首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >PNAS Plus: The ZBED6–IGF2 axis has a major effect on growth of skeletal muscle and internal organs in placental mammals
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PNAS Plus: The ZBED6–IGF2 axis has a major effect on growth of skeletal muscle and internal organs in placental mammals

机译:PNAS Plus:ZBED6-IGF2轴对胎盘哺乳动物骨骼肌和内部器官的生长有重要影响

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摘要

A single nucleotide substitution in the third intron of insulin-like growth factor 2 (IGF2) is associated with increased muscle mass and reduced subcutaneous fat in domestic pigs. This mutation disrupts the binding of the ZBED6 transcription factor and leads to a threefold up-regulation of IGF2 expression in pig skeletal muscle. Here, we investigated the biological significance of ZBED6–IGF2 interaction in the growth of placental mammals using two mouse models, ZBED6 knock-out (Zbed6−/−) and Igf2 knock-in mice that carry the pig IGF2 mutation. These transgenic mice exhibit markedly higher serum IGF2 concentrations, higher growth rate, increased lean mass, and larger heart, kidney, and liver; no significant changes were observed for white adipose tissues. The changes in body and lean mass were most pronounced in female mice. The phenotypic changes were concomitant with a remarkable up-regulation of Igf2 expression in adult tissues. Transcriptome analysis of skeletal muscle identified differential expression of genes belonging to the extracellular region category. Expression analysis using fetal muscles indicated a minor role of ZBED6 in regulating Igf2 expression prenatally. Furthermore, transcriptome analysis of the adult skeletal muscle revealed that this elevated expression of Igf2 was derived from the P1 and P2 promoters. The results revealed very similar phenotypic effects in the Zbed6 knock-out mouse and in the Igf2 knock-in mouse, showing that the effect of ZBED6 on growth of muscle and internal organs is mediated through the binding site in the Igf2 gene. The results explain why this ZBED6 binding site is extremely well conserved among placental mammals.
机译:胰岛素样生长因子2(IGF2)第三内含子中的单核苷酸取代与家猪的肌肉量增加和皮下脂肪减少有关。这种突变破坏ZBED6转录因子的结合,并导致猪骨骼肌中IGF2表达的三倍上调。在这里,我们使用两种携带猪的小鼠模型ZBED6敲除(Zbed6 -/-)和Igf2敲入小鼠,研究了ZBED6-IGF2相互作用在胎盘哺乳动物生长中的生物学意义。 IGF2突变。这些转基因小鼠表现出明显更高的血清IGF2浓度,更高的生长速度,增加的瘦肉质量以及更大的心脏,肾脏和肝脏。没有观察到白色脂肪组织的显着变化。雌性小鼠的体重和瘦体重变化最为明显。表型变化与成人组织中Igf2表达的显着上调同时发生。骨骼肌的转录组分析确定了属于细胞外区域类别的基因的差异表达。使用胎儿肌肉进行的表达分析表明,ZBED6在产前调节Igf2表达中的作用很小。此外,成年骨骼肌的转录组分析显示,Igf2的这种升高的表达源自P1和P2启动子。结果显示在Zbed6敲除小鼠和Igf2敲入小鼠中非常相似的表型作用,表明ZBED6对肌肉和内脏器官生长的作用是通过Igf2基因的结合位点介导的。结果解释了为什么该ZBED6结合位点在胎盘哺乳动物中极为保守。

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