Shibata M, Ono H, Hikasa H, Shinga J, Taira M
Laboratory of Molecular Embryology, Department of Biological Sciences, Graduate School of Science, University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, 113-0033, Tokyo, Japan.
Mech Dev. 2000 Sep;96(2):243-6. doi: 10.1016/s0925-4773(00)00399-3.
The Spemann organizer can be subdivided into head- and trunk-inducing tissues along the anteroposterior axis (Mangold, 1933. Naturwiisenschaften 43, 761-766; Spemann, 1931. Wilhelm Roux Arch. Entwicklungsmech. Org. 123, 389-517). Recent studies have suggested that head formation is brought about by repression of both Wnt and BMP signalling (Glinka et al., 1998. Nature 391, 357-362; Glinka et al., 1997. Nature 389, 517-519). Several Wnt inhibitors secreted from the head organizer region have been identified in Xenopus, such as Cerberus (Bouwmeester et al., 1996. Nature 382, 595-601), Frzb-1 (Leyns et al., 1997. Cell 88, 747-756; Lin et al., 1997. Proc. Natl. Acad. Sci. USA 94, 11196-11200), and Dkk-1 (Glinka et al., 1998. Nature 391, 357-362), supporting this two-inhibitor model. To isolate genes expressed in the head organizer, we screened a prechordal plate cDNA library by sequencing and expression pattern, and isolated the Xenopus ortholog of chick crescent encoding a Frizzled-like domain that is related to Wnt-binding regions of the Frizzled-family proteins. Expression of Xenopus crescent was first detected in the Spemann organizer region at the early gastrula stage and later in prechordal plate cells lining the boundary of mesoderm and ectoderm layers and in the anterior endoderm. At tailbud stages, the expression in the endomesoderm region was diminished, while expression in the pronephros became detectable. In animal cap assays, crescent gene was synergistically upregulated by coexpression of Xlim1, Ldb1, and Siamois, but not by Activin treatment.
施佩曼组织者可沿前后轴细分为诱导头部和躯干的组织(曼戈尔德,1933年。《自然科学》43,761 - 766;施佩曼,1931年。《威廉·鲁克斯发育机制杂志》123,389 - 517)。最近的研究表明,头部的形成是通过抑制Wnt和BMP信号传导实现的(格林卡等人,1998年。《自然》391,357 - 362;格林卡等人,1997年。《自然》389,517 - 519)。在非洲爪蟾中已鉴定出几种从头部组织者区域分泌的Wnt抑制剂,如Cerberus(鲍梅斯特等人,1996年。《自然》382,595 - 601)、Frzb - 1(莱因斯等人,1997年。《细胞》88,747 - 756;林等人,1997年。《美国国家科学院院刊》94,11196 - 11200)和Dkk - 1(格林卡等人,1998年。《自然》391,357 - 362),支持了这种双抑制剂模型。为了分离在头部组织者中表达的基因,我们通过测序和表达模式筛选了前索板cDNA文库,并分离出了鸡新月基因的非洲爪蟾直系同源基因,该基因编码一个与卷曲蛋白家族蛋白的Wnt结合区域相关的卷曲样结构域。非洲爪蟾新月基因的表达最初在原肠胚早期的施佩曼组织者区域被检测到,随后在中胚层和外胚层层边界的前索板细胞以及前端内胚层中被检测到。在尾芽期,内胚层区域的表达减弱,而在 pronephros 中的表达变得可检测到。在动物帽实验中,新月基因通过共表达Xlim1、Ldb1和暹罗鳄蛋白而协同上调,但激活素处理则不能。