The Notch intracellular domain integrates signals from Wnt, Hedgehog, TGFβ/BMP and hypoxia pathways

被引:198
作者
Borggrefe, Tilman [1 ]
Lauth, Matthias [2 ]
Zwijsen, An [3 ,4 ]
Huylebroeck, Danny [5 ]
Oswald, Franz [6 ]
Giaimo, Benedetto Daniele [1 ]
机构
[1] Univ Giessen, Inst Biochem, Giessen, Germany
[2] Univ Marburg, Inst Mol Biol & Tumor Res, D-35032 Marburg, Germany
[3] Katholieke Univ Leuven, WB Ctr Biol Dis, Leuven, Belgium
[4] Katholieke Univ Leuven, Dept Human Genet, Leuven, Belgium
[5] Erasmus Univ, Dept Cell Biol, Med Ctr, NL-3000 DR Rotterdam, Netherlands
[6] Univ Med Ctr Ulm, Dept Internal Med 1, Ulm, Germany
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH | 2016年 / 1863卷 / 02期
关键词
Notch signal transduction; Post-translational modifications; Methylation; Hydroxylation; Signaling crosstalk; Transcription factor Hes1; QUANTITATIVE PHOSPHOPROTEOMIC ANALYSIS; EPITHELIAL-MESENCHYMAL TRANSITION; ANKYRIN REPEAT DOMAIN; GAMMA-SECRETASE; STEM-CELL; WNT/BETA-CATENIN; SONIC-HEDGEHOG; TRANSCRIPTIONAL COACTIVATOR; SEGMENTATION CLOCK; ENDOTHELIAL NOTCH;
D O I
10.1016/j.bbamcr.2015.11.020
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Notch signaling is a highly conserved signal transduction pathway that regulates stem cell maintenance and differentiation in several organ systems. Upon activation, the Notch receptor is proteolytically processed, its intracellular domain (NICD) translocates into the nucleus and activates expression of target genes. Output, strength and duration of the signal are tightly regulated by post-translational modifications. Here we review the intracellular post-translational regulation of Notch that fine-tunes the outcome of the Notch response. We also describe how crosstalk with other conserved signaling pathways like the Wnt, Hedgehog, hypoxia and TGF beta/BMP pathways can affect Notch signaling output. This regulation can happen by regulation of ligand, receptor or transcription factor expression, regulation of protein stability of intracellular key components, usage of the same cofactors or coregulation of the same key target genes. Since carcinogenesis is often dependent on at least two of these pathways, a better understanding of their molecular crosstalk is pivotal. (C) 2015 The Authors. Published by Elsevier B.V. This is an open access article under the CC BY-NC-ND license.
引用
收藏
页码:303 / 313
页数:11
相关论文
共 187 条
[1]
Notch destabilises maternal β-catenin and restricts dorsal-anterior development in Xenopus [J].
Acosta, Helena ;
Lopez, Silvia L. ;
Revinski, Diego R. ;
Carrasco, Andres E. .
DEVELOPMENT, 2011, 138 (12) :2567-2579
[2]
Androutsellis-Theotokis A, 2006, NATURE, V442, P823, DOI 10.1038/nature04940
[3]
Wnt5a Controls Notch1 Signaling through CaMKII-mediated Degradation of the SMRT Corepressor Protein [J].
Ann, Eun-Jung ;
Kim, Hwa-Young ;
Seo, Mi-Sun ;
Mo, Jung-Soon ;
Kim, Mi-Yeon ;
Yoon, Ji-Hye ;
Ahn, Ji-Seon ;
Park, Hee-Sae .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2012, 287 (44) :36814-36829
[4]
Notch signaling: Cell fate control and signal integration in development [J].
Artavanis-Tsakonas, S ;
Rand, MD ;
Lake, RJ .
SCIENCE, 1999, 284 (5415) :770-776
[5]
Hypoxia Promotes Uveal Melanoma Invasion through Enhanced Notch and MAPK Activation [J].
Asnaghi, Laura ;
Lin, Michael H. ;
Lim, Kah Suan ;
Lim, Kah Jing ;
Tripathy, Arushi ;
Wendeborn, Murilo ;
Merbs, Shannath L. ;
Handa, James T. ;
Sodhi, Akrit ;
Bar, Eli E. ;
Eberhart, Charles G. .
PLOS ONE, 2014, 9 (08)
[6]
Alk1 and Alk5 inhibition by Nrp1 controls vascular sprouting downstream of Notch [J].
Aspalter, Irene Maria ;
Gordon, Emma ;
Dubrac, Alexandre ;
Ragab, Anan ;
Narloch, Jarek ;
Vizan, Pedro ;
Geudens, Ilse ;
Collins, Russell Thomas ;
Franco, Claudio Areias ;
Abrahams, Cristina Luna ;
Thurston, Gavin ;
Fruttiger, Marcus ;
Rosewell, Ian ;
Eichmann, Anne ;
Gerhardt, Holger .
NATURE COMMUNICATIONS, 2015, 6
[7]
Id sustains Hes1 expression to inhibit precocious neurogenesis by releasing negative autoregulation of Hes1 [J].
Bai, Ge ;
Sheng, Nengyin ;
Xie, Zhihui ;
Bian, Wei ;
Yokota, Yoshifumi ;
Benezra, Robert ;
Kageyama, Ryoichiro ;
Guillemot, Francois ;
Jing, Naihe .
DEVELOPMENTAL CELL, 2007, 13 (02) :283-297
[8]
Phosphoproteomics Identifies Driver Tyrosine Kinases in Sarcoma Cell Lines and Tumors [J].
Bai, Yun ;
Li, Jiannong ;
Fang, Bin ;
Edwards, Arthur ;
Zhang, Guolin ;
Bui, Marilyn ;
Eschrich, Steven ;
Altiok, Soner ;
Koomen, John ;
Haura, Eric B. .
CANCER RESEARCH, 2012, 72 (10) :2501-2511
[9]
Large-scale characterization of HeLa cell nuclear phosphoproteins [J].
Beausoleil, SA ;
Jedrychowski, M ;
Schwartz, D ;
Elias, JE ;
Villén, J ;
Li, JX ;
Cohn, MA ;
Cantley, LC ;
Gygi, SP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (33) :12130-12135
[10]
Robustness in angiogenesis: Notch and BMP shaping waves [J].
Beets, Karen ;
Huylebroeck, Danny ;
Moya, Ivan M. ;
Umans, Lieve ;
Zwijsen, An .
TRENDS IN GENETICS, 2013, 29 (03) :140-149