首页> 外文期刊>FEBS Letters >Origin of the interferon‐inducible (2′‐5′)oligoadenylate synthetases: cloning of the (2′‐5′)oligoadenylate synthetase from the marine sponge Geodia cydonium
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Origin of the interferon‐inducible (2′‐5′)oligoadenylate synthetases: cloning of the (2′‐5′)oligoadenylate synthetase from the marine sponge Geodia cydonium

机译:干扰素诱导的(2'-5')寡腺苷酸合成酶的起源:从海洋海绵Geodia cydonium克隆(2'-5')寡腺苷酸合成酶

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>In vertebrates cytokines mediate innate (natural) immunity and protect them against viral infections. The cytokine interferon causes the induction of the (2′-5′)oligoadenylate synthetase [(2-5)A synthetase], whose product, (2′-5′)oligoadenylate, activates the endoribonuclease L which in turn degrades (viral) RNA. Three isoforms of (2-5)A synthetases exist, form I (40–46 kDa), form II (69 kDa), and form III (100 kDa). Until now (2-5)A synthetases have only been cloned from birds and mammals. Here we describe the cloning of the first putative invertebrate (2-5)A synthetase from the marine sponge Geodia cydonium. The deduced amino acid sequence shows signatures characteristic for (2-5)A synthetases of form I. Phylogenetic analysis of the putative sponge (2-5)A synthetase indicates that it diverged first from a common ancestor of the hitherto known members of (vertebrate) (2-5)A synthetases I, (2-5)A synthetases II and III. Moreover, it is suggested that the (2-5)A synthetases II and III evolved from this common ancestor (very likely) by gene duplication. Together with earlier results on the existence of the (2′-5′)oligoadenylates in G. cydonium, the data presented here demonstrate that also invertebrates, here sponges, are provided with the (2-5)A system. At present, it is assumed that this system might be involved in growth control, including control of apoptosis, and acquired its additional function in innate immune response in evolutionarily younger animals, in vertebrates.
机译:>在脊椎动物中,细胞因子介导先天性(天然)免疫力并保护其免受病毒感染。细胞因子干扰素引起(2'-5')寡腺苷酸合成酶[(2-5)A合成酶]的诱导,其产物(2'-5')寡腺苷酸激活内切核糖核酸酶L,而后者降解(病毒)。 RNA。存在(2-5)A合成酶的三种同工型,形式I(40-46 kDa),形式II(69 kDa)和形式III(100 kDa)。迄今为止,仅从鸟类和哺乳动物中克隆了(2-5)A个合成酶。在这里,我们描述了从海洋海绵克隆第一个推定的无脊椎动物(2-5)A合成酶。推导的氨基酸序列显示了形式I的(2-5)A合成酶的特征性特征。推定海绵(2-5)A合成酶的系统发育分析表明,它首先与(脊椎动物的)迄今已知成员的共同祖先不同(2-5)A合成酶I,(2-5)A合成酶II和III。此外,建议(2-5)A合成酶II和III通过基因复制从该共同祖先进化(非常可能)。与早期的结果有关在(em)G中存在(2'-5')寡腺苷酸。 cy ,此处显示的数据表明(2-5)A系统也提供了无脊椎动物,这里是海绵。目前,假设该系统可能参与生长控制,包括细胞凋亡的控制,并在脊椎动物的进化年轻动物中获得其在先天免疫应答中的附加功能。

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