In silico evidence that substitution of glycine for valine (p.G8V) in a common variant of TMPRSS2 isoform 1 increases accessibility to an endocytic signal: Implication for SARS-cov-2 entry into host cells and susceptibility to COVID-19

被引:1
作者
Calcagnile, Matteo [1 ]
Damiano, Fabrizio [1 ]
Lobreglio, Giambattista [2 ]
Siculella, Luisa [3 ]
Bozzetti, Maria Pia [1 ]
Forgez, Patricia [4 ]
Malgoyre, Alexandra [5 ,6 ,7 ]
Libert, Nicolas [6 ,8 ]
Bucci, Cecilia [3 ]
Alifano, Marco [9 ,10 ]
Alifano, Pietro [1 ,3 ]
机构
[1] Univ Salento, Dept Biol & Environm Sci & Technol, Lecce, Italy
[2] Vito Fazzi Gen Hosp, Clin Pathol & Microbiol Unit, I-73100 Lecce, Italy
[3] Univ Salento, Dept Expt Med, Lecce, Italy
[4] Univ Paris, INSERM UMR S T3S 1124, INSERM UMR-S 1124 T3S, Eq 5 CELLULAR HOMEOSTASIS, Campus St Germain, Paris, France
[5] French Armed Forces Biomed Res Inst IRBA, Bretigny Sur Orge, France
[6] French Armed Forces Hlth Serv, Ecole Val Grace, Paris, France
[7] Univ Paris Saclay, Lab Biol Exercice Performance & St LBEPS, F-91025 Evry, France
[8] French Armed Forces Hlth Serv, Hop Instruction Armees, Marseille, France
[9] Univ Paris, Cochin Hosp, APHP Ctr, Thorac Surg Dept, Paris, France
[10] Univ Paris, Cordeliers Res Ctr, INSERM U1138, Team Canc Immune Control & Escape, Paris, France
关键词
COVID-19; SARS-CoV-2; TMPRSS2; Single nucleotide polymorphism; RESPIRATORY SYNDROME CORONAVIRUS; SERINE-PROTEASE; PEP-FOLD; ACE2; GENE; TRANSMEMBRANE; PEPTIDE; CLONING; SPIKE;
D O I
10.1016/j.biochi.2024.05.004
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The TMPRSS2 protease plays a key role in the entry of the SARS-CoV-2 into cells. The TMPRSS2 gene is highly polymorphic in humans, and some polymorphisms may affect the susceptibility to COVID-19 or disease severity. rs75603675 (c.23G > T) is a missense variant that causes the replacement of glycine with valine at position 8 (p.G8V) in the TMPRSS2 isoform 1. According to GnomAD v4.0.0 database, the allele frequency of the rs75603675 on a global scale is 38.10 %, and range from 0.92 % in East Asian to 40.77 % in non-Finnish European (NFE) population. We analyzed the occurrence of the rs75603675 in two cohorts of patients, the first with severe/critical COVID-19 enrolled in a French hospital (42 patients), and the second with predominantly asymptomatic/pauci-symptomatic/mild COVID-19 enrolled in an Italian hospital (69 patients). We found that the TMPRSS2-c.23T minor allele frequency was similar in the two cohorts, 46.43 % and 46.38 %, respectively, and higher than the frequency in the NFE population (40.77 %). Chi-square test provided significant results (p < 0.05) when the genotype data ( TMPRSS2- c.23T/c.23T homozygotes & thorn; TMPRSS2-c.23G/c.23T heterozygotes vs. TMPRSS2-c.23G/c.23G homozygotes) of the two patient groups were pooled and compared to the expected data for the NFE population, suggesting a possible pathogenetic mechanism of the p.G8V substitution. We explored the possible effects of the p.G8V substitution and found that the N-terminal region of the TMPRSS2 isoform 1 contains a signal for clathrin/AP-2-dependent endocytosis. In silico analysis predicted that the p.G8V substitution may increase the accessibility to the endocytic signal, which could help SARS-CoV-2 enter cells. (c) 2024 Elsevier B.V. and Soci & eacute;t & eacute; Fran & ccedil;aise de Biochimie et Biologie Mol & eacute;culaire (SFBBM). All rights are reserved, including those for text and data mining, AI training, and similar technologies.
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页码:89 / 98
页数:10
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