Deciphering the stem cell machinery as a basis for understanding the molecular mechanism underlying reprogramming

被引:10
作者
Bosnali, Manal [1 ,2 ]
Muenst, Bernhard [1 ,2 ]
Thier, Marc [1 ,2 ]
Edenhofer, Frank [1 ,2 ]
机构
[1] Univ Bonn, Life & Brain Ctr, Inst Reconstruct Neurobiol, Stem Cell Engn Grp, D-53105 Bonn, Germany
[2] Univ Bonn, Hertie Fdn, D-53105 Bonn, Germany
关键词
Stem cell; Pluripotency; Differentiation; Non-coding RNA; Reprogramming; Cancer; Germ cell; TRANSCRIPTIONAL REGULATORY CIRCUITRY; PLURIPOTENCY SUSTAINING FACTOR; PRIMORDIAL GERM-CELLS; SELF-RENEWAL; POU-DOMAIN; SMALL RNAS; ES CELLS; DEVELOPMENTAL REGULATORS; DNA METHYLATION; MOUSE EMBRYO;
D O I
10.1007/s00018-009-0095-2
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
Stem cells provide fascinating prospects for biomedical applications by combining the ability to renew themselves and to differentiate into specialized cell types. Since the first isolation of embryonic stem (ES) cells about 30 years ago, there has been a series of groundbreaking discoveries that have the potential to revolutionize modern life science. For a long time, embryos or germ cell-derived cells were thought to be the only source of pluripotency-a dogma that has been challenged during the last decade. Several findings revealed that cell differentiation from (stem) cells to mature cells is not in fact an irreversible process. The molecular mechanism underlying cellular reprogramming is poorly understood thus far. Identifying how pluripotency maintenance takes place in ES cells can help us to understand how pluripotency induction is regulated. Here, we review recent advances in the field of stem cell regulation focusing on key transcription factors and their functional interplay with non-coding RNAs.
引用
收藏
页码:3403 / 3420
页数:18
相关论文
共 160 条
[1]   The functions of animal microRNAs [J].
Ambros, V .
NATURE, 2004, 431 (7006) :350-355
[2]   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
[3]   Mouse ES cells express endogenous shRNAs, siRNAs, and other Microprocessor-independent, Dicer-dependent small RNAs [J].
Babiarz, Joshua E. ;
Ruby, J. Graham ;
Wang, Yangming ;
Bartel, David P. ;
Blelloch, Robert .
GENES & DEVELOPMENT, 2008, 22 (20) :2773-2785
[4]   MicroRNAs: Genomics, biogenesis, mechanism, and function (Reprinted from Cell, vol 116, pg 281-297, 2004) [J].
Bartel, David P. .
CELL, 2007, 131 (04) :11-29
[5]   A mammalian microRNA cluster controls DNA methylation and telomere recombination via Rbl2-dependent regulation of DNA methyltransferases [J].
Benetti, Roberta ;
Gonzalo, Susana ;
Jaco, Isabel ;
Munoz, Purificacion ;
Gonzalez, Susana ;
Schoeftner, Stefan ;
Murchison, Elizabeth ;
Andl, Thomas ;
Chen, Taiping ;
Klatt, Peter ;
Li, En ;
Serrano, Manuel ;
Millar, Sarah ;
Hannon, Gregory ;
Blasco, Maria A. .
NATURE STRUCTURAL & MOLECULAR BIOLOGY, 2008, 15 (03) :268-279
[6]   Dicer is essential for mouse development [J].
Bernstein, E ;
Kim, SY ;
Carmell, MA ;
Murchison, EP ;
Alcorn, H ;
Li, MZ ;
Mills, AA ;
Elledge, SJ ;
Anderson, KV ;
Hannon, GJ .
NATURE GENETICS, 2003, 35 (03) :215-217
[7]   Leukemia inhibitory factor-dependent transcriptional activation in embryonic stem cells [J].
Boeuf, H ;
Hauss, C ;
DeGraeve, F ;
Baran, N ;
Kedinger, C .
JOURNAL OF CELL BIOLOGY, 1997, 138 (06) :1207-1217
[8]   Generation of transducible versions of transcription factors Oct4 and Sox2 [J].
Bosnali, Manal ;
Edenhofer, Frank .
BIOLOGICAL CHEMISTRY, 2008, 389 (07) :851-861
[9]   Polycomb complexes repress developmental regulators in murine embryonic stem cells [J].
Boyer, LA ;
Plath, K ;
Zeitlinger, J ;
Brambrink, T ;
Medeiros, LA ;
Lee, TI ;
Levine, SS ;
Wernig, M ;
Tajonar, A ;
Ray, MK ;
Bell, GW ;
Otte, AP ;
Vidal, M ;
Gifford, DK ;
Young, RA ;
Jaenisch, R .
NATURE, 2006, 441 (7091) :349-353
[10]   Core transcriptional regulatory circuitry in human embryonic stem cells [J].
Boyer, LA ;
Lee, TI ;
Cole, MF ;
Johnstone, SE ;
Levine, SS ;
Zucker, JR ;
Guenther, MG ;
Kumar, RM ;
Murray, HL ;
Jenner, RG ;
Gifford, DK ;
Melton, DA ;
Jaenisch, R ;
Young, RA .
CELL, 2005, 122 (06) :947-956