
Evangelia Koutelou, PhD
Department of Epigenetics and Molecular Carcinogenesis, Division of Discovery Science
Present Title & Affiliation
Primary Appointment
Assistant Professor, Department of Epigenetics and Molecular Carcinogenesis, Division of Discovery Science, The University of Texas MD Anderson Cancer Center, Houston, TX
Research Interests
I have a strong interest in understanding the molecular pathways that underlie developmental processes, with a special focus on the epigenetic regulation of intercellular communication. During my graduate training with Drs. Joan and Ron Conaway at the Stowers Institute, I defined the functions of Neurl1, a mouse ortholog of Drosophila Neur, as an E3 ubiquitin ligase that monoubiquitinates Jagged1, but not other mammalian Notch ligands. My findings provided new insights into the functions of Neurl1 at the plasma membrane in regulating the signaling activity of Jagged1.
As a postdoctoral fellow and now an Assistant Professor in Sharon Dent’s lab at the M.D. Anderson Cancer Center, I have focused on defining the functions of USP22, a component of the SAGA complex linked to human disease and cancer, combining mouse genetics with genome-wide profiling of chromatin states and gene expression. USP22 is a deubiquitinase that targets histone H2B (H2Bub1) as well as non-histone substrates. To define the functions of this enzyme in vivo, I have created both null mutations in USP22 and mutations in the catalytic site in mice. My studies have revealed an unexpected function for USP22 in the development of placenta vasculature. As the development of the placenta shares many of the same processes involved in cancer formation or progression, my findings will provide new insights as to how overexpression of USP22 contributes to aggressive, therapy-resistant cancers.
Education & Training
Degree-Granting Education
2006 | University of Crete - Stowers Institute for Medical Research, Iraklio - Kansas City, Missouri, US, Molecular Biology and Biomedicine, Ph.D |
2001 | University of Crete, Iraklio, GR, Molecular Biology and Biomedicine, M.S |
1999 | University of Crete, Iraklio, GR, Biology, BS |
Postgraduate Training
2013-2013 | Cold Spring Harbor Course, Mouse Development, Stem Cells and Cancer, Cold Spring Harbor Laboratory, Cold Spring Harbor, New York |
2008-2013 | Research Fellowship, Epigenetics, MD Anderson Cancer Center, Houston, Texas |
2007-2008 | Research Fellowship, Stowers Institute for Medical Research, Kansas City, Missouri |
Experience & Service
Academic Appointments
Instructor, Department of Epigenetics and Molecular Carcinogenesis, The University of Texas MD Anderson Cancer Center, Smithville, Texas, TX, 2013 - 2021
Institutional Committee Activities
Chair, Genetics and Epigenetics Communications Committee, 2023 - Present
Member, Genetics and Epigenetics Communications Committee, 2022 - 2023
Honors & Awards
Extra-mural Predoctoral Fellowship, Propondis |
Selected Publications
Peer-Reviewed Articles
- Kuang X, Salinger A, Benavides F, Muller WJ, Dent SYR, Koutelou E. USP22 overexpression fails to augment tumor formation in MMTV-ERBB2 mice but loss of function impacts MMTV promoter activity. PLoS One 19(1):e0290837, 2024. e-Pub 2024. PMID: 38236941.
- Kuang X, McAndrew MJ, Mustachio LM, Chen YC, Atanassov BS, Lin K, Lu Y, Shen J, Salinger A, Macatee T, Dent SYR, Koutelou E. Usp22 Overexpression Leads to Aberrant Signal Transduction of Cancer-Related Pathways but Is Not Sufficient to Drive Tumor Formation in Mice. Cancers (Basel) 13(17), 2021. e-Pub 2021. PMID: 34503086.
- Farria AT, Plummer JB, Salinger AP, Shen J, Lin K, Lu Y, McBride KM, Koutelou E, Dent SYR. Transcriptional Activation of MYC-Induced Genes by GCN5 Promotes B-cell Lymphomagenesis. Cancer Res 80(24):5543-5553, 2020. e-Pub 2020. PMID: 33168647.
- Koutelou E, Wang L, Schibler AC, Chao HP, Kuang X, Lin K, Lu Y, Shen J, Jeter CR, Salinger A, Wilson M, Chen YC, Atanassov BS, Tang DG, Dent SYR. USP22 controls multiple signaling pathways that are essential for vasculature formation in the mouse placenta. Development 146(4), 2019. e-Pub 2019. PMID: 30718289.
- Wang L, Koutelou E, Hirsch C, McCarthy R, Schibler A, Lin K, Lu Y, Jeter C, Shen J, Barton MC, Dent SYR. GCN5 Regulates FGF Signaling and Activates Selective MYC Target Genes during Early Embryoid Body Differentiation. Stem Cell Reports 10(1):287-299, 2018. e-Pub 2017. PMID: 29249668.
- Atanassov BS, Mohan RD, Lan X, Kuang X, Lu Y, Lin K, McIvor E, Li W, Zhang Y, Florens L, Byrum SD, Mackintosh SG, Calhoun-Davis T, Koutelou E, Wang L, Tang DG, Tackett AJ, Washburn MP, Workman JL, Dent SY. ATXN7L3 and ENY2 coordinate activity of multiple H2B deubiquitinases important for cellular proliferation and tumor growth. Mol Cell 62(4):558-71, 2016. e-Pub 2016. PMID: 27132940.
- Schibler A, Koutelou E, Tomida J, Wilson-Pham M, Wang L, Lu Y, Cabrera AP, Chosed RJ, Li W, Li B, Shi X, Wood RD, Dent SY. Histone H3K4 methylation regulates deactivation of the Spindle Assembly Checkpoint through direct binding of Mad2. Genes Dev 30(10):1187-97, 2016. e-Pub 2016. PMID: 27198228.
- Lan X, Koutelou E, Schibler AC, Chen YC, Grant PA, Dent SY. The pathogenic ATXN7-92Q indirectly impairs SAGA deubiquitinating activity. Mol Cell Biol 35(10):1777-87, 2015. e-Pub 2015. PMID: 25755283.
- Wilson MA, Koutelou E, Hirsch C, Akdemir K, Schibler A, Barton MC, Dent SY. Ubp8 and SAGA regulate Snf1 AMP kinase activity. Mol Cell Biol 31(15):3126-35, 2011. e-Pub 2011. PMID: 21628526.
- Koutelou E, Hirsch CL, Dent SY. Multiple faces of the SAGA complex. Curr Opin Cell Biol 22(3):374-82, 2010. e-Pub 2010. PMID: 20363118.
- Koutelou E, Sato S, Tomomori-Sato C, Florens L, Swanson SK, Washburn MP, Kokkinaki M, Conaway RC, Conaway JW, Moschonas NK. Neuralized-like 1 (Neurl1) targeted to the plasma membrane by N-myristoylation regulates the Notch ligand Jagged1. J Biol Chem 283(7):3846-53, 2008. e-Pub 2007. PMID: 18077452.
- Pavlopoulos E, Kokkinaki M, Koutelou E, Mitsiadis TA, Prinos P, Delidakis C, Kilpatrick MW, Tsipouras P, Moschonas NK. Cloning, chromosomal organization and expression analysis of Neurl, the mouse homolog of Drosophila melanogaster neuralized gene. Biochim Biophys Acta 1574(3):375-82, 2002. PMID: 11997106.
Invited Articles
- Koutelou E, Dent SYR. Navigating EMT with COMPASS and PRC2. Nat Cell Biol 24(4):412-414, 2022. PMID: 35411082.
- Chen YC, Koutelou E, Dent SYR. Now open: Evolving insights to the roles of lysine acetylation in chromatin organization and function. Mol Cell 82(4):716-727, 2022. e-Pub 2022. PMID: 35016034.
- Koutelou E, Farria AT, Dent SYR. Complex functions of Gcn5 and Pcaf in development and disease. Biochim Biophys Acta Gene Regul Mech 1864(2):194609, 2021. e-Pub 2020. PMID: 32730897.
Other Articles
- Butler JS, Koutelou E, Schibler AC, Dent SY Histone-modifying enzymes: regulators of developmental decisions and drivers of human disease. Epigenomics 4(2):163-77, 2012. PMID: 22449188.
- Atanassov BS, Koutelou E, Dent SY The role of deubiquitinating enzymes in chromatin regulation. FEBS Lett 585(13):2016-23, 2011. PMID: 20974139.
Selected Presentations & Talks
Local Presentations
- 2023. Usp22 loss of function leads to Purkinje cells degeneration and glial deregulation in the cerebellum of adult mice. Conference. Center for Cancer Epigenetics Retreat. Round Top, TX, US.
- 2018. Usp22 controls cancer related signaling pathways that are essential for placenta vasculature formation. Conference. UTMDACC. Round Top, TX, US.
- 2016. Placental vascular failure upon Usp22 loss reveals connections to signaling cascades important in cancer. Conference. UTMDACC. Round Top, TX, US.
- 2015. USP22, a SAGA component with ubiquitin protease activity, is required for proper placentation and affects cellular motility and vasculature. Conference. G&D EMC Fall Joint Retreat, UTMDACC. Montgomery, TX, US.
- 2015. USP22, a SAGA component with ubiquitin protease activity, is required for proper placentation and affects cellular motility and vasculature. Conference. UTMDACC. Houston, TX, US.
- 2015. USP22, a SAGA component with ubiquitin protease activity, is required for labyrinth formation in the developing placenta. Conference. Cancer Center for Epigenetics Retreat, UTMDACC. Roundtop, TX, US.
- 2015. USP22, a SAGA component with ubiquitin protease activity, is required for labyrinth formation in the developing placenta. Conference. G&D EMC Spring Joint Retreat, UTMDACC. Navasota, TX, US.
- 2014. Defining USP22 functions in mouse embryogenesis. Conference. G&D EMC Joint Retreat, UTMDACC. New Braunfels, TX, US.
- 2013. USP22, a SAGA component with ubiquitin protease activity, is required at early mouse embryonic stages for proper placentation and neurogenesis. Conference. Lost Pines Conference. Smithville, TX, US.
- 2013. USP22, a SAGA component with ubiquitin protease activity, is required for embryonic mouse development. Conference. Cancer Center for Epigenetics Retreat. Roundtop, TX, US.
- 2012. USP22, a SAGA component with ubiquitin protease activity, is required for embryonic mouse development. Conference. Lost Pines Conference. Smithville, TX, US.
- 2012. USP22, a SAGA component with ubiquitin protease activity, is required for embryonic mouse development. Conference. Cancer Center for Epigenetics Retreat. Roundtop, TX, US.
- 2010. USP22, a SAGA component with ubiquitin protease activity, is required for embryonic mouse development. Conference. Cancer Center for Epigenetics Retreat. Houston, TX, US.
Regional Presentations
- 2019. Placental failure upon Usp22 loss reveals connections to signaling cascades important in cancer. Conference. Livestrong Cancer Institute. Austin, TX, US.
National Presentations
- 2023. USP22 Regulates Signaling Cascades in Development and Disease. Invited. United Scientific Group. Houston, TX, US.
- 2021. Genetic studies of Usp22 functions in Development and Disease. Poster. Genetics, Development and Evolutionary Biology. Kansas City, Missouri, US.
- 2021. Oncogenic Functions of SAGA complex. Conference. ASBMB. Virtual, US.
- 2021. USP22 controls multiple signaling pathways in development and disease. Conference. AACR. Virtual, US.
- 2020. SAGA functions in development and disease. Conference. CSHL. Virtual, US.
- 2019. Usp22 controls cancer related signaling pathways that are essential for placenta vasculature formation. Conference. Southwest Society for Dev Biology. Aurora, CO, US.
- 2018. Usp22 controls cancer related signaling pathways that are essential for vasculature formation in the placenta. Conference. University of Miami. Miami, FL, US.
- 2018. Usp22 controls cancer related signaling pathways that are essential for vasculature formation. Conference. Cold Spring Harbor Laboratory. Cold Spring Harbor, NY, US.
- 2016. Placental vascular failure upon Usp22 loss reveals connections to signaling cascades important in cancer. Conference. Genetics Society of America. Orlando, FL, US.
- 2016. USP22, a SAGA component with ubiquitin protease activity, is required for labyrinth formation in the developing placenta. Invited. Abcam. Austin, TX, US.
- 2012. Targeted modifications of mouse USP22 gene, a SAGA component that is required for embryonic development, with zinc-finger nucleases technology. Invited. SIGMA-Aldrich. St. Louis, MO, US.
- 2012. USP22, a SAGA component with ubiquitin protease activity, is required for embryonic mouse development. Conference. Cold Spring Harbor Laboratory. Cold Spring Harbor, NY, US.
- 2010. USP22, a SAGA component with ubiquitin protease activity, is required for embryonic mouse development. Conference. FASEB SRC. Snowmass, CO, US.
- 2004. Mouse Neuralized Acts as an E3 Ubiquitin Ligase. Conference. ASBMB. Boston, MA, US.
International Presentations
- 2024. Usp22 regulates signaling cascades in development and disease. Invited. Valencia, ES.
- 2023. Usp22 loss of function leads to Purkinje cells degeneration and glial deregulation in the cerebellum of adult mice. Conference. Keystone Symposia. Victoria, CA.
- 2019. Usp22 controls cancer related signaling pathways that are essential for placenta vasculature formation. Conference. Gordon Research Conference. Hong-Kong, CN.
- 2014. The pathogenic ATXN7-92Q indirectly impairs SAGA deubiquitinating activity. Conference. EMBL. Heidelberg, DE.
- 2007. Neuralized-like1 targeted to the plasma membrane by N-myristoylation regulates the Notch ligand Jagged1. Conference. The Notch Meeting. Athens, GR.
- 2003. Functional analysis of the mammalian Neuralized gene. Conference. International Summer School sponsored by FEBS. Spetsai, GR.
Grant & Contract Support
Title: | The function and regulation of alternative polyadenylation in urothelial cell differentiation |
Funding Source: | NIH |
Role: | Research Assistant Professor |
Title: | Genetic and Molecular Definition of Histone Modifying Enzyme Functions |
Funding Source: | NIH/NIGMS |
Role: | Co-I |
Title: | Defining USP22 Functions During Mammalian Development |
Funding Source: | NIH/NICHD |
Role: | Co-I |
Title: | Defining USP22 Functions During Mammalian Development |
Funding Source: | NIH/NIGMS |
Role: | Co-I |
Title: | Defining the role of Usp22, a binding partner of Atxn7 in the pathogenesis of spinocerebellar ataxia 7 |
Funding Source: | National Ataxia Foundation |
Role: | PI |
Patient Reviews
CV information above last modified February 11, 2025