Regulated subset of G1 growth-control genes in response to derepression by the Wnt pathway

被引:129
作者
Baek, SH
Kioussi, C
Briata, P
Wang, DG
Nguyen, HD
Ohgi, KA
Glass, CK
Wynshaw-Boris, A
Rose, DW
Rosenfeld, MG
机构
[1] Univ Calif San Diego, Howard Hughes Med Inst, La Jolla, CA 92093 USA
[2] Univ Calif San Diego, Dept Med, La Jolla, CA 92093 USA
[3] Univ Calif San Diego, Dept Cellular & Mol Med, La Jolla, CA 92093 USA
[4] Univ Calif San Diego, Dept Pediat, La Jolla, CA 92093 USA
[5] Univ Calif San Diego, Ctr Canc, La Jolla, CA 92093 USA
[6] Ist Nazl Ric Canc, I-16132 Genoa, Italy
关键词
D O I
10.1073/pnas.0330217100
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Pitx2 is a bicoid-related homeodomain factor that is required for effective cell type-specific proliferation directly activating a specific growth-regulating gene cyclin D2. Here, we report that Pitx2, in response to the Wnt/beta-catenin pathway and growth signals, also can regulate c-Myc and cyclin D1. Investigation of molecular mechanisms required for Pitx2-dependent proliferation, in these cases, further supports a nuclear role for beta-catenin in preventing the histone deacetylase 1-dependent inhibitory functions of several DNA-binding transcriptional repressors, potentially including E2F4/p130 pocket protein inhibitory complex, as well as lymphoid enhancer factor 1 and Pitx2, by dismissal of histone deacetylase 1 and loss of its enzymatic activity. Thus, beta-catenin plays a signal-integrating role in Wnt- and growth factor-dependent proliferation events in mammalian development by both derepressing several classes of repressors and by activating Pitx2, regulating the activity of several growth control genes.
引用
收藏
页码:3245 / 3250
页数:6
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