IR@PKUHSC  > 北京大学基础医学院  > 细胞生物学系
学科主题基础医学
Does not hUTP14a promoter form a regulation feedback loop with P53?
Zhang, Jingyi1; Guo, Yafei2; Du, Xiaojuan2; Xing, Baocai1
关键词Hutp14a Luciferase Activity Promoter P53 Transcription Factor
刊名CHINESE JOURNAL OF CANCER RESEARCH
2014-04-01
DOI10.3978/j.issn.1000-9604.2014.03.03
26期:2页:159-165
收录类别SCI
文章类型Article
WOS标题词Science & Technology
类目[WOS]Oncology
资助者Beijing Municipal Natural Science Foundation ; National Natural Science Foundation of China ; National Basic Research Program of China (973 program) ; National High Technology Research and Development Program of China (863 Program) ; Beijing Municipal Natural Science Foundation ; National Natural Science Foundation of China ; National Basic Research Program of China (973 program) ; National High Technology Research and Development Program of China (863 Program)
研究领域[WOS]Oncology
关键词[WOS]UBIQUITIN LIGASE ; DEGRADATION ; CANCER ; PIRH2 ; GENE ; MDM2 ; COP1
英文摘要

Objective: We previously found that hUTP14a binds P53 and promotes P53 degradation. However, if hUTP14a is a downstream gene of P53 remains to be determined. This study aimed to identify the promoter of hUTP14a and investigate if hUTP14a is regulated by P53.

Methods: The hUTP14a promoter region was cloned into pGL3-Basic-luciferase reporter plasmid to get pGL3-hUTP14a-luc. The reporter plasmid was transfected into 293T cells and luciferase activity was evaluated by the Dual-Luciferase Reporter Assay System. Putative transcription factors were identified through searching MatInspector Professional and Algorismica i Genetica databases. Either pGL3-hUTP14a-luc or p21 promoter reporter plasmid was co-transfected with increasing dose of p53 plasmid, and luciferase activity was evaluated. A series of deletion constructs of pGL3-hUTP14a-luc were constructed and minimal promoter region of hUTP14a was determined. Differences of the luciferase activities between different groups were assessed by statistical analysis.

Results: The hUTP14a gene promoter reporter construct was correctly cloned and was demonstrated to possess promoter activity. The transcription of hUTP14a was not regulated by P53. The minimal promoter region of hUTP14a gene is located between -203 to -100 of the transcription initiation site.

Conclusion: Unlike other P53-interacting proteins such as MDM2, Pirh2 and Cop I which promote P53 degradation and whose transcriptions are regulated by P53, does not hUTP14a transcription form a regulation feedback loop with P53.

语种英语
所属项目编号7122032 ; 81071672 ; 2010CB529303 ; 2008AA02Z131
资助者Beijing Municipal Natural Science Foundation ; National Natural Science Foundation of China ; National Basic Research Program of China (973 program) ; National High Technology Research and Development Program of China (863 Program) ; Beijing Municipal Natural Science Foundation ; National Natural Science Foundation of China ; National Basic Research Program of China (973 program) ; National High Technology Research and Development Program of China (863 Program)
WOS记录号WOS:000335622200006
Citation statistics
Cited Times:1[WOS]   [WOS Record]     [Related Records in WOS]
文献类型期刊论文
条目标识符http://ir.bjmu.edu.cn/handle/400002259/55507
Collection北京大学基础医学院_细胞生物学系
作者单位1.Peking Univ Canc Hosp & Inst, Dept Hepat Biliary & Pancreat Surg 1, Key Lab Carcinogenesis & Translat Res, Minist Educ, Beijing 100142, Peoples R China
2.Peking Univ Hlth Sci Ctr, Dept Cell Biol, Beijing 100191, Peoples R China
Recommended Citation
GB/T 7714
Zhang, Jingyi,Guo, Yafei,Du, Xiaojuan,et al. Does not hUTP14a promoter form a regulation feedback loop with P53?[J]. CHINESE JOURNAL OF CANCER RESEARCH,2014,26(2):159-165.
APA Zhang, Jingyi,Guo, Yafei,Du, Xiaojuan,&Xing, Baocai.(2014).Does not hUTP14a promoter form a regulation feedback loop with P53?.CHINESE JOURNAL OF CANCER RESEARCH,26(2),159-165.
MLA Zhang, Jingyi,et al."Does not hUTP14a promoter form a regulation feedback loop with P53?".CHINESE JOURNAL OF CANCER RESEARCH 26.2(2014):159-165.
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