Onai Takayuki, Sasai Noriaki, Matsui Masaru, Sasai Yoshiki
Organogenesis and Neurogenesis Group, Center for Developmental Biology, RIKEN, Kobe 650-0047, Japan.
Dev Cell. 2004 Jul;7(1):95-106. doi: 10.1016/j.devcel.2004.06.004.
Here we show that XsalF, a frog homolog of the Drosophila homeotic selector spalt, plays an essential role for the forebrain/midbrain determination in Xenopus. XsalF overexpression expands the domain of forebrain/midbrain genes and suppresses midbrain/hindbrain boundary (MHB) markers and anterior hindbrain genes. Loss-of-function studies show that XsalF is essential for the expression of the forebrain/midbrain genes and for the repression of the caudal genes. Interestingly, XsalF functions by antagonizing canonical Wnt signaling, which promotes caudalization of neural tissues. XsalF is required for anterior-specific expressions of GSK3beta and Tcf3, genes encoding antagonistic effectors of Wnt signaling. Loss-of-function phenotypes of GSK3beta and Tcf3 mimic those of XsalF while injections of GSK3beta and Tcf3 rescue loss-of-function phenotypes of XsalF. These findings suggest that the forebrain/midbrain-specific gene XsalF negatively controls cellular responsiveness to posteriorizing Wnt signals by regulating region-specific GSK3beta and Tcf3 expression.
我们在此表明,XsalF是果蝇同源异型选择基因spalt的青蛙同源物,在非洲爪蟾的前脑/中脑决定中起关键作用。XsalF的过表达扩大了前脑/中脑基因的区域,并抑制中脑/后脑边界(MHB)标记物和前脑后部基因。功能丧失研究表明,XsalF对于前脑/中脑基因的表达以及尾部基因的抑制至关重要。有趣的是,XsalF通过拮抗经典Wnt信号发挥作用,经典Wnt信号促进神经组织的尾部化。XsalF是GSK3β和Tcf3前侧特异性表达所必需的,GSK3β和Tcf3是编码Wnt信号拮抗效应物的基因。GSK3β和Tcf3的功能丧失表型与XsalF的相似,而注射GSK3β和Tcf3可挽救XsalF的功能丧失表型。这些发现表明,前脑/中脑特异性基因XsalF通过调节区域特异性GSK3β和Tcf3的表达,对细胞对尾部化Wnt信号的反应性进行负调控。