• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

参与病毒引发的 II 型跨膜丝氨酸蛋白酶的进化历史。

Evolutionary history of type II transmembrane serine proteases involved in viral priming.

机构信息

Scientific Institute IRCCS E. MEDEA, Bioinformatics, 23842, Bosisio Parini, Italy.

出版信息

Hum Genet. 2022 Nov;141(11):1705-1722. doi: 10.1007/s00439-022-02435-y. Epub 2022 Feb 5.

DOI:10.1007/s00439-022-02435-y
PMID:35122525
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8817155/
Abstract

Type II transmembrane serine proteases (TTSPs) are a family of trypsin-like membrane-anchored serine proteases that play key roles in the regulation of some crucial processes in physiological conditions, including cardiac function, digestion, cellular iron homeostasis, epidermal differentiation, and immune responses. However, some of them, in particular TTSPs expressed in the human airways, were identified as host factors that promote the proteolytic activation and spread of respiratory viruses such as influenza virus, human metapneumovirus, and coronaviruses, including SARS-CoV-2. Given their involvement in viral priming, we hypothesized that members of the TTSP family may represent targets of positive selection, possibly as the result of virus-driven pressure. Thus, we investigated the evolutionary history of sixteen TTSP genes in mammals. Evolutionary analyses indicate that most of the TTSP genes that have a verified role in viral proteolytic activation present signals of pervasive positive selection, suggesting that viral infections represent a selective pressure driving the evolution of these proteases. We also evaluated genetic diversity in human populations and we identified targets of balancing selection in TMPRSS2 and TMPRSS4. This scenario may be the result of an ancestral and still ongoing host-pathogen arms race. Overall, our results provide evolutionary information about candidate functional sites and polymorphic positions in TTSP genes.

摘要

II 型跨膜丝氨酸蛋白酶(TTSPs)是一类胰凝乳蛋白酶样的膜锚定丝氨酸蛋白酶,在生理条件下的一些关键过程的调节中发挥着关键作用,包括心脏功能、消化、细胞铁稳态、表皮分化和免疫反应。然而,其中一些蛋白酶,特别是在人类气道中表达的 TTSPs,被鉴定为促进呼吸道病毒(如流感病毒、人类偏肺病毒和冠状病毒,包括 SARS-CoV-2)的蛋白水解激活和传播的宿主因素。鉴于它们在病毒引发中的作用,我们假设 TTSP 家族的成员可能是正选择的靶点,可能是病毒驱动压力的结果。因此,我们研究了哺乳动物中十六种 TTSP 基因的进化历史。进化分析表明,大多数在病毒蛋白水解激活中具有验证作用的 TTSP 基因存在普遍正选择的信号,表明病毒感染是驱动这些蛋白酶进化的选择压力。我们还评估了人类群体中的遗传多样性,并在 TMPRSS2 和 TMPRSS4 中鉴定了平衡选择的靶点。这种情况可能是祖先和仍在进行的宿主-病原体军备竞赛的结果。总的来说,我们的研究结果提供了关于 TTSP 基因候选功能位点和多态性位置的进化信息。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d36/8817155/c390991842dc/439_2022_2435_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d36/8817155/50f11d321b25/439_2022_2435_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d36/8817155/b8b370a331e5/439_2022_2435_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d36/8817155/b5381a36b53d/439_2022_2435_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d36/8817155/c390991842dc/439_2022_2435_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d36/8817155/50f11d321b25/439_2022_2435_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d36/8817155/b8b370a331e5/439_2022_2435_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d36/8817155/b5381a36b53d/439_2022_2435_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d36/8817155/c390991842dc/439_2022_2435_Fig4_HTML.jpg

相似文献

1
Evolutionary history of type II transmembrane serine proteases involved in viral priming.参与病毒引发的 II 型跨膜丝氨酸蛋白酶的进化历史。
Hum Genet. 2022 Nov;141(11):1705-1722. doi: 10.1007/s00439-022-02435-y. Epub 2022 Feb 5.
2
The Proteolytic Activation of (H3N2) Influenza A Virus Hemagglutinin Is Facilitated by Different Type II Transmembrane Serine Proteases.不同的II型跨膜丝氨酸蛋白酶促进甲型流感病毒(H3N2)血凝素的蛋白水解激活。
J Virol. 2016 Apr 14;90(9):4298-4307. doi: 10.1128/JVI.02693-15. Print 2016 May.
3
TMPRSS2 and TMPRSS4 facilitate trypsin-independent spread of influenza virus in Caco-2 cells.TMPRSS2 和 TMPRSS4 促进了流感病毒在 Caco-2 细胞中的无胰蛋白酶依赖性扩散。
J Virol. 2010 Oct;84(19):10016-25. doi: 10.1128/JVI.00239-10. Epub 2010 Jul 14.
4
Inhibitors of type II transmembrane serine proteases in the treatment of diseases of the respiratory tract - A review of patent literature.II 型跨膜丝氨酸蛋白酶抑制剂在治疗呼吸道疾病中的应用——专利文献综述。
Expert Opin Ther Pat. 2020 Nov;30(11):807-824. doi: 10.1080/13543776.2020.1817390. Epub 2020 Oct 12.
5
Intracellular autoactivation of TMPRSS11A, an airway epithelial transmembrane serine protease.跨膜丝氨酸蛋白酶 11A(TMPRSS11A)的细胞内自动激活,一种气道上皮细胞跨膜丝氨酸蛋白酶。
J Biol Chem. 2020 Sep 4;295(36):12686-12696. doi: 10.1074/jbc.RA120.014525. Epub 2020 Jul 15.
6
The role of type II transmembrane serine protease-mediated signaling in cancer.II型跨膜丝氨酸蛋白酶介导的信号传导在癌症中的作用。
FEBS J. 2017 May;284(10):1421-1436. doi: 10.1111/febs.13971. Epub 2016 Dec 24.
7
TMPRSS11D and TMPRSS13 Activate the SARS-CoV-2 Spike Protein.TMPRSS11D 和 TMPRSS13 激活 SARS-CoV-2 刺突蛋白。
Viruses. 2021 Feb 28;13(3):384. doi: 10.3390/v13030384.
8
TMPRSS4, a type II transmembrane serine protease, as a potential therapeutic target in cancer.跨膜丝氨酸蛋白酶 4(TMPRSS4),一种 II 型跨膜丝氨酸蛋白酶,作为癌症的潜在治疗靶点。
Exp Mol Med. 2023 Apr;55(4):716-724. doi: 10.1038/s12276-023-00975-5. Epub 2023 Apr 3.
9
DESC1 and MSPL activate influenza A viruses and emerging coronaviruses for host cell entry.DESC1和MSPL激活甲型流感病毒和新出现的冠状病毒以进入宿主细胞。
J Virol. 2014 Oct;88(20):12087-97. doi: 10.1128/JVI.01427-14. Epub 2014 Aug 13.
10
Host serine proteases TMPRSS2 and TMPRSS11D mediate proteolytic activation and trypsin-independent infection in group A rotaviruses.宿主丝氨酸蛋白酶TMPRSS2和TMPRSS11D介导A组轮状病毒的蛋白水解激活和非胰蛋白酶依赖性感染。
J Virol. 2021 May 10;95(11). doi: 10.1128/JVI.00398-21. Epub 2021 Mar 24.

引用本文的文献

1
CRISPR-Cas9 genetic screens reveal regulation of TMPRSS2 by the Elongin BC-VHL complex.CRISPR-Cas9基因筛选揭示了Elongin BC-VHL复合物对TMPRSS2的调控作用。
Sci Rep. 2025 Apr 7;15(1):11907. doi: 10.1038/s41598-025-95644-0.
2
From N-0385 to N-0920: Unveiling a Host-Directed Protease Inhibitor with Picomolar Antiviral Efficacy against Prevalent SARS-CoV-2 Variants.从N-0385到N-0920:揭示一种对流行的SARS-CoV-2变体具有皮摩尔抗病毒效力的宿主导向蛋白酶抑制剂。
J Med Chem. 2025 Apr 10;68(7):7119-7136. doi: 10.1021/acs.jmedchem.4c02468. Epub 2025 Mar 31.
3
Identification of potent TMPRSS4 inhibitors through structural modeling and molecular dynamics simulations.

本文引用的文献

1
SARS-CoV-2-host proteome interactions for antiviral drug discovery.SARS-CoV-2 宿主蛋白组与抗病毒药物发现的相互作用。
Mol Syst Biol. 2021 Nov;17(11):e10396. doi: 10.15252/msb.202110396.
2
TMPRSS11D and TMPRSS13 Activate the SARS-CoV-2 Spike Protein.TMPRSS11D 和 TMPRSS13 激活 SARS-CoV-2 刺突蛋白。
Viruses. 2021 Feb 28;13(3):384. doi: 10.3390/v13030384.
3
CD147-spike protein is a novel route for SARS-CoV-2 infection to host cells.CD147-刺突蛋白是 SARS-CoV-2 感染宿主细胞的新途径。
通过结构建模和分子动力学模拟鉴定有效的跨膜丝氨酸蛋白酶4(TMPRSS4)抑制剂。
Sci Rep. 2025 Jan 22;15(1):2748. doi: 10.1038/s41598-025-86961-5.
4
Molecular basis of TMPRSS2 recognition by Paeniclostridium sordellii hemorrhagic toxin.梭菌属 Paeniclostridium 出血毒素识别 TMPRSS2 的分子基础。
Nat Commun. 2024 Mar 4;15(1):1976. doi: 10.1038/s41467-024-46394-6.
5
Type II Transmembrane Serine Proteases as Modulators in Adipose Tissue Phenotype and Function.II型跨膜丝氨酸蛋白酶作为脂肪组织表型和功能的调节因子
Biomedicines. 2023 Jun 23;11(7):1794. doi: 10.3390/biomedicines11071794.
6
Identification of Embryonic Chicken Proteases Activating Newcastle Disease Virus and Their Roles in the Pathogenicity of Virus Used as Vaccine.鉴定禽类胚胎中能激活新城疫病毒的蛋白酶及其在用作疫苗病毒的致病性中的作用。
J Virol. 2023 May 31;97(5):e0032423. doi: 10.1128/jvi.00324-23. Epub 2023 Apr 12.
Signal Transduct Target Ther. 2020 Dec 4;5(1):283. doi: 10.1038/s41392-020-00426-x.
4
Expression and co-expression analyses of TMPRSS2, a key element in COVID-19.TMPRSS2 的表达和共表达分析,COVID-19 的关键因素。
Eur J Clin Microbiol Infect Dis. 2021 Feb;40(2):451-455. doi: 10.1007/s10096-020-04089-y. Epub 2020 Nov 27.
5
SARS-CoV-2 Infection Boosts Antiviral Effector in COVID-19 Patients.严重急性呼吸综合征冠状病毒2感染增强了新冠肺炎患者的抗病毒效应器。
iScience. 2020 Oct 23;23(10):101585. doi: 10.1016/j.isci.2020.101585. Epub 2020 Sep 23.
6
Broad host range of SARS-CoV-2 predicted by comparative and structural analysis of ACE2 in vertebrates.通过比较和结构分析脊椎动物 ACE2 预测 SARS-CoV-2 的广泛宿主范围。
Proc Natl Acad Sci U S A. 2020 Sep 8;117(36):22311-22322. doi: 10.1073/pnas.2010146117. Epub 2020 Aug 21.
7
Evolutionary Arms Race between Virus and Host Drives Genetic Diversity in Bat Severe Acute Respiratory Syndrome-Related Coronavirus Spike Genes.病毒和宿主之间的进化军备竞赛驱动了蝙蝠严重急性呼吸综合征相关冠状病毒刺突基因的遗传多样性。
J Virol. 2020 Sep 29;94(20). doi: 10.1128/JVI.00902-20.
8
Intracellular autoactivation of TMPRSS11A, an airway epithelial transmembrane serine protease.跨膜丝氨酸蛋白酶 11A(TMPRSS11A)的细胞内自动激活,一种气道上皮细胞跨膜丝氨酸蛋白酶。
J Biol Chem. 2020 Sep 4;295(36):12686-12696. doi: 10.1074/jbc.RA120.014525. Epub 2020 Jul 15.
9
Host-Virus Arms Races Drive Elevated Adaptive Evolution in Viral Receptors.宿主-病毒军备竞赛推动病毒受体的适应性进化。
J Virol. 2020 Jul 30;94(16). doi: 10.1128/JVI.00684-20.
10
Cell entry mechanisms of SARS-CoV-2.SARS-CoV-2 的细胞进入机制。
Proc Natl Acad Sci U S A. 2020 May 26;117(21):11727-11734. doi: 10.1073/pnas.2003138117. Epub 2020 May 6.