Howard E W, Newman L A, Oleksyn D W, Angerer R C, Angerer L M
Department of Biology, University of Rochester, Rochester, NY 14627, USA.
Development. 2001 Feb;128(3):365-75. doi: 10.1242/dev.128.3.365.
Localization of nuclear beta-catenin initiates specification of vegetal fates in sea urchin embryos. We have identified SpKrl, a gene that is activated upon nuclear entry of beta-catenin. SpKrl is upregulated when nuclear beta-catenin activity is increased with LiCl and downregulated in embryos injected with molecules that inhibit beta-catenin nuclear function. LiCl-mediated SpKrl activation is independent of protein synthesis, indicating that SpKrl is a direct target of beat-catenin and TCF. Embryos in which SpKrl translation is inhibited with morpholino antisense oligonucleotides lack endoderm. Conversely, SpKrl mRNA injection rescues some vegetal structures in beta-catenin-deficient embryos. SpKrl negatively regulates expression of the animalizing transcription factor, SpSoxB1. We propose that SpKrl functions in patterning the vegetal domain by suppressing animal regulatory activities.
细胞核中β-连环蛋白的定位启动了海胆胚胎中植物性命运的特化。我们鉴定出了SpKrl,这是一个在β-连环蛋白进入细胞核后被激活的基因。当用LiCl增加细胞核β-连环蛋白活性时,SpKrl被上调,而在注射抑制β-连环蛋白核功能的分子的胚胎中则被下调。LiCl介导的SpKrl激活不依赖于蛋白质合成,这表明SpKrl是β-连环蛋白和TCF的直接靶标。用吗啉代反义寡核苷酸抑制SpKrl翻译的胚胎缺乏内胚层。相反,注射SpKrl mRNA可挽救β-连环蛋白缺陷胚胎中的一些植物性结构。SpKrl负向调节动物性转录因子SpSoxB1的表达。我们提出,SpKrl通过抑制动物调节活性在植物性区域的模式形成中发挥作用。