Ohta Kunimasa, Kuriyama Sei, Okafuji Tatsuya, Gejima Ryu, Ohnuma Shin-ichi, Tanaka Hideaki
Department of Developmental Neurobiology, Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan.
Development. 2006 Oct;133(19):3777-86. doi: 10.1242/dev.02579. Epub 2006 Aug 30.
Three classes of signaling molecule, VG1, WNT and BMP, play crucial roles in axis formation in the chick embryo. Although VG1 and WNT signals have a pivotal function in inducing the primitive streak and Hensen's node in the embryo midline, their action is complemented by that of BMP antagonists that protect the prospective axial tissue from the inhibitory influence of BMPs secreted from the periphery. We have previously reported that a secreted factor, chick Tsukushi (TSK), is expressed in the primitive streak and Hensen's node, where it works as a BMP antagonist. Here, we describe a new crucial function for TSK in promoting formation of the primitive streak and Hensen's node by positively regulating VG1 activity. We provide evidence that TSK directly binds VG1 in vitro, and that TSK and VG1 functionally interact in axis formation, as shown by biological assays performed in chick and Xenopus embryos. Furthermore, we show that alternative splicing of TSK RNA leads to the formation of two isoforms (TSKA, originally designated as TSK, and TSKB) that differ in their C-terminal region. Biochemical and biological assays indicate that TSKB is a much weaker BMP antagonist than TSKA, although both isoforms efficiently interact with VG1. Remarkably, although both TSKA and TSKB are expressed throughout the early extending primitive streak, their expression patterns diverge during gastrulation. TSKA expression concentrates in Hensen's node, a well-known source of anti-BMP signals, whereas TSKB accumulates in the middle primitive streak (MPS), a region known to work as a node-inducing center where VG1 expression is also specifically localized. Loss-of-function experiments demonstrate that TSKB, but not TSKA, function is required in the MPS for induction of Hensen's node. Taken together, these results indicate that TSK isoforms play a crucial role in chick axis formation by locally modulating VG1 and BMP activities during gastrulation.
三类信号分子,即VG1、WNT和BMP,在鸡胚的轴形成过程中发挥着关键作用。尽管VG1和WNT信号在诱导胚胎中线的原条和亨氏结方面具有关键功能,但它们的作用由BMP拮抗剂的作用所补充,这些拮抗剂保护预期的轴组织免受外周分泌的BMP的抑制影响。我们之前报道过,一种分泌因子,鸡的筑波蛋白(TSK),在原条和亨氏结中表达,在那里它作为一种BMP拮抗剂发挥作用。在这里,我们描述了TSK在通过正向调节VG1活性促进原条和亨氏结形成方面的一个新的关键功能。我们提供证据表明TSK在体外直接结合VG1,并且TSK和VG1在轴形成过程中功能相互作用,这在鸡和非洲爪蟾胚胎中进行的生物学试验中得到了证明。此外,我们表明TSK RNA的可变剪接导致形成两种异构体(TSKA,最初命名为TSK,和TSKB),它们在C端区域有所不同。生化和生物学试验表明,尽管两种异构体都能有效地与VG1相互作用,但TSKB作为BMP拮抗剂的作用比TSKA弱得多。值得注意的是,尽管TSKA和TSKB在早期延伸的原条中都有表达,但它们在原肠胚形成过程中的表达模式有所不同。TSKA的表达集中在亨氏结,这是一个众所周知的抗BMP信号源,而TSKB则聚集在中胚层原条(MPS),这是一个已知的作为结诱导中心的区域,VG1的表达也特异性地定位于此。功能丧失实验表明,在MPS中诱导亨氏结需要TSKB而不是TSKA的功能。综上所述,这些结果表明TSK异构体在鸡胚轴形成过程中通过在原肠胚形成期间局部调节VG1和BMP活性发挥关键作用。