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对哺乳动物细胞中的线粒体基因组进行重新设计。

Re-engineering the mitochondrial genomes in mammalian cells.

作者信息

Yoon Young Geol, Koob Michael D, Yoo Young Hyun

机构信息

Mitochondria Hub Regulation Center and Department of Anatomy and Cell Biology, Dong-A University, Busan, Korea.

出版信息

Anat Cell Biol. 2010 Jun;43(2):97-109. doi: 10.5115/acb.2010.43.2.97. Epub 2010 Jun 30.

Abstract

Mitochondria are subcellular organelles composed of two discrete membranes in the cytoplasm of eukaryotic cells. They have long been recognized as the generators of energy for the cell and also have been known to associate with several metabolic pathways that are crucial for cellular function. Mitochondria have their own genome, mitochondrial DNA (mtDNA), that is completely separated and independent from the much larger nuclear genome, and even have their own system for making proteins from the genes in this mtDNA genome. The human mtDNA is a small (~16.5 kb) circular DNA and defects in this genome can cause a wide range of inherited human diseases. Despite of the significant advances in discovering the mtDNA defects, however, there are currently no effective therapies for these clinically devastating diseases due to the lack of technology for introducing specific modifications into the mitochondrial genomes and for generating accurate mtDNA disease models. The ability to engineer the mitochondrial genomes would provide a powerful tool to create mutants with which many crucial experiments can be performed in the basic mammalian mitochondrial genetic studies as well as in the treatment of human mtDNA diseases. In this review we summarize the current approaches associated with the correction of mtDNA mutations in cells and describe our own efforts for introducing engineered mtDNA constructs into the mitochondria of living cells through bacterial conjugation.

摘要

线粒体是真核细胞细胞质中由两层离散膜组成的亚细胞细胞器。长期以来,它们一直被认为是细胞的能量产生者,并且也已知与对细胞功能至关重要的几种代谢途径相关。线粒体有自己的基因组,即线粒体DNA(mtDNA),它与大得多的核基因组完全分离且独立,甚至有自己从该mtDNA基因组中的基因制造蛋白质的系统。人类mtDNA是一种小的(约16.5 kb)环状DNA,该基因组中的缺陷可导致多种遗传性人类疾病。然而,尽管在发现mtDNA缺陷方面取得了重大进展,但由于缺乏将特定修饰引入线粒体基因组以及生成准确的mtDNA疾病模型的技术,目前对于这些具有临床破坏性的疾病尚无有效的治疗方法。对线粒体基因组进行工程改造的能力将提供一个强大的工具,用于创建突变体,利用这些突变体可以在基础哺乳动物线粒体遗传学研究以及人类mtDNA疾病治疗中进行许多关键实验。在这篇综述中,我们总结了当前与细胞中mtDNA突变校正相关的方法,并描述了我们自己通过细菌接合将工程化mtDNA构建体引入活细胞线粒体的努力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d31/2998782/104ce92d1365/acb-43-97-g001.jpg

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