Inter-cellular variation in DNA content of Entamoeba histolytica originates from temporal and spatial uncoupling of cytokinesis from the nuclear cycle.

Inter-cellular variation in DNA content of Entamoeba histolytica originates from temporal and spatial uncoupling of cytokinesis from the nuclear cycle.
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DOI:
10.1371/journal.pntd.0000409
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发表时间:
2009
影响因子:
3.8
通讯作者:
Lohia A
Lohia A
中科院分区:
医学2区
文献类型:
--
作者:
Mukherjee C;Majumder S;Lohia A

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Accumulation of multiple copies of the genome in a single nucleus and several nuclei in a single cell has previously been noted in Entamoeba histolytica, contributing to the genetic heterogeneity of this unicellular eukaryote. In this study, we demonstrate that this genetic heterogeneity is an inherent feature of the cell cycle of this organism. Chromosome segregation occurs on a variety of novel microtubular assemblies including multi-polar spindles. Cytokinesis in E. histolytica is completed by the mechanical severing of a thin cytoplasmic bridge, either independently or with the help of neighboring cells. Importantly, cytokinesis is uncoupled from the nuclear division cycle, both temporally and spatially, leading to the formation of unequal daughter cells. Sorting of euploid and polyploid cells showed that each of these sub-populations acquired heterogeneous DNA content upon further growth. Our study conclusively demonstrates that genetic heterogeneity originates from the unique mode of cell division events in this protist. Proliferating eukaryotic cells regulate their DNA synthesis, chromosome segregation, and cell division with great precision so that daughter cells are genetically identical. Our study demonstrates that in proliferating cells of the protist pathogen Entamoeba histolytica re-duplication of DNA followed by segregation on atypical and diverse microtubular structures is frequently observed. In this parasite, cell division is erratic, so that each daughter cell may contain one or more nuclei and sometimes no nuclei. This uncoupling of cell cycle events and survival of daughter cells with unequal DNA contents leads to genetic heterogeneity in E. histolytica. Our study highlights the inherent plasticity of the Entamoeba genome and the ability of this protist to survive in the absence of strict regulatory mechanisms that are a hallmark of the eukaryotic cell cycle.
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