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Melissa Harrison

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Assistant Professor

6204B Biochemical Sciences Building
440 Herny Mall
Madison WI 53706
Postal address click here

Fax: (608) 262-5253

Lab: (608) 262-0484

Office: (608) 262-2382




  • A.B. 1998, Harvard University;
  • Ph.D. 2006, M.I.T. (H.R. Horvitz);
  • Postdoctoral Fellow 2006-2011, University of California, Berkeley (M.R. Botchan and T.W. Cline).

Honors & Awards

  • Howard Hughes Predoctoral Fellow, 1999-2004;
  • American Cancer Society Postdoctoral Fellow, 2007-2010.

Research Interests

Development and differentiation are driven by coordinated changes in gene expression. Early zygotic development is controlled by maternally contributed mRNAs and proteins, and transcriptional activation of the zygotic genome is delayed until hours after fertilization. This delayed transcriptional activation is a nearly universal phenomenon in all metazoans. Immediately following fertilization, the genome undergoes epigenetic reprogramming to allow for the transition from a specified germ cell to the pluripotent cells of the early embryo. The zygotic genome remains transcriptionally quiescent during these initial stages. Only at later cell cycles is widespread zygotic transcription initiated. This zygotic genome activation is tightly coordinated with the degradation of maternally provided mRNAs at the maternal-to-zygotic transition (MZT). Thus during this discrete developmental time point the transcriptional profile of the developing embryo undergoes a monumental reorganization.

While most of the genome is silenced prior to the MZT, a small subset of genes is expressed. These genes control fundamental processes essential for the future development of the organism and allow for progression through the MZT. Despite the fact that these developmental events are common from plants to vertebrates, little is currently known about the factors that regulate zygotic genome activation at the MZT or the mechanisms that allow for the selective transcription of a handful of genes at earlier time points. An understanding of these mechanisms will provide insights into how the genomes of pluripotent cells in general, including embryonic, cancer and induced-pluripotent stem cells, maintain their broad developmental potential while being poised to differentiate.

We use Drosophila melanogaster to study these phenomena using a wide variety of tools including biochemistry, genetics, molecular biology, genomics, and cell biology. Broadly, we are seeking to understand three outstanding questions: (1) why most of the genome is not transcribed until many nuclear divisions after fertilization, (2) how a small number of genes are expressed when the remainder of the genome is not, and (3) what triggers the widespread activation of the zygotic genome at the MZT.

Publications of Note

Gratz, S.J., Cummings, A.M., Nguyen, J.N., Hamm, D.C., Donohue, L.K., Harrison, M.M., Wildonger, J., and O'Connor-Giles, K.M. (2013) Genome Engineering of Drosophila with the CRISPR RNA-Guided Cas9 Nuclease. Genetics. 194:1029-1035.

Harrison, M.M., Li, X.Y. Kaplan, T., Botchan, M.R., and M.B. Eisen. (2011) Zelda Binding in the Early Drosophila melanogaster Embryo Marks Regions Subsequently Activated at the Maternal-to-Zygotic Transistion. PLoS Genet. 7:e1002266

Tabuchi, T.M., Deplancke, B., Osato, N., Zhu, L.J., Barrasa, I.M., Harrison, M.M., Horvitz, H.R., Walhout, A.J. and K.A. Hagstrom. (2011) Chromosome-Biased Binding and Gene Regulation by the Caenorhabditis elegans DRM Complex. PLoS Genet. 7:e1002074.

Cline, T.W., Dorsett, M., Sun, S., Harrison, M.M., Dines, J., Sefton, L., and L. Megna. (2010) Evolution of the Drosophila feminizing switch gene Sex-lethal. Genetics. 186:1321-1336.

Harrison, M.M., Botchan, M.R. and T.W. Cline. (2010) Grainyhead and Zelda compete for binding to the promoters of the earliest-expressed Drosophila genes. Dev Biol. 345: 248-255.

Harrison, M.M., Lu, X. and H.R. Horvitz. (2007) LIN-61, one of two Caenorhabditis elegans malignant-brain-tumor-repeat-containing proteins, acts with DRM and NuRD-like protein complexes in vulval development but not in certain other biological processes. Genetics. 176: 255-271.

Harrison, M.M., Ceol, C.J., Lu, X., and H.R. Horvitiz. (2006) Some C. elegans class B synMuv proteins encode a conserved LIN-35 Rb-containing complex distinct from a NuRD-like complex. Proc Natl Acad Sci USA. 103: 16782-16787.

Ceol, C.J., Stegmeier, F., Harrison, M.M., and H.R. Horvitz. (2006) New classes of genes that act as negative regulators of let-60 Ras signaling in Caenorhabditis elegans. Genetics. 173: 709-726.

Davison, E.M., Harrison, M.M., Walhout, A.J., Vidal, M., and H.R. Horvitiz. (2005) lin-8, which antagonizes Caenorhabditis elegans Ras-mediated vulval induction, encodes a novel nuclear protein that interacts with the LIN-35 Rb protein. Genetics. 171: 1017-1031.

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University of Wisconsin - Department of Biomolecular Chemistry
First published: 08/08/2013 Last updated:03 December 2011 Email Biomolecular Chemistry
Copyright © 2009 The Board of Regents of the University of Wisconsin System


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