首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >Regulation of DLK1 by the maternally expressed miR-379/miR-544 cluster may underlie callipyge polar overdominance inheritance
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Regulation of DLK1 by the maternally expressed miR-379/miR-544 cluster may underlie callipyge polar overdominance inheritance

机译:母体表达的miR-379 / miR-544簇对DLK1的调控可能是Callipyge极性优势遗传的基础

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摘要

Inheritance of the callipyge phenotype in sheep is an example of polar overdominance inheritance, an unusual mode of inheritance. To investigate the underlying molecular mechanism, we profiled the expression of the genes located in the Delta-like 1 homolog (Dlk1)–type III iodothyronine deiodinase (Dio3) imprinting region in mice. We found that the transcripts of the microRNA (miR) 379/miR-544 cluster were highly expressed in neonatal muscle and paralleled the expression of the Dlk1. We then determined the in vivo role of the miR-379/miR-544 cluster by establishing a mouse line in which the cluster was ablated. The maternal heterozygotes of young mutant mice displayed a hypertrophic tibialis anterior muscle, extensor digitorum longus muscle, gastrocnemius muscle, and gluteus maximus muscle and elevated expression of the DLK1 protein. Reduced expression of DLK1 was mediated by miR-329, a member of this cluster. Our results suggest that maternal expression of the imprinted miR-379/miR-544 cluster regulates paternal expression of the Dlk1 gene in mice. We therefore propose a miR-based molecular working model for polar overdominance inheritance.
机译:绵羊中的愈伤组织表型的遗传是极度优势遗传的一个例子,这是一种不寻常的遗传方式。为了研究潜在的分子机制,我们分析了小鼠中位于Delta-like 1同源物(Dlk1)-III型碘甲状腺素脱碘酶(Dio3)印迹区域的基因的表达。我们发现,microRNA(miR)379 / miR-544簇的转录本在新生儿肌肉中高度表达,并与Dlk1的表达平行。然后,我们通过建立消融该簇的小鼠品系来确定miR-379 / miR-544簇的体内作用。年轻的突变小鼠的母体杂合子表现出肥大的胫前肌,长指趾伸肌,腓肠肌和臀大肌以及DLK1蛋白的表达升高。 DLK1的表达减少是由该簇成员miR-329介导的。我们的结果表明,印记的miR-379 / miR-544簇的母体表达调节小鼠Dlk1基因的父本表达。因此,我们提出了一个基于miR的极性主导遗传分子工作模型。

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