生物
十指瘫痪
信号转导
细胞生物学
丝氨酸
磷酸化
激酶
蛋白激酶A
细胞质
分子生物学
基因
生物化学
表型
影像盘
作者
Stuart J. Newfeld,Arun Mehra,Matthew A. Singer,Jeffrey L. Wrana,Liliana Attisano,William M Gelbart
出处
期刊:Development
[The Company of Biologists]
日期:1997-08-15
卷期号:124 (16): 3167-3176
被引量:90
标识
DOI:10.1242/dev.124.16.3167
摘要
ABSTRACT Mothers against dpp (Mad) is the prototype of a family of genes required for signaling by TGF-β related ligands. In Drosophila, Mad is specifically required in cells responding to Decapentaplegic (DPP) signals. We further specify the role of Mad in DPP-mediated signaling by utilizing tkvQ199D, an activated form of the DPP type I receptor serine-threonine kinase thick veins (tkv). In the embryonic midgut, tkvQ199D mimics DPP-mediated inductive interactions. Homozygous Mad mutations block signaling by tkvQ199D. Appropriate responses to signaling by tkvQ199D are restored by expression of MAD protein in DPP-target cells. Endogenous MAD is phosphorylated in a ligand-dependent manner in Drosophila cell culture. DPP overexpression in the embryonic midgut induces MAD nuclear accumulation; after withdrawal of the overexpressed DPP signal, MAD is detected only in the cytoplasm. However, in three different tissues and developmental stages actively responding to endogenous DPP, MAD protein is detected in the cytoplasm but not in the nucleus. From these observations, we discuss possible roles for MAD in a DPP-dependent serine-threonine kinase signal transduction cascade integral to the proper interpretation of DPP signals.
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