Hollemann T, Chen Y, Grunz H, Pieler T
Georg-August-Universität Göttingen, Institut für Biochemie und Molekulare Zellbiologie, Humboldtallee 23, D-37073 Göttingen, Germany.
EMBO J. 1998 Dec 15;17(24):7361-72. doi: 10.1093/emboj/17.24.7361.
The competence of a cell to respond to the signalling molecule retinoic acid (RA) is thought to depend largely on its repertoire of cognate zinc finger nuclear receptors. XCYP26 is an RA hydroxylase that is expressed differentially during early Xenopus development. In Xenopus embryos, XCYP26 can rescue developmental defects induced by application of exogenous RA, suggesting that the enzymatic modifications introduced inhibit RA signalling activities in vivo. Alterations in the expression pattern of a number of different molecular markers for neural development induced upon ectopic expression of XCYP26 reflect a primary function of RA signalling in hindbrain development. Progressive inactivation of RA signalling results in a stepwise anteriorization of the molecular identity of individual rhombomeres. The expression pattern of XCYP26 during gastrulation appears to define areas within the prospective neural plate that develop in response to different concentrations of RA. Taken together, these observations appear to reflect an important regulatory function of XCYP26 for RA signalling; XCYP26-mediated modification of RA modulates its signalling activity and helps to establish boundaries of differentially responsive and non-responsive territories.
细胞对信号分子视黄酸(RA)作出反应的能力在很大程度上被认为取决于其同源锌指核受体的组成。XCYP26是一种RA羟化酶,在非洲爪蟾早期发育过程中差异表达。在非洲爪蟾胚胎中,XCYP26能够挽救因施加外源性RA而诱导的发育缺陷,这表明引入的酶促修饰在体内抑制了RA信号活性。在XCYP26异位表达时,多种不同神经发育分子标记的表达模式发生改变,这反映了RA信号在后脑发育中的主要功能。RA信号的逐步失活导致各个菱脑节分子身份的逐步向前化。原肠胚形成期间XCYP26的表达模式似乎确定了前神经板内响应不同浓度RA而发育的区域。综上所述,这些观察结果似乎反映了XCYP26对RA信号的重要调节功能;XCYP26介导的RA修饰调节其信号活性,并有助于建立差异反应和无反应区域的边界。