The epigenetic network regulating muscle development and regeneration

被引:93
作者
Palacios, D
Puri, PL
机构
[1] ICBTE, Fdz A Cesalpino, Gene Express Lab, Dulbecco Telethon Inst, Rome, Italy
[2] Burnham Inst, La Jolla, CA 92037 USA
关键词
D O I
10.1002/jcp.20489
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
This review focuses on our current knowledge of the epigenetic changes regulating gene expression at the chromatin and DNA level, independently on the primary DNA sequence, to reprogram the nuclei of muscle precursors during developmental myogenesis and muscle regeneration. These epigenetic marks provide the blueprint by which the extra-cellular cues are interpreted at the nuclear level by the transcription machinery to select the repertoire of tissue-specific genes to be expressed. The reversibility of some of these changes necessarily reflects the dynamic nature of skeletal myogenesis, which entails the progression through two antagonistic processes - proliferation and differentiation. Other epigenetic modifications are instead associated to events conventionally considered as irreversible - e.g. maintenance of lineage commitment and terminal differentiation. However, recent results Support the possibility that these events can be reversed, at least upon certain experimental conditions, thereby revealing a dynamic nature of many of the epigenetic modifications underlying skeletal myogenesis. The elucidation of the epigenetic network that regulates transcription during developmental myogenesis and muscle regeneration might provide the information instrumental to devise pharmacological interventions toward selective manipulation of gene expression to promote regeneration of skeletal Muscles and possibly other tissue.
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页码:1 / 11
页数:11
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共 198 条
[71]   CORRELATION OF TERMINAL CELL-CYCLE ARREST OF SKELETAL-MUSCLE WITH INDUCTION OF P21 BY MYOD [J].
HALEVY, O ;
NOVITCH, BG ;
SPICER, DB ;
SKAPEK, SX ;
RHEE, J ;
HANNON, GJ ;
BEACH, D ;
LASSAR, AB .
SCIENCE, 1995, 267 (5200) :1018-1021
[72]   Activation of the transcription factor MEF2C by the MAP kinase p38 in inflammation [J].
Han, J ;
Jiang, Y ;
Li, Z ;
Kravchenko, VV ;
Ulevitch, RJ .
NATURE, 1997, 386 (6622) :296-299
[73]   Brahma links the SWI/SNF chromatin-remodeling complex with MeCP2-dependent transcriptional silencing [J].
Harikrishnan, KN ;
Chow, MZ ;
Baker, EK ;
Pal, S ;
Bassal, S ;
Brasacchio, D ;
Wang, L ;
Craig, JM ;
Jones, PL ;
Sif, S ;
El-Osta, A .
NATURE GENETICS, 2005, 37 (03) :254-264
[74]   Identification and characterization of a family of mammalian methyl-CpG binding proteins [J].
Hendrich, B ;
Bird, A .
MOLECULAR AND CELLULAR BIOLOGY, 1998, 18 (11) :6538-6547
[75]   EXPRESSION OF THE MUSCLE REGULATORY FACTOR-MRF4 DURING SOMITE AND SKELETAL MYOFIBER DEVELOPMENT [J].
HINTERBERGER, TJ ;
SASSOON, DA ;
RHODES, SJ ;
KONIECZNY, SF .
DEVELOPMENTAL BIOLOGY, 1991, 147 (01) :144-156
[76]   IL-4 acts as a myoblast recruitment factor during mammalian muscle growth [J].
Horsley, V ;
Jansen, KM ;
Mills, ST ;
Pavlath, GK .
CELL, 2003, 113 (04) :483-494
[77]   Rb is required for progression through myogenic differentiation but not maintenance of terminal differentiation [J].
Hub, MS ;
Parker, MH ;
Scimè, A ;
Parks, R ;
Rudnicki, MA .
JOURNAL OF CELL BIOLOGY, 2004, 166 (06) :865-876
[78]   Epigenetic instability in ES cells and cloned mice [J].
Humpherys, D ;
Eggan, K ;
Akutsu, H ;
Hochedlinger, K ;
Rideout, WM ;
Biniszkiewicz, D ;
Yanagimachi, R ;
Jaenisch, R .
SCIENCE, 2001, 293 (5527) :95-97
[79]   Hematopoietic potential of stem cells isolated from murine skeletal muscle [J].
Jackson, KA ;
Mi, TJ ;
Goodell, MA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (25) :14482-14486
[80]   Severe global DNA hypomethylation blocks differentiation and induces histone hyperacetylation in embryonic stem cells [J].
Jackson, M ;
Krassowska, A ;
Gilbert, N ;
Chevassut, T ;
Forrester, L ;
Ansell, J ;
Ramsahoye, B .
MOLECULAR AND CELLULAR BIOLOGY, 2004, 24 (20) :8862-8871