ADVS Faculty
Mirella Meyer-Ficca
Animal, Dairy and Veterinary Sciences
Reproductive Biology and Toxicology, Environmental Exposures, Epigenetic Influence
Research Assistant Professor
Educational Background
PhD, Human Genetics, Virology, Eberhard-Karls-University of Tuebingen, 2002 Dissertation
Analyses of Cytotoxicity of the Cardiotropic Coxsackievirus B3 and Development of Strategies for Immortalization of human Cardiomyocytes
MS, Biology (Genetics, Human Genetics, Zoology) and Chemistry (Organic Chemistry), University of Kaiserslautern, 1997 Thesis
Molecular Cytogenetic Analysis of Spermiogenesis in the Rat
Biography
Between 1992 and 1997, I studied Biology and Chemistry at the University of Kaiserslautern (TU Kaiserslautern), Germany, and 1997 received the German Diploma in Biology (equivalent to M.S., with major focus on Genetics, Human Genetics and Organic Chemistry). For graduate training and doctoral research I moved to the Eberhard-Karls-University of Tübingen and the University Hospital of Tübingen, Germany, where I focused on Virology and Human Genetics, and received my Ph.D. degree (Dr.rer.nat., Doctorate in Natural Sciences) in 2002. In 2002, I joined the University of Arizona (Arizona Cancer Center and College of Pharmacy, Department of Pharmacology and Toxicology) as post-doctoral research associate and received further training in Cancer Biology and Toxicology. Between 2005 and 2013, I worked as a Senior Research Investigator at the University of Pennsylvania, conducting research in the fields of Male Reproductive Biology and Toxicology. In 2013, I joined Utah State University as Research Assistant Professor in the Department of Animal, Dairy and Veterinary Sciences and the School of Veterinary Medicine, where I teaches Veterinary Toxicology.Teaching Interests
- Veterinary Toxicology
- Reproductive Toxicology
Research Interests
My main research interest is to understand how environmental factors (e.g. exposure to toxicants, dietary conditions, oxidative stressors, etc.) can change the germ-line epigenome, and thus indirectly gene regulation in offspring, and influence their health and disease.
The epigenome comprises additional levels of structural and biochemical information superimposed to the primary DNA sequence information, such as nuclear architecture and genome organization, DNA methylation, posttranslational modification the chromatin associated proteins, e.g. histones, and small RNAs. Epigenetic control appears to be for the development of complex and often late-onset diseases, such as cancer, diabetes and autism.
My lab is particularly interested in exposures that occur during the prenatal phase of germ cell development. In other words, we focus on this central question: How does exposure of a pregnant mother to adverse environmental factors influence the germ-line epigenome of the developing offspring?
A thorough understanding of the relevant mechanisms will help us to develop adequate lifestyle choices and pharmacological interventions that can improve human and animal health, which is our long-term goal.
Contact Information
Office Hours: Call or Email for Appointment
Go toOffice Location: Center for Biotechnology 213
DialPhone: 435-797-1685
SendEmail: Mirella.Meyer@usu.edu
Awards
Invited Speaker, 2017
Testis Workshop 2017 / American Society of Andrology2017 ADVS Department Undergraduate Research Mentor of the Year , 2017
ADVS DepartmentSusan Heyner Award for Excellence in Research, 2011
Center for Research on Reproduction and Women’s Health, University of Pennsylvania, Philadelphia, PennsylvaniaTravel Award, 2011
American Society for AndrologySpecial Recognition Award in Basic Science, 2004
American Association for Cancer ResearchTravel Award, 2004
The Fujihara Foundation of SciencePublications - Books & Book Chapters
- Meyer, R., Meyer-Ficca, M., Jacobson, E.L, Jacobson, M.K, (2004). Enzymes in poly(ADP-ribose) metabolism: Poly(ADP-ribosyl)ation. Landes Bioscience
Book Chapters
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Publications - Fact Sheets
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Publications - Curriculum
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Publications - Journal Articles
- Meyer-Ficca, M., Kirkland, J., (2016). NUTRITION INFORMATION BRIEFS - Niacin. Advances in Nutrition, 556-557. doi: doi:10.3945/an.115.011239.
- Douglas, H.F, Southwood, L.L, Meyer-Ficca, M., Hart, S.K, Meyer, R., (2015). Journal of Veterinary Emergency and Critical Care. , 25:4, 528-37. doi: doi: 10.1111/vec.12316
- Bryant, J.M, Donahue, G., Wang, X., Meyer-Ficca, M., Luense, L.J, Weller, A.H, Bartolomei, M.S, Blobel, G.A, Meyer, R., Garcia, B.A, Berger, S.L, (2015). Characterization of BRD4 during mammalian postmeiotic sperm development.. Molecular and cellular biology, 35:8, 1433-48.
- Meyer-Ficca, M., Ihara, M., Bader, J.J, Leu, N.A, Beneke, S., Meyer, R., (2015). Spermatid head elongation with normal nuclear shaping requires ADP-ribosyltransferase PARP11 (ARTD11) in mice.. Biology of reproduction, 92:3, 80.
- Ihara, M., Meyer-Ficca, M., Leu, N.A, Rao, S., Li, F., Gregory, B.D, Zalenskaya, I.A, Schultz, R.M, Meyer, R., (2014). Paternal poly(ADP-ribose) metabolism modulates retention of inheritable sperm histones and early embryonic gene expression. PLOS Genetics, doi: 10.1371/journal.pgen.1004317
- Bryant, J.M, Meyer-Ficca, M., Dang, V.M, Berger, S.L, Meyer, R., (2013). Separation of spermatogenic cell types using STA-PUT velocity sedimentation. J Vis Exp80
- Meyer-Ficca, M., Lonchar, J.D, Ihara, M., Bader, J.J, Meyer, R., (2013). Alteration of poly(ADP-ribose) metabolism affects murine sperm nuclear architecture by impairing pericentric heterochromatin condensation. Chromosoma, 122:4, 319–335.
- Meyer-Ficca, M., Meyer, R., (2011). Genetic approaches to targeting multiple PARP genes in a mammalian genome. Methods Mol. Biol., 780, 349–376.
- Meyer-Ficca, M., Lonchar, J.D, Ihara, M., Meistrich, M.L, Austin, C.A, Meyer, R., (2011). Poly(ADP-ribose) polymerases PARP1 and PARP2 modulate topoisomerase II beta (TOP2B) function during chromatin condensation in mouse spermiogenesis. Biol. Reprod., 84:5, 900–909.
- Meyer-Ficca, M., Ihara, M., Lonchar, J.D, Meistrich, M.L, Austin, C.A, Min, W., Wang, Z.Q, Meyer, R., (2011). Poly(ADP-ribose) metabolism is essential for proper nucleoprotein exchange during mouse spermiogenesis. Biol. Reprod., 84:2, 218–228.
- Whatcott, C.J, Meyer-Ficca, M., Meyer, R., Jacobson, M.K, (2009). A specific isoform of poly(ADP-ribose) glycohydrolase is targeted to the mitochondrial matrix by a N-terminal mitochondrial targeting sequence. Exp. Cell Res., 315:20, 3477–3485.
- Meyer-Ficca, M., Lonchar, J., Credidio, C., Ihara, M., Li, Y., Wang, Z.Q, Meyer, R., (2009). Disruption of poly(ADP-ribose) homeostasis affects spermiogenesis and sperm chromatin integrity in mice. Biol. Reprod., 81:1, 46–55.
- Meyer, R., Meyer-Ficca, M., Whatcott, C.J, Jacobson, E.L, Jacobson, M.K, (2007). Two small enzyme isoforms mediate mammalian mitochondrial poly(ADP-ribose) glycohydrolase (PARG) activity. Exp. Cell Res., 313:13, 2920–2936.
- Gao, H., Coyle, D.L, Meyer-Ficca, M., Meyer, R., Jacobson, E.L, Wang, Z.Q, Jacobson, M.K, (2007). Altered poly(ADP-ribose) metabolism impairs cellular responses to genotoxic stress in a hypomorphic mutant of poly(ADP-ribose) glycohydrolase. Exp. Cell Res., 313:5, 984–996.
- Meyer-Ficca, M., Meyer, R., Jacobson, E.L, Jacobson, M.K, (2005). Poly(ADP-ribose) polymerases: managing genome stability. Int. J. Biochem. Cell Biol., 37:5, 920–926.
- Meyer-Ficca, M., Scherthan, H., Burkle, A., Meyer, R., (2005). Poly(ADP-ribosyl)ation during chromatin remodeling steps in rat spermiogenesis. Chromosoma, 114:1, 67–74.
- Meyer-Ficca, M., Meyer, R., Kaiser, H., Brack, A.R, Kandolf, R., Kupper, J.H, (2004). Comparative analysis of inducible expression systems in transient transfection studies. Anal. Biochem., 334:1, 9–19.
- Cortes, U., Tong, W.M, Coyle, D.L, Meyer-Ficca, M., Meyer, R., Petrilli, V., Herceg, Z., Jacobson, E.L, Jacobson, M.K, Wang, Z.Q, (2004). Depletion of the 110-kilodalton isoform of poly(ADP-ribose) glycohydrolase increases sensitivity to genotoxic and endotoxic stress in mice. Mol. Cell. Biol., 24:16, 7163–7178.
- Meyer, R., Meyer-Ficca, M., Kaiser, H., Selinka, H.C, Kandolf, R., Kupper, J.H, (2004). Plasmid-based generation of recombinant coxsackievirus B3 particles carrying capsid gene replacement replicons. Virus Res., 104:1, 17–26.
- Meyer-Ficca, M., Meyer, R., Coyle, D.L, Jacobson, E.L, Jacobson, M.K, (2004). Human poly(ADP-ribose) glycohydrolase is expressed in alternative splice variants yielding isoforms that localize to different cell compartments. Exp. Cell Res., 297:2, 521–532.
- Meyer, R., Meyer-Ficca, M., Jacobson, E.L, Jacobson, M.K, (2003). Human poly(ADP-ribose) glycohydrolase (PARG) gene and the common promoter sequence it shares with inner mitochondrial membrane translocase 23 (TIM23). Gene, 314, 181–190.
- Hans, M.A, Muller, M., Meyer-Ficca, M., Burkle, A., Kupper, J.H, (1999). Overexpression of dominant negative PARP interferes with tumor formation of HeLa cells in nude mice: evidence for increased tumor cell apoptosis in vivo.. Oncogene, 18:50, 7010-5.
- Meyer-Ficca, M., Muller-Navia, J., Scherthan, H., (1998). Clustering of pericentromeres initiates in step 9 of spermiogenesis of the rat (Rattus norvegicus) and contributes to a well defined genome architecture in the sperm nucleus. Journal of Cell Science, 111:10, 1363-70.
- Meyer, R., Meyer-Ficca, M., Kupper, J., (2016). Adenoviral vectors for modulation 1 of poly(ADP-ribose) polymerase-1 2 (PARP1) – dependent DNA repair 3 as a predictive tool for chemotherapy. Journal of Cellular Biotechnology / IOS Press, 2:1, 57-68. doi: DOI 10.3233/JCB-15026
Academic Journal
Professional Journal
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Publications - Literary Journal
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Publications - MultiMedia
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Publications - Technical Reports
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Publications - Translations & Transcripts
Publications - Other
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