An unusual activity of mycobacterial MutT1 Nudix hydrolase domain as a protein phosphatase regulates nucleoside diphosphate kinase function.

IF 2.7 3区 生物学 Q3 MICROBIOLOGY
Journal of Bacteriology Pub Date : 2025-01-31 Epub Date: 2024-12-11 DOI:10.1128/jb.00314-24
Elhassan Ali Fathi Emam, Koyel Roy, Devendra Pratap Singh, Deepak K Saini, Umesh Varshney
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引用次数: 0

Abstract

MutT proteins are Nudix hydrolases characterized by the presence of a Nudix box, GX5EX7REUXEEXGU, where U is a bulky hydrophobic residue and X is any residue. Major MutT proteins hydrolyze 8-oxo-(d)GTP (8-oxo-GTP or 8-oxo-dGTP) to the corresponding 8-oxo-(d)GMP, preventing their incorporation into nucleic acids. Mycobacterial MutT1 comprises an N-terminal domain (NTD) harboring the Nudix box motif, and a C-terminal domain (CTD) harboring the RHG histidine phosphatase motif. Interestingly, unlike other MutTs, the MutT1 hydrolyses the mutagenic 8-oxo-(d)GTP to the corresponding 8-oxo-(d)GDP. Nucleoside diphosphate kinase (NDK), a conserved protein, carries out reversible conversion of (d)NDPs to (d)NTPs through phospho-NDK (NDK-Pi) intermediate. Recently, we showed that NDK-Pi converts 8-oxo-dGDP to 8-oxo-dGTP and escalates A to C mutations in a MutT-deficient Escherichia coli. We now show that both Mycobacterium tuberculosis MutT1 and Mycobacterium smegmatis MutT1, through their NTD (Nudix hydrolase motifs) function as protein phosphatase to regulate the levels of NDK-Pi and prevent it from catalyzing conversion of (d)NDPs to (d)NTPs (including conversion of 8-oxo-dGDP to 8-oxo-dGTP). To corroborate this function, we show that MsmMutT1 decreases A to C mutations in E. coli under the conditions of EcoNDK overexpression.IMPORTANCEMutT proteins, having a Nudix box domain, hydrolyze the mutagenic 8-oxo-dGTP to 8-oxo-dGMP. However, mycobacterial MutT (MutT1) comprises an N-terminal domain (NTD) harboring a Nudix box, and a C-terminal domain (CTD) harboring an RHG histidine phosphatase. Unlike other MutTs, mycobacterial MutT1 hydrolyses 8-oxo-dGTP to 8-oxo-dGDP. Nucleoside diphosphate kinase (NDK), a conserved protein, converts 8-oxo-dGDP to 8-oxo-dGTP through phospho-NDK (NDK-Pi) intermediate and escalates A to C mutations. Here, we show that the mycobacterial MutT1 is unprecedented in that its NTD (Nudix box), functions as protein phosphatase to regulate NDK-Pi levels and prevents it from converting dNDPs to dNTPs (including 8-oxo-dGDP to 8-oxo-dGTP conversion). In addition, mycobacterial MutT1 decreases A to C mutations in Escherichia coli under the conditions of NDK overexpression.

分枝杆菌MutT1 Nudix水解酶结构域作为蛋白磷酸酶的异常活性调节核苷二磷酸激酶的功能。
MutT蛋白是Nudix水解酶,其特征是存在一个Nudix盒子,GX5EX7REUXEEXGU,其中U是一个大的疏水残基,X是任何残基。主要的MutT蛋白将8-oxo-(d)GTP (8-oxo-GTP或8-oxo- dgtp)水解为相应的8-oxo-(d)GMP,阻止其掺入核酸。分枝杆菌MutT1包括一个包含Nudix盒基序的n端结构域(NTD)和一个包含RHG组氨酸磷酸酶基序的c端结构域(CTD)。有趣的是,与其他MutTs不同,MutT1将诱变的8-oxo-(d)GTP水解为相应的8-oxo-(d)GDP。核苷二磷酸激酶(NDK)是一种保守蛋白,通过磷酸化-NDK (NDK- pi)中间体将(d)NDPs可逆转化为(d)NTPs。最近,我们发现NDK-Pi在缺乏mutt的大肠杆菌中将8-oxo-dGDP转化为8-oxo-dGTP,并将A突变升级为C突变。我们现在发现结核分枝杆菌MutT1和耻垢分枝杆菌MutT1通过其NTD (Nudix水解酶基元)作为蛋白磷酸酶调节NDK-Pi的水平,并阻止NDK-Pi催化(d)NDPs向(d)NTPs的转化(包括8-oxo-dGDP向8-oxo-dGTP的转化)。为了证实这一功能,我们发现在EcoNDK过表达的条件下,MsmMutT1减少了大肠杆菌中A到C的突变。重要的是,具有Nudix盒结构域的emutt蛋白可以将8-oxo-dGTP水解为8-oxo-dGMP。然而,分枝杆菌MutT (MutT1)包括一个包含Nudix box的n端结构域(NTD)和一个包含RHG组氨酸磷酸酶的c端结构域(CTD)。与其他mutt不同,分枝杆菌mut1将8-oxo-dGTP水解为8-oxo-dGDP。核苷二磷酸激酶(NDK)是一种保守蛋白,通过磷酸化NDK (NDK- pi)中间体将8-oxo-dGDP转化为8-oxo-dGTP,并将a突变升级为C突变。在这里,我们发现分枝杆菌MutT1是前所未有的,因为它的NTD (Nudix box)作为蛋白磷酸酶调节NDK-Pi水平,并阻止它将ndps转化为dntp(包括8-oxo-dGDP到8-oxo-dGTP的转化)。此外,在NDK过表达的条件下,分枝杆菌MutT1减少了大肠杆菌中A到C的突变。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Bacteriology
Journal of Bacteriology 生物-微生物学
CiteScore
6.10
自引率
9.40%
发文量
324
审稿时长
1.3 months
期刊介绍: The Journal of Bacteriology (JB) publishes research articles that probe fundamental processes in bacteria, archaea and their viruses, and the molecular mechanisms by which they interact with each other and with their hosts and their environments.
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