生物
23号公路
酪氨酸磷酸化
基因
酪氨酸
突变体
磷酸化
基因表达
受体
分子生物学
氨基酸
突变
基因表达调控
受体酪氨酸激酶
细胞生物学
遗传学
生物化学
抗体
免疫球蛋白E
作者
John J. Ryan,Lisa J. McReynolds,Achsah Keegan,Lu-Hai Wang,Evan S. Garfein,Paul B. Rothman,Keats Nelms,William E. Paul
出处
期刊:Immunity
[Cell Press]
日期:1996-02-01
卷期号:4 (2): 123-132
被引量:158
标识
DOI:10.1016/s1074-7613(00)80677-9
摘要
IL-4 causes hematopoietic cells to proliferate and express a series of genes, including CD23. We examined whether IL-4-mediated growth, as measured by 4PS phosphorylation, and gene induction were similarly controlled. Studies of M12.4.1 cells expressing human IL-4R truncation mutants indicated that the region between amino acids 557–657 is necessary for full gene expression, which correlated with Stat6 DNA binding activity. This region was not required for 4PS phosphorylation. Tyrosine-to-phenylalanine mutations in the interval between amino acids 557–657 revealed that as long as one tyrosine remained unmutated, CD23 was fully induced. When all three tyrosines were mutated, the receptor was unable to induce CD23. The results indicate that growth regulation and gene expression are principally controlled by distinct regions of IL-4R.
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