Frand, Alison R. - University of California, Los Angeles

个人简介

Alison joined the faculty of the Department of Biological Chemistry in the David Geffen School of Medicine at UCLA in March of 2007. She began studying the molting cycle of C. elegans as a post-doctoral research associate in the laboratory of Gary Ruvkun at Harvard Medical School. Her graduate research in Chris Kaiser's lab at the Massachusetts Institute of Technology defined an essential pathway for protein disulfide bond formation in the endoplasmic reticulum of yeast. Alison earned her bachelor degree from Cornell University, where she worked in the laboratory of Tom Fox.

研究领域

Genetic Analysis of the Molting Cycle of C. elegans Our lab is interested in the molting cycle of the model nematode C. elegans. Molting is the hallmark of the ecdysozoan clade that encompasses all animals with an external skeleton. Ecdysozoans periodically shed and remake their skeleton in order to grow. The molting cycle typically involves extensive communication among neuroendocrine centers in the brain and peripheral tissues remodeled during molting. Although the endocrine control of molting is best understood in insects, neuroendocrine circuits that start, stop, and set the pace of the molting cycle are not well understood in any organism. Every molt involves the coordinated, transient remodeling of tissues spread throughout the body. Epidermal cells fully remodel the local extracellular matrix (ECM) in addition to cell-ECM and cell-cell attachments. Particular epidermal cells also divide like stem cells near the time of the molt. Because the external skeleton of nematodes is a collagenous ECM similar to human skin and connective tissue, mechanisms for renewal of the worm skeleton will likely apply to ECM homeostasis in vertebrates, a process essential for normal development and wound repair. Faulty interactions among cells and the ECM promote the metastasis of tumors and also contribute to pathologies of skin and connective tissue in humans, including Marfan syndrome and certain muscular dystrophies. Use of the model nematode C. elegans provides an exemplary opportunity to study the endocrine and enzymatic regulation of molting in an organism amenable to functional genomic, genetic, and cell biological analysis. In prior work, we identified scores of genes required for shedding the old skeleton through a genome-wide, reverse genetic screen using RNA-interference (RNAi). Fusions to GFP showed that eight of the genes are expressed in epidermal cells that synthesize the cuticle, in a pulse before ecdysis. These and other genes identified in our screen may contribute to remodeling of the exoskeleton. Through our ongoing analysis of the C. elegans molting cycle, we expect to discover conserved signaling pathways and enzymatic cascades that promote remodeling of collagenous extracellular matrices. We further expect to find novel mechanisms for the neuroendocrine regulation of animal development and behavior. In addition, our research will identify potential targets for new drugs for diseases caused by parasitic nematodes currently affecting over 140 million people living primarily in tropical regions.

近期论文

查看导师新发文章（温馨提示：请注意重名现象，建议点开原文通过作者单位确认）

Kelley, M., Yochem, J., Krieg, M., Calixto, A., Heiman, M.G., Kuzmanov, A., Meli, V., Chalfie, M., Goodman, M.B., Shaham, S., Frand, A.R. and Fay, D.S. (2015) FBN-1, a Fibrillin-Related Protein, Is Required for Resistance of the Epidermis to Mechanical Deformation During C. elegans Embryogenesis. eLife, 4:e06565. Chin, R.M., Fu, X., Pai, M.Y., Vergnes, L., Hwang, H., Deng, G., Diep, S., Lomenick, B., Meli, V.S., Monsalve, G.C., Hu, E., Whelan, S.A., Wang, J.X., Jung, G., Solis, G.M., Fazlollahi, F., Kaweeteerawat, C., Quach, A., Nili, M., Krall, A.S., Godwin, H.A., Chang, H.R., Faull, K.F., Guo, F., Jiang, M., Trauger, S.A., Saghatelian, A., Braas, D., Christofk, H.R., Clarke, C.F., Teitell, M.A., Petrascheck, M., Reue, K., Jung, M.E., Frand, A.R., and Huang, J. (2014) The Metabolite α-Ketoglutarate Extends Lifespan by Inhibiting ATP Synthase and TOR. Nature, 510:397-401. Monsalve, G.C., and Frand, A.R. (2012) Toward a Unified Model of Developmental Timing: A “Molting” Approach. Worm, 1:1-10. Gomez, F., Monsalve, G.C., Tse, V., Saiki, R., Weng. E., Lee, L., Srinivasan, C., Frand, A.R., and Clarke, C.F. (2012) Delayed Accumulation of Intestinal Coliform Bacteria Enhances Life Span and Stress Resistance in Caenorhabditis elegans Fed Respiratory Feficient E. coli. BMC Microbiology, 12:300. Moissiard, G., Cokus, S.J., Cary, J., Feng, S., Billi, A.C., Stroud, H., Husmann, D., Zhan, Y., Lajoie, B.R., McCord, R.P., Hale, C.J., Feng, W., Michaels, S.D., Frand, A.R., Pellegrini, M., Dekker, J., Kim, J.K., and Jacobsen, S. (2012) MORC Family ATPases Required for Heterochromatin Condensation and Gene Silencing. Science, 336:1448-65. Monsalve, G.C., Van Buskirk, C., and Frand, A.R. (2011) LIN-42/PERIOD Controls Cyclical and Developmental Progression of C. elegans Molts. Current Biology, 21:2033-45. Russel, S.E., Frand, A.R., and Ruvkun, G. (2011) Regulation of the C. elegans Molt by pqn-47. Developmental Biology, 21: 360: 297-309.