- B.S., University of Wyoming, 1999
- Ph.D., University of Utah, 2006
- Postdoc, UC Santa Cruz, 2007-2012
207-288-9880 ext 477
Germ cells are the progenitors of reproductive cells, and the only cells in sexually reproducing animals that have the potential to give rise to all of the cell types of each subsequent generation. In our lab, we want to understand how these totipotent and immortal properties are conferred. Part of the answer comes from special aggregates called “germ granules” that are found just outside the nucleus of germ cells. Recent research has shown that germ granules play a critical role in maintaining the totipotent and immortal properties of the germline. Take away an organism’s germ granules and it will become sterile. In some organisms, introducing germ granules in cells outside of the germline will restore cellular immortality and totipotency, and will reprogram them into germline stem cells.
Germ granules are conserved in their appearance, subcellular localization, and composition from worms to humans. Because of this, we are able to quickly ascertain the mechanisms by which germ granules function by studying them in a small roundworm called C. elegans. This well-established model organism is responsible for much of what we know about developmental genetics in humans. Using fluorescence microscopy, germ granules (called P granules in C. elegans) can be observed in the germ line of transparent worms at all stages of development. The genetic power of C. elegans combined with its short 3-day generation time and transparency offers an opportunity to study the function of germ granules that isn’t feasible in more complex model organisms.
A focus of our research is to understand the biophysical properties of germ granules, how they are assembled, and the components that affect their subcellular distribution. We have shown that germ granules are held together by weak hydrophobic interactions, and that they extend the size exclusion barrier of the nuclear pore complex out into the cytoplasm of germ cells. Here germ granules create a specialized microenvironment that facilitates post-transcriptional processing events that are exclusive to the germline. We are continuing to investigate the specifics of those processing events to understand how they are used to maintain the totipotent and immortal properties of germ cells, and how these mechanisms can be applied to unlocking stem cell-like properties in other cell types.
MDI Biological Laboratory President Kevin Strange Awarded $12 Million NIH Grant
Press Release · June 28, 2018
An Interview with Susan Strome
Development · March 15, 2018
What Lava Lamps and Vinaigrette Can Teach Us About Cell Biology
Nature · March 14, 2018
MDI Biological Laboratory Recognizes Undergraduates of 2017 Summer Fellowship Program
Kennebec Journal · August 30, 2017
MDI Biological Laboratory Celebrates Banner Year
Mount Desert Islander · August 2, 2017
Introduction to the MDI Biological Laboratory’s Center for Science Entrepreneurship
Regenerative Medicine Network · March 7, 2017
‘A Geneticist’s Toolkit’ to be Subject of MDI Science Café
Press Release · January 27, 2017
How Do Germline Cells Maintain Immortality?
Press Release · July 15, 2015
MDI Biological Laboratory Scientist Receives $1.7 Million for Stem Cell Research
Press Release · May 1, 2015
Artists and Scientists Discuss Their Common Path at July 1 Science Café
Press Release · June 19, 2013
ELLI-1, a novel germline protein, modulates RNAi activity and P-granules accumulation in Caenorhabditis elegans. Andralojc, K.M., Campbell, A.C., Kelly, A.L., Terrey, M., Tanner, P.C., Gans, I.M., Senter-Zapata, M.J., Khokhar, E.S., & Updike, D.L. PLoS Genetics. 2017 13(2):e1006611.
PQN-75 is expressed in the pharyngeal gland cells of Caenorhabditis elegans and is dispensable for germline development. Rochester, J.D., Tanner, P.C., Sharp, C.S., Andralojc, K.M., & Updike, D.L. Biology Open 2017 6(9):1355-1363.
Comparative biology of tissue repair, regeneration and aging. Coffman, J.A., Rieger, S., Rogers, A.N., Updike, D.L., & Yin, V.P. npj Regenerative Medicine. 2016 (1).
A forward genetic screen for suppressors of somatic P granules in C. elegans. Kelly, A. L., Senter-Zapata, M. J., Campbell, A. C., Lust, H. E., Theriault, M. E. Andralojc, K. M., & Updike, D.L. G3, 2015 (5),2209-2215.
Specifying and Protecting Germ Cell Fate. Strome S. & Updike D.L. Nature Reviews Molecular Cell Biology. 2015 16(7), 206-216.
CSR-1 and P granules suppress sperm-specific transcription in the C. elegans germline. Campbell AC, Updike DL – Development. 2015 May 15.
Germ-Granule Components Prevent Somatic Development in the C. elegans Germline. Updike DL, Knutson AK, Egelhofer TA, Campbell AC, Strome S – Curr Biol. 2014 Apr 15.
P granules extend the nuclear pore complex environment in the C. elegans Germline. Updike DL, Hachey SJ, Kreher J, Strome S – J Cell Biol. 2012 Mar 21.
P-granule assembly and function in Caenorhabditis elegans germ cells. Updike DL & Strome S – J. Androl. 2010 Jan-Feb.
A genomewide RNAi screen for genes that affect the stability, distribution and function of P granules in C. elegans. Updike DL & Strome S – Genetics 2009 Dec.
Come work with C. elegans and learn genetics! Summer INBRE and NSF REU fellows have used both forward and reverse genetics to isolate new C. elegans genes that regulate germ-granule biogenesis. Our lab uses a number of molecular and genetic techniques, along with stereo and fluorescence microscopy, to map and characterize these novel genes. Each student is partnered with an experienced technician that will assist them on their project. At the end of the summer, students present their findings in a poster or a talk session at the student symposium.
GSBSE students: We are looking for graduate students. Please contact me to discuss potential rotation projects.