Moon Anne M, Guris Deborah L, Seo Ji-heui, Li Leiming, Hammond Jennetta, Talbot Amy, Imamoto Akira
Department of Pediatrics, University of Utah School of Medicine, Salt Lake City, Utah 84112, USA.
Dev Cell. 2006 Jan;10(1):71-80. doi: 10.1016/j.devcel.2005.12.003.
Deletions on chromosome 22q11.21 disrupt pharyngeal and cardiac development and cause DiGeorge and related human syndromes. CRKL (CRK-Like) lies within 22q11.21, and Crkl-/- mice have phenotypic features of 22q11 deletion (del22q11) syndromes. While human FGF8 does not localize to 22q11, deficiency of Fgf8 also generates many features of del22q11 syndrome in mice. Since Fgf8 signals via receptor-type tyrosine kinases, and Crk family adaptor proteins transduce intracellular signals downstream of tyrosine kinases, we investigated whether Crkl mediates Fgf8 signaling. In addition to discovering genetic interactions between Crkl and Fgf8 during morphogenesis of structures affected in del22q11 syndrome, we found that Fgf8 induces tyrosine phosphorylation of FgfRs 1 and 2 and their binding to Crkl. Crkl is required for normal cellular responses to Fgf8, including survival and migration, Erk activation, and target gene expression. These findings provide mechanistic insight into disrupted intercellular interactions in the pathogenesis of malformations seen in del22q11 syndrome.
22号染色体q11.21区域的缺失会破坏咽和心脏的发育,并导致迪格奥尔格综合征及相关人类综合征。CRKL(类CRK)位于22q11.21区域内,Crkl基因敲除小鼠具有22q11缺失(del22q11)综合征的表型特征。虽然人类FGF8并不定位于22q11,但Fgf8基因缺陷也会在小鼠中产生许多del22q11综合征的特征。由于Fgf8通过受体型酪氨酸激酶发出信号,而Crk家族衔接蛋白在酪氨酸激酶下游转导细胞内信号,我们研究了Crkl是否介导Fgf8信号传导。除了发现在del22q11综合征所影响结构的形态发生过程中Crkl与Fgf8之间的遗传相互作用外,我们还发现Fgf8可诱导FgfRs 1和2的酪氨酸磷酸化及其与Crkl的结合。Crkl是细胞对Fgf8正常细胞反应所必需的,包括存活和迁移、Erk激活以及靶基因表达。这些发现为深入了解del22q11综合征中所见畸形发病机制中细胞间相互作用的破坏提供了机制性见解。