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使用高分辨率的倒置显微镜对小鼠胚胎的结构异常进行表型分析。

Phenotyping structural abnormalities in mouse embryos using high-resolution episcopic microscopy.

机构信息

Centre for Anatomy and Cell Biology & MIC, Medical University of Vienna, 1090 Wien, Austria.

MRC National Institute for Medical Research, London NW7 1AA, UK.

出版信息

Dis Model Mech. 2014 Oct;7(10):1143-52. doi: 10.1242/dmm.016337.

DOI:10.1242/dmm.016337
PMID:25256713
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4174525/
Abstract

The arrival of simple and reliable methods for 3D imaging of mouse embryos has opened the possibility of analysing normal and abnormal development in a far more systematic and comprehensive manner than has hitherto been possible. This will not only help to extend our understanding of normal tissue and organ development but, by applying the same approach to embryos from genetically modified mouse lines, such imaging studies could also transform our knowledge of gene function in embryogenesis and the aetiology of developmental disorders. The International Mouse Phenotyping Consortium is coordinating efforts to phenotype single gene knockouts covering the entire mouse genome, including characterising developmental defects for those knockout lines that prove to be embryonic lethal. Here, we present a pilot study of 34 such lines, utilising high-resolution episcopic microscopy (HREM) for comprehensive 2D and 3D imaging of homozygous null embryos and their wild-type littermates. We present a simple phenotyping protocol that has been developed to take advantage of the high-resolution images obtained by HREM and that can be used to score tissue and organ abnormalities in a reliable manner. Using this approach with embryos at embryonic day 14.5, we show the wide range of structural abnormalities that are likely to be detected in such studies and the variability in phenotypes between sibling homozygous null embryos.

摘要

简单可靠的小鼠胚胎 3D 成像方法的出现,使得人们有可能以前所未有的系统和全面的方式分析正常和异常发育。这不仅有助于扩展我们对正常组织和器官发育的理解,而且通过将相同的方法应用于来自基因修饰小鼠系的胚胎,这种成像研究也可以改变我们对胚胎发生中基因功能和发育障碍病因的认识。国际小鼠表型分析联盟正在协调对覆盖整个小鼠基因组的单基因敲除进行表型分析的工作,包括对那些被证明是胚胎致死的敲除系进行发育缺陷的特征描述。在这里,我们利用高分辨率倒置显微镜(HREM)对纯合子缺失胚胎及其野生型同窝仔鼠进行全面的 2D 和 3D 成像,对 34 条这样的线进行了试点研究。我们提出了一种简单的表型分析方案,该方案利用 HREM 获得的高分辨率图像,并可用于可靠地对组织和器官异常进行评分。使用这种方法对胚胎进行 14.5 天的研究,我们展示了在这种研究中可能检测到的广泛的结构异常以及同窝纯合子缺失胚胎之间表型的可变性。

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Deciphering the Mechanisms of Developmental Disorders (DMDD): a new programme for phenotyping embryonic lethal mice.解析发育障碍的机制(DMDD):表型胚胎致死小鼠的新项目。
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Bloomsbury report on mouse embryo phenotyping: recommendations from the IMPC workshop on embryonic lethal screening.
ZSCAN10 缺陷导致一种具有特征性耳面畸形的神经发育障碍。
Brain. 2024 Jul 5;147(7):2471-2482. doi: 10.1093/brain/awae058.
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Genetic determinants of micronucleus formation in vivo.体内微核形成的遗传决定因素。
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