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鉴定影响七种人类 APOBEC3 蛋白对 LINE-1 限制的分子特征。

Characterization of molecular attributes that influence LINE-1 restriction by all seven human APOBEC3 proteins.

机构信息

Department of Biochemistry, Microbiology and Immunology, Faculty of Medicine, University of Ottawa, Ottawa, Ontario, Canada.

Human Health Therapeutics Portfolio, National Research Council of Canada, Ottawa, Ontario, Canada.

出版信息

Virology. 2018 Jul;520:127-136. doi: 10.1016/j.virol.2018.05.015. Epub 2018 May 31.

Abstract

LINE-1 (L1) is a non-long terminal repeat (LTR) retrotransposon inserted throughout the human genome. APOBEC3 (A3) proteins are part of a network of host intrinsic defenses capable of restricting retroviruses and the replication of L1 retroelements. These enzymes inactivate retroviruses primarily through deamination of single-stranded viral DNA. In contrast, only A3A deaminates L1 DNA, while the other six A3 proteins restrict L1 to varying degrees through yet poorly defined mechanisms. Here we provide further insight into the molecular attributes of L1 restriction by A3 proteins. We specifically investigated the roles of A3 protein oligomerization, interactions with RNA and their binding to the various L1 proteins. Our results show that compromising the ability of A3 proteins to oligomerize or interact with a nucleic acid substrate diminished L1 restriction to varying degrees. However the efficiency of their binding to L1 proteins did not predict restriction or the potency of the restriction.

摘要

LINE-1 (L1) 是一种非长末端重复 (LTR) 逆转录转座子,插入人类基因组的各个部位。APOBEC3 (A3) 蛋白是宿主固有防御网络的一部分,能够限制逆转录病毒和 L1 逆转录元件的复制。这些酶主要通过脱氨酶作用使单链病毒 DNA 失活。相比之下,只有 A3A 使 L1 DNA 脱氨,而其他六种 A3 蛋白通过尚未明确定义的机制在不同程度上限制 L1。在这里,我们通过 A3 蛋白进一步深入了解 L1 限制的分子特征。我们特别研究了 A3 蛋白寡聚化、与 RNA 的相互作用及其与各种 L1 蛋白结合的作用。我们的结果表明,削弱 A3 蛋白的寡聚化或与核酸底物相互作用的能力会在不同程度上降低 L1 的限制。然而,它们与 L1 蛋白结合的效率并不能预测限制或限制的效力。

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