Ding Xue

Molecular, Cellular & Developmental Biology;
Member of the Center for Neuroscience

Department of Molecular, Cellular & Developmental Biology, Campus Box 347
MCDB Addition A320C
University of Colorado at Boulder
Boulder, CO 80309-0347

email: xue@spot.colorado.edu
Phone: 303-492-0271
FAX: 303-492-7744
Website: http://mcdb.colorado.edu/labs/xue/

Dr. Xue is a Professor of Molecular, Cellular, and Developmental Biology at the University of Colorado at Boulder. He received his Ph.D. in 1993 from Columbia University and was a postdoctoral fellow at MIT from 1994-1997 before he joined the faculty at the University of Colorado at Boulder in the Fall of 1997. Dr. Xue has received numerous awards including Helen Hay Whitney Foundation postdoctoral fellowship, the Searle Scholar Award, the Burroughs Wellcome Fund Career Award, and the Sandler Program for Asthma Research Early Excellence Award.


Dr. Xue's main research interests lie in studying the mechanisms of programmed cell death (or apoptosis) and various human diseases such as neurodegenerative diseases, cancer, and autoimmune disorders that are caused by abnormal apopotosis. He has been using genetic, molecular, biochemical, and structural biological approaches to study the mechanisms that control, activate and execute programmed cell death in the nematode C. elegans and in mammals, with a focus on studying the regulation and activation of neuronal cell deaths. His laboratory recently identified more than 15 genes that act downstream of the C. elegans cell death protease CED-3 to execute programmed cell death and at least eight new genes that control sexually dimorphic apoptosis, which is an ancient developmental process crucial for the reproduction of animal species.

Selected Publications:

Parrish, J., Li, L., Klotz, K., Ledwich, D., Wang, X.D., and Xue, D. (2001). C. elegans mitochondrial endonuclease G is important for apoptosis. Nature 412, 90-94.

Wang, X.C., Yang, C.L., Cai, J.J., Shi, Y.G., and Xue, D. (2002). Mechanisms of AIF-mediated apoptotic DNA degradation in Caenorhabditis elegans. Science 298, 1587-1592.

Wang, X.C., Wu, Y.C., Fadok, V., Lee, M.C., Gengyo-Ando, K., Cheng, L.C., Ledwich, D., Hsu, P.K., Chen, J.Y., Chou, B.K., Henson, P., Mitani, S., and Xue, D. (2003). Cell Corpse Engulfment Mediated by C. elegans Phosphatidylserine Receptor Through CED-5 and CED-12. Science 302, 1563-1566.


Parrish, J. and Xue, D. (2003). Functional genomic analysis of apoptotic DNA degradation in C. elegans. Mol. Cell 11, 987-996.


Kokel, D., Li, Y.H., Qin, J., and Xue, D. (2006). The non-genotoxic carcinogens naphthalene and para-dichlorobenzene suppress apoptosis in C. elegans. Nature Chemical Biology 2, 338-345.


Wang, X.C., Wang, J., Gengyo-Ando, K., Gu, L.C., Sun, C.L., Yang, C.L., Shi, Y., Kobayashi, T., Shi, Y.G., Mitani, S., Xie, X.S., and Xue, D. (2007). "C. elegans mitochondrial factor WAH-1 promotes phosphatidylserine externalization in apoptotic cells through phospholipid scramblase SCRM-1". Nature Cell Biology 9, 541-549..