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ORC4 在去除鼠红白血病(MEL)细胞中的作用类似于在卵母细胞极体挤出中的作用。

The role of ORC4 in enucleation of Murine Erythroleukemia (MEL) cells is similar to that in oocyte polar body extrusion.

机构信息

Department of Anatomy, Biochemistry, and Physiology, John A. Burns School of Medicine, University of Hawaii at Manoa, 1960 East-West Rd., University of Hawaii , Honolulu, HI, USA 96822.

出版信息

Syst Biol Reprod Med. 2020 Dec;66(6):378-386. doi: 10.1080/19396368.2020.1822458. Epub 2020 Sep 24.

Abstract

The Origin Replication Complex subunit 4 (ORC4) is one in six subunits of the Origin Replication Complexes (ORCs) which is essential for initiating licensing at DNA replication origins and recruiting adaptor molecules necessary for various cellular processes. Previously, we reported that ORC4 also plays a vital role in polar body extrusion (PBE) during oogenesis in which half the chromosomes are extruded from the oocyte. We hypothesized that ORC4 might play a broader role in chromatin elimination. We tested its role in enucleation during the development of erythrocytes. Murine erythroleukemia (MEL) cells can be propagated in culture indefinitely and can be induced to enucleate their DNA by treatment with Vacuolin-1, thereby mimicking normal erythrocyte enucleation. We found that ORC4 appeared around the nuclei of the MEL cells with Vacuolin-1 treatment, gradually increasing in thickness before enucleation. We then tested whether ORC4 was required for MEL enucleation by down regulating ORC4 with siRNA-ORC4 during Vacuolin-1 treatment and found that this prevented MEL enucleation. These data are consistent with the model that ORC4 is required for erythroblast enucleation just as it is for oocyte PBE. They suggest a new model in which ORC4 expression is a marker for the initiation to the enucleation pathway.

摘要

Origin 复制复合体亚基 4(ORC4)是 Origin 复制复合体(ORC)的六个亚基之一,对于在 DNA 复制起点起始许可和招募各种细胞过程所需的衔接分子至关重要。先前,我们报道 ORC4 也在卵母细胞中挤出一半染色体的卵子发生中的极体挤出(PBE)中发挥重要作用。我们假设 ORC4 可能在染色质消除中发挥更广泛的作用。我们在红细胞发育过程中检测了其去核作用。鼠红白血病(MEL)细胞可以在培养中无限期繁殖,并通过用 Vacuolin-1 处理来诱导其核 DNA 去核,从而模拟正常红细胞去核。我们发现 ORC4 在 Vacuolin-1 处理时出现在 MEL 细胞核周围,在去核前逐渐变厚。然后,我们通过在 Vacuolin-1 处理期间用 siRNA-ORC4 下调 ORC4 来测试 ORC4 是否是 MEL 去核所必需的,发现这阻止了 MEL 去核。这些数据与 ORC4 对于卵母细胞 PBE 中极体挤出以及对于红细胞母细胞去核都必需的模型一致。它们提出了一个新模型,其中 ORC4 表达是核出途径起始的标志物。

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本文引用的文献

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