Intracellular localization of the catalytic subunit from cyclic AMP-dependent protein kinase in mutant Chinese hamster ovary cells deficient in this enzyme.

C V Byus, W H Fletcher
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Abstract

A direct cytochemical procedure that specifically locates free catalytic subunits (C) from cAMP-dependent protein kinase has been used to follow the kinetics of kinase dissociation in parental Chinese hamster ovary cells (CHO 10001) and 4 mutant CHO cell lines variously deficient in this enzyme (CHO 10215, 10248, 10260, 10265) (1-5). When cultures of wild-type cells were stimulated with 8BrcAMP a time- and dose-dependent dissociation of kinase was observed. The catalytic unit appeared first in the cytoplasm and nucleolus and with time in the nucleoplasm as well. At peak protein kinase activation (30 min) more than 80% of the cells possessed abundant C in all of these subcellular compartments. The data indicate that both the type I and type II isozymes of the cAMP-dependent protein kinase are localized in similar areas of the cell. Stimulation of the mutant cell lines with 8-BrcAMP revealed that they each contained activatable kinase, determined cytochemically, that paralleled in amount the total assayable protein kinase determined biochemically (1-6). There were differences in the basal (unstimulated) levels of free C in the mutants relative to each other and to wild-type cells. For example, wild-type and mutants 10248, and 10260 had barely detectable cytoplasmic catalytic-subunit in unstimulated cultures whereas mutant 10215 possessed a significant amount of free C. Upon stimulation with 8-BrcAMP, the subcellular distribution of C was in all cases similar; although there were significant quantitative disparities between the wild type and various mutant cell lines. All cell lines examined had roughly equivalent amounts of nucleolar C but differed predominantly in the quantity of cytoplasmic kinase. Specifically, two of the mutant lines (10260 and 10248) contained barely detectable amounts of nucleoplasmic C whereas the other mutants had moderate (10265) to near normal (10215) amounts of nucleoplasmic enzyme. Mutants having only type I isozyme (10248) and those with only type II isozyme (10265) gave similar patterns of free C localization after 8BrcAMP stimulation.

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环amp依赖性蛋白激酶在缺乏该酶的突变体中国仓鼠卵巢细胞中的细胞内定位。
一种直接的细胞化学方法可以定位camp依赖性蛋白激酶的游离催化亚基(C),用于跟踪亲代中国仓鼠卵巢细胞(CHO 10001)和4种不同程度缺乏该酶的突变CHO细胞系(CHO 10215, 10248, 10260, 10265)的激酶解离动力学(1-5)。当用8BrcAMP刺激野生型细胞培养时,观察到激酶的解离具有时间和剂量依赖性。催化单元首先出现在细胞质和核仁中,随着时间的推移也出现在核质中。在蛋白激酶激活的峰值(30分钟),超过80%的细胞在所有这些亚细胞区室中都具有丰富的C。这些数据表明,camp依赖性蛋白激酶的I型和II型同工酶都位于细胞的相似区域。用8-BrcAMP刺激突变细胞系显示,它们都含有细胞化学测定的可活化激酶,其数量与生化测定的可测定蛋白激酶总量相似(1-6)。突变体中游离C的基础(未受刺激的)水平相对于其他突变体和野生型细胞存在差异。例如,野生型和突变体10248和10260在未刺激培养中几乎检测不到细胞质催化亚基,而突变体10215具有大量的游离C。在8-BrcAMP刺激下,C的亚细胞分布在所有情况下都是相似的;尽管在野生型和各种突变细胞系之间存在显著的数量差异。所有细胞系的核仁C含量大致相当,但细胞质激酶的含量主要不同。具体来说,两个突变系(10260和10248)含有几乎无法检测到的核质C,而其他突变系的核质酶含量中等(10265)至接近正常(10215)。仅具有I型同工酶(10248)的突变体和仅具有II型同工酶(10265)的突变体在8BrcAMP刺激后具有相似的游离C定位模式。
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