Functional diversity among Notch1, Notch2, and Notch3 receptors

被引:91
作者
Shimizu, K
Chiba, S
Saito, T
Kumano, K
Hamada, Y
Hirai, H
机构
[1] Univ Tokyo, Grad Sch Med, Dept Hematol & Oncol, Tokyo, Japan
[2] Univ Tokyo, Grad Sch Med, Dept Cell Therapy & Transplantat Med, Tokyo, Japan
[3] Natl Inst Basic Biol, Okazaki, Aichi 444, Japan
关键词
Notch; activated Notch; HES1; HES5; RBP-J kappa; reporter assay;
D O I
10.1006/bbrc.2002.6528
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
To clarify functional diversities among the Notch receptors, we generated truncated forms of Notch1, Notch2, and Notch3 comprising the intracellular domain (aN1, aN2, and aN3) and investigated their transcriptional activities for HES1 and HES5 promoters driving the luciferase reporter gene (HES1-Luc and HES5-Luc). The reporter assays demonstrated that the transcriptional activities of aNs were markedly different from each other and dependent on the promoters examined. Furthermore, relative activities between some aN and another for each promoter were altered by the expression level of RBP-Jkappa. We also found that the activities of aN1 and aN3 were reduced by coexpression of aN2. These observations suggest that each Notch receptor has a diverse role in the downstream gene expression and that the levels of HES1 and HES5 gene expression are complexly determined by various factors, such as the type and combination of the Notch receptors which confer the downstream signals and the expression level of RBP-Jkappa. (C) 2002 Elsevier Science (USA).
引用
收藏
页码:775 / 779
页数:5
相关论文
共 50 条
[31]   RUNX3 directly interacts with intracellular domain of Notch1 and suppresses Notch signaling in hepatocellular carcinoma cells [J].
Gao, Juan ;
Chen, Yu ;
Wu, Kai-Chun ;
Liu, Jie ;
Zhao, Yan-Qiu ;
Pan, Yang-Lin ;
Du, Rui ;
Zheng, Guo-Rong ;
Xiong, Yi-Min ;
Xu, Hua-Lin ;
Fan, Dai-Ming .
EXPERIMENTAL CELL RESEARCH, 2010, 316 (02) :149-157
[32]   Regulation of Notch1/NICD and Hes1 Expressions by GSK-3α/β [J].
Jin, Yun Hye ;
Kim, Hangun ;
Oh, Minsoo ;
Ki, Hyunkyung ;
Kim, Kwonseop .
MOLECULES AND CELLS, 2009, 27 (01) :15-19
[33]   Decreasing Notch/Hes1 pathway associated with abnormal Notch1/NICD transduction in diabetic mice [J].
Yu, Tao ;
Min, Xiao-Hui ;
Chen, Qi-Kui .
JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY, 2013, 28 :153-154
[34]   The Expression of Notch 1 and Notch 3 in Gallbladder Cancer and Their Clinicopathological Significance [J].
Liu, Luyao ;
Yang, Zhu-lin ;
Wang, Chunwei ;
Miao, Xiongying ;
Liu, Zhiyu ;
Li, Daiqiang ;
Zou, Qiong ;
Li, Jinghe ;
Liang, Lufeng ;
Zeng, Guixiang ;
Chen, Senlin .
PATHOLOGY & ONCOLOGY RESEARCH, 2016, 22 (03) :483-492
[35]   The Notch1 transcriptional activation domain is required for development and reveals a novel role for Notch1 signaling in fetal hematopoietic stem cells [J].
Gerhardt, Dawson M. ;
Pajcini, Kostandin V. ;
D'altri, Teresa ;
Tu, LiLi ;
Jain, Rajan ;
Xu, Lanwei ;
Chen, Michael J. ;
Rentschler, Stacey ;
Shestova, Olga ;
Wertheim, Gerald B. ;
Tobias, John W. ;
Kluk, Michael ;
Wood, Antony W. ;
Aster, Jon C. ;
Gimotty, Phyllis A. ;
Epstein, Jonathan A. ;
Speck, Nancy ;
Bigas, Anna ;
Pear, Warren S. .
GENES & DEVELOPMENT, 2014, 28 (06) :576-593
[36]   Aspartate mutations in presenilin and γ-secretase inhibitors both impair Notch1 proteolysis and nuclear translocation with relative preservation of Notch1 signaling [J].
Berezovska, O ;
Jack, C ;
McLean, P ;
Aster, JC ;
Hicks, C ;
Xia, WM ;
Wolfe, MS ;
Kimberly, WT ;
Weinmaster, G ;
Selkoe, DJ ;
Hyman, BT .
JOURNAL OF NEUROCHEMISTRY, 2000, 75 (02) :583-593
[37]   Instability of Notch1 and Delta1 mRNAs and reduced Notch activity in vertebrate neuroepithelial cells undergoing S-phase [J].
Cisneros, Elsa ;
Latasa, Maria Jesus ;
Garcia-Flores, Marta ;
Frade, Jose Maria .
MOLECULAR AND CELLULAR NEUROSCIENCE, 2008, 37 (04) :820-831
[38]   Transition of Cleaved Notch1 and Gene Expression Changes in Myeloblastic Leukemia Cells Stimulated with Notch Ligands [J].
Fu, Lu ;
Katsube, Ken-Ichi ;
Tohda, Shuji .
ANTICANCER RESEARCH, 2009, 29 (10) :3967-3970
[39]   Notch1 ligand signaling pathway activated in cervical cancer: poor prognosis with high-level JAG1/Notch1 [J].
Yousif, Nasser Ghaly ;
Sadiq, Alaa Muhammad ;
Yousif, Maitham G. ;
Al-Mudhafar, Rihab H. ;
Al-Baghdadi, Jinan J. ;
Hadi, Najah .
ARCHIVES OF GYNECOLOGY AND OBSTETRICS, 2015, 292 (04) :899-904
[40]   Loss of intestinal crypt progenitor cells owing to inactivation of both Notch1 and Notch2 is accompanied by derepression of CDK inhibitors p27Kip1 and p57Kip2 [J].
Riccio, Orbicia ;
van Gijn, Marielle E. ;
Bezdek, April C. ;
Pellegrinet, Luca ;
van Es, Johan H. ;
Zimber-Strobl, Ursula ;
Strobl, Lothar J. ;
Honjo, Tasuku ;
Clevers, Hans ;
Radtke, Freddy .
EMBO REPORTS, 2008, 9 (04) :377-383