapy. Were selected genes that showed a ratio higher than ± 0.5 in all 6 patients. RESULTS: Microarray analysis showed that preoperative radiotherapy significantly up-regulated 31 genes and down-regulated 6 genes. According to the Gene Ontology project classification, these genes are involved in protein metabolism (ADAMDEC1 ; AKAP7 ; CAPN5 ; CLIC5 ; CPE ; CREB3L1 ; NEDD4L ; RAB27A), ion transport (AKAP7 ; ATP2A3 ; CCL28 ; CLIC5 ; F2RL2 ; NEDD4L ; SLC6A8), transcription (AKAP7 ; CREB3L1 ; ISX ; PAB-PC1L ; TXNIP), signal transduction (CAPN5 ; F2RL2 ; RA- B27A ; TNFRSF11A), cell adhesion (ADAMDEC1 ; PXDN ; SPON1 ; S100A2), immune response (CCL28 ; PXDN ; TNFRSF11A) and apoptosis (ITM2C ; PDCD4 ; PVT1). Up-regulation of 3 genes (CCL28 ; CLIC5 ; PDCD4) was detected by 2 different probes and up-regulation of 2 genes (RAB27A ; TXNIP) by 3 probes. CONCLUSION: Micro-arrays can efficiently assess early transcriptomic changes during preoperative radiotherapy for rectal cancer, and may help better understand tumor radioresistance. 展开更多
关键词 CCL28 clic5 PDCD4 RAB27A TXNIP Protein METABOLISM CELL ADHESION CELL migration SPON1 CARBOXYPEPTIDASE E
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