DOI QR코드

DOI QR Code

Gene expression profiles of skin from cyclin dependent kinases 5-knockdown mice

  • Shanshan Yang (College of Animal Science and Technology, Hebei Normal University of Science & Technology) ;
  • Dingxing Jiao (College of Animal Science and Technology, Hebei Normal University of Science & Technology) ;
  • Tao Song (College of Animal Science and Technology, Hebei Normal University of Science & Technology) ;
  • Ping Rui (College of Animal Science and Technology, Hebei Normal University of Science & Technology) ;
  • Ruiwen Fan (College of Veterinary Medicine, Shanxi Agricultural University) ;
  • Zengjun Ma (College of Animal Science and Technology, Hebei Normal University of Science & Technology)
  • Received : 2023.07.04
  • Accepted : 2023.10.02
  • Published : 2024.04.01

Abstract

Objective: This study aimed to identify genes regulated by cyclin dependent kinases 5 (CDK5) that participate in hair pigmentation in mice. Methods: The mRNA expression profiles of skin samples from CDK5-knockdown mice were constructed using high-throughput RNA sequencing and compared with those of wild-type mice. Results: In total, 8,002 known genes were differentially expressed between CDK5-knockdown and wild-type mice. Of these, 3,658 were upregulated and 4,344 were downregulated in the skin of CDK5-knockdown mice. An additional 318 previously unknown genes were also differentially expressed, with 171 downregulated and 147 upregulated genes in the skin of CDK5-knockdown mice. Of the known genes expressed in mouse skin, 80 were associated with hair color, with 61 showing lower expression and 19 exhibiting higher expression in skin of CDK5-knockdown mice. Importantly, the expression of the tyrosinase-related protein 1 (TYRP1) and the calcium signaling pathway were also found to be regulated by CDK5, suggesting that pigmentation is regulated by CDK5 via the calcium signaling pathway and TYRP1. Conclusion: The transcriptome profiles obtained from the skin of CDK5-knockdown mice compared to wild-type mice provide a valuable resource to help understand the mechanism by which CDK5 regulates melanogenesis in mice and other animals.

Keywords

Acknowledgement

This work was supported by the Scientific Research Fund of the Hebei Normal Unixersity of Science and Technology (Grant number: 2023YB003) and Special Project for Basic Scientific Research of Provincial Universities (Grant number: 2023JK02).

References

  1. Crepaldi P, Nicoloso L. SNPs in coat colour genes in goats. Ital J Anim Sci 2007;6:91-3. https://doi.org/10.4081/ijas.2007.1s.91
  2. Lamoreux ML, Wakamatsu K, Ito S. Interaction of major coat color gene functions in mice as studied by chemical analysis of eumelanin and pheomelanin. Pigment Cell Res 2001;14:23-31. https://doi.org/10.1034/j.1600-0749.2001.140105.x
  3. Bunge R, Thomas DL, Nash TG, Lupton CJ. Performance of hair breeds and prolific wool breeds of sheep in southern Illinois: wool production and fleece quality. J Anim Sci 1996;74:25-30. https://doi.org/10.2527/1996.74125x
  4. Kidson SH, Fabian BC. The effect of temperature on tyrosinase activity in Himalayan mouse skin. J Exp Zool 1981;215:91-7. https://doi.org/10.1002/jez.1402150111
  5. Barsh G, Cotsarelis G. How hair gets its pigment. Cell 2007;130:779-81. https://doi.org/10.1016/j.cell.2007.08.032
  6. Croce AC, Scolari F. Characterization of spontaneous melanization by fluorescence spectroscopy: a basis for analytical application to biological substrates. Biology (Basel) 2023;12:433. https://doi.org/10.3390/biology12030433
  7. Debbache J, Zaidi MR, Davis S, et al. In vivo role of alternative splicing and serine phosphorylation of the microphthalmia-associated transcription factor. Genetics 2012;191:133-44. https://doi.org/10.1534/genetics.111.135996
  8. Anello M, Daverio MS, Rodriguez SS, et al. The ASIP gene in the llama (Lama glama): alternative transcripts, expression and relation with color phenotypes. Gene 2022;809:146018. https://doi.org/10.1016/j.gene.2021.146018
  9. Dhariwala FA, Rajadhyaksha MS. An unusual member of the Cdk family: Cdk5. Cell Mol Neurobiol 2008;28:351-69. https://doi.org/10.1007/s10571-007-9242-1
  10. Shupp A, Casimiro MC, Pestell RG. Biological functions of CDK5 and potential CDK5 targeted clinical treatments. Oncotarget 2017;8:17373-82. https://doi.org/10.18632/oncotarget.14538
  11. Fan R, Dong Y, Cao J, et al. Gene expression profile in white alpaca (Vicugna pacos) skin. Animal 2011;5:1157-61. https://doi.org/10.1017/S1751731111000280
  12. Dong C, Yang S, Fan R, et al. Functional role of cyclin-dependent kinase 5 in the regulation of melanogenesis and epidermal structure. Sci Rep 2017;7:13783. https://doi.org/10.1038/s41598-017-12567-1
  13. Livak KJ, Schmittgen TD. Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) method. Methods 2001;25:402-8. https://doi.org/10.1006/meth.2001.1262
  14. Audic S, Claverie JM. The significance of digital gene expression profiles. Genome Res 1997;7:986-95. https://doi.org/10.1101/gr.7.10.986
  15. Hearing VJ, Tsukamoto K. Enzymatic control of pigmentation in mammals. FASEB J 1991;5:2902-9. https://doi.org/10.1096/fasebj.5.14.1752358
  16. Wiriyasermkul P, Moriyama S, Nagamori S. Membrane transport proteins in melanosomes: regulation of ions for pigmentation. Biochim Biophys Acta Biomembr 2020;1862:183318. https://10.1016/j.bbamem.2020.183318
  17. Ito S, Wakamatsu K, Ozeki H. Chemical analysis of melanins and its application to the study of the regulation of melanogenesis. Pigment Cell Res 2000;13(S8):103-9. https://doi.org/10.1034/j.1600-0749.13.s8.19.x
  18. Passeron T, Valencia JC, Bertolotto C, Hearing VJ. SOX9 is a key player in ultraviolet B-induced melanocyte differentiation and pigmentation. Proc Natl Acad Sci USA 2007;104:13984-9. https://doi.org/10.1073/pnas.0705117104
  19. Hemesath TJ, Steingrimsson E, McGill G, et al. Microphthalmia, a critical factor in melanocyte development, defines a discrete transcription factor family. Genes Dev 1994;8:2770-80. https://doi.org/10.1101/gad.8.22.2770
  20. Medic S, Ziman M. PAX3 expression in normal skin melanocytes and melanocytic lesions (naevi and melanomas). PloS one 2010;5:e9977. https://doi.org/10.1371/journal.pone.0009977
  21. Cheung, M., Briscoe, J. Neural crest development is regulated by the transcription factor Sox9. Development 2003;130:5681-93. https://doi.org/10.1242/dev.00808
  22. Murisier F, Beermann F. Genetics of pigment cells: lessons from the tyrosinase gene family. Histol Histopathol 2006;21:567-78. https://doi.org/10.14670/HH-21.567
  23. Kuzumaki T, Matsuda A, Wakamatsu K, Ito S, Ishikawa K. Eumelanin biosynthesis is regulated by coordinate expression of tyrosinase and tyrosinase-related protein-1 genes. Exp Cell Res 1993;207:33-40. https://doi.org/10.1006/excr.1993.1159
  24. Sarangarajan R, Boissy RE. Tyrp1 and oculocutaneous albinism type 3. Pigment Cell Res 2001;14:437-44. https://doi.org/10.1034/j.1600-0749.2001.140603.x
  25. Schallreuter-Wood KU, Pittelkow MR, Swanson NN. Defective calcium transport in vitiliginous melanocytes. Arch Dermatol Res 1996;288:11-3. https://doi.org/10.1007/BF02505036
  26. Carsberg CJ, Jones KT, Sharpe GR, Friedmann PS. Intracellular calcium modulates the responses of human melanocytes to melanogenic stimuli. J Dermatol Sci 1995;9:157-64. https://doi.org/10.1016/0923-1811(94)00372-l
  27. Maeda K, Tomita Y, ukuda M, Tagami H. Effects of staurosporine, PMA and A23187 on human melanocyte cultures with dibutyryl cyclic AMP. Br J Dermatol 1992;126:118-24. https://doi.org/10.1111/j.1365-2133.1992.tb07807.x
  28. Buffey JA, Hill SE, Bleehen SS, Thody AJ, Neil SM. Evidence for a calcium/calmodulin involvement in density-dependent melanogenesis in murine B16 melanoma cells. Pigment Cell Res 1991;4:112-9. https://doi.org/10.1111/j.1600-0749.1991.tb00427.x