James Dahlberg

Position title: Professor Emeritus

Email: dahlberg@wisc.edu

Phone: (608) 262-1459

4260B Biochemical Sciences Building
440 Henry Mall, Madison, WI 53706

james Dahlberg

• BA 1962, Haverford College
• PhD 1966, University of Chicago
• Postdoctoral 1966-68, MRC Laboratory of Molecular Biology, Cambridge (F. Sanger), 1968-69, Universite de Geneve (R. Epstein).

Honors & Awards

• Eli Lilly Award for Biol. Chem., 1974
• H.I. Romnes Faculty Research Fellowship, 1976
• Haverford College Philips Visitor, 1977, 1998
• Macy Scholar Award, 1979-80
• Fellow, American Association for the Advancement of Science, 1982
• Frederick Sanger Professorship, 1991
• American Academy of Arts and Sciences, 1993
• National Academy of Sciences, 1996
• U. Chicago Alumni Achievement Award, 1992
• American Academy of Microbiologists, 1997
• President, RNA Society, 1997
• U.W. Hilldale Professor, 1997
• Buzzati-Traverso Award for Molecular Biology, Italian Nat. Res. Council, 1998
• NIH Merit Award, 1998
• European Molecular Biology Organization, Foreign Associate, 1998
• Hilldale Award, 2002;
• Distinguished Service Award, University of Chicago, 2003
• Emeritus Professor of Biomolecular Chemistry, 2005
• Science Advisor to the Governor of Wisconsin, Hon. James E. Doyle, 2007-2010
• Board of Trustees, Morgridge Institute for Research, 2009-
• Interim Executive Director, Morgridge Institute for Research, Madison, 2012-13
• Wisconsin Medical Alumni Association Basic Sciences Emeritus Faculty Award, 2015

Research Interests

Research in my laboratory focuses on RNA biology. We have used several model systems, including bacteria, mammalian tissue culture cells and frogs to learn about the synthesis, transport and function of a variety of RNA molecules.

Our current focus, in collaberation with Elsebet Lund, is on the mechanism and control of microRNA processing, and the function of miRNAs during early development in Xenopus laevis oocytes and early embryos. MiRNAs are short (~22 nucleotides) molecules found in metazoans, which control the stability and function of messenger RNAs. We have shown that in early frog embryos miR-427 promotes the deadenylation and destabilization of certain maternally inherited mRNAs, preparing the embryo for a subsequent stage of development. This experimentally manipulatible system has allowed us to ask detailed questions about the assembly and function of RNPs that contain miRNA.

We recently showed that frog oocytes and early embryos are deficient in Ago proteins, resulting in non-specific inhibition of miRNA maturation by siRNAs. Also, the lack of Ago2 activity explains why these embryos cannot carry out RNAi. However, we have found that we can use this powerful targeted gene knock-out method by supplementing the system with exogenous human Ago2 protein; this discovery now allows us to investigate the roles of specific proteins early in development.