Suppr超能文献

使用编辑工具纠正遗传性表观遗传缺陷。

Correction of Heritable Epigenetic Defects Using Editing Tools.

机构信息

Stem Cell Research Laboratory, Medical Genetics Institute Shaare Zedek Medical Center, Jerusalem 91031, Israel.

School of Medicine, The Hebrew University, Campus Ein Kerem, Jerusalem 91120, Israel.

出版信息

Int J Mol Sci. 2021 Apr 12;22(8):3966. doi: 10.3390/ijms22083966.

Abstract

Epimutations refer to mistakes in the setting or maintenance of epigenetic marks in the chromatin. They lead to mis-expression of genes and are often secondary to germline transmitted mutations. As such, they are the cause for a considerable number of genetically inherited conditions in humans. The correction of these types of epigenetic defects constitutes a good paradigm to probe the fundamental mechanisms underlying the development of these diseases, and the molecular basis for the establishment, maintenance and regulation of epigenetic modifications in general. Here, we review the data to date, which is limited to repetitive elements, that relates to the applications of key editing tools for addressing the epigenetic aspects of various epigenetically regulated diseases. For each approach we summarize the efforts conducted to date, highlight their contribution to a better understanding of the molecular basis of epigenetic mechanisms, describe the limitations of each approach and suggest perspectives for further exploration in this field.

摘要

表观突变是指染色质中表观遗传标记的设定或维持出现错误。它们导致基因的异常表达,通常是种系遗传突变的结果。因此,它们是人类许多遗传性疾病的原因。这些类型的表观遗传缺陷的纠正为探究这些疾病发生的基本机制以及一般来说建立、维持和调节表观遗传修饰的分子基础提供了一个很好的范例。在这里,我们回顾了迄今为止仅限于重复元件的相关数据,这些数据涉及到关键编辑工具在解决各种受表观遗传调控的疾病的表观遗传方面的应用。对于每种方法,我们总结了迄今为止所做的努力,强调了它们对更好地理解表观遗传机制的分子基础的贡献,描述了每种方法的局限性,并为该领域的进一步探索提出了展望。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09fc/8070094/cad7bc398161/ijms-22-03966-g001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验