Warrior, Rahul - University of California, Irvine - Department of Developmental and Cell Biology

研究领域

Molecular genetic analysis of nuclear migration and growth factor signaling in Drosophila We use Drosophila genetics, molecular and cellular techniques to study three mechanisms critical for normal development: (1) How extracellular proteoglycans (HSPGs) affect growth factor (especially BMP) signaling (2) How cells respond transcriptionally to Bone Morphogenetic Protein (BMP) ligands and (3) How a genetic pathway regulates the position and movement of the nucleus within a cell. The genes and pathways involved in these processes are evolutionarily conserved, and when disrupted in humans, cause congenital defects and disease. Warrior Lab ResearchProteoglycans in development: HSPGs are extracellular macromolecules found on virtually every cell in eumetazoans. They are composed of a core protein covalently linked to long unbranched stretches of repeating glycosaminoglycan (GAG) sugar chains that bind and modulate the signaling efficiency of many growth factor ligands. In humans mutations that affect HSPG function are implicated in developmental defects and cancer. We have found that in flies, activity of the GAG chain co-polymerases EXT1 (Ttv) and EXT2 (Sotv) is required for BMP, Wg and Hh signaling. More recently we showed that GAG synthesis is developmentally regulated through a novel translational control mechanism that we are now trying to understand. Transcriptional response to BMPs: For several years we have studied Schnurri (Shn), a zinc finger DNA-binding protein cloned and characterized in collaboration with Dr. Kavita Arora that enables cells to respond to BMP signals. Shn is essential for BMP signaling in Drosophila and is homologous to the human transcription factors Shn1, Shn2 and Shn3. We have found that Shn interacts with the BMP-specific Smad, Mad, in response to BMP pathway activation and can mediate either transcriptional activation or repression depending on the cellular context. Interestingly, we found that the human ortholog Shn1, can also act in BMP signaling in vertebrates, and does so by binding to very similar cis-elements. We continue to use genetic, molecular and mathematical approaches to study the role of Shn in BMP signaling. Nuclear migration: In most differentiated cells the nucleus is usually present at a defined subcellular position and maintained there through an active process that is not well understood. We have characterized two genes, Drosophila nudC (DnudC), and Drosophila Lissencephaly1 (DLis1) that are critical components of an evolutionarily conserved pathway regulating nuclear migration. These genes act by affecting the activity of the minus-end directed microtubule motor cytoplasmic dynein. Mutations in the human Lis1 homolog cause a birth defect Miller-Dieker Lissencephaly. This syndrome results from failure of embryonic neuronal migration, suggesting a link between nuclear and neuronal movement. We are currently focused (i) understanding the link between DLis1 and the motor complex in nuclear migration, (ii) identifying other genes in the nuclear migration pathway that may play regulatory or structural roles.

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Moua P, Fullerton D, Serbus LR, Warrior R, Saxton WM. (2011) Kinesin-1 tail autoregulation and microtubule-binding regions function in saltatory transport but not ooplasmic streaming. Development 138, 1087-1092 Haruta, T., Warrior, R., Yonemura, S., and Oda, H. (2010). The proximal half of the Drosophila E-cadherin extracellular region is dispensable for many cadherin-dependent events but necessary for ventral furrow formation. Genes to Cells, 15, 193-208 Wang, Y., Mijares, M., Gall, M.D., Turan, T., Javier, A., Bornemann, D.J., Manage, K., and Warrior, R. (2010) Drosophila variable nurse cells encodes arrest defective 1 (ARD1), the catalytic subunit of the major N-terminal acetyltransferase complex. Dev Dyn. 239(11):2813-27. Aguilar-Roca, N., Williams, A., Warrior, R., O’Dowd, D. K. (2009) Two minute training in class significantly increases the use of professional formatting in student to faculty email correspondence. International Journal for the Scholarship of Teaching and Learning, Vol 3, No. 1. http://www.georgiasouthern.edu/ijsotl Lawrence, R., Olson, S.K., Steele, R.E., Wang, L., Warrior, R., Cummings, R.D., Esko, J.D. (2008). Evolutionary differences in glycosaminoglycan fine structure detected by quantitative glycan reductive isotope labeling. J Biol Chem. 283 (48):33674-84 Yao, L.C., Phin, S., Cho, J., Rushlow C., Arora, K.* and Warrior R.*. (2008) Dpp on the brink(er). Development 2008 135:1205. *Communicating authors. Yao, L.C., Phin, S., Cho, J., Rushlow, C., Arora, K.* and Warrior, R.* (2008) Multiple modular promoter elements drive graded brinker expression in response to the Dpp morphogen gradient. Development. 135, 1039-1047. *Communicating authors. Bornemann, D., Park, S., Phin, S and Warrior, R. (2008) A translational block to HSPG synthesis permits BMP signaling in the early Drosophila embryo. Development, epub Feb 6. Yao, L-C., Blitz, I. L., Peiffer D. A., Phin, S., Wang, Y., Ogata, S., Cho, K. W. Y., Arora, K and Warrior R. (2006) Schnurri transcription factors from Drosophila and vertebrates can mediate BMP signaling through a phylogenetically conserved mechanism. Development. 133, 4025-4034. Brugger SM., Merrill AE., Torres-Vazquez J., Wu N., Ting MC., Cho JY., Dobias SL., Yi SE., Lyons K., Bell JR., Arora K., Warrior R., Maxson R. (2004) A phylogenetically conserved cis-regulatory module in the Msx2 promoter is sufficient for BMP-dependent transcription in murine and Drosophila embryos. Development. 131, 5153-5165. Bornemann DJ., Duncan JE., Staatz W., Selleck S., Warrior R. (2004) Abrogation of heparan sulfate synthesis in Drosophila disrupts the Wingless, Hedgehog and Decapentaplegic signaling pathways. Development. 131, 1927-1938. Duncan, J. and Warrior, R. (2002) The cytoplasmic dynein and kinesin motors have interdependent roles in patterning the Drosophila oocyte. Current Biology 12, 1982-1991. Reviewed in R. S. Cohen. Oocyte patterning: Dynein and Kinesin, Inc. Current Biology (2002) 12 R797-799