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本文引用的文献

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BIME2, a novel gene required for interhomolog meiotic recombination in the protist model organism Tetrahymena.BIME2,一种在原生生物模式生物四膜虫中同源染色体减数分裂重组所必需的新基因。
Chromosome Res. 2017 Oct;25(3-4):291-298. doi: 10.1007/s10577-017-9563-y. Epub 2017 Aug 12.
2
Cell cycle transcription control: DREAM/MuvB and RB-E2F complexes.细胞周期转录调控:DREAM/MuvB复合物与RB-E2F复合物
Crit Rev Biochem Mol Biol. 2017 Dec;52(6):638-662. doi: 10.1080/10409238.2017.1360836. Epub 2017 Aug 11.
3
Nonsense-mediated mRNA decay in Tetrahymena is EJC independent and requires a protozoa-specific nuclease.四膜虫中无义介导的mRNA降解不依赖外显子连接复合体,且需要一种原生动物特异性核酸酶。
Nucleic Acids Res. 2017 Jun 20;45(11):6848-6863. doi: 10.1093/nar/gkx256.
4
A Zip3-like protein plays a role in crossover formation in the SC-less meiosis of the protist .一种类似Zip3的蛋白质在原生生物无联会复合体减数分裂的交叉形成过程中发挥作用。
Mol Biol Cell. 2017 Mar 15;28(6):825-833. doi: 10.1091/mbc.E16-09-0678. Epub 2017 Jan 18.
5
E2fl1 is a meiosis-specific transcription factor in the protist Tetrahymena thermophila.E2fl1是嗜热栖热四膜虫中的一种减数分裂特异性转录因子。
Cell Cycle. 2017 Jan 2;16(1):123-135. doi: 10.1080/15384101.2016.1259779. Epub 2016 Nov 28.
6
DREAMs make plant cells to cycle or to become quiescent.DREAMs 使植物细胞循环或静止。
Curr Opin Plant Biol. 2016 Dec;34:100-106. doi: 10.1016/j.pbi.2016.10.002. Epub 2016 Nov 3.
7
Structural basis for LIN54 recognition of CHR elements in cell cycle-regulated promoters.细胞周期调控启动子中 CHR 元件的 LIN54 识别的结构基础。
Nat Commun. 2016 Jul 28;7:12301. doi: 10.1038/ncomms12301.
8
Cdk3, a conjugation-specific cyclin-dependent kinase, is essential for the initiation of meiosis in Tetrahymena thermophila.Cdk3是一种具有特异性结合作用的细胞周期蛋白依赖性激酶,对嗜热四膜虫减数分裂的起始至关重要。
Cell Cycle. 2016 Sep 16;15(18):2506-14. doi: 10.1080/15384101.2016.1207838. Epub 2016 Jul 15.
9
Cyc17, a meiosis-specific cyclin, is essential for anaphase initiation and chromosome segregation in Tetrahymena thermophila.Cyc17是一种减数分裂特异性细胞周期蛋白,对嗜热四膜虫的后期起始和染色体分离至关重要。
Cell Cycle. 2016 Jul 17;15(14):1855-64. doi: 10.1080/15384101.2016.1188238. Epub 2016 May 18.
10
DNA double-strand break formation and repair in Tetrahymena meiosis.四膜虫减数分裂过程中DNA双链断裂的形成与修复
Semin Cell Dev Biol. 2016 Jun;54:126-34. doi: 10.1016/j.semcdb.2016.02.021. Epub 2016 Feb 16.

一种 DP 样转录因子蛋白与 E2fl1 相互作用,调节嗜热四膜虫减数分裂。

A DP-like transcription factor protein interacts with E2fl1 to regulate meiosis in Tetrahymena thermophila.

机构信息

a Key Laboratory of Aquatic Biodiversity and Conservation , Institute of Hydrobiology , Chinese Academy of Sciences , Wuhan , People's Republic of China.

b University of Chinese Academy of Sciences , Beijing , People's Republic of China.

出版信息

Cell Cycle. 2018;17(5):634-642. doi: 10.1080/15384101.2018.1431595. Epub 2018 Apr 4.

DOI:10.1080/15384101.2018.1431595
PMID:29417875
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5969552/
Abstract

Evolutionarily conserved E2F family transcription factors regulate the cell cycle via controlling gene expression in a wide range of eukaryotes. We previously demonstrated that the meiosis-specific transcription factor E2fl1 had an important role in meiosis in the model ciliate Tetrahymena thermophila. Here, we report that expression of another E2F family transcription factor gene DPL2 correlates highly with that of E2FL1. Similar to e2fl1Δ cells, dpl2Δ cells undergo meiotic arrest prior to anaphase I, with the five chromosomes adopting an abnormal tandem arrangement. Immunofluorescence staining and immunoprecipitation experiments demonstrate that Dpl2 and E2fl1 form a complex during meiosis. We previously identified several meiotic regulatory proteins in T. thermophila. Cyc2 and Tcdk3 may cooperate to initiate meiosis and Cyc17 is essential for initiating meiotic anaphase. We investigate the relationship of these regulators with Dpl2 and E2fl1, and then construct a meiotic regulatory network by measuring changes in meiotic genes expression in knockout cells. We conclude that the E2fl1/Dpl2 complex plays a central role in meiosis in T. thermophila.

摘要

进化上保守的 E2F 家族转录因子通过在广泛的真核生物中控制基因表达来调节细胞周期。我们之前证明,减数分裂特异性转录因子 E2fl1 在模式纤毛虫嗜热四膜虫的减数分裂中具有重要作用。在这里,我们报告另一个 E2F 家族转录因子基因 DPL2 的表达与 E2FL1 的表达高度相关。与 e2fl1Δ 细胞相似,dpl2Δ 细胞在第一次减数分裂后期之前经历减数分裂停滞,五个染色体呈现异常串联排列。免疫荧光染色和免疫沉淀实验表明,Dpl2 和 E2fl1 在减数分裂过程中形成复合物。我们之前在嗜热四膜虫中鉴定了几种减数分裂调节蛋白。Cyc2 和 Tcdk3 可能合作启动减数分裂,而 Cyc17 对于启动减数分裂后期是必不可少的。我们研究了这些调节剂与 Dpl2 和 E2fl1 的关系,然后通过测量敲除细胞中减数分裂基因表达的变化来构建减数分裂调节网络。我们得出结论,E2fl1/Dpl2 复合物在嗜热四膜虫的减数分裂中起核心作用。