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A Polymer Physics Investigation of the Architecture of the Murine Orthologue of the 7q11.23 Human Locus

机译:7q11.23人类基因座的小鼠直系同源物的体系结构的高分子物理研究。

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摘要

In the last decade, the developments of novel technologies, such as Hi-C or GAM methods, allowed to discover that chromosomes in the nucleus of mammalian cells have a complex spatial organization, encompassing the functional contacts between genes and regulators. In this work, we review recent progresses in chromosome modeling based on polymer physics to understand chromatin structure and folding mechanisms. As an example, we derive in mouse embryonic stem cells the full 3D structure of the Bmp7 locus, a genomic region that plays a key role in osteoblastic differentiation. Next, as an application to Neuroscience, we present the first 3D model for the mouse orthologoue of the Williams–Beuren syndrome 7q11.23 human locus. Deletions and duplications of the 7q11.23 region generate neurodevelopmental disorders with multi-system involvement and variable expressivity, and with autism. Understanding the impact of such mutations on the rewiring of the interactions of genes and regulators could be a new key to make sense of their related diseases, with potential applications in biomedicine.
机译:在过去的十年中,诸如Hi-C或GAM方法等新技术的发展使人们发现哺乳动物细胞核中的染色体具有复杂的空间组织,涵盖了基因与调节子之间的功能性联系。在这项工作中,我们回顾了基于聚合物物理学的染色体建模的最新进展,以了解染色质的结构和折叠机制。例如,我们从小鼠胚胎干细胞中衍生出Bmp7基因座的完整3D结构,这是在成骨细胞分化中起关键作用的基因组区域。接下来,作为对神经科学的应用,我们为Williams-Beuren综合征7q11.23人基因座提出了小鼠正统的第一个3D模型。 7q11.23区域的缺失和重复会产生神经发育障碍,并伴有多系统参与和可变表达,并伴有自闭症。了解此类突变对基因与调节剂相互作用重新关联的影响可能是弄清其相关疾病的新钥匙,并可能在生物医学中得到应用。

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