Characterization of enhancer fragments in Drosophila robo2

References

• Rajagopalan S, Nicolas E, Vivancos V, et al. Crossing the midline: roles and regulation of Robo receptors. Neuron. 2000a;28(3):767–777.
   PubMed Web of Science ®Google Scholar
• Rajagopalan S, Vivancos V, Nicolas E, et al. 2000b Selecting a longitudinal pathway: robo receptors specify the lateral position of axons in the Drosophila CNS. Cell. 2000b;103(7):1033–1045.
   PubMed Web of Science ®Google Scholar
• Simpson JH, Kidd T, Bland KS, et al. Short-range and long-range guidance by slit and its Robo receptors. Robo and Robo2 play distinct roles in midline guidance. Neuron. 2000a;28(3):753–766.
   PubMed Web of Science ®Google Scholar
• Simpson JH, Bland KS, Fetter RD, et al. Short-range and long-range guidance by slit and its Robo receptors: a combinatorial code of Robo receptors controls lateral position. Cell. 2000b;103(7):1019–1032.
   PubMed Web of Science ®Google Scholar
• Spitzweck B, Brankatschk M, Dickson BJ. Distinct protein domains and expression patterns confer divergent axon guidance functions for drosophila robo receptors. Cell. 2010;140(3):409–420.
   PubMed Web of Science ®Google Scholar
• Evans TA, Bashaw GJ. Functional diversity of Robo receptor immunoglobulin domains promotes distinct axon guidance decisions. Curr Biol. 2010;20(6):567–572.
   PubMed Web of Science ®Google Scholar
• Evans TA, Santiago C, Arbeille E, et al. Robo2 acts in trans to inhibit Slit-Robo1 repulsion in pre-crossing commissural axons. Elife. 2015;4:e08407.
   PubMed Web of Science ®Google Scholar
• Nüsslein-Volhard C, Wieschaus E, Kluding H. Mutations affecting the pattern of the larval cuticle in Drosophila melanogaster I. Zygotic loci on the second chromosome. Roux Arch Dev Biol. 1984;193(5):267–282.
   Google Scholar
• Schimmelpfeng K, Gögel S, Klämbt C. The function of leak and kuzbanian during growth cone and cell migration. Mech Dev. 2001;106(1-2):25–36.
   PubMed Web of Science ®Google Scholar
• Santiago C, Labrador J-P, Bashaw GJ. The homeodomain transcription factor Hb9 controls axon guidance in Drosophila through the regulation of Robo receptors. Cell Rep. 2014;7(1):153–165.
   PubMed Web of Science ®Google Scholar
• Kraut R, Zinn K. Roundabout 2 regulates migration of sensory neurons by signaling in trans. Curr Biol. 2004;14(15):1319–1329.
   PubMed Web of Science ®Google Scholar
• Ordan E, Volk T. A non-signaling role of Robo2 in tendons is essential for Slit processing and muscle patterning. Development. 2015;142(20): 3512–3518. DOI:10.1242/dev.128157.
   Google Scholar
• Santiago-Martínez E, Soplop NH, Kramer SG. Lateral positioning at the dorsal midline: slit and Roundabout receptors guide Drosophila heart cell migration. Proc Natl Acad Sci USA. 2006;103(33):12441–12446.
   PubMed Web of Science ®Google Scholar
• Englund C, Steneberg P, Falileeva L, et al. Attractive and repulsive functions of Slit are mediated by different receptors in the Drosophila trachea. Development. 2002;129(21):4941–4951.
   PubMed Web of Science ®Google Scholar
• Parsons L, Harris K-L, Turner K, et al. Roundabout gene family functions during sensory axon guidance in the drosophila embryo are mediated by both Slit-dependent and Slit-independent mechanisms. Dev Biol. 2003;264(2):363–375.
   PubMed Web of Science ®Google Scholar
• Kramer SG, Kidd T, Simpson JH, et al. Switching repulsion to attraction: changing responses to slit during transition in mesoderm migration. Science. 2001;292(5517):737–740.
   PubMed Web of Science ®Google Scholar
• Weyers JJ, Milutinovich AB, Takeda Y, et al. A genetic screen for mutations affecting gonad formation in Drosophila reveals a role for the slit/robo pathway. Dev Biol. 2011;353(2):217–228.
   PubMed Web of Science ®Google Scholar
• Biteau B, Jasper H. Slit/Robo signaling regulates cell fate decisions in the intestinal stem cell lineage of Drosophila. Cell Rep. 2014;7(6):1867–1875.
   PubMed Web of Science ®Google Scholar
• Sasse S, Klämbt C. Repulsive epithelial cues direct glial migration along the nerve. Dev Cell. 2016;39(6):696–707.
   PubMed Web of Science ®Google Scholar
• Stine RR, Greenspan LJ, Ramachandran KV, et al. Coordinate regulation of stem cell competition by slitrobo and JAK-STAT signaling in the Drosophila testis. In: Buszczak M, editor. PLoS Genet. 2014;10(11):e1004713.
   PubMed Web of Science ®Google Scholar
• Brierley DJ, Blanc E, Reddy OV, et al. Dendritic targeting in the leg neuropil of Drosophila: the role of midline signalling molecules in generating a myotopic map. PLoS Biol. 2009;7(9):e1000199.
   PubMed Web of Science ®Google Scholar
• Mellert DJ, Knapp J-M, Manoli DS, et al. Midline crossing by gustatory receptor neuron axons is regulated by fruitless, doublesexand the Roundabout receptors. Development. 2010;137(2):323–332.
   PubMed Web of Science ®Google Scholar
• Jenett A, Rubin GM, Ngo T-TB, et al. A GAL4-driver line resource for Drosophila Neurobiology. Cell Rep. 2012;2(4):991–1001.
   PubMed Web of Science ®Google Scholar
• Pfeiffer B D, Jenett A, Hammonds AS, et al. Tools for neuroanatomy and neurogenetics in Drosophila. Proc Natl Acad Sci USA. 2008;105(28):9715–9720.
   PubMed Web of Science ®Google Scholar
• Port F, Chen H-M, Lee T, et al. Optimized CRISPR/Cas tools for efficient germline and somatic genome engineering in Drosophila. Proc Natl Acad Sci USA. 2014;111(29):E2967–76.
   Google Scholar
• Howard LJ, Reichert MC, Evans TA. The Slit-binding Ig1 domain is required for multiple axon guidance activities of Drosophila Robo2. Genesis. 2021;59(9):e23443.
   PubMed Web of Science ®Google Scholar
• Hayashi S, Ito K, Sado Y, et al. GETDB, a database compiling expression patterns and molecular locations of a collection of gal4 enhancer traps. Genesis. 2002;34(1-2):58–61.
   PubMed Web of Science ®Google Scholar
• Patel NH. Imaging neuronal subsets and other cell types in whole-mount Drosophila embryos and larvae using antibody probes. Methods Cell Biol. 1994;44:445–487.
   PubMed Web of Science ®Google Scholar
• Haase A, Stern M, Wächtler K, et al. A tissue-specific marker of Ecdysozoa. Dev Genes Evol. 2001;211(8):428–433.
   PubMed Web of Science ®Google Scholar
• Jan LY, Jan Y-N. Antibodies to horseradish peroxidase as specific neuronal markers in Drosophila and in grasshopper embryos. Proc Natl Acad Sci USA. 1982;79(8):2700–2704.
   PubMed Web of Science ®Google Scholar
• Grenningloh G, Rehm EJ, Goodman CS. Genetic analysis of growth cone guidance in Drosophila: fasciclin II functions as a neuronal recognition molecule. Cell. 1991;67(1):45–57.
   PubMed Web of Science ®Google Scholar
• Schindelin J, Arganda-Carreras I, Frise E, et al. Fiji: an open-source platform for biological-image analysis. Nat Methods. 2012;9(7):676–682.
   PubMed Web of Science ®Google Scholar
• Ito K, Urban J, Technau GM. Distribution, classification, and development ofDrosophila glial cells in the late embryonic and early larval ventral nerve cord. Roux Arch Dev Biol. Rouxs Arch. Dev. Biol. 1995;204(5):284–307.
   PubMedGoogle Scholar
• Gorczyca MG, Phillis RW, Budnik V. The role of tinman, a mesodermal cell fate gene, in axon pathfinding during the development of the transverse nerve in Drosophila.10. Development. 1994;120(8):2143–2152.
   PubMed Web of Science ®Google Scholar
• Noordermeer J N, Kopczynski CC, Fetter RD, et al. Wrapper, a novel member of the Ig superfamily, is expressed by midline glia and is required for them to ensheath commissural axons in Drosophila. Neuron. 1998;21(5):991–1001.
   PubMed Web of Science ®Google Scholar
• Brown HE, Reichert MC, Evans TA. Slit binding via the Ig1 domain is essential for midline repulsion by drosophila robo1 but dispensable for receptor expression. Localization, and Regulation in Vivo. G3: Genes|Genomes|Genetics. 2015;5(11):2429–2439.
   Google Scholar
• Kidd T, Brose K, Mitchell KJ, et al. Roundabout controls axon crossing of the CNS midline and defines a novel subfamily of evolutionarily conserved guidance receptors. Cell. 1998b;92(2):205–215.
   PubMed Web of Science ®Google Scholar
• Keleman K, Rajagopalan S, Cleppien D, et al. Comm sorts robo to control axon guidance at the Drosophila midline. Cell. 2002;110(4):415–427.
   PubMed Web of Science ®Google Scholar
• Keleman K, Ribeiro C, Dickson BJ. Comm function in commissural axon guidance: cell-autonomous sorting of Robo in vivo. Nat Neurosci. 2005;8(2):156–163.
   PubMed Web of Science ®Google Scholar
• Kidd T, Russell C, Goodman CS, et al. Dosage-sensitive and complementary functions of roundabout and commissureless control axon crossing of the CNS midline. Neuron. 1998a;20(1):25–33.
   PubMed Web of Science ®Google Scholar