Epigenetic patterns of embryonic and adult stem cells

被引:42
作者
Bloushtain-Qimron, Noga [1 ,3 ,4 ]
Yao, Jun [1 ,2 ]
Shipitsin, Michail [1 ,2 ]
Maruyama, Reo [1 ,2 ]
Polyak, Kornelia [1 ,2 ]
机构
[1] Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Boston, MA USA
[3] Ben Gurion Univ Negev, Fac Hlth Sci, Shraga Segal Dept Microbiol & Immunol, Beer Sheva, Israel
[4] Ben Gurion Univ Negev, Canc Res Ctr, IL-84105 Beer Sheva, Israel
关键词
stem cells; epigenetics; DNA methylation; chromatin; HUMAN MAMMARY-GLAND; HISTONE DEACETYLASE ACTIVITY; BREAST-CANCER CELLS; DNA METHYLATION; PROGENITOR CELLS; SELF-RENEWAL; DEVELOPMENTAL REGULATORS; CELLULAR-DIFFERENTIATION; POLYCOMB COMPLEXES; IN-VITRO;
D O I
10.4161/cc.8.6.7938
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Embryonic stem (ES) cells are pluripotent cells that differentiate into all cell types of the organism. In adult, multipotent tissue-specific stem cells undergo multi-lineage differentiation to preserve normal tissue homeostasis and repair potential injuries. The maintenance of stem cells and their differentiation follows defined epigenetic programs, including DNA methylation, histone modifications and small non-coding RNAs that result in gene expression, morphologic and functional changes. Recently, we reported for the first time the comprehensive characterization of the in vivo gene expression and DNA methylation profiles of four distinct populations of normal human mammary epithelial cells and the identification of cell type-specific DNA methylation patterns with clinical relevance. Our results together with other studies suggest an important role for epigenetic regulation in stem cell self-renewal, pluripotency and differentiation, and imply that abnormalities in these processes may play a role in tumor initiation and progression.
引用
收藏
页码:809 / 817
页数:9
相关论文
共 87 条
[1]  
ADEI OM, 2008, CURR TOP MED CHEM, V8, P841
[2]   Prospective identification of tumorigenic breast cancer cells [J].
Al-Hajj, M ;
Wicha, MS ;
Benito-Hernandez, A ;
Morrison, SJ ;
Clarke, MF .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (07) :3983-3988
[3]   Stem cells in the skin: waste not, Wnt not [J].
Alonso, L ;
Fuchs, E .
GENES & DEVELOPMENT, 2003, 17 (10) :1189-1200
[4]  
Alvi AJ, 2003, BREAST CANCER RES, V5, DOI [10.1186/bcr563, 10.1186/bcr547]
[5]   Epigenetic characterization of hematopoietic stem cell differentiation using miniChIP and bisulfite sequencing analysis [J].
Attema, Joanne L. ;
Papathanasiou, Peter ;
Forsberg, E. Camilla ;
Xu, Jian ;
Smale, Stephen T. ;
Weissman, Irving L. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2007, 104 (30) :12371-12376
[6]   Chromatin signatures of pluripotent cell lines [J].
Azuara, V ;
Perry, P ;
Sauer, S ;
Spivakov, M ;
Jorgensen, HF ;
John, RM ;
Gouti, M ;
Casanova, M ;
Warnes, G ;
Merkenschlager, M ;
Fisher, AG .
NATURE CELL BIOLOGY, 2006, 8 (05) :532-U189
[7]   Epigenetic gene silencing in cancer - a mechanism for early oncogenic pathway addiction? [J].
Baylin, SB ;
Ohm, JE .
NATURE REVIEWS CANCER, 2006, 6 (02) :107-116
[8]   A bivalent chromatin structure marks key developmental genes in embryonic stem cells [J].
Bernstein, BE ;
Mikkelsen, TS ;
Xie, XH ;
Kamal, M ;
Huebert, DJ ;
Cuff, J ;
Fry, B ;
Meissner, A ;
Wernig, M ;
Plath, K ;
Jaenisch, R ;
Wagschal, A ;
Feil, R ;
Schreiber, SL ;
Lander, ES .
CELL, 2006, 125 (02) :315-326
[9]   The mammalian epigenome [J].
Bernstein, Bradley E. ;
Meissner, Alexander ;
Lander, Eric S. .
CELL, 2007, 128 (04) :669-681
[10]   High-throughput DNA methylation profiling using universal bead arrays [J].
Bibikova, M ;
Lin, ZW ;
Zhou, LX ;
Chudin, E ;
Garcia, EW ;
Wu, B ;
Doucet, D ;
Thomas, NJ ;
Wang, YH ;
Vollmer, E ;
Goldmann, T ;
Seifart, C ;
Jiang, W ;
Barker, DL ;
Chee, MS ;
Floros, J ;
Fan, JB .
GENOME RESEARCH, 2006, 16 (03) :383-393