Neural cell fate analysis in zebrafish using olig2 BAC transgenics (original) (raw)
References
Kimmel CB, Warga RM, Kane DA (1994). Cell cycles and clonal strings during formation of the zebrafish central nervous system. Development 120: 265–276. Google Scholar
Papan C, Campos-Ortega JA (1997). A clonal analysis of spinal cord development in the zebrafish. Dev Genes Evol 207: 71–81. Google Scholar
Papan C, Campos-Ortega JA (1999). Region-specific cell clones in the developing spinal cord of the zebrafish. Dev Genes Evol 209: 135–144. Google Scholar
Eisen JS, Pike SH, Romancier B (1990). An identified motoneuron with variable fates in embryonic zebrafish. J Neurosci 10: 34–43. Google Scholar
Eisen JS (1992). The role of interactions in determining cell fate of two identified motoneurons in the embryonic zebrafish. Neuron 8: 231–240. Google Scholar
Eisen JS (1991). Determination of primary motoneuron identity in developing zebrafish embryos. Science 252: 569–572. Google Scholar
Appel B, Korzh V, Glasgow E, Thor S, Edlund T, Dawid IB, Eisen JS (1995). Motoneuron fate specification revealed by patterned LIM homeobox gene expression in embryonic zebrafish. Development 121: 4117–4125. Google Scholar
Appel B, Givan LA, Eisen JS (2001). Delta-Notch signaling and lateral inhibition in zebrafish spinal cord development. BMC Dev Biol 1: 13. Google Scholar
Bernhardt RR, Patel CK, Wilson SW, Kuwada JY (1992). Axonal trajectories and distribution of GABAergic spinal neurons in wildtype and mutant zebrafish lacking floor plate cells. J Comp Neurol 326: 263–272. Google Scholar
Bernhardt RR, Chitnis AB, Lindamer L, Kuwada JY (1990). Identification of spinal neurons in the embryonic and larval zebrafish. J Comp Neurol 302: 603–616. Google Scholar
Hale ME, Ritter DA, Fetcho JR (2001). A confocal study of spinal interneurons in living larval zebrafish. J Comp Neurol 437: 1–16. Google Scholar
Brand M, Heisenberg CP, Jiang YJ, Beuchle D, Lun K, Furutani-Seiki M, Granato M, Haffter P, Hammerschmidt M, Kane DA, Kelsh RN, Mullins MC, Odenthal J, van Eeden FJ, Nusslein-Volhard C (1996). Mutations in zebrafish genes affecting the formation of the boundary between midbrain and hindbrain. Development 123: 179–190. Google Scholar
Schier AF, Neuhauss SC, Harvey M, Malicki J, Solnica-Krezel L, Stainier DY, Zwartkruis F, Abdelilah S, Stemple DL, Rangini Z, Yang H, Driever W (1996). Mutations affecting the development of the embryonic zebrafish brain. Development 123: 165–178. Google Scholar
Jiang YJ, Brand M, Heisenberg CP, Beuchle D, Furutani-Seiki M, Kelsh RN, Warga RM, Granato M, Haffter P, Hammerschmidt M, Kane DA, Mullins MC, Odenthal J, van Eeden FJ, Nusslein-Volhard C (1996). Mutations affecting neurogenesis and brain morphology in the zebrafish, Danio rerio. Development 123: 205–216. Google Scholar
Udvadia AJ, Linney E (2003). Windows into development: historic, current, and future perspectives on transgenic zebrafish. Dev Biol 256: 1–17. Google Scholar
Koster RW, Fraser SE (2001). Direct imaging of in vivo neuronal migration in the developing cerebellum. Curr Biol 11: 1858–1863. Google Scholar
Gilmour DT, Maischein HM, Nusslein-Volhard C (2002). Migration and function of a glial subtype in the vertebrate peripheral nervous system. Neuron 34: 577–588. Google Scholar
Neumann CJ, Nuesslein-Volhard C (2000). Patterning of the zebrafish retina by a wave of sonic hedgehog activity. Science 289: 2137–2139. Google Scholar
Picker A, Scholpp S, Bohli H, Takeda H, Brand M (2002). A novel positive transcriptional feedback loop in midbrain-hindbrain boundary development is revealed through analysis of the zebrafish pax2.1 promoter in transgenic lines. Development 129: 3227–3239. Google Scholar
Jessen JR, Meng A, McFarlane RJ, Paw BH, Zon LI, Smith GR, Lin S (1998). Modification of bacterial artificial chromosomes through chistimulated homologous recombination and its application in zebrafish transgenesis. Proc Natl Acad Sci USA 95: 5121–5126. Google Scholar
Lee EC, Yu D, Martinez de Velasco J, Tessarollo L, Swing DA, Court DL, Jenkins NA, Copeland NG (2001). A highly efficient Escherichia coli-based chromosome engineering system adapted for recombinogenic targeting and subcloning of BAC DNA. Genomics 73: 56–65. Google Scholar
Westerfield M (2000). The Zebrafish Book. Eugene, Oregon, USA: University of Oregon Press. Google Scholar
Hauptmann G, Gerster T (2000). Multicolor whole-mount in situ hybridization. Methods Mol Biol 137: 139–148. Google Scholar
Yu D, Ellis HM, Lee EC, Jenkins NA, Copeland NG, Court DL (2000). An efficient recombination system for chromosome engineering in Escherichia coli. Proc Natl Acad Sci USA 97: 5978–5983. Google Scholar
Langenberg T, Brand M, Cooper MS (2003). Imaging brain development and organogenesis in zebrafish using immobilized embryonic explants. Developmental Dynamics. In press.
Lu QR, Sun T, Zhu Z, Ma N, Garcia M, Stiles CD, Rowitch DH (2002). Common developmental requirement for Olig function indicates a motor neuron/oligodendrocyte connection. Cell 109: 75–86. Google Scholar
Lu QR, Yuk D, Alberta JA, Zhu Z, Pawlitzky I, Chan J, McMahon AP, Stiles CD, Rowitch DH (2000). Sonic hedgehog - regulated oligodendrocyte lineage genes encoding bHLH proteins in the mammalian central nervous system. Neuron 25: 317–329. Google Scholar
Mizuguchi R, Sugimori M, Takebayashi H, Kosako H, Nagao M, Yoshida S, Nabeshima Y, Shimamura K, Nakafuku M (2001). Combinatorial roles of olig2 and neurogenin2 in the coordinated induction of pan-neuronal and subtype-specific properties of motoneurons. Neuron 31: 757–771. Google Scholar
Novitch BG, Chen AI, Jessell TM (2001). Coordinate regulation of motor neuron subtype identity and pan-neuronal properties by the bHLH repressor Olig2. Neuron 31: 773–789. Google Scholar
Park H, Mehta A, Richardson JS, Appel B (2002). olig2 is required for zebrafish primary motor neuron and oligodendrocyte development. Developmental Biology 248: 356–368. Google Scholar
Sun T, Echelard Y, Lu R, Yuk D, Kaing S, Stiles CD, Rowitch DH (2001). Olig bHLH proteins interact with homeodomain proteins to regulate cell fate acquisition in progenitors of the ventral neural tube. Curr Biol 11: 1413–1420. Google Scholar
Takebayashi H, Nabeshima Y, Yoshida S, Chisaka O, Ikenaka K (2002). The basic helix-loop-helix factor olig2 is essential for the development of motoneuron and oligodendrocyte lineages. Curr Biol 12: 1157–1163. Google Scholar
Takebayashi H, Yoshida S, Sugimori M, Kosako H, Kominami R, Nakafuku M, Nabeshima Y (2000). Dynamic expression of basic helix-loop-helix Olig family members: implication of Olig2 in neuron and oligodendrocyte differentiation and identification of a new member, Olig3. Mech Dev 99: 143–148. Google Scholar
Zhou Q, Wang S, Anderson DJ (2000). Identification of a novel family of oligodendrocyte lineage-specific basic helix-loop-helix transcription factors. Neuron 25: 331–343. Google Scholar
Zhou Q, Choi G, Anderson DJ (2001). The bHLH transcription factor Olig2 promotes oligodendrocyte differentiation in collaboration with Nkx2.2. Neuron 31: 791–807. Google Scholar
Zhou Q, Anderson DJ (2002). The bHLH transcription factors OLIG2 and OLIG1 couple neuronal and glial subtype specification. Cell 109: 61–73. Google Scholar