...
首页> 外文期刊>Development >LvTbx2/3: a T-box family transcription factor involved in formation of the oral/aboral axis of the sea urchin embryo.
【24h】

LvTbx2/3: a T-box family transcription factor involved in formation of the oral/aboral axis of the sea urchin embryo.

机译:LvTbx2 / 3:一个T-box家族转录因子,参与海胆胚胎的口腔/口腔轴的形成。

获取原文
获取原文并翻译 | 示例

摘要

T-box family transcription factors have been identified in many organisms and are frequently associated with patterning events during embryonic development. With an interest in the molecular basis of patterning in the sea urchin embryo, we identified several members of the T-box family in Lytechinus variegatus. Here, we report the cloning and characterization of an ortholog of the Tbx2/3 subfamily, LvTbx2/3. To characterize the spatial distribution of LvTbx2/3 protein throughout sea urchin embryogenesis, a polyclonal antiserum was generated. Nuclear localization of LvTbx2/3 initiated at the mesenchyme blastula stage and protein was present into the pluteus stage. Localization was asymmetric throughout this period and costaining with marker genes indicated that asymmetry was about the oral/aboral (O/A) axis. Asymmetric distribution of LvTbx2/3 was observed in the aboral territories of all three germ layers. In the skeletogenic mesoderm lineage, LvTbx2/3 expression was dynamic because expression appearedinitially in all skeletogenic mesenchyme cells (PMCs) but, subsequently, became refined solely to the aboral ones during skeletogenesis. To determine if the aboral expression of LvTbx2/3 is linked between germ layers, and to place LvTbx2/3 in the sequence of events that specifies the O/A axis, the effects of a series of perturbations to O/A polarity on LvTbx2/3 expression in each germ layer were examined. Preventing the nuclear localization of beta-catenin, pharmacological disruption of the O/A axis with NiCl(2), overexpression of BMP2/4 and disruption of the extracellular matrix all blocked LvTbx2/3 expression in all germ layers. This indicates that expression of LvTbx2/3 in the aboral territories of each germ layer is a common aspect of O/A specification, downstream of the molecular events that specify the axis. Furthermore, blocking the nuclear localization of beta-catenin, overexpression of BMP2/4 and disruption of the extracellular matrix also prevented the oral (stomodael) expression of LvBrachyury (LvBrac) protein, indicating that the O/A axis is established by a complex series of events. Last, the function of LvTbx2/3 in the formation of the O/A axis was characterized by examining the phenotypic consequences of ectopic expression of LvTbx2/3 mRNA on embryonic development and the expression of marker genes that identify specific germ layers and tissues. Ectopic expression of LvTbx2/3 produced profound morphogenetic defects in derivatives of each germ layer with no apparent loss in specification events in those tissues. This indicates that LvTbx2/3 functions as a regulator of morphogenetic movements in the aboral compartments of the ectoderm, endoderm and mesoderm.
机译:T-box家族转录因子已在许多生物中得到鉴定,并经常与胚胎发育过程中的模式事件相关。对海胆胚胎中形成图案的分子基础感兴趣,我们鉴定了变异天蛾(Lytechinus variegatus)T-box家族的几个成员。在这里,我们报告的Tbx2 / 3亚科,LvTbx2 / 3的直系同源基因的克隆和表征。为了表征整个海胆胚胎发生过程中LvTbx2 / 3蛋白的空间分布,生成了多克隆抗血清。 LvTbx2 / 3的核定位在间充质囊期开始,蛋白质存在于发育期。在此期间,本地化是不对称的,与标记基因共同鉴定表明不对称性大约在口腔/口腔(O / A)轴上。 LvTbx2 / 3的不对称分布在所有三个胚层的北方区域都被观察到。在骨骼形成性中胚层谱系中,LvTbx2 / 3表达是动态的,因为表达最初出现在所有骨骼生成性间充质细胞(PMC)中,但随后在骨骼生成过程中仅被提纯为aboral。为了确定LvTbx2 / 3的基因表达是否在胚芽层之间链接,并将LvTbx2 / 3置于指定O / A轴的事件序列中,对LvTbx2 / 3的一系列O / A极性扰动的影响检查每个细菌层中的3个表达。防止β-catenin的核定位,NiCl(2)的O / A轴的药理学破坏,BMP2 / 4的过表达和细胞外基质的破坏都阻止了LvTbx2 / 3在所有细菌层的表达。这表明LvTbx2 / 3在每个细菌层的硼质领土中的表达是O / A规范的一个共同方面,在指定轴的分子事件的下游。此外,阻断β-catenin的核定位,BMP2 / 4的过表达和细胞外基质的破坏也阻止了LvBrachyury(LvBrac)蛋白的口服(胃祖细胞)表达,表明O / A轴是由一个复杂的序列建立的事件。最后,LvTbx2 / 3在O / A轴形成中的功能通过检查LvTbx2 / 3 mRNA异位表达对胚胎发育的表型后果以及识别特定细菌层和组织的标志物基因的表达来表征。 LvTbx2 / 3的异位表达在每个胚层的衍生物中产生了深刻的形态发生缺陷,而这些组织中的规格事件没有明显的损失。这表明LvTbx2 / 3充当外胚层,内胚层和中胚层的房室中形态发生运动的调节剂。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号