Regulation of cell lineage specification by the retinoblastoma tumor suppressor

被引:29
作者
Skapek, S. X.
Pan, Y-R
Lee, E. Y-H P.
机构
[1] St Jude Childrens Res Hosp, Dept Hematol Oncol, Memphis, TN 38105 USA
[2] Univ Calif Irvine, Dept Biol Chem, Irvine, CA 92717 USA
[3] Univ Calif Irvine, Dept Dev & Cell Biol, Irvine, CA 92717 USA
关键词
tumor suppressor gene; retinoblastoma susceptibility gene; cellular differentiation;
D O I
10.1038/sj.onc.1209710
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
Early studies of the retinoblastoma gene (RB) have uncovered its critical role as a regulator of the G(1)/S cell cycle phase progression. Surprisingly, genetic approaches in mammals and nematodes have also shown RB controls cell lineage specification and aspects of differentiation. The RB gene product accomplishes this by diverse mechanisms such as by interacting with tissue-specific transcription factors, enhancing RNA interference, and modifying chromatin structure. We review recent studies uncovering novel mechanisms by which RB works in several cell lineages and we provide perspectives on how these new findings might relate to RB tumor suppression.
引用
收藏
页码:5268 / 5276
页数:9
相关论文
共 99 条
[1]   Myeloid development is selectively disrupted in PU.1 null mice [J].
Anderson, KL ;
Smith, KA ;
Conners, K ;
McKercher, SR ;
Maki, RA ;
Torbett, BE .
BLOOD, 1998, 91 (10) :3702-3710
[2]   LEK1 is a potential inhibitor of pocket protein-mediated cellular processes [J].
Ashe, M ;
Lil, PPA ;
Dees, E ;
Price, KL ;
Bader, D .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (01) :664-676
[3]   Binding of pRB to the PHD protein RBP2 promotes cellular differentiation [J].
Benevolenskaya, EV ;
Murray, HL ;
Branton, P ;
Young, RA ;
Kaelin, WG .
MOLECULAR CELL, 2005, 18 (06) :623-635
[4]   A pRb-independent mechanism preserves the postmitotic state in terminally differentiated skeletal muscle cells [J].
Camarda, G ;
Siepi, F ;
Pajalunga, D ;
Bernardini, C ;
Rossi, R ;
Montecucco, A ;
Meccia, E ;
Crescenzi, M .
JOURNAL OF CELL BIOLOGY, 2004, 167 (03) :417-423
[5]   XNP-1/ATR-X acts with RB, HP1 and the NuRD complex during larval development in C. elegans [J].
Cardoso, C ;
Couillault, C ;
Mignon-Ravix, C ;
Millet, A ;
Ewbank, JJ ;
Fontés, M ;
Pujol, N .
DEVELOPMENTAL BIOLOGY, 2005, 278 (01) :49-59
[6]   EXPRESSION OF RECESSIVE ALLELES BY CHROMOSOMAL MECHANISMS IN RETINOBLASTOMA [J].
CAVENEE, WK ;
DRYJA, TP ;
PHILLIPS, RA ;
BENEDICT, WF ;
GODBOUT, R ;
GALLIE, BL ;
MURPHREE, AL ;
STRONG, LC ;
WHITE, RL .
NATURE, 1983, 305 (5937) :779-784
[7]   FOXC2 is a winged helix gene that counteracts obesity, hypertriglyceridemia, and diet-induced insulin resistance [J].
Cederberg, A ;
Gronning, LM ;
Ahrén, B ;
Taskén, K ;
Carlsson, P ;
Enerbäck, S .
CELL, 2001, 106 (05) :563-573
[8]   dpl-1 DP and efl-1 E2F act with lin-35 Rb to antagonize Ras signaling in C-elegans vulval development [J].
Ceol, CJ ;
Horvitz, HR .
MOLECULAR CELL, 2001, 7 (03) :461-473
[9]   Cell-specific effects of RB or RB/p107 loss on retinal development implicate an intrinsically death-resistant cell-of-origin in retinoblastoma [J].
Chen, D ;
Livne-Bar, I ;
Vanderluit, JL ;
Slack, RS ;
Agochiya, M ;
Bremner, R .
CANCER CELL, 2004, 5 (06) :539-551
[10]   Molecular cloning and developmental expression of mouse p130, a member of the retinoblastoma gene family [J].
Chen, G ;
Guy, CT ;
Chen, HW ;
Hu, NP ;
Lee, EYHP ;
Lee, WH .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (16) :9567-9572