Wang, Jiyong

Fellow - Laboratory Genetics and Genomics

Wang, Jiyong

After receiving his Ph.D. degree from China Agricultural University in Beijing, China, Dr. Wang joined Columbia University in New York City as a postdoctoral fellow, where he studied the field of epigenetics. By transitioning to work in the clinical laboratories, he was attracted to the diagnosis of genetic disorders by utilizing the cytogenetic and molecular methods. He specialized in developing new approaches and testing and interpreting the data for clinical diagnostics of human diseases by leveraging next-generation sequencing and conventional Sanger sequencing analyses, as well as other molecular methodologies. In 2020, he continued to pursue his career goal in clinical genetic medicine through the Laboratory Genetics and Genomics fellowship at GGC. Currently, he is training in interpreting the diagnostic results of both cytogenetic and molecular tests, as well as developing novel tests for clinical use.

Contact Information

Office: (864)-388-1816


  • B.S., Bioengineering, Dalian University of Technology, Dalian, Liaoning, China, 2006
  • Ph.D., Microbiology, China Agricultural University, Beijing, China, 2011
  • Fellow, Laboratory Genetics and Genomics, Greenwood Genetic Center, 2020-present

Selected Publications

  • Zhurinsky, J., Salas-Pino, S., Iglesias-Romero, A., Torres-Mendez, A., Knapp, B., Flor-Parra, I., Wang, J., Bao, K., Jia, S., Chang, F., Daga, R. (2019) Effects of the Microtubule Nucleator Mto1 on Chromosomal Movement, DNA Repair, and Sister Chromatid Cohesion in Fission Yeast. Mol Biol Cell. 30(21):2695-2708
  • Zhang, Y. #, Shan, C.#, Wang, J.#, Bao K.#, Tong, L.*, and Jia, S.* (2017). Molecular basis for the role of oncogenic histone mutations in modulating H3K36 methylation. Molecular basis for the role of oncogenic histone mutations in modulating H3K36 methylation. Sci Rep. 2017 Mar 3;7:43906. (# co-first author).
  • Wang, J., Cohen, A.L., Letian, A., Tadeo, X., Moresco, J.J., Liu, J., Yates, J.R., Qiao, F., and Jia, S. (2016). The proper connection between shelterin components regulates telomeric heterochromatin assembly. Genes Dev. 30,827-839.
  • Wang, J., and Jia, S. New insights into the regulation of heterochromatin. (2016).Trends in Genetics. 32, 284-294. Shan, C.#, Wang, J.#, Xu K.#, Chen, H., Andrews, S., Moresco, J. J., Yates, J. R., Nagy, P. L., Tong, L.*, and Jia, S.* (2016). Histone H3K9M mutation traps a H3K9 methyltransferase to block heterochromatin spreading. eLife 5:e17903. (# co-first author).
  • Wang, J., Reddy, B.D., and Jia, S. (2015). Rapid epigenetic adaptation to uncontrolled heterochromatin spreading. eLife 4, 1–17.
  • Wang, J., Tadeo, X., Hou, H., Andrews, S., Moresco, J.J., Yates, J.R., Nagy, P.L., and Jia, S. (2014a). Tls1 regulates splicing of shelterin components to control telomeric heterochromatin assembly and telomere length. Nucleic Acids Res. 1–14.
  • Wang, J., Lawry, S.T., Cohen, A.L., and Jia, S. (2014b). Chromosome boundary elements and regulation of heterochromatin spreading. Cell. Mol. Life Sci. 71, 4841-4852.
  • Wang, J., Tadeo, X., Hou, H., Tu, P.G., Thompson, J., Yates, J.R., and Jia, S. (2013). Epe1 recruits BET family bromodomain protein Bdf2 to establish heterochromatin boundaries. Genes Dev. 27, 1886–1902.
  • Tadeo, X., Wang, J., Kallgren, S.P., Liu, J., Reddy, B.D., Qiao, F., and Jia, S. (2013). Elimination of shelterin components bypasses RNAi for pericentric heterochromatin assembly. Genes Dev. 27, 2489–2499.
  • Hou, H., Zhou, Z., Wang, Y., Wang, J., Kallgren, S.P., Kurchuk, T., Miller, E. a, Chang, F., and Jia, S. (2012). Csi1 links centromeres to the nuclear envelope for centromere clustering. J. Cell Biol. 199, 735–744.
  • Wang, J., Hu, Q., Chen, H., Zhou, Z., Li, W., Wang, Y., Li S., and He Q. (2010). Role of Individual Subunits of the Neurospora crassa CSN Complex in Regulation of Deneddylation and Stability of Cullin Proteins. PLoS Genet 6 (12) e1001232.
  • Xu, H., Wang, J., Hu, Q., Quan, Y., Chen, H., Cao, Y., Li, C., Wang, Y., and He, Q. (2010). DCAF26, an adaptor protein of Cul4-based E3, is essential for DNA methylation in Neurospora crassa. PLoS Genet 6 (11) ,e1001132.
  • Zhao, Y., Shen, Y., Yang, S., Wang, J., Hu, Q., Wang, Y., and He, Q. (2010). Ubiquitin ligase components Cullin4 and DDB1 are essential for DNA methylation in Neurospora crassa. J Biol Chem 285, 4355-4365.

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