LeSueur J A, Graff J M
Center for Developmental Biology, UT Southwestern Medical Center, NB 5.208, Dallas, TX 75235-9133, USA.
Development. 1999 Jan;126(1):137-46. doi: 10.1242/dev.126.1.137.
The Spemann organizer induces neural tissue, dorsalizes mesoderm and generates a second dorsal axis. We report the isolation and characterization of Smad10, which has all three of these Spemann activities. Smad10 is expressed at the appropriate time to transduce Spemann signals endogenously. Like the organizer, Smad10 generates anterior and posterior neural tissues. Smad10 appears to function downstream of the Spemann organizer, consistent with a role in mediating organizer-derived signals. Interestingly, Smad10, unlike previously characterized mediators of Spemann activity, does not appear to block BMP signals. This finding, coupled with the functional activity and expression profile, suggests that Smad10 mediates Spemann action in a novel manner.
施佩曼组织者诱导神经组织形成,使中胚层背化并产生第二条背轴。我们报告了Smad10的分离与特性,它具有施佩曼的所有这三种活性。Smad10在适当的时间表达,以内源性转导施佩曼信号。与组织者一样,Smad10可产生前后神经组织。Smad10似乎在施佩曼组织者的下游发挥作用,这与它在介导组织者衍生信号中的作用一致。有趣的是,与先前鉴定的施佩曼活性介质不同,Smad10似乎并不阻断骨形态发生蛋白(BMP)信号。这一发现,再加上其功能活性和表达谱,表明Smad10以一种新的方式介导施佩曼的作用。