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Genome-wide identification, organization, and expression profiles of the chicken fibroblast growth factor genes in public databases and Vietnamese indigenous Ri chickens against highly pathogenic avian influenza H5N1 virus infection

  • Anh Duc Truong (Department of Biochemistry and Immunology, National Institute of Veterinary Research) ;
  • Ha Thi Thanh Tran (Department of Biochemistry and Immunology, National Institute of Veterinary Research) ;
  • Nhu Thi Chu (Department of Biochemistry and Immunology, National Institute of Veterinary Research) ;
  • Huyen Thi Nguyen (Department of Biochemistry and Immunology, National Institute of Veterinary Research) ;
  • Thi Hao Vu (Department of Biochemistry and Immunology, National Institute of Veterinary Research) ;
  • Yeojin Hong (Department of Animal Science and Technology, Chung-Ang University) ;
  • Ki-Duk Song (The Animal Molecular Genetics and Breeding Center and Department of Animal Biotechnology, JeonBuk National University) ;
  • Hoang Vu Dang (Department of Biochemistry and Immunology, National Institute of Veterinary Research) ;
  • Yeong Ho Hong (Department of Animal Science and Technology, Chung-Ang University)
  • Received : 2022.07.16
  • Accepted : 2022.09.16
  • Published : 2023.04.01

Abstract

Objective: Fibroblast growth factors (FGFs) play critical roles in embryo development, and immune responses to infectious diseases. In this study, to investigate the roles of FGFs, we performed genome-wide identification, expression, and functional analyses of FGF family members in chickens. Methods: Chicken FGFs genes were identified and analyzed by using bioinformatics approach. Expression profiles and Hierarchical cluster analysis of the FGFs genes in different chicken tissues were obtained from the genome-wide RNA-seq. Results: A total of 20 FGF genes were identified in the chicken genome, which were classified into seven distinct groups (A-F) in the phylogenetic tree. Gene structure analysis revealed that members of the same clade had the same or similar exon-intron structure. Chromosome mapping suggested that FGF genes were widely dispersed across the chicken genome and were located on chromosomes 1, 4-6, 9-10, 13, 15, 28, and Z. In addition, the interactions among FGF proteins and between FGFs and mitogen-activated protein kinase (MAPK) proteins are limited, indicating that the remaining functions of FGF proteins should be further investigated in chickens. Kyoto encyclopedia of genes and genomes pathway analysis showed that FGF gene interacts with MAPK genes and are involved in stimulating signaling pathway and regulating immune responses. Furthermore, this study identified 15 differentially expressed genes (DEG) in 21 different growth stages during early chicken embryo development. RNA-sequencing data identified the DEG of FGFs on 1- and 3-days post infection in two indigenous Ri chicken lines infected with the highly pathogenic avian influenza virus H5N1 (HPAIV). Finally, all the genes examined through quantitative real-time polymerase chain reaction and RNA-Seq analyses showed similar responses to HPAIV infection in indigenous Ri chicken lines (R2 = 0.92-0.95, p<0.01). Conclusion: This study provides significant insights into the potential functions of FGFs in chickens, including the regulation of MAPK signaling pathways and the immune response of chickens to HPAIV infections.

Keywords

Acknowledgement

This research is funded by the National Research Foundation grant (NRF-2021R1A2C2005236) of the Republic of Korea.

References

  1. Olapoju SO, Adejobi OI, Le Thi X. Fibroblast growth factor 21; review on its participation in vascular calcification pathology. Vascul Pharmacol 2020;125-126:106636. https://doi.org/10.1016/j.vph.2019.106636 
  2. Forough R, Weylie B, Patel C, et al. Role of AKT/PKB signaling in fibroblast growth factor-1 (FGF-1)-induced angiogenesis in the chicken chorioallantoic membrane (CAM). J Cell Biochem 2005;94:109-16. https://doi.org/10.1002/jcb.20274 
  3. Choi JW, Kim S, Kim TM, et al. Basic fibroblast growth factor activates MEK/ERK cell signaling pathway and stimulates the proliferation of chicken primordial germ cells. PLoS One 2010;5:e12968. https://doi.org/10.1371/journal.pone.0012968 
  4. Wu YF, Zhang DD, Liu SY, et al. C-Type natriuretic peptide dampens fibroblast growth factor-23 expression through MAPK signaling pathway in human mesangial cells. J Interferon Cytokine Res 2018;38:500-9. https://doi.org/10.1089/jir.2018.0051 
  5. Wang X, Zhu Y, Sun C, et al. Feedback activation of basic fibroblast growth factor signaling via the wnt/beta-catenin pathway in skin fibroblasts. Front Pharmacol 2017;8:32. https://doi.org/10.3389/fphar.2017.00032 
  6. Li S, Guo X, Zhang T, et al. Fibroblast growth factor 21 ameliorates high glucose-induced fibrogenesis in mesangial cells through inhibiting STAT5 signaling pathway. Biomed Pharmacother 2017;93:695-704. https://doi.org/10.1016/j.biopha.2017.06.100 
  7. Yang PH, Zhu JX, Huang YD, et al. Human basic fibroblast growth factor inhibits tau phosphorylation via the PI3K/Akt-GSK3beta signaling pathway in a 6-hydroxydopamine-induced model of Parkinson's disease. Neurodegener Dis 2016;16:357-69. https://doi.org/10.1159/000445871 
  8. Borland CZ, Schutzman JL, Stern MJ. Fibroblast growth factor signaling in Caenorhabditis elegans. Bioessays 2001;23:1120-30. https://doi.org/10.1002/bies.10007 
  9. Duszynski RJ, Topczewski J, LeClair EE. Divergent requirements for fibroblast growth factor signaling in zebrafish maxillary barbel and caudal fin regeneration. Dev Growth Differ 2013;55:282-300. https://doi.org/10.1111/dgd.12035 
  10. Zhan DC, Shen YS, Zhao YR, Meng FJ. Efficacy and safety of basic fibroblast growth factor in the treatment of burns: Protocol for a systematic review and meta-analysis of randomized controlled trials. Medicine (Baltimore) 2019;98:e15102. https://doi.org/10.1097/MD.0000000000015102 
  11. Gallegos TF, Kamei CN, Rohly M, Drummond IA. Fibroblast growth factor signaling mediates progenitor cell aggregation and nephron regeneration in the adult zebrafish kidney. Dev Biol 2019;454:44-51. https://doi.org/10.1016/j.ydbio.2019.06.011 
  12. Schofer C, Frei K, Weipoltshammer K, Wachtler F. The apical ectodermal ridge, fibroblast growth factors (FGF-2 and FGF-4) and insulin-like growth factor I (IGF-I) control the migration of epidermal melanoblasts in chicken wing buds. Anat Embryol (Berl) 2001;203:137-46. https://doi.org/10.1007/s004290000148 
  13. Dono R, Zeller R. Cell-type-specific nuclear translocation of fibroblast growth factor-2 isoforms during chicken kidney and limb morphogenesis. Dev Biol 1994;163:316-30. https://doi.org/10.1006/dbio.1994.1151 
  14. Wang M, Zhang C, Huang C, et al. Regulation of fibroblast growth factor 8 (FGF8) in chicken embryonic stem cells differentiation into spermatogonial stem cells. J Cell Biochem 2018;119:2396-407. https://doi.org/10.1002/jcb.26402 
  15. Munoz-Sanjuan I, Simandl BK, Fallon JF, Nathans J. Expression of chicken fibroblast growth factor homologous factor (FHF)-1 and of differentially spliced isoforms of FHF-2 during development and involvement of FHF-2 in chicken limb development. Development 1999;126:409-21. https://doi.org/10.1242/dev.126.2.409 
  16. Kurose H, Bito T, Adachi T, Shimizu M, Noji S, Ohuchi H. Expression of Fibroblast growth factor 19 (Fgf19) during chicken embryogenesis and eye development, compared with Fgf15 expression in the mouse. Gene Expr Patterns 2004;4:687-93. https://doi.org/10.1016/j.modgep.2004.04.005 
  17. Frohns F, Mager M, Layer PG. Basic fibroblast growth factor increases the precursor pool of photoreceptors, but inhibits their differentiation and apoptosis in chicken retinal reaggregates. Eur J Neurosci 2009;29:1931-42. https://doi.org/10.1111/j.1460-9568.2009.06738.x 
  18. Kent WJ. BLAT--the BLAST-like alignment tool. Genome Res 2002;12:656-64. https://doi.org/10.1101/gr.229202 
  19. Bailey TL, Boden M, Buske FA, et al. MEME SUITE: tools for motif discovery and searching. Nucleic Acids Res 2009;37:W202-8. https://doi.org/10.1093/nar/gkp335 
  20. Tamura K, Stecher G, Peterson D, Filipski A, Kumar S. MEGA6: molecular evolutionary genetics analysis version 6.0. Mol Biol Evol 2013;30:2725-9. https://doi.org/10.1093/molbev/mst197 
  21. Bui VN, Ogawa H, Trinh DQ, et al. Genetic characterization of an H5N1 avian influenza virus from a vaccinated duck flock in Vietnam. Virus Genes 2014;49:278-85. https://doi.org/10.1007/s11262-014-1089-1 
  22. OIE. Chapter 3.3.4: Avian influenza (infection with avian influenza viruses) (NB: Version adopted in May 2015). Pari, France: OIE; 2018. 
  23. Reed LJ, Muench H. A simple method of estimating fifty per cent endpoints. Am J Epidemiol 1938;27:493-97. https://doi.org/10.1093/oxfordjournals.aje.a118408 
  24. Vu TH, Hong Y, Truong AD, et al. Cytokine-cytokine receptor interactions in the highly pathogenic avian influenza H5N1 virus-infected lungs of genetically disparate Ri chicken lines. Anim Biosci 2022;35:367-76. https://doi.org/10.5713/ab.21.0163 
  25. Hwang YS, Seo M, Lee BR, et al. The transcriptome of early chicken embryos reveals signaling pathways governing rapid asymmetric cellularization and lineage segregation. Development 2018;145:dev157453. https://doi.org/10.1242/dev.157453 
  26. Trapnell C, Williams BA, Pertea G, et al. Transcript assembly and quantification by RNA-Seq reveals unannotated transcripts and isoform switching during cell differentiation. Nat Biotechnol 2010;28:511-5. https://doi.org/10.1038/nbt.1621 
  27. Szklarczyk D, Morris JH, Cook H, et al. The STRING database in 2017: quality-controlled protein-protein association networks, made broadly accessible. Nucleic Acids Res 2017;45:D362-8. https://doi.org/10.1093/nar/gkw937 
  28. Livak KJ, Schmittgen TD. Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) method. Methods (San Diego, Calif.) 2001;25:402-8. https://doi.org/10.1006/meth.2001.1262 
  29. Ruiz-Narvaez EA, Haddad SA, Lunetta KL, et al. Gene-based analysis of the fibroblast growth factor receptor signaling pathway in relation to breast cancer in African American women: the AMBER consortium. Breast Cancer Res Treat 2016;155:355-63. https://doi.org/10.1007/s10549-015-3672-0 
  30. Jiang L, Zhang S, Dong C, et al. Genome-wide identification, phylogeny, and expression of fibroblast growth genes in common carp. Gene 2016;578:225-31. https://doi.org/10.1016/j.gene.2015.12.027 
  31. Bagchi M, Ireland M, Katar M, Maisel H. Heat shock proteins of chicken lens. J Cell Biochem 2001;82:409-14. https://doi.org/10.1002/jcb.1168 
  32. Munaim SI, Klagsbrun M, Toole BP. Developmental changes in fibroblast growth factor in the chicken embryo limb bud. Proc Natl Acad Sci USA 1988;85:8091-3. https://doi.org/10.1073/pnas.85.21.8091 
  33. Consigli SA, Joseph-Silverstein J. Immunolocalization of basic fibroblast growth factor during chicken cardiac development. J Cell Physiol 1991;146:379-85. https://doi.org/10.1002/jcp.1041460307 
  34. Mattoo RL. The roles of fibroblast growth factor (FGF)-23, alpha-klotho and furin protease in calcium and phosphate homeostasis: a mini-review. Indian J Clin Biochem 2014;29:8-12. https://doi.org/10.1007/s12291-013-0324-1 
  35. Chen G, Qiu H, Ke S, Hu S, Yu S, Zou S. The fibroblast growth factor receptor 2-mediated extracellular signal-regulated kinase 1/2 signaling pathway plays is important in regulating excision repair cross-complementary gene 1 expression in hepatocellular carcinoma. Biomed Rep 2013;1:604-8. https://doi.org/10.3892/br.2013.96 
  36. Jeong W, Lee J, Bazer FW, Song G, Kim J. Fibroblast growth factor 4-induced migration of porcine trophectoderm cells is mediated via the AKT cell signaling pathway. Mol Cell Endocrinol 2016;419:208-16. https://doi.org/10.1016/j.mce.2015.10.020 
  37. Charoenngam N, Rujirachun P, Holick MF, Ungprasert P. Oral vitamin D3 supplementation increases serum fibroblast growth factor 23 concentration in vitamin D-deficient patients: a systematic review and meta-analysis. Osteoporos Int 2019;30:2183-93. https://doi.org/10.1007/s00198-019-05102-7 
  38. Tsai WC, Wu HY, Peng YS, et al. Effects of lower versus higher phosphate diets on fibroblast growth factor-23 levels in patients with chronic kidney disease: a systematic review and meta-analysis. Nephrol Dial Transplant 2018;33:1977-83. https://doi.org/10.1093/ndt/gfy005