Murine cortactin is phosphorylated in response to fibroblast growth factor-1 on tyrosine residues late in the G1 phase of the BALB/c 3T3 cell cycle.

Murine cortactin is phosphorylated in response to fibroblast growth factor-1 on tyrosine residues late in the G1 phase of the BALB/c 3T3 cell cycle.
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发表时间:
1993-11
期刊:
The Journal of biological chemistry
影响因子:
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通讯作者:
X. Zhan;X. Hu;B. Hampton;W. Burgess;R. Friesel;T. Maciag
X. Zhan;X. Hu;B. Hampton;W. Burgess;R. Friesel;T. Maciag
中科院分区:
其他
文献类型:
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作者:
X. Zhan;X. Hu;B. Hampton;W. Burgess;R. Friesel;T. Maciag

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我们先前报道BALB/c 3 T3细胞需要长时间暴露于成纤维细胞生长因子(FGF)-1以刺激最大DNA合成,并且该事件与G1后期新蛋白质的酪氨酸磷酸化相关,包括称为p80/p85的蛋白质(Zhan,X.,Hu,X.,弗里茨河,和Maciag,T.(1993)J.Biol.Chem.268,9611-9620)。我们已纯化,测序,并克隆了cDNA编码p80/p85和报告,它是小鼠同源的鸡corneum基因和人造血特异性-1基因家族的成员。对FGF-1反应的m-皮质素-酪氨酸磷酸化的免疫化学分析显示了一种双相磷酸化模式,即弱的即刻早期和强的中期至晚期G1反应蛋白。由于鸡corneum基因最初是作为v-Src的底物分离的,FGF-1可能影响其他细胞相关酪氨酸激酶的酶活性,这些酪氨酸激酶利用p80/p85(corneum)作为多肽底物。
We have previously reported that BALB/c 3T3 cells require a prolonged exposure to fibroblast growth factor (FGF)-1 for the stimulation of maximal DNA synthesis, and this event correlates with the tyrosine phosphorylation of novel proteins late in G1 including a protein termed p80/p85 (Zhan, X., Hu, X., Friesel, R., and Maciag, T. (1993) J. Biol. Chem. 268, 9611-9620). We have purified, sequenced, and cloned the cDNA encoding p80/p85 and report that it is the murine homolog of the chicken cortactin gene and a member of the human hematopoietic specific-1 gene family. Immunochemical analysis of m-cortactin-tyrosine phosphorylation in response to FGF-1 demonstrates a biphasic phosphorylation pattern both as a weak immediate-early and strong mid to late G1 response protein. Because the chicken cortactin gene was originally isolated as a substrate for v-Src, FGF-1 may influence the enzymatic activity of other cell-associated tyrosine kinases which utilize p80/p85 (cortactin) as a polypeptide substrate.