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Development, Vol 116, Issue 4 855-863, Copyright © 1992 by Company of Biologists
JOURNAL ARTICLES |
CQ Doe
Department of Cell and Structural Biology, University of Illinois, Urbana 61801.
The first step in generating cellular diversity in the Drosophila central nervous system is the formation of a segmentally reiterated array of neural precursor cells, called neuroblasts. Subsequently, each neuroblast goes through an invariant cell lineage to generate neurons and/or glia. Using molecular lineage markers, I show that (1) each neuroblast forms at a stereotyped time and position; (2) the neuroblast pattern is indistinguishable between thoracic and abdominal segments; (3) the development of individual neuroblasts can be followed throughout early neurogenesis; (4) gene expression in a neuroblast can be reproducibly modulated during its cell lineage; (5) identified ganglion mother cells form at stereotyped times and positions; and (6) the cell lineage of four well-characterized neurons can be traced back to two identified neuroblasts. These results set the stage for investigating neuroblast specification and the mechanisms controlling neuroblast cell lineages.
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J Broadus and C. Doe Evolution of neuroblast identity: seven-up and prospero expression reveal homologous and divergent neuroblast fates in Drosophila and Schistocerca Development, January 12, 1995; 121(12): 3989 - 3996. [Abstract] [PDF] |
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E. Spana, C Kopczynski, C. Goodman, and C. Doe Asymmetric localization of numb autonomously determines sibling neuron identity in the Drosophila CNS Development, January 11, 1995; 121(11): 3489 - 3494. [Abstract] [PDF] |
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C. Austin, D. Feldman, J. Ida, and C. Cepko Vertebrate retinal ganglion cells are selected from competent progenitors by the action of Notch Development, January 11, 1995; 121(11): 3637 - 3650. [Abstract] [PDF] |
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E. Spana and C. Doe The prospero transcription factor is asymmetrically localized to the cell cortex during neuroblast mitosis in Drosophila Development, January 10, 1995; 121(10): 3187 - 3195. [Abstract] [PDF] |
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X Cui and C. Doe The role of the cell cycle and cytokinesis in regulating neuroblast sublineage gene expression in the Drosophila CNS Development, January 10, 1995; 121(10): 3233 - 3243. [Abstract] [PDF] |
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M. Martin-Bermudo, A Carmena, and F Jimenez Neurogenic genes control gene expression at the transcriptional level in early neurogenesis and in mesectoderm specification Development, January 1, 1995; 121(1): 219 - 224. [Abstract] [PDF] |
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B Jennings, A Preiss, C Delidakis, and S Bray The Notch signalling pathway is required for Enhancer of split bHLH protein expression during neurogenesis in the Drosophila embryo Development, January 12, 1994; 120(12): 3537 - 3548. [Abstract] [PDF] |
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T Bossing and G. Technau The fate of the CNS midline progenitors in Drosophila as revealed by a new method for single cell labelling Development, January 7, 1994; 120(7): 1895 - 1906. [Abstract] [PDF] |
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K. Bhat and P Schedl The Drosophila miti-mere gene, a member of the POU family, is required for the specification of the RP2/sibling lineage during neurogenesis Development, January 6, 1994; 120(6): 1483 - 1501. [Abstract] [PDF] |
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J. Skeath, G. Panganiban, and S. Carroll The ventral nervous system defective gene controls proneural gene expression at two distinct steps during neuroblast formation in Drosophila Development, January 6, 1994; 120(6): 1517 - 1524. [Abstract] [PDF] |
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Y Zhang, A Ungar, C Fresquez, and R Holmgren Ectopic expression of either the Drosophila gooseberry-distal or proximal gene causes alterations of cell fate in the epidermis and central nervous system Development, January 5, 1994; 120(5): 1151 - 1161. [Abstract] [PDF] |
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B Kramatschek and J. Campos-Ortega Neuroectodermal transcription of the Drosophila neurogenic genes E(spl) and HLH-m5 is regulated by proneural genes Development, January 4, 1994; 120(4): 815 - 826. [Abstract] [PDF] |
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T. Menne and C Klambt The formation of commissures in the Drosophila CNS depends on the midline cells and on the Notch gene Development, January 1, 1994; 120(1): 123 - 133. [Abstract] [PDF] |
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Q Chu-LaGraff and C. Doe Neuroblast specification and formation regulated by wingless in the Drosophila CNS Science, September 17, 1993; 261(5128): 1594 - 1597. [Abstract] [PDF] |
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X Yang, S Yeo, T Dick, and W Chia The role of a Drosophila POU homeo domain gene in the specification of neural precursor cell identity in the developing embryonic central nervous system. Genes & Dev., March 1, 1993; 7(3): 504 - 516. [Abstract] [PDF] |
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G Udolph, A Prokop, T Bossing, and G. Technau A common precursor for glia and neurons in the embryonic CNS of Drosophila gives rise to segment-specific lineage variants Development, January 7, 1993; 118(3): 765 - 775. [Abstract] [PDF] |
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M. Martin-Bermudo, F Gonzalez, M Dominguez, I Rodriguez, M Ruiz-Gomez, S Romani, J Modolell, and F Jimenez Molecular characterization of the lethal of scute genetic function Development, January 7, 1993; 118(3): 1003 - 1012. [Abstract] [PDF] |
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T Gutjahr, N. Patel, X Li, C. Goodman, and M Noll Analysis of the gooseberry locus in Drosophila embryos: gooseberry determines the cuticular pattern and activates gooseberry neuro Development, January 5, 1993; 118(1): 21 - 31. [Abstract] [PDF] |
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X. Cui and C. Q. Doe ming is expressed in neuroblast sublineages and regulates gene expression in the Drosophila central nervous system Development, December 1, 1992; 116(4): 943 - 952. [Abstract] [PDF] |
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X. Shao, K. Koizumi, N. Nosworthy, D.-P. Tan, W. Odenwald, and M. Nirenberg Regulatory DNA required for vnd/NK-2 homeobox gene expression pattern in neuroblasts PNAS, January 8, 2002; 99(1): 113 - 117. [Abstract] [Full Text] [PDF] |
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