1887

Abstract

is a known human pathogen that causes the airborne infectious disease tuberculosis (TB). Every year TB infects millions of people worldwide. The emergence of multi-drug resistant (MDR), extensively drug resistant (XDR) and totally drug resistant (TDR) strains against the first- and second-line anti-TB drugs has created an urgent need for the development and implementation of new drug strategies. In this study, the complete genomes of 174 strains of are analysed to understand the evolution of molecular drug target (MDT) genes. Phylogenomic placements of strains depicted close association and temporal clustering. Selection pressure analysis by deducing the ratio of non-synonymous to synonymous substitution rates () in 51 MDT genes of the 174 . strains led to categorizing these genes into diversifying (D, >0.70), moderately diversifying (MD, =0.35–0.70) and stabilized (S, <0.35) genes. The genes and were identified as diversifying, and , and were identified as stabilized genes. Furthermore, sequence similarity networks were drawn that supported these divisions. In the multiple sequence alignments of diversifying and stabilized proteins, previously reported resistance mutations were checked to predict sensitive and resistant strains of . Finally, to delineate the potential of stabilized or least diversified genes/proteins as anti-TB drug targets, protein–protein interactions of MDT proteins with human proteins were analysed. We predict that (=0.29), a stabilized gene that encodes the most host-interacting protein, KasA, should serve as a potential drug target for the treatment of TB.

  • This is an open-access article distributed under the terms of the Creative Commons Attribution NonCommercial License.
Loading

Article metrics loading...

/content/journal/mgen/10.1099/mgen.0.000542
2021-03-22
2024-04-20
Loading full text...

Full text loading...

/deliver/fulltext/mgen/7/3/mgen000542.html?itemId=/content/journal/mgen/10.1099/mgen.0.000542&mimeType=html&fmt=ahah

References

  1. Pai M, Behr MA, Dowdy D, Dheda K, Divangahi M et al. Tuberculosis. Nat Rev Dis Primers 2016; 2:16076 [View Article][PubMed]
    [Google Scholar]
  2. Koch A, Mizrahi V. Mycobacterium tuberculosis. Trends Microbiol 2018; 26:555–556 [View Article][PubMed]
    [Google Scholar]
  3. WHO Global Tuberculosis Report Geneva: World Health Organization; 2019
    [Google Scholar]
  4. Velayati AA, Masjedi MR, Farnia P, Tabarsi P, Ghanavi J et al. Emergence of new forms of totally drug-resistant tuberculosis bacilli: super extensively drug-resistant tuberculosis or totally drug-resistant strains in Iran. Chest 2009; 136:420–425
    [Google Scholar]
  5. Klopper M, Warren RM, Hayes C, Gey van Pittius NC, Streicher EM et al. Emergence and spread of extensively and totally drug-resistant tuberculosis, South Africa. Emerg Infect Dis 2013; 19:449–455
    [Google Scholar]
  6. Udwadia Z. Totally drug resistant-tuberculosis in India: the bad just got worse. J Assoc Chest Physicians 2016; 4:41–42 [View Article]
    [Google Scholar]
  7. Hameed HMA, Islam MM, Chhotaray C, Wang C, Liu Y et al. Molecular targets related drug resistance mechanisms in MDR-, XDR-, and TDR-Mycobacterium tuberculosis strains. Front Cell Infect Microbiol 2018; 8:114
    [Google Scholar]
  8. Bloemberg GV, Keller PM, Stucki D, Trauner A, Borrell S et al. Acquired resistance to bedaquiline and delamanid in therapy for tuberculosis. N Engl J Med 2015; 373:1986–1988
    [Google Scholar]
  9. Singh P, Kumari R, Lal R. Bedaquiline: fallible hope against drug-resistant tuberculosis. Indian J Microbiol 2017; 57:371–377
    [Google Scholar]
  10. Polsfuss S, Hofmann-Thiel S, Merker M, Krieger D, Niemann S et al. Emergence of low-level delamanid and bedaquiline resistance during extremely drug-resistant tuberculosis treatment. Clin Infect Dis 2019; 69:1229–1231
    [Google Scholar]
  11. Simner PJ, Antar AAR, Hao S, Gurtowski J, Tamma PD et al. Antibiotic pressure on the acquisition and loss of antibiotic resistance genes in Klebsiella pneumoniae . J Antimicrob Chemother 2018; 73:1796–1803
    [Google Scholar]
  12. Cole ST, Brosch R, Parkhill J, Garnier T, Churcher C et al. Deciphering the biology of Mycobacterium tuberculosis from the complete genome sequence. Nature 1998; 393:537–544
    [Google Scholar]
  13. Rodriguez-Castillo JG, Pino C, Nino LF, Rozo JC, Llerena-Polo C et al. Comparative genomic analysis of Mycobacterium tuberculosis Beijing-like strains revealed specific genetic variations associated with virulence and drug resistance. Infect Genet Evol 2017; 54:314–323
    [Google Scholar]
  14. Zimpel CK, Brandao PE, de Souza Filho AF, de Souza RF, Ikuta CY et al. Complete genome sequencing of Mycobacterium bovis SP38 and comparative genomics of Mycobacterium bovis and M. tuberculosis strains. Front Microbiol 2017; 8:2389
    [Google Scholar]
  15. Palaniyandi K, Kumar N, Veerasamy M, Kabir Refaya A, Dolla C et al. Isolation and comparative genomics of Mycobacterium tuberculosis isolates from cattle and their attendants in South India. Sci Rep 2019; 9:17892
    [Google Scholar]
  16. Zhang H, Li D, Zhao L, Fleming J, Lin N et al. Genome sequencing of 161 Mycobacterium tuberculosis isolates from China identifies genes and intergenic regions associated with drug resistance. Nat Genet 2013; 45:1255–1260
    [Google Scholar]
  17. Nguyen L. Antibiotic resistance mechanisms in M. tuberculosis: an update. Arch Toxicol 2016; 90:1585–1604
    [Google Scholar]
  18. Pritchard L, Glover RH, Humphris S, Elphinstone JG, Toth IK. Genomics and taxonomy in diagnostics for food security: soft-rotting enterobacterial plant pathogens. Analytical Methods 2016; 8:12–24
    [Google Scholar]
  19. Saeed AI, Sharov V, White J, Li J, Liang W et al. TM4: a free, open-source system for microarray data management and analysis. Biotechniques 2003; 34:374–378
    [Google Scholar]
  20. Letunic I, Bork P. Interactive tree of life (iTOL) v3: an online tool for the display and annotation of phylogenetic and other trees. Nucleic Acids Res 44 2016W242–W245
    [Google Scholar]
  21. Delcher AL, Bratke KA, Powers EC, Salzberg SL. Identifying bacterial genes and endosymbiont DNA with Glimmer. Bioinformatics 2007; 23:673–679
    [Google Scholar]
  22. Aziz RK, Bartels D, Best AA, DeJongh M, Disz T et al. The RAST server: rapid annotations using subsystems technology. BMC Genomics 2008; 9:75
    [Google Scholar]
  23. Altschul SF, Gish W, Miller W, Myers EW, Lipman DJ. Basic local alignment search tool. J Mol Biol 1990; 215:403–410 [View Article][PubMed]
    [Google Scholar]
  24. Fukami K, Tateno Y. On the maximum likelihood method for estimating molecular trees: uniqueness of the likelihood point. J Mol Evol 1989; 28:460–464
    [Google Scholar]
  25. Kumar S, Stecher G, Li M, Knyaz C, Tamura K. MEGA X: molecular evolutionary genetics analysis across computing platforms. Mol Biol Evol 2018; 35:1547–1549
    [Google Scholar]
  26. Weaver S, Shank SD, Spielman SJ, Li M, Muse SV et al. Datamonkey 2.0: a modern web application for characterizing selective and other evolutionary processes. Mol Biol Evol 2018; 35:773–777
    [Google Scholar]
  27. R Core Team R: a language and environment for statistical computing Vienna: R Foundation for Statistical Computing; 2015 https://www.R-project.org/
  28. Hall TA. BioEdit: a user-friendly biological sequence alignment editor and analysis program for windows 95/98/NT. Nucl Acids Symp 1999; 41:95–98
    [Google Scholar]
  29. Li W, Godzik A. Cd-hit: a fast program for clustering and comparing large sets of protein or nucleotide sequences. Bioinformatics 2006; 22:1658–1659 [View Article][PubMed]
    [Google Scholar]
  30. Shannon P, Markiel A, Ozier O, Baliga NS, Wang JT et al. Cytoscape: a software environment for integrated models of biomolecular interaction networks. Genome Res 2003; 13:2498–2504
    [Google Scholar]
  31. Zhang Y, Skolnick J. TM-align: a protein structure alignment algorithm based on TM-score. Nucleic Acids Res 2005; 33:2302–2309
    [Google Scholar]
  32. Aranda B, Achuthan P, Alam-Faruque Y, Armean I, Bridge A et al. The IntAct molecular interaction database in 2010. Nucleic Acids Res 2010; 38:D525–D531 [View Article][PubMed]
    [Google Scholar]
  33. Ceol A, Chatr Aryamontri A, Licata L, Peluso D, Briganti L et al. MINT, the molecular interaction database: 2009 update. Nucleic Acids Res 2010; 38:D532–D539 [View Article][PubMed]
    [Google Scholar]
  34. Stark C, Breitkreutz B-J, Chatr-Aryamontri A, Boucher L, Oughtred R et al. The BioGRID interaction database: 2011 update. Nucleic Acids Res 2011; 39:D698–D704 [View Article][PubMed]
    [Google Scholar]
  35. Bader GD, Betel D, Hogue CW. BIND: the biomolecular interaction network database. Nucleic Acids Res 2003; 31:248–250
    [Google Scholar]
  36. Lew JM, Kapopoulou A, Jones LM, Cole ST. TubercuList – 10 years after. Tuberculosis 2011; 91:1–7 [View Article][PubMed]
    [Google Scholar]
  37. Zhu L, Zhong J, Jia X, Liu G, Kang Y et al. Precision methylome characterization of Mycobacterium tuberculosis complex (MTBC) using PacBio single-molecule real-time (SMRT) technology. Nucleic Acids Res 2016; 44:730–743 [View Article][PubMed]
    [Google Scholar]
  38. Madhavilatha GK, Joseph BV, Paul LK, Kumar RA, Hariharan R et al. Whole-genome sequences of two clinical isolates of Mycobacterium tuberculosis from Kerala, South India. J Bacteriol 2012; 194:4430 [View Article][PubMed]
    [Google Scholar]
  39. Saelens JW, Lau-Bonilla D, Moller A, Xet-Mull AM, Medina N et al. Annotated genome sequences of 16 lineage 4 Mycobacterium tuberculosis strains from Guatemala. Genome Announc 2018; 6:e00024-18 [View Article][PubMed]
    [Google Scholar]
  40. Bloom BR, Murray CJ. Tuberculosis: commentary on a reemergent killer. Science 1992; 257:1055–1064
    [Google Scholar]
  41. Moazed D, Noller HF. Interaction of antibiotics with functional sites in 16S ribosomal RNA. Nature 1987; 327:389–394
    [Google Scholar]
  42. Barnes PF, Bloch AB, Davidson PT, Snider DE. Tuberculosis in patients with human immunodeficiency virus infection. N Engl J Med 1991; 324:1644–1650 [View Article][PubMed]
    [Google Scholar]
  43. Snider DE, Roper WL. The new tuberculosis. N Engl J Med 1992; 326:703–705 [View Article][PubMed]
    [Google Scholar]
  44. Honore N, Cole ST. Streptomycin resistance in mycobacteria. Antimicrob Agents Chemother 1994; 38:238–242
    [Google Scholar]
  45. Okamoto S, Tamaru A, Nakajima C, Nishimura K, Tanaka Y et al. Loss of a conserved 7-methylguanosine modification in 16S rRNA confers low-level streptomycin resistance in bacteria. Mol Microbiol 2007; 63:1096–1106
    [Google Scholar]
  46. Zhang Y, Mitchison D. The curious characteristics of pyrazinamide: a review. Int J Tuberc Lung Dis 2003; 7:6–21
    [Google Scholar]
  47. Cheng SJ, Thibert L, Sanchez T, Heifets L, Zhang Y. pncA mutations as a major mechanism of pyrazinamide resistance in Mycobacterium tuberculosis: spread of a monoresistant strain in Quebec, Canada. Antimicrob Agents Chemother 2000; 44:528–532
    [Google Scholar]
  48. Khan MT, Malik SI, Ali S, Masood N, Nadeem T et al. Pyrazinamide resistance and mutations in pncA among isolates of Mycobacterium tuberculosis from Khyber Pakhtunkhwa, Pakistan. BMC Infect Dis 2019; 19:116
    [Google Scholar]
  49. Rawat R, Whitty A, Tonge PJ. The isoniazid-NAD adduct is a slow, tight-binding inhibitor of InhA, the Mycobacterium tuberculosis enoyl reductase: adduct affinity and drug resistance. Proc Natl Acad Sci USA 2003; 100:13881–13886
    [Google Scholar]
  50. Wong CF, Shin J, Subramanian Manimekalai MS, Saw WG, Yin Z et al. AhpC of the mycobacterial antioxidant defense system and its interaction with its reducing partner thioredoxin-C. Sci Rep 2017; 7:5159
    [Google Scholar]
  51. Wengenack NL, Rusnak F. Evidence for isoniazid-dependent free radical generation catalyzed by Mycobacterium tuberculosis KatG and the isoniazid-resistant mutant KatG(S315T). Biochemistry 2001; 40:8990–8996
    [Google Scholar]
  52. Wang H-W, Chung C-H, Ma T-Y, Wong H. Roles of alkyl hydroperoxide reductase subunit C (AhpC) in viable but nonculturable Vibrio parahaemolyticus . Appl Environ Microbiol 2013; 79:3734–3743 [View Article][PubMed]
    [Google Scholar]
  53. Springer B, Master S, Sander P, Zahrt T, McFalone M et al. Silencing of oxidative stress response in Mycobacterium tuberculosis: expression patterns of ahpC in virulent and avirulent strains and effect of ahpC inactivation. Infect Immun 2001; 69:5967–5973
    [Google Scholar]
  54. Cheng XF, Jiang C, Zhang M, Xia D, Chu LL et al. Mycobacterial interspersed repetitive unit can predict drug resistance of Mycobacterium tuberculosis in China. Front Microbiol 2016; 7:378
    [Google Scholar]
  55. Singh V, Mani I, Chaudhary DK, Somvanshi P. The β-ketoacyl-ACP synthase from Mycobacterium tuberculosis as potential drug targets. Curr Med Chem 2011; 18:1318–1324 [View Article][PubMed]
    [Google Scholar]
  56. Gurumurthy M, Mukherjee T, Dowd CS, Singh R, Niyomrattanakit P et al. Substrate specificity of the deazaflavin-dependent nitroreductase from Mycobacterium tuberculosis responsible for the bioreductive activation of bicyclic nitroimidazoles. FEBS J 2012; 279:113–125 [View Article][PubMed]
    [Google Scholar]
  57. Lee BM, Harold LK, Almeida DV, Afriat-Jurnou L, Aung HL et al. Predicting nitroimidazole antibiotic resistance mutations in Mycobacterium tuberculosis with protein engineering. PLoS Pathog 2020; 16:e1008287
    [Google Scholar]
  58. Hoffmann H, Kohl TA, Hofmann-Thiel S, Merker M, Beckert P et al. Delamanid and bedaquiline resistance in Mycobacterium tuberculosis ancestral Beijing genotype causing extensively drug-resistant tuberculosis in a Tibetan refugee. Am J Respir Crit Care Med 2016; 193:337–340
    [Google Scholar]
  59. Baulard AR, Betts JC, Engohang-Ndong J, Quan S, McAdam RA et al. Activation of the pro-drug ethionamide is regulated in mycobacteria. J Biol Chem 2000; 275:28326–28331
    [Google Scholar]
  60. Donald PR, McIlleron H. Antibuerculosis drugs. Tuberculosis: a Comprehensive Clinincal Reference 2009 pp 608–617
    [Google Scholar]
  61. Willand N, Dirie B, Carette X, Bifani P, Singhal A et al. Synthetic EthR inhibitors boost antituberculous activity of ethionamide. Nat Med 2009; 15:537–544
    [Google Scholar]
  62. Morlock GP, Metchock B, Sikes D, Crawford JT, Cooksey RC. ethA, inhA, and katG loci of ethionamide-resistant clinical Mycobacterium tuberculosis isolates. Antimicrob Agents Chemother 2003; 47:3799–3805
    [Google Scholar]
  63. Vilchèze C, Jacobs WR. Resistance to isoniazid and ethionamide in Mycobacterium tuberculosis: genes, mutations, and causalities. Microbiol Spectr 2014; 2:MGM2-0014-2013 [View Article][PubMed]
    [Google Scholar]
  64. Dookie N, Rambaran S, Padayatchi N, Mahomed S, Naidoo K. Evolution of drug resistance in Mycobacterium tuberculosis: a review on the molecular determinants of resistance and implications for personalized care. J Antimicrob Chemother 2018; 73:1138–1151
    [Google Scholar]
  65. Mortimer TD, Weber AM, Pepperell CS. Signatures of selection at drug resistance loci in Mycobacterium tuberculosis . mSystems 2018; 3:e00108-17 [View Article][PubMed]
    [Google Scholar]
  66. Copp JN, Akiva E, Babbitt PC, Tokuriki N. Revealing unexplored sequence-function space using sequence similarity networks. Biochemistry 2018; 57:4651–4662
    [Google Scholar]
  67. Finken M, Krischner P, Meier A, Wrede A, Bottger EC. Molecular basis of streptomycin resistance in Mycobacterium tuberculosis: alterations of the ribosomal protein S12 gene and point mutations within a functional 16S ribosomal RNA pseudoknot. Mol Microbiol 1993; 9:1239–1246
    [Google Scholar]
  68. Hlaing YM, Tongtawe P, Tapchaisri P, Thanongsaksrikul J, Thawornwan U et al. Mutations in streptomycin resistance genes and their relationship to streptomycin resistance and lineage of Mycobacterium tuberculosis Thai isolates. Tuberc Respir Dis 2017; 80:159–168
    [Google Scholar]
  69. Sun Y-J, Luo J-T, Wong S-Y, Lee ASG. Analysis of rpsL and rrs mutations in Beijing and non-Beijing streptomycin-resistant Mycobacterium tuberculosis isolates from Singapore. Clin Microbiol Infect 2010; 16:287–289 [View Article][PubMed]
    [Google Scholar]
  70. Tudó G, Rey E, Borrell S, Alcaide F, Codina G et al. Characterization of mutations in streptomycin-resistant Mycobacterium tuberculosis clinical isolates in the area of Barcelona. J. Antimicrob 2010; 65:2341–2346
    [Google Scholar]
  71. Ilin AI, Kulmanov ME, Korotetskiy IS, Islamov RA, Akhmetova GK et al. Genomic insight into mechanisms of reversion of antibiotic resistance in multidrug resistant Mycobacterium tuberculosis induced by a nanomolecular iodine-containing complex FS-1. Front Cell Infect Microbiol 2017; 7:151 [View Article][PubMed]
    [Google Scholar]
  72. Ilin AI, Kulmanov ME, Korotetskiy IS, Lankina MV, Akhmetova GK et al. Constraints of drug resistance in Mycobacterium tuberculosis - prospects for pharmacological reversion of susceptibility to antibiotics. Open Conf Proc J 2017; 8:33–43 [View Article]
    [Google Scholar]
  73. Wong SY, Lee JS, Kwak HK, Via LE, Boshoff HIM et al. Mutations in gidB confer low-level streptomycin resistance in Mycobacterium tuberculosis . Antimicrob Agents Chemother 2011; 55:2515–2522 [View Article][PubMed]
    [Google Scholar]
  74. Perdigão J, Macedo R, Machado D, Silva C, Jordão L et al. GidB mutation as a phylogenetic marker for Q1 cluster Mycobacterium tuberculosis isolates and intermediate-level streptomycin resistance determinant in Lisbon, Portugal. Clin Microbiol Infect 2014; 20:O278–O284 [View Article][PubMed]
    [Google Scholar]
  75. Verma JS, Gupta Y, Nair D, Manzoor N, Rautela RS et al. Evaluation of gidB alterations responsible for streptomycin resistance in Mycobacterium tuberculosis . J Antimicrob Chemother 2014; 69:2935–2941 [View Article][PubMed]
    [Google Scholar]
  76. Jagielski T, Ignatowska H, Bakuła Z, Dziewit L, Napiorkowska A et al. Screening for streptomycin resistance-conferring mutations in Mycobacterium tuberculosis clinical isolates from Poland. PLoS One 2014; 9:e100078
    [Google Scholar]
  77. Sun H, Zhang C, Xiang L, Pi R, Guo Z et al. Characterization of mutations in streptomycin-resistant Mycobacterium tuberculosis isolates in Sichuan, China and the association between Beijing-lineage and dual-mutation in gidB. Tuberculosis 2016; 96:102–106
    [Google Scholar]
  78. Mestdagh M, Fonteyne PA, Realini L, Rossau R, Jannes G et al. Relationship between pyrazinamide resistance, loss of pyrazinamidase activity, and mutations in the pncA locus in multidrug-resistant clinical isolates of Mycobacterium tuberculosis . Antimicrobial Agents Chemother 1999; 43:2317–2319
    [Google Scholar]
  79. Juréen P, Werngren J, Toro JC, Hoffner S. Pyrazinamide resistance and pncA gene mutations in Mycobacterium tuberculosis . Antimicrobial Agents Chemother 2008; 52:1852–1854
    [Google Scholar]
  80. Karmakar M, Rodrigues CHM, Horan K, Denholm JT, Ascher DB. Structure guided prediction of pyrazinamide resistance mutations in pncA. Sci Rep 2020; 10:1875
    [Google Scholar]
  81. Karmakar M, Globan M, Fyfe JAM, Stinear TP, Johnson PDR et al. Analysis of a novel pncA mutation for susceptibility to pyrazinamide therapy. Am J Respir Crit Care Med 2018; 198:541–544 [View Article][PubMed]
    [Google Scholar]
  82. Chiu Y-C, Huang S-F, Yu K-W, Lee Y-C, Feng J-Y et al. Characteristics of pncA mutations in multidrug-resistant tuberculosis in Taiwan. BMC Infect Dis 2011; 11:240 [View Article][PubMed]
    [Google Scholar]
  83. Sreevatsan S, Pan X, Zhang Y, Deretic V, Musser JM. Analysis of the oxyR-ahpC region in isoniazid-resistant and -susceptible Mycobacterium tuberculosis complex organisms recovered from diseased humans and animals in diverse localities. Antimicrob Agents Chemother 1997; 41:600–606 [View Article][PubMed]
    [Google Scholar]
  84. Brossier F, Veziris N, Truffot-Pernot C, Jarlier V, Sougakoff W. Molecular investigation of resistance to the antituberculous drug ethionamide in multidrug-resistant clinical isolates of Mycobacterium tuberculosis . Antimicrobial Chemother 2011; 55:355–360
    [Google Scholar]
  85. Lee BM, Harold LK, Almeida DV, Afriat-Jurnou L, Aung HL et al. Predicting nitroimidazole antibiotic resistance mutations in Mycobacterium tuberculosis with protein engineering. PLoS Pathog 2020; 16:e1008287
    [Google Scholar]
  86. Ramirez LMN, Vargas KQ, Diaz G. Whole genome sequencing for the analysis of drug resistant strains of Mycobacterium tuberculosis: a systematic review for bedaquiline and delamanid. Antibiotics 2020; 9:133
    [Google Scholar]
  87. Zhang F, Li S, Wen S, Zhang T, Shang Y et al. Comparison of in vitro susceptibility of mycobacteria against PA-824 to identify key residues of Ddn, the deazoflavin-dependent nitroreductase from Mycobacterium tuberculosis . Infect Drug Resist 2020; 13:815–822
    [Google Scholar]
  88. Kirstein M, Sanz L, Quiñones S, Moscat J, Diaz-Meco MT et al. Cross-talk between different enhancer elements during mitogenic induction of the human stromelysin-1 gene. J Biol Chem 1996; 271:18231–18236
    [Google Scholar]
  89. Rekdal C, Sjottem E, Johansen T. The nuclear factor SPBP contains different functional domains and stimulates the activity of various transcriptional activators. J Biol Chem 2000; 275:40288–40300
    [Google Scholar]
  90. Dunn C, Wiltshire C, MacLaren A, Gillespie DAF. Molecular mechanism and biological functions of c-Jun N-terminal kinase signalling via the c-Jun transcription factor. Cellular Signalling 2002; 14:585–593
    [Google Scholar]
  91. Tan NY, Khachigian LM. Sp1 phosphorylation and its regulation of gene transcription. Mol Cell Biol 2009; 29:2483–2488
    [Google Scholar]
  92. Scott FL, Stec B, Pop C, Dobaczewska MK, Lee JJ et al. The Fas-FADD death domain complex structure unravels signalling by receptor clustering. Nature 2009; 457:1019–1022
    [Google Scholar]
  93. Shen Y, Song Z, Lu X, Ma Z, Lu C et al. Fas signaling-mediated TH9 cell differentiation favors bowel inflammation and antitumor functions. Nat Commun 2019; 10:2924
    [Google Scholar]
  94. Vafiadaki E, Arvanitis DA, Pagakis SN, Papalouka V, Sanoudou D et al. The anti-apoptotic protein HAX-1 interacts with SERCA2 and regulates its protein levels to promote cell survival. Mol Biol Cell 2009; 20:306–318
    [Google Scholar]
  95. Chen HY, Sharma BB, Yu L, Zuberi R, Weng IC et al. Role of galectin-3 in mast cell functions: galectin-3-deficient mast cells exhibit impaired mediator release and defective JNK expression. J Immunol 2006; 177:4991–4997
    [Google Scholar]
  96. Haudek KC, Spronk KJ, Voss PG, Patterson RJ, Wang JL et al. Dynamics of galectin-3 in the nucleus and cytoplasm. Biochim Biophys Acta 2010; 1800:181–189
    [Google Scholar]
  97. Dai SY, Nakagawa R, Itoh A, Murakami H, Kashio Y et al. Galectin-9 induces maturation of human monocyte-derived dendritic cells. J Immunol 2005; 175:2974–2981
    [Google Scholar]
  98. Beinke S, Robinson MJ, Hugunin M, Ley SC. Lipopolysaccharide activation of the TPL-2/MEK/extracellular signal-regulated kinase mitogen-activated protein kinase cascade is regulated by IκB kinase-induced proteolysis of NF-κB1 p105. Mol Cell Biol 2004; 24:9658–9667 [View Article]
    [Google Scholar]
  99. Adachi H, Tsujimoto M. FEEL-1, a novel scavenger receptor with in vitro bacteria-binding and angiogenesis-modulating activities. J Biol Chem 2002; 277:34264–34270
    [Google Scholar]
  100. Abrahams KA, Chung C, Ghidelli-Disse S, Rullas J, Rebollo-López MJ et al. Identification of KasA as the cellular target of an anti-tubercular scaffold. Nat Commun 2016; 7:12581 [View Article]
    [Google Scholar]
http://instance.metastore.ingenta.com/content/journal/mgen/10.1099/mgen.0.000542
Loading
/content/journal/mgen/10.1099/mgen.0.000542
Loading

Data & Media loading...

Supplements

Supplementary material 1

PDF

Supplementary material 2

EXCEL

Supplementary material 3

EXCEL
This is a required field
Please enter a valid email address
Approval was a Success
Invalid data
An Error Occurred
Approval was partially successful, following selected items could not be processed due to error