Establishment of the dorsal-ventral axis in Xenopus embryos coincides with the dorsal enrichment of dishevelled that is dependent on cortical rotation.

Establishment of the dorsal-ventral axis in Xenopus embryos coincides with the dorsal enrichment of dishevelled that is dependent on cortical rotation.
复制标题

DOI:
10.1083/jcb.146.2.427
复制
发表时间:
1999-07-26
期刊:
The Journal of cell biology
影响因子:
--
通讯作者:
Moon RT
Moon RT
中科院分区:
其他
文献类型:
--
作者:
Miller JR;Rowning BA;Larabell CA;Yang-Snyder JA;Bates RL;Moon RT

文献摘要

参考文献

被引文献

相似文献

Examination of the subcellular localization of Dishevelled (Dsh) in fertilized Xenopus eggs revealed that Dsh is associated with vesicle-like organelles that are enriched on the prospective dorsal side of the embryo after cortical rotation. Dorsal enrichment of Dsh is blocked by UV irradiation of the vegetal pole, a treatment that inhibits development of dorsal cell fates, linking accumulation of Dsh and specification of dorsal cell fates. Investigation of the dynamics of Dsh localization using Dsh tagged with green fluorescent protein (Dsh-GFP) demonstrated that Dsh-GFP associates with small vesicle-like organelles that are directionally transported along the parallel array of microtubules towards the prospective dorsal side of the embryo during cortical rotation. Perturbing the assembly of the microtubule array with D2O, a treatment that promotes the random assembly of the array and the dorsalization of embryos, randomizes translocation of Dsh-GFP. Conversely, UV irradiation of the vegetal pole abolishes movement of Dsh-GFP. Finally, we demonstrate that overexpression of Dsh can stabilize β-catenin in Xenopus. These data suggest that the directional translocation of Dsh along microtubules during cortical rotation and its subsequent enrichment on the prospective dorsal side of the embryo play a role in locally activating a maternal Wnt pathway responsible for establishing dorsal cell fates in Xenopus.
DOI: 10.1016/0925-4773(96)00546-1
发表时间: 1996-07-01
影响因子: 2.6
作者:
Schneider, S;Steinbeisser, H;Hausen, P
通讯作者: Hausen, P
DOI: 10.1101/gad.10.21.2805
发表时间: 1996-11-01
影响因子: 10.5
作者:
Hoppler, S;Brown, JD;Moon, RT
通讯作者: Moon, RT
DOI: 10.1016/0092-8674(94)90069-8
发表时间: 1994-12-02
期刊: CELL
影响因子: 64.5
作者:
HEASMAN, J;CRAWFORD, A;WYLIE, C
通讯作者: WYLIE, C
DOI: 10.1093/emboj/16.13.3797
发表时间: 1997-07-01
期刊: EMBO JOURNAL
影响因子: 11.4
作者:
Aberle, H;Bauer, A;Kemler, R
通讯作者: Kemler, R
DOI: 10.1074/jbc.272.40.24735
发表时间: 1997-10-03
影响因子: 4.8
作者:
Orford, K;Crockett, C;Byers, SW
通讯作者: Byers, SW