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Peptidylglycine-α-amidating monooxygenase activity and protein are lower in copper-deficient rats and suckling copper-deficient mice

机译:缺铜大鼠和哺乳期缺铜小鼠的肽基甘氨酸-α-酰胺化单加氧酶活性和蛋白质较低

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摘要

Peptidylglycine-α-amidating monooxygenase (PAM) is a copper-dependent enzyme involved in peptide posttranslational activation. Dietary Cu deficiency (Cu−) was studied to determine if lower PAM activity was due to reduction in protein or cofactor limitation. PAM activity was lower in cardiac atria of Cu− rats than Cu-adequate (Cu+) rats and there was a 50% equivalent reduction in PAM protein. No reduction in Cu− rat midbrain PAM protein was detected although PAM activity was reduced 40%. In 12-day-old (P12) mouse pups derived from dams that began Cu deficiency on day 7 of gestation, there was a parallel reduction in brain PAM activity and protein of 40–50%. PAM mRNA levels assessed in atria and brains from Cu+ and Cu− rats and mice were not altered by dietary treatment, suggesting a posttranscriptional mechanism for lower PAM protein when Cu is limiting in the cell, perhaps due to enhanced apoprotein turnover.
机译:肽基甘氨酸-α酰胺化单加氧酶(PAM)是一种铜依赖性酶,参与肽后翻译激活。对饮食中的铜缺乏症(Cu-)进行了研究,以确定较低的PAM活性是否是由于蛋白质或辅因子限制的减少所致。在Cu-大鼠的心脏心房中,PAM活性低于铜充足(Cu +)大鼠,PAM蛋白降低了50%。尽管PAM活性降低了40%,但未检测到Cu-大鼠中脑PAM蛋白降低。在源自母鼠的12天大(P12)幼崽于妊娠的第7天开始出现铜缺乏症时,其脑PAM活性和蛋白质降低了40%至50%。饮食治疗未改变Cu +和Cu-大鼠和老鼠的心房和大脑中PAM mRNA的水平,这表明当铜限制在细胞内时,可能是由于脱辅基蛋白更新增加而导致PAM蛋白降低的转录后机制。

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