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Identification of the Long-Sought Leptin in Chicken and Duck: Expression Pattern of the Highly GC-Rich Avian leptin Fits an Autocrine/Paracrine Rather Than Endocrine Function

机译:鸡和鸭中长期瘦素的鉴定:富含GC的禽瘦蛋白的表达模式比内分泌功能更适合自分泌/旁分泌

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More than 20 years after characterization of the key regulator of mammalian energy balance, leptin, we identified the leptin (LEP) genes of chicken (Gallus gallus) and duck (Anas platyrhynchos). The extreme guanine-cytosine content (similar to 70%), the location in a genomic region with low-complexity repetitive and palindromic sequence elements, the relatively low sequence conservation, and low level of expression have hampered the identification of these genes until now. In vitro-expressed chicken and duck leptins specifically activated signaling through the chicken leptin receptor in cell culture. In situ hybridization demonstrated expression of LEP mRNA in granular and Purkinje cells of the cerebellum, anterior pituitary, and in embryonic limb buds, somites, and branchial arches, suggesting roles in adult brain control of energy balance and during embryonic development. The expression patterns of LEP and the leptin receptor (LEPR) were explored in chicken, duck, and quail (Coturnix japonica) using RNA-sequencing experiments available in the Short Read Archive and by quantitative RT-PCR. In adipose tissue, LEP and LEPR were scarcely transcribed, and the expression level was not correlated to adiposity. Our identification of the leptin genes in chicken and duck genomes resolves a long lasting controversy regarding the existence of leptin genes in these species. This identification was confirmed by sequence and structural similarity, conserved exon-intron boundaries, detection in numerous genomic, and transcriptomic datasets and characterization by PCR, quantitative RT-PCR, in situ hybridization, and bioassays. Our results point to an autocrine/paracrine mode of action for bird leptin instead of being a circulating hormone as in mammals.
机译:在确定了哺乳动物能量平衡的关键调节因子瘦素的20多年后,我们鉴定了鸡(Gallus gallus)和鸭(Anas platyrhynchos)的瘦素(LEP)基因。迄今为止,鸟嘌呤-胞嘧啶的含量极高(约70%),重复性和回文序列元素低复杂性的基因组区域中的位置,较低的序列保守性和低表达水平一直阻碍了这些基因的鉴定。体外表达的鸡和鸭瘦蛋白通过细胞培养物中的鸡瘦蛋白受体特异性激活信号传导。原位杂交表明LEP mRNA在小脑,垂体前叶的颗粒细胞和Purkinje细胞中,以及在胚胎肢芽,体节和branch弓中表达,提示在成人大脑控制能量平衡和胚胎发育过程中的作用。使用Short Read Archive中的RNA测序实验和定量RT-PCR探索了在鸡,鸭和鹌鹑(Coturnix japonica)中LEP和瘦蛋白受体(LEPR)的表达模式。在脂肪组织中,几乎不转录LEP和LEPR,并且表达水平与肥胖无关。我们对鸡和鸭基因组中瘦素基因的鉴定解决了有关这些物种中瘦素基因存在的长期争议。通过序列和结构相似性,保守的外显子-内含子边界,在许多基因组和转录组数据集中的检测以及通过PCR,定量RT-PCR,原位杂交和生物测定的表征,证实了这种鉴定。我们的研究结果表明,鸟瘦蛋白的自分泌/旁分泌作用方式不同于哺乳动物中的循环激素。

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