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细胞质锚定的桥粒芯蛋白在非洲爪蟾中诱导出类似WNT的表型。

Cytoplasmically anchored plakoglobin induces a WNT-like phenotype in Xenopus.

作者信息

Merriam J M, Rubenstein A B, Klymkowsky M W

机构信息

University of Colorado, Boulder 80309-0347, USA.

出版信息

Dev Biol. 1997 May 1;185(1):67-81. doi: 10.1006/dbio.1997.8550.

Abstract

Plakoglobin is one of two vertebrate proteins closely related to the Drosophila segment polarity gene product armadillo. Overexpression of plakoglobin induces neural axis duplication in Xenopus and the exogenous plakoglobin is localized to nuclei (Karnovsky, A., and Klymkowsky, M. W., Proc. Natl. Acad. Sci. USA 92, 4255, 1995; Rubenstein, A., et al., Dev. Genet., 1997, in press). We have carried out a series of experiments to test whether the nuclear localization of plakoglobin is required for its inductive effects. Prior to the midblastula transition exogenous plakoglobin is cytoplasmic and concentrated in the cortical regions of blastomeres; after the midblastula transition exogenous plakoglobin accumulates in embryonic nuclei. The addition of a "nuclear localization sequence" does not change the timing of plakoglobin's nuclear localization, suggesting that it is anchored in the cytoplasm prior to the midblastula transition. Next, we constructed two "membrane-anchored" forms of plakoglobin. These are exclusively cytoplasmic; yet both were as effective at producing a "Wnt-like" axis duplication as were "free," unfettered forms of plakoglobin. Moreover, expression of anchored plakoglobins had no apparent effect on the cytoplasmic or nuclear levels of beta-catenin. These data indicate that plakoglobin can act cytoplasmically to generate a WNT-like phenotype. Taken together with the ventralizing effects of a mutant from of the XTcf-3 transcription factor, described by Molenaar et al. Cell 86, 391, 1996, we speculate that in the early Xenopus embryo, activation of plakoglobin (or beta-catenin) inhibits the activity of XTcf-3 or a XTcf-3-like factor.

摘要

桥粒斑珠蛋白是两种与果蝇体节极性基因产物犰狳密切相关的脊椎动物蛋白之一。桥粒斑珠蛋白的过表达会诱导非洲爪蟾的神经轴重复,并且外源性桥粒斑珠蛋白定位于细胞核(卡尔诺夫斯基,A.,和克莱姆科夫斯基,M. W.,《美国国家科学院院刊》92,4255,1995;鲁宾斯坦,A.,等人,《发育遗传学》,1997,待发表)。我们进行了一系列实验,以测试桥粒斑珠蛋白的核定位是否是其诱导作用所必需的。在囊胚中期转变之前,外源性桥粒斑珠蛋白位于细胞质中,并集中在卵裂球的皮质区域;在囊胚中期转变之后,外源性桥粒斑珠蛋白积累在胚胎细胞核中。添加“核定位序列”并不会改变桥粒斑珠蛋白核定位的时间,这表明它在囊胚中期转变之前锚定在细胞质中。接下来,我们构建了两种“膜锚定”形式的桥粒斑珠蛋白。它们仅存在于细胞质中;然而,两者在产生“Wnt样”轴重复方面与“游离”、不受束缚形式的桥粒斑珠蛋白一样有效。此外,锚定的桥粒斑珠蛋白的表达对β-连环蛋白的细胞质或核水平没有明显影响。这些数据表明,桥粒斑珠蛋白可以在细胞质中发挥作用,以产生WNT样表型。结合莫伦纳尔等人(《细胞》86,391,1996)所描述的XTcf-3转录因子突变体的腹侧化作用,我们推测在早期非洲爪蟾胚胎中,桥粒斑珠蛋白(或β-连环蛋白)的激活会抑制XTcf-3或类似XTcf-3因子的活性。

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