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布氏锥虫线粒体DNA聚合酶ID的动态定位

Dynamic localization of Trypanosoma brucei mitochondrial DNA polymerase ID.

作者信息

Concepción-Acevedo Jeniffer, Luo Juemin, Klingbeil Michele M

机构信息

Department of Microbiology, University of Massachusetts, Amherst, Massachusetts, USA.

出版信息

Eukaryot Cell. 2012 Jul;11(7):844-55. doi: 10.1128/EC.05291-11. Epub 2012 Jan 27.

Abstract

Trypanosomes contain a unique form of mitochondrial DNA called kinetoplast DNA (kDNA) that is a catenated network composed of minicircles and maxicircles. Several proteins are essential for network replication, and most of these localize to the antipodal sites or the kinetoflagellar zone. Essential components for kDNA synthesis include three mitochondrial DNA polymerases TbPOLIB, TbPOLIC, and TbPOLID). In contrast to other kDNA replication proteins, TbPOLID was previously reported to localize throughout the mitochondrial matrix. This spatial distribution suggests that TbPOLID requires redistribution to engage in kDNA replication. Here, we characterize the subcellular distribution of TbPOLID with respect to the Trypanosoma brucei cell cycle using immunofluorescence microscopy. Our analyses demonstrate that in addition to the previously reported matrix localization, TbPOLID was detected as discrete foci near the kDNA. TbPOLID foci colocalized with replicating minicircles at antipodal sites in a specific subset of the cells during stages II and III of kDNA replication. Additionally, the TbPOLID foci were stable following the inhibition of protein synthesis, detergent extraction, and DNase treatment. Taken together, these data demonstrate that TbPOLID has a dynamic localization that allows it to be spatially and temporally available to perform its role in kDNA replication.

摘要

锥虫含有一种独特形式的线粒体DNA,称为动质体DNA(kDNA),它是由微小环和大环组成的连环网络。几种蛋白质对网络复制至关重要,其中大多数定位于反位或动基体鞭毛区。kDNA合成的必需成分包括三种线粒体DNA聚合酶TbPOLIB、TbPOLIC和TbPOLID。与其他kDNA复制蛋白不同,此前报道TbPOLID定位于整个线粒体基质。这种空间分布表明,TbPOLID需要重新分布才能参与kDNA复制。在这里,我们使用免疫荧光显微镜来描述TbPOLID在布氏锥虫细胞周期中的亚细胞分布。我们的分析表明,除了先前报道的基质定位外,还在kDNA附近检测到TbPOLID为离散的焦点。在kDNA复制的II期和III期,在特定的细胞亚群中,TbPOLID焦点与反位的复制微小环共定位。此外,在蛋白质合成受到抑制、用去污剂提取和进行DNase处理后,TbPOLID焦点仍然稳定。综上所述,这些数据表明,TbPOLID具有动态定位,使其能够在空间和时间上发挥其在kDNA复制中的作用。

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