Mice lacking microRNAs in Pax8-expressing cells develop hypothyroidism and end-stage renal failure

IF 2.946 Q3 Biochemistry, Genetics and Molecular Biology BMC Molecular Biology Pub Date : 2016-04-18 DOI:10.1186/s12867-016-0064-x
Malte P. Bartram, Elena Amendola, Thomas Benzing, Bernhard Schermer, Gabriella de Vita, Roman-Ulrich Müller
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引用次数: 14

Abstract

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.

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.

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.

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在表达pax8的细胞中缺乏microrna的小鼠会发生甲状腺功能减退和终末期肾功能衰竭
在过去的十年中,非编码rna得到了越来越多的关注。从21世纪初开始,第一大群被系统表征的非编码rna是小的寡核苷酸——即所谓的microrna (miRNAs)。到目前为止,我们已经了解到microRNAs在大多数生物过程中是必不可少的,包括器官发生和器官结构和功能的维持。microRNAs在许多器官发育中的作用已被广泛研究,到目前为止,大多数研究集中在心脏或大脑等器官,而microRNAs在复杂上皮器官的发育和维持中的作用尚不清楚。此外,大多数关于上皮器官中microRNA功能的分析都采用了RNAse III Dicer的条件敲除小鼠模型来消除microRNA的生物发生。然而,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独立模型来进一步了解miRNA依赖过程的复杂生物学。在这里,我们分析了microrna依赖的转录控制在表达pax8的上皮细胞中的作用。Pax8是一种对上皮器官发育至关重要的转录因子。通过将条件diggeorge综合征关键区域8 (Dgcr8) fl/fl小鼠与Pax8Cre小鼠杂交,miRNA机制被破坏。Dgcr8/Drosha复合物在细胞核中加工pri- mirna,然后将其作为pre- mirna输出到细胞质中,由Dicer进一步成熟。Dgcr8 ? fl / fl;Pax8Cre + ?由于Pax8表达组织中mirna的缺失,基因敲除小鼠过早死亡,出现大量甲状腺功能减退和终末期肾病。pax8cre介导的diggeorge综合征关键区8 (Dgcr8)的条件性缺失,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,体重大量减少,最终导致肾衰竭和动物死亡。这些数据提供了使用Dicer独立模型进一步了解mirna在器官稳态中的重要性。
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来源期刊
BMC Molecular Biology
BMC Molecular Biology 生物-生化与分子生物学
CiteScore
4.80
自引率
0.00%
发文量
0
审稿时长
>12 weeks
期刊介绍: BMC Molecular Biology is an open access journal publishing original peer-reviewed research articles in all aspects of DNA and RNA in a cellular context, encompassing investigations of chromatin, replication, recombination, mutation, repair, transcription, translation and RNA processing and function.
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