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首页> 外文期刊>BMC Molecular Biology >Mice lacking microRNAs in Pax8-expressing cells develop hypothyroidism and end-stage renal failure
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Mice lacking microRNAs in Pax8-expressing cells develop hypothyroidism and end-stage renal failure

机译:Pax8表达细胞中缺少microRNA的小鼠发展为甲状腺功能减退症和终末期肾衰竭

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Background Non-coding RNAs have gained increasing attention during the last decade. The first large group of non-coding RNAs to be characterized systematically starting at the beginning of the 21st century were small oligonucleotides—the so-called microRNAs (miRNAs). By now we have learnt that microRNAs are indispensable for most biological processes including organogenesis and maintenance of organ structure and function. The role of microRNAs has been studied extensively in the development of a number of organs, so far most studies focussed on e.g. the heart or the brain whilst the role of microRNAs in the development and maintenance of complex epithelial organs is less well understood. Furthermore most analyses regarding microRNA function in epithelial organs employed conditional knockout mouse models of the RNAse III Dicer to abrogate microRNA biogenesis. However, there is increasing evidence for Dicer to have multiple functions independent from microRNA maturation. Therefore Dicer independent models are needed to gain further insight into the complex biology of miRNA dependent processes. Results Here we analyze the contribution of microRNA-dependent transcriptional control in Pax8-expressing epithelial cells. Pax8 is a transcription factor that is crucial to the development of epithelial organs. The miRNA machinery was disrupted by crossing conditional DiGeorge syndrome critical region 8 (Dgcr8) fl/fl mice to Pax8Cre mice. The Dgcr8/Drosha complex processes pri-miRNAs in the nucleus before they are exported as pre-miRNAs for further maturation by Dicer in the cytoplasm. Dgcr8 fl/fl; Pax8Cre +?knockout mice died prematurely, developed massive hypothyroidism and end stage renal disease due to a loss of miRNAs in Pax8 expressing tissue. Conclusion Pax8Cre -mediated conditional loss of DiGeorge syndrome critical region 8 (Dgcr8), an essential component of the nuclear machinery that is required for microRNA biogenesis, resulted in severe hypothyroidism, massively reduced body weight and ultimately led to renal failure and death of the animals. These data provide further insight into the importance of miRNAs in organ homeostasis using a Dicer independent model.
机译:背景技术在过去十年中,非编码RNA受到越来越多的关注。从21世纪初开始系统地表征的第一批非编码RNA是小的寡核苷酸-所谓的microRNA(miRNA)。到目前为止,我们已经了解到,microRNA对于大多数生物学过程都是必不可少的,包括器官发生以及器官结构和功能的维持。在许多器官的发育中已经对microRNA的作用进行了广泛的研究,到目前为止,大多数研究都集中在例如心脏或大脑,而microRNA在复杂上皮器官的发育和维持中的作用则鲜为人知。此外,有关上皮器官中microRNA功能的大多数分析都采用了RNAse III Dicer的条件敲除小鼠模型来消除microRNA生物发生。但是,越来越多的证据表明Dicer具有独立于microRNA成熟的多种功能。因此,需要Dicer独立模型来深入了解miRNA依赖过程的复杂生物学。结果在这里,我们分析了表达Pax8的上皮细胞中microRNA依赖性转录控制的作用。 Pax8是一种转录因子,对上皮器官的发育至关重要。通过将条件DiGeorge综合征关键区域8(Dgcr8)fl / fl小鼠与Pax8Cre小鼠杂交,破坏了miRNA的机制。 Dgcr8 / Drosha复合物在细胞核中加工pri-miRNA,然后将其作为pre-miRNA输出,以供Dicer在细胞质中进一步成熟。 Dgcr8 fl / fl; Pax8Cre +基因敲除小鼠因表达Pax8的组织中的miRNA缺失而过早死亡,发展为甲状腺功能减退症和晚期肾病。结论Pax8Cre介导的DiGeorge综合征关键区域8(Dgcr8)的条件性丢失,这是microRNA生物发生所必需的核机制的重要组成部分,导致严重的甲状腺功能减退症,大量减轻体重,最终导致肾脏衰竭和动物死亡。这些数据使用Dicer独立模型进一步揭示了miRNA在器官稳态中的重要性。

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