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赖氨酸甲基转移酶EhPKMT2参与了.的体外毒力。 (原文此处不完整,翻译可能存在信息缺失)

Lysine Methyltransferase EhPKMT2 Is Involved in the In Vitro Virulence of .

作者信息

Munguía-Robledo Susana, Orozco Esther, García-Rivera Guillermina, Bolaños Jeni, Valdés Jesús, Azuara-Licéaga Elisa, Rodríguez Mario Alberto

机构信息

Center for Research and Advanced Studies of the IPN, Department of Infectomics and Molecular Pathogenesis, National Polytechnic Institute, Mexico City 07360, Mexico.

Center for Research and Advanced Studies of the IPN, Department of Biochemistry, National Polytechnic Institute, Mexico City 07360, Mexico.

出版信息

Pathogens. 2023 Mar 17;12(3):474. doi: 10.3390/pathogens12030474.

DOI:10.3390/pathogens12030474
PMID:36986396
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10058465/
Abstract

Lysine methylation, a posttranslational modification catalyzed by protein lysine methyltransferases (PKMTs), is involved in epigenetics and several signaling pathways, including cell growth, cell migration and stress response, which in turn may participate in virulence of protozoa parasites. , the etiologic agent of human amebiasis, has four PKMTs (EhPKMT1 to EhPKMT4), but their role in parasite biology is unknown. Here, to obtain insight into the role of EhPKMT2, we analyzed its expression level and localization in trophozoites subjected to heat shock and during phagocytosis, two events that are related to amoeba virulence. Moreover, the effect of EhPKMT2 knockdown on those activities and on cell growth, migration and cytopathic effect was investigated. The results indicate that this enzyme participates in all these cellular events, suggesting that it could be a potential target for development of novel therapeutic strategies against amebiasis.

摘要

赖氨酸甲基化是一种由蛋白质赖氨酸甲基转移酶(PKMTs)催化的翻译后修饰,参与表观遗传学和多种信号通路,包括细胞生长、细胞迁移和应激反应,这些反过来可能参与原生动物寄生虫的毒力。溶组织内阿米巴,人类阿米巴病的病原体,有四种PKMTs(EhPKMT1至EhPKMT4),但其在寄生虫生物学中的作用尚不清楚。在这里,为了深入了解EhPKMT2的作用,我们分析了其在热休克处理的滋养体以及吞噬过程中的表达水平和定位,这两个事件与变形虫的毒力有关。此外,还研究了EhPKMT2敲低对这些活动以及细胞生长、迁移和细胞病变效应的影响。结果表明,这种酶参与了所有这些细胞事件,表明它可能是开发针对阿米巴病的新型治疗策略的潜在靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0544/10058465/6c98c1c4a4e5/pathogens-12-00474-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0544/10058465/f1d887003f05/pathogens-12-00474-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0544/10058465/9a905d9f7dfd/pathogens-12-00474-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0544/10058465/17eb2d896690/pathogens-12-00474-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0544/10058465/837caca36540/pathogens-12-00474-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0544/10058465/7a85871aff06/pathogens-12-00474-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0544/10058465/21ef5f6ba65e/pathogens-12-00474-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0544/10058465/f52f4ae55143/pathogens-12-00474-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0544/10058465/6c98c1c4a4e5/pathogens-12-00474-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0544/10058465/f1d887003f05/pathogens-12-00474-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0544/10058465/9a905d9f7dfd/pathogens-12-00474-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0544/10058465/17eb2d896690/pathogens-12-00474-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0544/10058465/837caca36540/pathogens-12-00474-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0544/10058465/7a85871aff06/pathogens-12-00474-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0544/10058465/21ef5f6ba65e/pathogens-12-00474-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0544/10058465/f52f4ae55143/pathogens-12-00474-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0544/10058465/6c98c1c4a4e5/pathogens-12-00474-g008.jpg

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本文引用的文献

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Life (Basel). 2022 Mar 2;12(3):362. doi: 10.3390/life12030362.
2
Set1-mediated H3K4 methylation is required for virulence by regulating intracellular level of reactive oxygen species.组蛋白 H3K4 甲基化的 Set1 介导对于调节细胞内活性氧水平的毒力是必需的。
Virulence. 2021 Dec;12(1):2648-2658. doi: 10.1080/21505594.2021.1980988.
3
Functions of SMYD proteins in biological processes: What do we know? An updated review.
SMYD 蛋白在生物过程中的功能:我们了解多少?更新综述。
Arch Biochem Biophys. 2021 Nov 15;712:109040. doi: 10.1016/j.abb.2021.109040. Epub 2021 Sep 20.
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Set7/9 controls proliferation and genotoxic drug resistance of NSCLC cells.Set7/9 控制非小细胞肺癌细胞的增殖和遗传毒性药物耐药性。
Biochem Biophys Res Commun. 2021 Oct 1;572:41-48. doi: 10.1016/j.bbrc.2021.07.086. Epub 2021 Jul 31.
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Histone H3K4 Methyltransferases as Targets for Drug-Resistant Cancers.组蛋白H3K4甲基转移酶作为耐药性癌症的靶点
Biology (Basel). 2021 Jun 25;10(7):581. doi: 10.3390/biology10070581.
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DIM5/KMT1 controls fungal insect pathogenicity and genome stability by methylation of histone H3K4, H3K9 and H3K36.DIM5/KMT1 通过组蛋白 H3K4、H3K9 和 H3K36 的甲基化来控制真菌的昆虫致病性和基因组稳定性。
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The atypical protein arginine methyltrasferase of Entamoeba histolytica (EhPRMTA) is involved in cell proliferation, heat shock response and in vitro virulence.溶组织内阿米巴的非典型精氨酸甲基转移酶(EhPRMTA)参与细胞增殖、热休克反应和体外毒力。
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