Evidence that dorsal-ventral differences in gap junctional communication in the early Xenopus embryo are generated by β-catenin independent of cell adhesion effects

被引:19
作者
Krufka, A
Johnson, RG
Wylie, CC
Heasman, J
机构
[1] Univ Minnesota, Dept Genet & Cell Biol, St Paul, MN 55108 USA
[2] Univ Minnesota, Dept Cell Biol & Neuroanat, Minneapolis, MN 55455 USA
关键词
D O I
10.1006/dbio.1998.8951
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Gap junctional communication (GJC) is regulated in the early Xenopus embryo and quantitative differences in functional communication correlate with the specification of the dorsal-ventral axis. To address the mechanism that is responsible for regulating this differential communication, we investigated the function of beta-catenin during the formation of the dorsal-ventral axis in Xenopus embryos by blocking its synthesis with antisense oligodeoxynucleotides. This method has previously been shown to reduce the level of beta-catenin in the early embryo, prior to zygotic transcription, and to inhibit the formation of the dorsal axis (Heasman et al., 1994, Cell 79, 791-803). We show here that antisense inhibition of beta-catenin synthesis also reduces GJC among cells in the dorsal hemisphere of 32-cell embryos to levels similar to those observed among ventral cells. Full-length beta-catenin mRNA can restore elevated levels of dorsal GJC when injected into beta-catenin-deficient oocytes, demonstrating the specificity of the beta-catenin depletion with the antisense oligonucleotides. Thus, endogenous beta-catenin is required for the observed differential GJC. This regulation of GJC is the earliest known action of the dorsal regulator, beta-catenin, in Xenopus development. Two lines of evidence, presented here, indicate that beta-catenin acts within the cytoplasm to regulate GJC, rather than through an effect on cell adhesion. First, when EP-cadherin is overexpressed and increased adhesion is observed, embryos display both a ventralized phenotype and reduced dye transfer. Second, a truncated form of beta-catenin (i.e., the ARM region), that lacks the cadherin-binding domain, restores dorsal GJC to beta-catenin-depleted embryos. Thus, beta-catenin appears to regulate GJC independent of its role in cell-cell adhesion, by acting within the cytoplasm through a signaling mechanism, (C) 1998 Academic Press.
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页码:92 / 102
页数:11
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