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德国小蠊(蜚蠊目:蜚蠊科)脂肪体中3-羟基-3-甲基戊二酰辅酶A合成酶和还原酶在卵黄发生期间的协同表达与活性

Coordinated expression and activity of 3-hydroxy-3-methylglutaryl coenzyme A synthase and reductase in the fat body of Blattella germanica (L.) during vitellogenesis.

作者信息

Casals N, Buesa C, Piulachs M D, Cabañó J, Marrero P F, Bellés X, Hegardt F G

机构信息

Unit of Biochemistry, University of Barcelona, School of Pharmacy, Spain.

出版信息

Insect Biochem Mol Biol. 1996 Sep-Oct;26(8-9):837-43. doi: 10.1016/s0965-1748(96)00044-6.

DOI:10.1016/s0965-1748(96)00044-6
PMID:9014330
Abstract

Levels of mRNA for the two 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) synthases, (HMG-S1 and HMG-S2), and for HMG-CoA reductase (HMG-R) of Blattella germanica were analyzed in the fat body during the first gonadotrophic cycle. HMG-S2 and HMG-R showed the highest mRNA levels on day 0 and decreased thereafter, whereas HMG-S1, showed faint expression. Western blot using specific antibodies for HMG-S1 and HMG-S2 showed no detectable levels for HMG-S1 but a clear pattern for HMG-S2. Both results point to a very limited role for HMG-CoA synthase-1 in B. germanica fat body that the functional enzyme in this organ is HMG-CoA synthase-2. HMG-CoA reductase and synthase proteins shared a cyclic pattern (maximum levels at day 4 and minimum levels on days 0 and 8), which was coincident with the pattern of activity. The delay between gene transcription and protein synthesis suggests a finely regulated translation mechanism. Moreover, the pattern of mevalonate synthesis parallels that of vitellogenin production, suggesting a coordinate mechanism between the mevalonate pathway and the production of vitellogenin.

摘要

在第一个促性腺周期中,分析了德国小蠊脂肪体中两种3-羟基-3-甲基戊二酰辅酶A(HMG-CoA)合酶(HMG-S1和HMG-S2)以及HMG-CoA还原酶(HMG-R)的mRNA水平。HMG-S2和HMG-R在第0天显示出最高的mRNA水平,此后下降,而HMG-S1表达微弱。使用针对HMG-S1和HMG-S2的特异性抗体进行的蛋白质印迹分析显示,未检测到HMG-S1的水平,但HMG-S2有明显的表达模式。这两个结果都表明HMG-CoA合酶-1在德国小蠊脂肪体中的作用非常有限,该器官中的功能酶是HMG-CoA合酶-2。HMG-CoA还原酶和合成酶蛋白呈现出周期性模式(第4天达到最高水平,第0天和第8天达到最低水平),这与活性模式一致。基因转录和蛋白质合成之间的延迟表明存在精细调节的翻译机制。此外,甲羟戊酸合成模式与卵黄蛋白原产生模式相似,表明甲羟戊酸途径与卵黄蛋白原产生之间存在协调机制。

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