Chen Hui-Jye, Lin Chung-Ming, Lin Chyuan-Sheng, Perez-Olle Raul, Leung Conrad L, Liem Ronald K H
Department of Pathology and Cell Biology, College of Physicians and Surgeons, Columbia University, New York, New York 10032, USA.
Genes Dev. 2006 Jul 15;20(14):1933-45. doi: 10.1101/gad.1411206. Epub 2006 Jun 30.
MACF1 (microtubule actin cross-linking factor 1) is a multidomain protein that can associate with microfilaments and microtubules. We found that MACF1 was highly expressed in neuronal tissues and the foregut of embryonic day 8.5 (E8.5) embryos and the head fold and primitive streak of E7.5 embryos. MACF1(-/-) mice died at the gastrulation stage and displayed developmental retardation at E7.5 with defects in the formation of the primitive streak, node, and mesoderm. This phenotype was similar to Wnt-3(-/-) and LRP5/6 double-knockout embryos. In the absence of Wnt, MACF1 associated with a complex that contained Axin, beta-catenin, GSK3beta, and APC. Upon Wnt stimulation, MACF1 appeared to be involved in the translocation and subsequent binding of the Axin complex to LRP6 at the cell membrane. Reduction of MACF1 with small interfering RNA decreased the amount of beta-catenin in the nucleus, and led to an inhibition of Wnt-induced TCF/beta-catenin-dependent transcriptional activation. Similar results were obtained with a dominant-negative MACF1 construct that contained the Axin-binding region. Reduction of MACF1 in Wnt-1-expressing P19 cells resulted in decreased T (Brachyury) gene expression, a DNA-binding transcription factor that is a direct target of Wnt/beta-catenin signaling and required for mesoderm formation. These results suggest a new role of MACF1 in the Wnt signaling pathway.
微管肌动蛋白交联因子1(MACF1)是一种多结构域蛋白,可与微丝和微管结合。我们发现MACF1在神经元组织以及胚胎第8.5天(E8.5)胚胎的前肠、E7.5胚胎的头褶和原条中高度表达。MACF1基因敲除(MACF1(-/-))小鼠在原肠胚形成阶段死亡,在E7.5时表现出发育迟缓,原条、节点和中胚层形成存在缺陷。这种表型与Wnt-3基因敲除(Wnt-3(-/-))和低密度脂蛋白受体相关蛋白5/6(LRP5/6)双敲除胚胎相似。在没有Wnt的情况下,MACF1与包含轴蛋白(Axin)、β-连环蛋白、糖原合成酶激酶3β(GSK3β)和腺瘤性息肉病 coli蛋白(APC)的复合物结合。在Wnt刺激下,MACF1似乎参与了Axin复合物向细胞膜上LRP6的转运及随后的结合。用小干扰RNA降低MACF1的表达量会减少细胞核中β-连环蛋白的含量,并导致Wnt诱导的T细胞因子(TCF)/β-连环蛋白依赖性转录激活受到抑制。用包含Axin结合区域的显性负性MACF1构建体也得到了类似结果。在表达Wnt-1的P19细胞中降低MACF1的表达量会导致T(短尾)基因表达减少,T基因是一种DNA结合转录因子,是Wnt/β-连环蛋白信号的直接靶点,也是中胚层形成所必需的。这些结果表明MACF1在Wnt信号通路中具有新的作用。