Cole T, Inglis A, Nagashima M, Schreiber G
Biochem Biophys Res Commun. 1985 Jan 31;126(2):719-24. doi: 10.1016/0006-291x(85)90244-x.
Rat major acute-phase alpha(1)protein (MAP) was characterized by determining its secondary structure, ligand binding and partial amino acid sequence. A cDNA clone expressing MAP and coding for the entire mature protein was isolated from a cDNA library in E. coli prepared from rat liver mRNA. By hybridization to nick translated cDNA, mRNA for MAP was found only in liver, where it increased 17-fold during acute inflammation. Constant proportions of rates of leucine incorporation into MAP over mRNA levels in liver indicated that the regulation of the synthesis of MAP is due to a change in the rate of synthesis and/or the stability of mRNA for MAP, but not the rate of its translation.
通过确定大鼠主要急性期α(1)蛋白(MAP)的二级结构、配体结合情况及部分氨基酸序列对其进行了表征。从大鼠肝脏mRNA制备的大肠杆菌cDNA文库中分离出一个表达MAP并编码整个成熟蛋白的cDNA克隆。通过与切口平移cDNA杂交发现,MAP的mRNA仅在肝脏中存在,在急性炎症期间其含量增加了17倍。肝脏中亮氨酸掺入MAP的速率与mRNA水平的比例恒定,这表明MAP合成的调节是由于MAP的mRNA合成速率和/或稳定性的变化,而非其翻译速率的改变。