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环磷酸腺苷受体1在生长中的盘基网柄菌细胞中的过表达。

Overexpression of the cAMP receptor 1 in growing Dictyostelium cells.

作者信息

Johnson R L, Vaughan R A, Caterina M J, Van Haastert P J, Devreotes P N

机构信息

Department of Biological Chemistry, School of Medicine, Johns Hopkins University, Baltimore, Maryland 21205.

出版信息

Biochemistry. 1991 Jul 16;30(28):6982-6. doi: 10.1021/bi00242a025.

DOI:10.1021/bi00242a025
PMID:1648967
Abstract

cAR1, the cAMP receptor expressed normally during the early aggregation stage of the Dictyostelium developmental program, has been expressed during the growth stage, when only low amounts of endogenous receptors are present. Transformants expressing cAR1 have 7-40 times over growth stage and 3-5-fold over aggregation stage levels of endogenous receptors. The high amounts of cAR1 protein expressed constitutively throughout early development did not drastically disrupt the developmental program; the onset of aggregation was delayed by 1-3 h, and then subsequent stages proceeded normally. The affinity of the expressed cAR1 was similar to that of the endogenous receptors in aggregation stage cells when measured either in phosphate buffer (two affinity states with Kd's of approximately 30 and 300 nM) or in 3 M ammonium sulfate (one affinity state with a Kd of 2-3 nM). When expressed during growth, cAR1 did not appear to couple to its normal effectors since these cells failed to carry out chemotaxis or to elevate cGMP or cAMP levels when stimulated with cAMP. However, cAMP stimulated phosphorylation, and loss of ligand binding of cAR1 did occur. Like aggregation stage control cells, the cAR1 protein shifted in apparent molecular mass from 40 to 43 kDa and became highly phosphorylated when exposed to cAMP. In addition, the number of surface cAMP binding sites in cAR1 cells was reduced by over 80% during prolonged cAMP stimulation. These results define a useful system to express altered cAR1 proteins and examine their regulatory functions.

摘要

cAR1是一种在盘基网柄菌发育程序早期聚集阶段正常表达的cAMP受体,在生长阶段也有表达,而此时内源性受体的含量很低。表达cAR1的转化体在生长阶段内源性受体水平的基础上增加了7 - 40倍,在聚集阶段增加了3 - 5倍。在整个早期发育过程中持续组成性表达的大量cAR1蛋白并没有严重扰乱发育程序;聚集的开始延迟了1 - 3小时,随后的阶段则正常进行。当在磷酸盐缓冲液(两种亲和力状态,Kd分别约为30和300 nM)或3 M硫酸铵(一种亲和力状态,Kd为2 - 3 nM)中测量时,表达的cAR1的亲和力与聚集阶段细胞中的内源性受体相似。当在生长期间表达时,cAR1似乎没有与其正常效应器偶联,因为这些细胞在用cAMP刺激时未能进行趋化作用或提高cGMP或cAMP水平。然而,cAMP刺激确实导致了磷酸化以及cAR1配体结合的丧失。与聚集阶段的对照细胞一样,cAR1蛋白在暴露于cAMP时表观分子量从40 kDa转变为43 kDa并变得高度磷酸化。此外,在长时间的cAMP刺激下,cAR1细胞表面cAMP结合位点的数量减少了80%以上。这些结果定义了一个有用的系统,可用于表达改变的cAR1蛋白并研究其调节功能。

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