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Compositional complexity of rods and rings

机译:杆和环的组成复杂性

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摘要

Rods and rings (RRs) are large linear- or circular-shaped structures typically described as polymers of IMPDH (inosine monophosphate dehydrogenase). They have been observed across a wide variety of cell types and species and can be induced to form by inhibitors of IMPDH. RRs are thought to play a role in the regulation of de novo guanine nucleotide synthesis; however, the function and regulation of RRs is poorly understood. Here we show that the regulatory GTPase, ARL2, a subset of its binding partners, and several resident proteins at the endoplasmic reticulum (ER) also localize to RRs. We also have identified two new inducers of RR formation: AICAR and glucose deprivation. We demonstrate that RRs can be disassembled if guanine nucleotides can be generated by salvage synthesis regardless of the inducer. Finally, we show that there is an ordered addition of components as RRs mature, with IMPDH first forming aggregates, followed by ARL2, and only later calnexin, a marker of the ER. These findings suggest that RRs are considerably more complex than previously thought and that the function(s) of RRs may include involvement of a regulatory GTPase, its effectors, and potentially contacts with intracellular membranes.
机译:杆和环(RRs)是大型线性或圆形结构,通常称为IMPDH(肌苷单磷酸脱氢酶)的聚合物。已在多种细胞类型和物种中观察到它们,并且可以通过IMPDH抑制剂诱导形成。 RR被认为在从头鸟嘌呤核苷酸合成的调节中起作用。然而,对RR的功能和调节知之甚少。在这里,我们显示出调节性GTPase,ARL2,其结合伴侣的一个子集以及在内质网(ER)上的一些驻留蛋白也位于RRs。我们还确定了RR形成的两个新诱因:AICAR和葡萄糖剥夺。我们证明,如果可以通过挽救合成产生鸟嘌呤核苷酸而与诱导物无关,则可以拆卸RR。最后,我们显示,随着RR的成熟,有序添加组分,IMPDH首先形成聚集体,然后是ARL2,然后才是ER的标志钙粘蛋白。这些发现表明RR比以前认为的要复杂得多,并且RR的功能可能包括调节性GTP酶,其效应子的参与以及潜在地与细胞内膜的接触。

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