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Molecular & Biomedical Sciences


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Faculty - Keith Hutchison

Phone: (207) 581-2827
Email/web: Send an Email

Professor of Biochemistry & Molecular Biology
1999 Presidential Outstanding Teaching Award
2001 Distinguished Maine Professor Award
2002 Maine Professor of the Year: Carnegie Foundation for the Advancement of Teaching and the Council for the Advancement and Support of Teaching

 

Education

Ph.D. (1974), Bacteriology, University of Wisconsin-Madison
M.S. (1972), Bacteriology, University of Wisconsin-Madison
A.B. (1969), Bacteriology, University of Connecticut

Research interests

Research in my laboratory currently is directed toward understanding control of the earliest moments of development using both the zebrafish and the mouse as model systems. In collaboration with Drs. Barbara Knowles and Joel Graber, at The Jackson Laboratory, we are using a combination of computational and experimental approaches to determine the signals in the 3′ UTR of transcripts that control poly-adenylation as well as other mRNA processing events (see Salisbury, Hutchison and Graber, 2006).

Our major research focus is on determining the genomic sequences responsible for reorganization and activation of the oocyte genome in the developing embryo using the activation of retrotransposons as our model system. Work in the Knowles laboratory had previously shown that over 10% of the transcripts in the mouse oocyte was from the MT class of mouse retrotransposons. There are over 15000 LTRs in the mouse genome and around 3000 intact MT elements. Some of the LTRs are also used to drive expression of normal mouse genes. Using a computational approach we have narrowed to number of possible MT elements being activated during oocyte development to 30 to 150 (see Peaston, Knowles and Hutchison, 2007). Once confirmed these loci can be compared with non-expressed loci for local and long-range cis-acting elements that control expression in the oocyte. We are also scanning the zebrafish genome for retrotransposons that may have a similar activation pattern. The zebrafish genome is less well characterized and the EST databases are not as complete as for the mouse. Nevertheless, the ease of working with embryos in the earliest stages of development make this an attractive system to explore

In times past:
As reflected in the list of publications, previous research in this laboratory was centered on control of gene expression in conifers, particularly in the formation of adventitious roots. Adventitious root formation has an absolute requirement for the addition of auxins. Rooting and non-rooting tissues show similar initial responses to the exogenous auxin. We have identified expansin, a cell wall modeling gene as one of those genes that are induced by exogenous auxin application. Using RT-PCR and northern blots we show that expression reaches its maximum in approximately 24 hours. Expression precedes root meristem organization but using in situ hybridization we have found that expression is located in those regions of the plant were roots are going to form. Expression can also be found in non-rooting epicotyl tissue but in this case expression is uniformally distributed, suggesting that asymmetry of expression may be a pre-requisite for root initials to form.

Publications

Image Description: Keith Hutchison

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Contact Information

Molecular & Biomedical Sciences
5735 Hitchner Hall
Orono, Maine 04469-5735
Phone: (207) 581-2810 | Fax: (207) 581-2801E-mail: Chair: gundersn@maine.edu
The University of Maine
Orono, Maine 04469
207.581.1110
A Member of the University of Maine System