Johnson's first published study examined the effects of intravertebral disc using cell implantation within sand rats. The study focused on a combination of histology,tissue culture,and immunocytochemistry. Her team used this study to determine if these rats were a good model organism for future research to start developing real-world cell therapy interventions.[2]
Currently,Johnson's research focuses on understanding gene regulation,chromatin modification,RNA splicing and how regulating splicing allows cells to respond to their environment.[3] Specifically,her group studied the spliceosome,a macromolecular "machine" made of five subunits that interacts with a pre-messenger RNA to produce an edited version,[4] leading to appropriate translation into proteins. Through her research,Johnson hopes to outline the functions of spliceosomes in RNA splicing in order to discover how mutations may lead to the development of certain illnesses.[5] Utilizing molecular genetic technology,her group provided evidence that spliceosome assembly around a nascent mRNA transcript is regulated by histone modifications in the chromatin of the transcribed region.[6][7] Johnson has also worked on identifying and developing the structure of tri-snRNPs,a small nuclear ribonucleoprotein found within spliceosomes. These snRNPs position mRNA components in the correct position for splicing.[5][8] Her work allowed for the visualization of the specific regions of interest on the spliceosome that play key roles in the RNA splicing process.[5] She presented this research to the RNA Society in 2016.
While her study of RNA splicing is ongoing,Johnson's 2020 study investigates the role of dopamine in regulating spinal reflexes (ANS),with a focus on how the autonomic nervous system influences this process. The study explores how the presence or absence of the ANS alters the responsiveness of spinal reflexes to dopamine.[9]
From 2003 to 2013,Johnson was a member of the University of California San Diego biological sciences faculty where she earned many awards,including the National Science Foundation (NSF) Presidential Early Career Award for Scientists and Engineers (PECASE) and the UCSD Chancellor's Associates Award for Excellence in Undergraduate Teaching.[10] Johnson joined the faculty of the University of California,Los Angeles in 2013 as the professor of molecular,cell,and developmental biology and holder of the Keith and Cecilia Terasaki Presidential Endowed Chair.[1] In 2014,she was named a Howard Hughes Medical Institute Professor,[10] and became the associate dean for inclusive excellence in the division of life sciences in 2015.[1] She was named dean of the UCLA Division of Life Sciences in 2020.[1]
Johnson has also focused on developing programs to create transformative learning experiences for undergraduates[11] including the UCLA-HHMI Pathways to Success Program.[12] The program is a comprehensive strategy to provide students with an authentic research experience early in their academic careers.[11] The program has three key components: (1) A research-based laboratory course which goes by CURL (Collaborative Undergraduate Research Lab),(2) a mentoring network that integrates peer and hierarchical mentoring,and (3) intensive learning communities.[11][1]
Awad, A. M., Venkataramanan, S., Nag, A., Galivanche, A. R., Bradley, M. C., Neves, L. T., Douglass, S., Clarke, C. F., & Johnson, T. L. (2017). Chromatin-remodeling SWI/SNF complex regulates coenzyme Q6 synthesis and a metabolic shift to respiration in yeast. The Journal of biological chemistry, 292(36), 14851–14866.[15]
Awad, Agape M, et al. “Nutrient Sensing and Mitochondrial Coenzyme Q Biosynthesis: Are They Connected by a Phosphatase?” The FASEB Journal, vol. 31, no. S1, 1 Apr. 2017. ResearchGate[16]
Barber, P. H., Hayes, T. B., Johnson, T. L., & Márquez-Magaña, L. (2020). Systemic racism in higher education. Science (American Association for the Advancement of Science), 369(6510), 1440–1441.[17]
Baumgartner, B. L., Bennett, M. R., Ferry, M., Johnson, T. L., Tsimring, L. S., & Hasty, J. (2011). Antagonistic gene transcripts regulate adaptation to new growth environments. Proceedings of the National Academy of Sciences of the United States of America, 108(52), 21087–21092.[18]
Brangwynne, C. P., & Johnson, T. L. (2013). The micro and macro of RNA function. Molecular biology of the cell, 24(6), 679.[19]
Buschemeyer, W. C., 3rd, Klink, J. C., Mavropoulos, J. C., Poulton, S. H., Demark-Wahnefried, W., Hursting, S. D., Cohen, P., Hwang, D., Johnson, T. L., & Freedland, S. J. (2010). Effect of intermittent fasting with or without caloric restriction on prostate cancer growth and survival in SCID mice. The Prostate, 70(10), 1037–1043.[20]
Carpentier, W. R., Charles, J. B., Shelhamer, M., Hackler, A. S., Johnson, T. L., Domingo, C. M. M., Sutton, J. P., Scott, G. B. I., & Wotring, V. E. (2018). Biomedical findings from NASA's Project Mercury: a case series. NPJ microgravity, 4, 6.[21] Fischer, H. H., Moore, S. L., Johnson, T. L., Everhart, R. M., Batal, H., & Davidsoni, A. J. (2017). Appointment reminders by text message in a safety net health care system: a pragmatic investigation. EGEMS (Washington, DC), 5(1), 20.[22]
Cheng, C. S., Johnson, T. L., & Hoffmann, A. (2008). Epigenetic control: slow and global, nimble and local. Genes & development, 22(9), 1110–1114.[23]
Davern, M., Lepkowski, J., Call, K. T., Arnold, N., Johnson, T. L., Goldsteen, K., Todd-Malmlov, A., & Blewett, L. A. (2004). Telephone service interruption weighting adjustments for state health insurance surveys. Inquiry: a journal of medical care organization, provision and financing, 41(3), 280–290.[24]
Davis-Turak, J. C., Allison, K., Shokhirev, M. N., Ponomarenko, P., Tsimring, L. S., Glass, C. K., Johnson, T. L., & Hoffmann, A. (2015). Considering the kinetics of mRNA synthesis in the analysis of the genome and epigenome reveals determinants of co-transcriptional splicing. Nucleic Acids Research, 43(2), 699–707.[25]
Davis-Turak, J., Johnson, T. L., & Hoffmann, A. (2018). Mathematical modeling identifies potential gene structure determinants of co-transcriptional control of alternative pre-mRNA splicing. Nucleic Acids Research, 46(20), 10598–10607.[26]
Davis-Turak, J., Johnson, T. L., & Hoffmann, A. (2019). Mathematical modeling identifies potential gene structure determinants of co-transcriptional control of alternative pre-mRNA splicing. Nucleic Acids Research, 47(3), 1602–1603.[27]
Edwards, S. R., & Johnson, T. L. (2019). Intron RNA sequences help yeast cells to survive starvation. Nature, 565(7741), 578–579.[28]
Gruber, H. E., Johnson, T. L., Leslie, K., Ingram, J. A., Martin, D., Hoelscher, G., Banks, D., Phieffer, L., Coldham, G., & Hanley, E. N., Jr (2002). Autologous intervertebral disc cell implantation: a model using Psammomys obesus, the sand rat. Spine, 27(15), 1626–1633. https://doi.org/10.1097/00007632-200208010-00007[29]
Gunderson, F. Q., & Johnson, T. L. (2009). Acetylation by the transcriptional coactivator Gcn5 plays a novel role in co-transcriptional spliceosome assembly. PLoS genetics, 5(10), e1000682.[30]
Gunderson, F. Q., Merkhofer, E. C., & Johnson, T. L. (2011). Dynamic histone acetylation is critical for cotranscriptional spliceosome assembly and spliceosomal rearrangements. Proceedings of the National Academy of Sciences of the United States of America, 108(5), 2004–2009.[31]
Hossain, M. A., Claggett, J. M., Nguyen, T., & Johnson, T. L. (2009). The cap binding complex influences H2B ubiquitination by facilitating splicing of the SUS1 pre-mRNA. RNA, 15(8), 1515–1527.[32]
Hossain, M. A., Rodriguez, C. M., & Johnson, T. L. (2011). Key features of the two-intron Saccharomyces cerevisiae gene SUS1 contribute to its alternative splicing. Nucleic Acids Research, 39(19), 8612–8627.[33]
Hossain, M. A., Chung, C., Pradhan, S. K., & Johnson, T. L. (2013). The yeast cap binding complex modulates transcription factor recruitment and establishes proper histone H3K36 trimethylation during active transcription. Molecular and cellular biology, 33(4), 785–799.[34]
Hossain, M. A., & Johnson, T. L. (2014). Using yeast genetics to study splicing mechanisms. Methods in molecular biology, 1126, 285–298.[35]
Hossain, M. A., Claggett, J. M., Edwards, S. R., Shi, A., Pennebaker, S. L., Cheng, M. Y., Hasty, J., & Johnson, T. L. (2016). Posttranscriptional Regulation of Gcr1 Expression and Activity Is Crucial for Metabolic Adjustment in Response to Glucose Availability. Molecular cell, 62(3), 346–358.[36]
Johnson, T. L., & Vilardell, J. (2012). Regulated pre-mRNA splicing: the ghostwriter of the eukaryotic genome. Biochimica et biophysica acta, 1819(6), 538–545.[37]
Johnson, T. L., Tulis, D. A., Keeler, B. E., Virag, J. A., Lust, R. M., & Clemens, S. (2013). The dopamine D3 receptor knockout mouse mimics aging-related changes in autonomic function and cardiac fibrosis. PloS one, 8(8), e74116.[38]
Johnson, T. L., Rinehart, D. J., Durfee, J., Brewer, D., Batal, H., Blum, J., Oronce, C. I., Melinkovich, P., & Gabow, P. (2015). For many patients who use large amounts of health care services, the need is intense yet temporary. Health affairs (Project Hope), 34(8), 1312–1319.[39]
Johnson, T. L., Brewer, D., Estacio, R., Vlasimsky, T., Durfee, M. J., Thompson, K. R., Everhart, R. M., Rinehart, D. J., & Batal, H. (2015). Augmenting Predictive Modeling Tools with Clinical Insights for Care Coordination Program Design and Implementation. EGEMS (Washington, DC), 3(1), 1181.[40]
Johnson, T. L., & Ares, M., Jr (2016). SMITten by the Speed of Splicing. Cell, 165(2), 265–267.[41]
Johnson, T. L., & Clemens, S. (2021). Differential dopamine modulation of spinal reflex amplitudes is associated with the presence or absence of the autonomic nervous system. Neuroscience letters, 742, 135514.[42]
Leung, C. S., & Johnson, T. L. (2018). The Exon Junction Complex: A Multitasking Guardian of the Transcriptome. Molecular cell, 72(5), 799–801.[43]
Leung, C. S., Douglass, S. M., Morselli, M., Obusan, M. B., Pavlyukov, M. S., Pellegrini, M., & Johnson, T. L. (2019). H3K36 Methylation and the Chromodomain Protein Eaf3 Are Required for Proper Cotranscriptional Spliceosome Assembly. Cell reports, 27(13), 3760–3769.e4.[44]
Lyu, S., Doroodchi, A., Xing, H., Sheng, Y., DeAndrade, M. P., Yang, Y., Johnson, T. L., Clemens, S., Yokoi, F., Miller, M. A., Xiao, R., & Li, Y. (2020). BTBD9 and dopaminergic dysfunction in the pathogenesis of restless legs syndrome. Brain structure & function, 225(6), 1743–1760.[45]
McKay, S. L., & Johnson, T. L. (2010). A bird's-eye view of post-translational modifications in the spliceosome and their roles in spliceosome dynamics. Molecular bioSystems, 6(11), 2093–2102.[46]
McKay, S. L., & Johnson, T. L. (2011). An investigation of a role for U2 snRNP spliceosomal components in regulating transcription. PloS one, 6(1), e16077.[47]
Merkhofer, E. C., & Johnson, T. L. (2012). U1 snRNA rewrites the "script". Cell, 150(1), 9–11.[48]
Merkhofer, E. C., Hu, P., & Johnson, T. L. (2014). Introduction to cotranscriptional RNA splicing. Methods in molecular biology, 1126, 83–96.[49]
Neves, L. T., Douglass, S., Spreafico, R., Venkataramanan, S., Kress, T. L., & Johnson, T. L. (2017). The histone variant H2A.Z promotes efficient cotranscriptional splicing in S. cerevisiae. Genes & development, 31(7), 702–717.[50]
Venkataramanan, S., Douglass, S., Galivanche, A. R., & Johnson, T. L. (2017). The chromatin remodeling complex Swi/Snf regulates splicing of meiotic transcripts in Saccharomyces cerevisiae. Nucleic Acids Research, 45(13), 7708–7721.[51]
Virag, J. A., Anderson, E. J., Kent, S. D., Blanton, H. D., Johnson, T. L., Moukdar, F., DeAntonio, J. H., Thayne, K., Ding, J. M., & Lust, R. M. (2013). Cardioprotection via preserved mitochondrial structure and function in the mPer2-mutant mouse myocardium. American journal of physiology. Heart and circulatory physiology, 305(4), H477–H483.[52]
↑ Buschemeyer, W. Cooper; Klink, Joseph C.; Mavropoulos, John C.; Poulton, Susan H.; Demark-Wahnefried, Wendy; Hursting, Stephen D.; Cohen, Pinchas; Hwang, David; Johnson, Tracy L.; Freedland, Stephen J. (2010-07-01). "Effect of intermittent fasting with or without caloric restriction on prostate cancer growth and survival in SCID mice". The Prostate. 70 (10): 1037–1043. doi:10.1002/pros.21136. ISSN1097-0045. PMID20166128.
↑ Davern, Michael; Lepkowski, James; Call, Kathleen Thiede; Arnold, Noreen; Johnson, Tracy L.; Goldsteen, Karen; Todd-Malmlov, April; Blewett, Lynn A. (2004). "Telephone service interruption weighting adjustments for state health insurance surveys". Inquiry: A Journal of Medical Care Organization, Provision and Financing. 41 (3): 280–290. doi:10.1177/004695800404100305. ISSN0046-9580. PMID15669746.
↑ Johnson, Tracy L.; Rinehart, Deborah J.; Durfee, Josh; Brewer, Daniel; Batal, Holly; Blum, Joshua; Oronce, Carlos I.; Melinkovich, Paul; Gabow, Patricia (2015). "For many patients who use large amounts of health care services, the need is intense yet temporary". Health Affairs. 34 (8): 1312–1319. doi:10.1377/hlthaff.2014.1186. ISSN2694-233X. PMID26240244.
↑ Johnson, Tracy L.; Clemens, Stefan (2021-01-18). "Differential dopamine modulation of spinal reflex amplitudes is associated with the presence or absence of the autonomic nervous system". Neuroscience Letters. 742 135514. doi:10.1016/j.neulet.2020.135514. ISSN1872-7972. PMID33227368.
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