β-catenin/Tcf-regulated transcription prior to the midblastula transition

被引:135
作者
Yang, J
Tan, CG
Darken, RS
Wilson, PA
Klein, PS [1 ]
机构
[1] Univ Penn, Sch Med, Dept Med Hematol Oncol, Philadelphia, PA 19104 USA
[2] Univ Penn, Sch Med, Howard Hughes Med Inst, Philadelphia, PA 19104 USA
[3] Cornell Univ, Weill Med Coll, Dept Cell Biol, New York, NY 10021 USA
来源
DEVELOPMENT | 2002年 / 129卷 / 24期
关键词
Wnt; beta-catenin; Tcf; LEF; midblastula transition; transcription; Xenopus embryo; lithium;
D O I
10.1242/dev.00150
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Following fertilization, the zygotic genome in many organisms is quiescent until the midblastula transition (MBT), when large-scale transcription begins. In Xenopus embryos, for example, transcription is believed to be repressed until the twelfth cell division. Thus, although dorsal-ventral patterning begins during the first cell cycle, little attention has been given to transcriptional regulation in pre-MBT development. We present evidence that regulated transcription begins during early cleavage stages and that the beta-catenin-Tcf complex is required for the transcription of the Xenopus nodal genes Xnr5 and Xnr6 as early as the 256-cell stage. Moreover, inhibition of beta-catenin/Tcf function can block dorsal development, but only if the inhibition begins early and is maintained throughout pre-MBT stages. Dorsal development can be rescued in ventralized embryos if Tcf-dependent transcription is activated prior to MBT, but activation of Tcf after MBT cannot rescue ventralized embryos, suggesting that beta-catenin/Tcf-dependent transcription is required prior to MBT for dorsal-ventral patterning in Xenopus.
引用
收藏
页码:5743 / 5752
页数:10
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