Penzel R, Oschwald R, Chen Y, Tacke L, Grunz H
Universität GH Essen, Department of Zoophysiology, Germany.
Int J Dev Biol. 1997 Oct;41(5):667-77.
Using the powerful RDA-PCR-technique we could identify a novel Xenopus specific Sox-gene (xSox3) a transcription factor closely related to the sox sub-group B, which contains a HMG box. In normogenesis the xSox3 gene is expressed in the presumptive central nervous system. Furthermore a maternal component is also found in oocytes and in early cleavage stages in the animal hemisphere only. By whole-mount in situ hybridization the first zygotic transcription activities can be detected in the late blastula in the dorsal ectoderm and the dorsal and lateral part of the marginal zone. The expression reaches the highest level atthe late gastrula till the late neurula and fades after stage 30. The expression is restricted from gastrulation onwards to the presumptive brain area and the lens epithelium. Furthermore we could show that the gene is expressed in isolated Spemann organizer with adjacent neuroectoderm. The signal can be suppressed by suramin treatment, which inhibits neural development and causes a shift of dorsal to ventral mesoderm. The treatment of whole embryos with LiCl and UV results in an overexpression or an inhibition of the expression, respectively. In exogastrulae (pseudo-exogastrulae) the gene is expressed in the close vicinity to the endomesoderm only, but not in the distal most part of the ectoderm. This result indicates that it is unlikely that the gene can be activated by planar signals. The gene can also be activated in dissociated gastrula ectoderm without mesodermal or neural inducers. That means that the gene can be expressed in ectodermal cells in a cell autonomous manner.
利用强大的RDA-PCR技术,我们鉴定出一种新的非洲爪蟾特异性Sox基因(xSox3),它是一种转录因子,与包含HMG盒的Sox B亚组密切相关。在正常发育过程中,xSox3基因在推定的中枢神经系统中表达。此外,仅在卵母细胞和动物半球的早期卵裂阶段也发现了母体成分。通过全胚胎原位杂交,可在囊胚后期的背侧外胚层以及边缘区的背侧和外侧部分检测到首次合子转录活性。该表达在原肠胚后期直至神经胚后期达到最高水平,并在第30阶段后消失。从原肠胚形成开始,该表达局限于推定的脑区和晶状体上皮。此外,我们还表明该基因在分离的施佩曼组织者及其相邻的神经外胚层中表达。信号可被苏拉明处理抑制,苏拉明会抑制神经发育并导致背侧中胚层向腹侧中胚层转变。用LiCl和紫外线处理整个胚胎分别导致该基因的过表达或表达抑制。在外胚层发育不全(假外胚层发育不全)中,该基因仅在内胚层附近表达,而不在外胚层的最远端部分表达。这一结果表明该基因不太可能被平面信号激活。该基因也可在没有中胚层或神经诱导物的解离原肠胚外胚层中被激活。这意味着该基因可以以细胞自主的方式在外胚层细胞中表达。