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本文引用的文献

1
The Toxoplasma gondii centrosome is the platform for internal daughter budding as revealed by a Nek1 kinase mutant.刚地弓形虫中心体是内部子芽出芽的平台,这是由 Nek1 激酶突变体揭示的。
J Cell Sci. 2013 Aug 1;126(Pt 15):3344-55. doi: 10.1242/jcs.123364. Epub 2013 May 31.
2
Csi1 illuminates the mechanism and function of Rabl configuration.Csi1 阐明了 Rabl 构型的机制和功能。
Nucleus. 2013 May-Jun;4(3):176-81. doi: 10.4161/nucl.24876. Epub 2013 May 1.
3
Evolutionary cell biology of chromosome segregation: insights from trypanosomes.染色体分离的进化细胞生物学:从锥虫获得的启示。
Open Biol. 2013 May 1;3(5):130023. doi: 10.1098/rsob.130023.
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Slk19 clusters kinetochores and facilitates chromosome bipolar attachment.Slk19 聚集着动粒并促进染色体的两极附着。
Mol Biol Cell. 2013 Mar;24(5):566-77. doi: 10.1091/mbc.E12-07-0552. Epub 2013 Jan 2.
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Exotic mitotic mechanisms.奇异的有丝分裂机制。
Open Biol. 2012 Dec 5;2(12):120140. doi: 10.1098/rsob.120140.
6
Cell division in Apicomplexan parasites is organized by a homolog of the striated rootlet fiber of algal flagella.锥虫类寄生虫的细胞分裂是由藻类鞭毛的横纹根纤维的同源物组织的。
PLoS Biol. 2012;10(12):e1001444. doi: 10.1371/journal.pbio.1001444. Epub 2012 Dec 11.
7
Csi1 links centromeres to the nuclear envelope for centromere clustering.Csi1 将着丝粒连接到核膜上,以实现着丝粒聚类。
J Cell Biol. 2012 Nov 26;199(5):735-44. doi: 10.1083/jcb.201208001. Epub 2012 Nov 19.
8
Cytoskeleton assembly in Toxoplasma gondii cell division.刚地弓形虫细胞分裂中的细胞骨架组装。
Int Rev Cell Mol Biol. 2012;298:1-31. doi: 10.1016/B978-0-12-394309-5.00001-8.
9
Plasmodium falciparum centromeres display a unique epigenetic makeup and cluster prior to and during schizogony.恶性疟原虫着丝粒在裂殖前和裂殖期间表现出独特的表观遗传学特征,并聚集在一起。
Cell Microbiol. 2012 Sep;14(9):1391-401. doi: 10.1111/j.1462-5822.2012.01803.x. Epub 2012 May 15.
10
Toxoplasma gondii chromodomain protein 1 binds to heterochromatin and colocalises with centromeres and telomeres at the nuclear periphery.刚地弓形虫染色质域蛋白 1 与异染色质结合,并在核周与着丝粒和端粒共定位。
PLoS One. 2012;7(3):e32671. doi: 10.1371/journal.pone.0032671. Epub 2012 Mar 9.

刚地弓形虫的动粒是中心体与中心锥(纺锤体极)结合所必需的。

The Toxoplasma gondii kinetochore is required for centrosome association with the centrocone (spindle pole).

作者信息

Farrell Megan, Gubbels Marc-Jan

机构信息

Department of Biology, Boston College, 140 Commonwealth Avenue, Higgins Hall 355, Chestnut Hill, MA, 02467, USA.

出版信息

Cell Microbiol. 2014 Jan;16(1):78-94. doi: 10.1111/cmi.12185. Epub 2013 Sep 10.

DOI:10.1111/cmi.12185
PMID:24015880
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3933516/
Abstract

The kinetochore is a multi-protein structure assembled on eukaryotic centromeres mediating chromosome attachment to spindle microtubules. Here we identified the kinetochore proteins Nuf2 and Ndc80 in the apicomplexan parasite Toxoplasma gondii. Localization revealed that kinetochores remain clustered throughout the cell cycle and colocalize with clustered centromeres at the centrocone, a structure containing the spindle pole embedded in the nuclear envelope. Pharmacological disruption of microtubules resulted in partial loss of some kinetochore and centromere clustering, indicating microtubules are necessary but not strictly required for kinetochore clustering. Generation of a TgNuf2 conditional knock-down strain revealed it is essential for chromosome segregation, but dispensable for centromere clustering. The centromeres actually remained associated with the centrocone suggesting microtubule binding is not required for their interaction with the spindle pole. The most striking observation upon TgNuf2 depletion was that the centrosome behaved normally, but that it lost its association with the centrocone. This suggests that microtubules are essential to maintain contact between the centrosome and chromosomes, and this interaction is critical for the partitioning of the nuclei into the two daughter parasites. Finally, genetic complementation experiments with mutated TgNuf2 constructs highlighted an apicomplexan-specific motif with a putative role in nuclear localization.

摘要

动粒是一种组装在真核生物着丝粒上的多蛋白结构,介导染色体与纺锤体微管的附着。在此,我们在顶复门寄生虫刚地弓形虫中鉴定出了动粒蛋白Nuf2和Ndc80。定位显示,动粒在整个细胞周期中都保持聚集状态,并与位于中心锥处聚集的着丝粒共定位,中心锥是一种包含嵌入核膜的纺锤极的结构。微管的药理学破坏导致一些动粒和着丝粒聚集部分丧失,表明微管对于动粒聚集是必要的,但并非严格必需。生成一个TgNuf2条件性敲低菌株表明,它对于染色体分离至关重要,但对于着丝粒聚集是可有可无的。着丝粒实际上仍与中心锥相关联,这表明微管结合对于它们与纺锤极的相互作用不是必需的。在TgNuf2缺失时最显著的观察结果是,中心体表现正常,但它失去了与中心锥的关联。这表明微管对于维持中心体与染色体之间的接触至关重要,并且这种相互作用对于将细胞核分配到两个子寄生虫中至关重要。最后,用突变的TgNuf2构建体进行的遗传互补实验突出了一个顶复门特异性基序,其在核定位中可能发挥作用。