Liang Н X, Liu Н W
School of Biomedical Engineering, Taiyuan University of Technology, Taiyuan, Shanxi, 030024 China.
lianghaixia456@hotmail. com.
Mol Biol (Mosk). 2019 May-Jun;53(3):446-455. doi: 10.1134/S0026898419030108.
Ran is an evolutionarily conserved GTPase crucial in regulating various cell divisions, including mitosis and meiosis. A previous study showed that the knockdown of RAN1 inhibited macronuclear amitosis with the abnormal organization of intramacronuclear microtubules in Tetrahymena thermophila. This study aimed to further investigate the effects of the inducible expression of wild-type Ran1 (Ran1WT), GTP-bound Ran1-mimetic (Ran1Q70L), and GDP-bound Ran1-mimetic (Ran1T25N) on cytoplasmic microtubule assembly during amitosis of T. thermophila, based on previous studies about their effects on intramacronuclear microtubule. The mutant strains of T. thermophila for inducible expression of Ran1WT/T25N/Q70L by Cd^(2+) were constructed. The inducibly expressed HA-Ran1Q70L/T25N distributed asymmetrically across the macronuclear envelope during amitosis. At the lower level of inducible expression, only Ran1T25N showed a significant decreasing effect on T. thermophila reproduction, macronuclear amitosis and cytokinesis. At the higher level of inducible expression, Ran1WT/Q70L/T25N inhibited T. thermophila reproduction, macronuclear amitosis and cytokinesis, and the inhibitive effect of Ran1T25N was the most significant. The inducible expression of Ran1WT/Q70L/T25N led to defects in amitosis and cytokinesis with abnormal cytoplasmic microtubule assembly. These results further confirmed the regulatory function of Ran1 on amitosis and suggested a novel role of Ran1 in cytokinesis and the alignment of cytoplasmic microtubules in T. thermophila.
Ran是一种在进化上保守的GTP酶,对调节包括有丝分裂和减数分裂在内的各种细胞分裂至关重要。先前的一项研究表明,RAN1的敲低会抑制嗜热四膜虫的大核无丝分裂,并导致大核内微管组织异常。本研究旨在基于先前关于野生型Ran1(Ran1WT)、GTP结合型Ran1模拟物(Ran1Q70L)和GDP结合型Ran1模拟物(Ran1T25N)对大核内微管影响的研究,进一步探究它们的诱导表达对嗜热四膜虫无丝分裂期间细胞质微管组装的影响。构建了通过Cd^(2+)诱导表达Ran1WT/T25N/Q70L的嗜热四膜虫突变株。在无丝分裂期间,诱导表达的HA-Ran1Q70L/T25N不对称地分布在大核膜上。在较低的诱导表达水平下,只有Ran1T25N对嗜热四膜虫的繁殖、大核无丝分裂和胞质分裂表现出显著的抑制作用。在较高的诱导表达水平下,Ran1WT/Q70L/T25N均抑制嗜热四膜虫的繁殖、大核无丝分裂和胞质分裂,其中Ran1T25N的抑制作用最为显著。Ran1WT/Q70L/T25N的诱导表达导致无丝分裂和胞质分裂缺陷,以及细胞质微管组装异常。这些结果进一步证实了Ran1对无丝分裂的调节功能,并揭示了Ran1在嗜热四膜虫胞质分裂和细胞质微管排列中的新作用。