Integration of Signaling Pathways with the Epigenetic Machinery in the Maintenance of Stem Cells

被引:25
作者
Fagnocchi, Luca [1 ]
Mazzoleni, Stefania [1 ]
Zippo, Alessio [1 ]
机构
[1] Fdn Ist Nazl Genet Mol Romeo & Enrica Invernizzi, I-20122 Milan, Italy
关键词
TRANSCRIPTIONAL REGULATORY CIRCUITRY; EMBRYONIC STEM; SELF-RENEWAL; HISTONE H3; LINKS INFLAMMATION; MOUSE EPIBLAST; FEEDBACK LOOP; GROUND-STATE; BETA-CATENIN; PLURIPOTENCY;
D O I
10.1155/2016/8652748
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Stem cells balance their self-renewal and differentiation potential by integrating environmental signals with the transcriptional regulatory network. The maintenance of cell identity and/or cell lineage commitment relies on the interplay of multiple factors including signaling pathways, transcription factors, and the epigenetic machinery. These regulatory modules are strongly interconnected and they influence the pattern of gene expression of stemcells, thus guiding their cellular fate. Embryonic stem cells (ESCs) represent an invaluable tool to study this interplay, being able to indefinitely self-renew and to differentiate towards all three embryonic germ layers in response to developmental cues. In this review, we highlight those mechanisms of signaling to chromatin, which regulate chromatin modifying enzymes, histone modifications, and nucleosome occupancy. In addition, we report the molecular mechanisms through which signaling pathways affect both the epigenetic and the transcriptional state of ESCs, thereby influencing their cell identity. We propose that the dynamic nature of oscillating signaling and the different regulatory network topologies through which those signals are encoded determine specific gene expression programs, leading to the fluctuation of ESCs among multiple pluripotent states or to the establishment of the necessary conditions to exit pluripotency.
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页数:13
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共 130 条
[1]   A module of negative feedback regulators defines growth factor signaling [J].
Amit, Ido ;
Citri, Ami ;
Shay, Tal ;
Lu, Yiling ;
Katz, Menachem ;
Zhang, Fan ;
Tarcic, Gabi ;
Siwak, Doris ;
Lahad, John ;
Jacob-Hirsch, Jasmine ;
Amariglio, Ninette ;
Vaisman, Nora ;
Segal, Eran ;
Rechavi, Gideon ;
Alon, Uri ;
Mills, Gordon B. ;
Domany, Eytan ;
Yarden, Yosef .
NATURE GENETICS, 2007, 39 (04) :503-512
[2]   Dynamic Nucleosome-Depleted Regions at Androgen Receptor Enhancers in the Absence of Ligand in Prostate Cancer Cells [J].
Andreu-Vieyra, Claudia ;
Lai, John ;
Berman, Benjamin P. ;
Frenkel, Baruch ;
Jia, Li ;
Jones, Peter A. ;
Coetzee, Gerhard A. .
MOLECULAR AND CELLULAR BIOLOGY, 2011, 31 (23) :4648-4662
[3]   A nucleosomal function for IκB kinase-α in NF-κB-dependent gene expression [J].
Anest, V ;
Hanson, JL ;
Cogswell, PC ;
Steinbrecher, KA ;
Strahl, BD ;
Baldwin, AS .
NATURE, 2003, 423 (6940) :659-663
[4]   Temporal Perturbation of the Wnt Signaling Pathway in the Control of Cell Reprogramming Is Modulated by TCFI [J].
Aulicino, Francesco ;
Theka, Ilda ;
Ombrato, Luigi ;
Lluis, Frederic ;
Cosma, Maria Pia .
STEM CELL REPORTS, 2014, 2 (05) :707-720
[5]   Multipotent cell lineages in early mouse development depend on SOX2 function [J].
Avilion, AA ;
Nicolis, SK ;
Pevny, LH ;
Perez, L ;
Vivian, N ;
Lovell-Badge, R .
GENES & DEVELOPMENT, 2003, 17 (01) :126-140
[6]   When Signaling Kinases Meet Histones and Histone Modifiers in the Nucleus [J].
Baek, Sung Hee .
MOLECULAR CELL, 2011, 42 (03) :274-284
[7]   An embryonic stem cell-like gene expression signature in poorly differentiated aggressive human tumors [J].
Ben-Porath, Ittai ;
Thomson, Matthew W. ;
Carey, Vincent J. ;
Ge, Ruping ;
Bell, George W. ;
Regev, Aviv ;
Weinberg, Robert A. .
NATURE GENETICS, 2008, 40 (05) :499-507
[8]   BRACHYURY and CDX2 Mediate BMP-Induced Differentiation of Human and Mouse Pluripotent Stem Cells into Embryonic and Extraembryonic Lineages [J].
Bernardo, Andreia S. ;
Faial, Tiago ;
Gardner, Lucy ;
Niakan, Kathy K. ;
Ortmann, Daniel ;
Senner, Claire E. ;
Callery, Elizabeth M. ;
Trotter, Matthew W. ;
Hemberger, Myriam ;
Smith, James C. ;
Bardwell, Lee ;
Moffett, Ashley ;
Pedersen, Roger A. .
CELL STEM CELL, 2011, 9 (02) :144-155
[9]   Activin/Nodal signaling and NANOG orchestrate human embryonic stem cell fate decisions by controlling the H3K4me3 chromatin mark [J].
Bertero, Alessandro ;
Madrigal, Pedro ;
Galli, Antonella ;
Hubner, Nina C. ;
Moreno, Inmaculada ;
Burks, Deborah ;
Brown, Stephanie ;
Pedersen, Roger A. ;
Gaffney, Daniel ;
Mendjan, Sasha ;
Pauklin, Siim ;
Vallier, Ludovic .
GENES & DEVELOPMENT, 2015, 29 (07) :702-717
[10]   Organoid Models of Human and Mouse Ductal Pancreatic Cancer [J].
Boj, Sylvia F. ;
Hwang, Chang-Il ;
Baker, Lindsey A. ;
Chio, Iok In Christine ;
Engle, Dannielle D. ;
Corbo, Vincenzo ;
Jager, Myrthe ;
Ponz-Sarvise, Mariano ;
Tiriac, Herve ;
Spector, Mona S. ;
Gracanin, Ana ;
Oni, Tobiloba ;
Yu, Kenneth H. ;
van Boxtel, Ruben ;
Huch, Meritxell ;
Rivera, Keith D. ;
Wilson, John P. ;
Feigin, Michael E. ;
Oehlund, Daniel ;
Handly-Santana, Abram ;
Ardito-Abraham, Christine M. ;
Ludwig, Michael ;
Elyada, Ela ;
Alagesan, Brinda ;
Biffi, Giulia ;
Yordanov, Georgi N. ;
Delcuze, Bethany ;
Creighton, Brianna ;
Wright, Kevin ;
Park, Youngkyu ;
Morsink, Folkert H. M. ;
Molenaar, I. Quintus ;
Rinkes, Inne H. Borel ;
Cuppen, Edwin ;
Hao, Yuan ;
Jin, Ying ;
Nijman, Isaac J. ;
Iacobuzio-Donahue, Christine ;
Leach, Steven D. ;
Pappin, Darryl J. ;
Hammell, Molly ;
Klimstra, David S. ;
Basturk, Olca ;
Hruban, Ralph H. ;
Offerhaus, George Johan ;
Vries, Robert G. J. ;
Clevers, Hans ;
Tuveson, David A. .
CELL, 2015, 160 (1-2) :324-338