首页> 美国卫生研究院文献>International Journal of Molecular Sciences >Characterization of a Leptin Receptor Paralog and Its Response to Fasting in Rainbow Trout (Oncorhynchus mykiss)
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Characterization of a Leptin Receptor Paralog and Its Response to Fasting in Rainbow Trout (Oncorhynchus mykiss)

机译:瘦蛋白受体寄生虫表征及其对虹鳟鱼禁食的反应(Oncorhynchus mykiss)

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摘要

Leptin is a cytokine that regulates appetite and energy expenditure, where in fishes it is primarily produced in the liver and acts to mobilize carbohydrates. Most fishes have only one leptin receptor (LepR/LepRA1), however, paralogs have recently been documented in a few species. Here we reveal a second leptin receptor (LepRA2) in rainbow trout that is 77% similar to trout LepRA1. Phylogenetic analyses show a salmonid specific genome duplication event as the probable origin of the second LepR in trout. Tissues distributions showed tissue specific expression of these receptors, with lepra1 highest in the ovaries, nearly 50-fold higher than lepra2. Interestingly, lepra2 was most highly expressed in the liver while hepatic lepra1 levels were low. Feed deprivation elicited a decline in plasma leptin, an increase in hepatic lepra2 by one week and remained elevated at two weeks, while liver expression of lepra1 remained low. By contrast, muscle lepra1 mRNA increased at one and two weeks of fasting, while adipose lepra1 was concordantly lower in fasted fish. lepra2 transcript levels were not affected in muscle and fat. These data show lepra1 and lepra2 are differentially expressed across tissues and during feed deprivation, suggesting paralog- and tissue-specific functions for these leptin receptors.
机译:瘦蛋白是一种调节食欲和能量消耗,其中在鱼类它在肝脏中主要产生并作用于动员碳水化合物的细胞因子。大多数鱼都只有一个瘦素受体(瘦素受体/ LepRA1),然而,旁系同源最近已在几个物种记录。在这里,我们揭示了在虹鳟鱼是类似于鳟鱼LepRA1 77%的第二瘦素受体(LepRA2)。系统发育分析显示鲑鱼特定基因组复制事件在鳟鱼第二瘦素受体的可能起源。组织分布表明这些受体的组织特异性表达,用lepra1在卵巢最高,有近50倍lepra2更高。有趣的是,lepra2是最高度在肝脏中表达,而肝lepra1水平很低。饲料剥夺引起血浆中瘦素的下降,由一个一周增加肝lepra2和两周仍然升高,而lepra1的肝表达仍然很低。相比之下,肌肉lepra1表达增加在禁食一两个星期,而脂肪lepra1在禁食鱼一致地低。 lepra2转录水平没有肌肉和脂肪的影响。这些数据表明lepra1和lepra2跨组织和饲料剥夺期间差异表达,这表明这些受体瘦素和paralog-组织特定功能。

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