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首页> 外文期刊>The Journal of Experimental Biology >Expression of Manduca sexta V-ATPase genes mvB, mvG and mvd is regulated by ecdysteroids
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Expression of Manduca sexta V-ATPase genes mvB, mvG and mvd is regulated by ecdysteroids

机译:蜕皮类固醇调节满天蛾V-ATPase基因mvB,mvG和mvd的表达

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V-ATPases are complex proteins consisting of a peripheral, ATP-hydrolysing V-1 complex and a membrane-bound H+-translocating V-0 complex. The plasma membrane V-ATPase from the tobacco hornworm (Mauduca sexta) midgut is made up of eight different V-1 and four different V-0 subunits. During starvation and moulting, V-ATPase activity decreases as a result of the dissociation of the V-1 complex from the V-0 complex. To determine whether subunit biosynthesis is reduced during periods of enzyme inactivity, we measured the transcript levels and transcriptional activities of V-ATPase genes. Northern blots revealed the downregulation of almost all V-ATPase transcripts during starvation. During moulting, transcript levels of the three V-ATPase genes examined, mvB, mvG and mvd, also decreased, and this decrease was negatively correlated with the titre of 20-hydroxyecdysone (20-HE) and positively correlated with the titre of juvenile hormone (JH). To test the biological significance of these correlations, we injected both hormones into feeding larvae and measured transcript levels several hours later. A short-term increase and a long-term decrease in levels of mRNA were observed after 20-HE injection, whereas JH injection had no significant effect. Immunohistochemical studies of the midgut epithelium revealed that 20-HE injection led to changes in goblet cell morphology and in the subcellular distribution of the Vi complex comparable with the situation during the moult and during starvation. Reporter gene assays in Sf21 cells using mvB, mvG and mvd promoters to initiate transcription of firefly luciferase led, after incubation of the cells with 20-HE, to results comparable with those obtained in the injection experiments. These findings suggest that putative ecdysone-responsive elements are present in all three promoters. Taken together, our results suggest that the expression of V-ATPase genes is controlled in a coordinated manner by ecdysteroids.
机译:V-ATP酶是复合蛋白,由外围的可水解ATP的V-1复合物和膜结合的H +-易位V-0复合物组成。来自烟草天蛾中肠的质膜V-ATP酶由八个不同的V-1和四个不同的V-0亚基组成。在饥饿和换毛期间,由于V-1复合物与V-0复合物解离,V-ATPase活性降低。为了确定酶无活性期间亚单位的生物合成是否减少,我们测量了V-ATPase基因的转录水平和转录活性。 Northern印迹显示饥饿期间几乎所有V-ATPase转录本均下调。在换羽过程中,检查的三个V-ATPase基因的转录水平mvB,mvG和mvd也降低了,并且这种降低与20-羟基蜕皮酮(20-HE)的效价呈负相关,与少年激素的效价呈正相关。 (JH)。为了测试这些相关性的生物学意义,我们在数小时后将两种激素都注入了饲料中的幼虫并测量了转录水平。注射20-HE后观察到mRNA水平的短期升高和长期降低,而JH注射则无显着影响。对中肠上皮的免疫组织化学研究显示,与蜕皮期和饥饿期相比,注射20-HE导致杯状细胞形态和Vi复合物亚细胞分布的变化。在用20-HE孵育细胞后,使用mvB,mvG和mvd启动子在Sf21细胞中进行记者基因检测,导致萤火虫荧光素酶转录,结果与注射实验中的结果相当。这些发现表明推定的蜕皮激素响应元件存在于所有三个启动子中。两者合计,我们的结果表明,蜕皮类固醇以协调的方式控制V-ATPase基因的表达。

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