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DDX1的底物特异性:一种人类DEAD盒蛋白

Substrate Specificities of DDX1: A Human DEAD-Box Protein.

作者信息

Moore Anthony F T, Berhie Yepeth, Weislow Isaac S, Koculi Eda

机构信息

Department of Chemistry, University of Central Florida, 4111 Libra Drive, Physical Sciences, Orlando, Florida 32816-2366, United States.

Department of Chemistry and Biochemistry, The University of Texas at El Paso, 500 W University Ave, Chemistry and Computer Science, El Paso, Texas 79902-5802, United States.

出版信息

ACS Omega. 2025 Jan 14;10(3):2598-2607. doi: 10.1021/acsomega.4c07522. eCollection 2025 Jan 28.

Abstract

DDX1 is a human DEAD-box RNA helicase involved in various stages of RNA metabolism, from transcription to decay, and is consequently implicated in many human diseases. The nucleotides hydrolyzed by DDX1 and the structures of the nucleic acids upon which it acts in cells remain largely unknown. In this study, we identify the nucleic acid sequences and structures that support DDX1's nucleotide hydrolysis activity and determine its nucleotide hydrolysis specificity. Our data demonstrate that DDX1 hydrolyzes only ATP and deoxy-ATP in the presence of RNA. The ATP hydrolysis activity of DDX1 is stimulated by single-stranded RNA molecules as short as ten nucleotides, a blunt-ended double-stranded RNA, double-stranded RNA/DNA hybrid, and single-stranded DNA. Under our experimental conditions, single-stranded DNA stimulates DDX1's ATPase activity to a smaller extent compared to the other RNA constructs or the RNA/DNA hybrid. Given DDX1's involvement in numerous critical cellular processes and its implication in various human diseases, determining its substrate specificity not only enhances our understanding of its function, but also facilitates the development of novel therapeutic approaches.

摘要

DDX1是一种人类DEAD盒RNA解旋酶,参与从转录到衰变的RNA代谢的各个阶段,因此与许多人类疾病有关。DDX1水解的核苷酸以及它在细胞中作用的核酸结构在很大程度上仍然未知。在这项研究中,我们确定了支持DDX1核苷酸水解活性的核酸序列和结构,并确定了其核苷酸水解特异性。我们的数据表明,DDX1在RNA存在的情况下仅水解ATP和脱氧ATP。DDX1的ATP水解活性受到短至十个核苷酸的单链RNA分子、平端双链RNA、双链RNA/DNA杂交体和单链DNA的刺激。在我们的实验条件下,与其他RNA构建体或RNA/DNA杂交体相比,单链DNA对DDX1的ATP酶活性的刺激程度较小。鉴于DDX1参与众多关键的细胞过程并与各种人类疾病有关,确定其底物特异性不仅能增强我们对其功能的理解,还能促进新型治疗方法的开发。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1666/11780465/75692f12bba2/ao4c07522_0001.jpg

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