0
Views
6
CrossRef citations to date
0
Altmetric
Transcriptional Regulation

A Rat Gene With Sequence Homology to the Drosophila Gene Hairy is Rapidly Induced by Growth Factors Known to Influence Neuronal Differentiation

, &
Pages 105-113 | Received 05 Aug 1992, Accepted 09 Oct 1992, Published online: 01 Apr 2023

REFERENCES

  • Anderson, D. J. 1990. The neural crest cell lineage problem: neuropoiesis? Neuron 3:1–12.
  • Artavanis-Tsakonas, S. 1988. The molecular biology of the Notch locus and the fine tuning of differentiation in Drosophila. Trends Genet. 4:95–100.
  • Baker, N. E. 1987. Molecular cloning of sequences from wingless, a segmentation polarity gene in Drosophila: the spatial distribution of a transcript in embryos. EMBO J. 6:1765–1773.
  • Bartel, D. P., Μ. Sheng, L. F. Lau, and Μ. E. Greenberg. 1989. Growth factors and membrane depolarization activate distinct programs of early response gene expression: dissociation of fos and jun induction. Genes Dev. 3:304–313.
  • Benezra, R., R. L. Davis, D. Lockhson, D. L. Turner, and H. Weintraub. 1990. The protein Id: a negative regulator of helixloop-helix DNA binding proteins. Cell 61:49–59.
  • Bier, E., H. Vaessin, S. Shepherd, L. Y. Jan, and Y. N. Jan. deadpan, an essential pan-neural gene in Drosophila, encodes a helix-loop-helix protein similar to the hairy gene product. Genes Dev., in press.
  • Boonstra, J., W. H. Moolenaar, P. H. Harrison, P. Moed, P. T. van der Saag, and S. W. Delaat. 1983. Ionic responses and growth stimulation induced by nerve growth factor and epidermal growth factor in rat pheochromocytoma (PC12) cells. J. Cell Biol. 97:92–98.
  • Botas, J., J. Moscoso del Prado, and A. Garcia-Bellido. 1982. Gene-dose titration analysis in the search of trans-regulatory genes in Drosophila. EMBO J. 1:307–310.
  • Cabrera, C. V., and Μ. C. Alonso. 1991. Transcriptional activation by heterodimers of the achaete-scute and daughterless gene products of Drosophila. EMBO J. 10:2965–2973.
  • Cabrera, C. V., A. Martinez-Arias, and Μ. Bate. 1987. The expression of three members of the achaete-scute gene complex correlates with neuroblast segregation in Drosophila. Cell 50:425–433.
  • Campos-Ortega, J. A. 1985. Genetics of early neurogenesis in Drosophila melanogaster. Trends Neurosci. 8:245–250.
  • Campos-Ortega, J. A., and Y. N. Jan. 1991. Genetic and molecular bases of neurogenesis in Drosophila melanogaster. Annu. Rev. Neurosci. 14:399–420.
  • Campuzano, S., and J. Modolell. 1992. Patterning of the Drosophila nervous system: the achaete-scute gene complex. Trends Genet. 8:202–208.
  • Carroll, S. B., and J. S. Whyte. 1989. The role of the hairy gene during Drosophila morphogenesis: stripes in imaginai discs. Genes Dev. 3:905–916.
  • Caudy, M., H. Vaessin, Μ. Brand, R. Tuma, L. Y. Jan, and Y. N. Jan. 1988. daughterless, a Drosophila gene essential for both neurogenesis and sex determination, has sequence similarities to myc and the achaete-scute complex. Cell 55:1061–1067.
  • Chomczynski, P., and N. Sacchi. 1987. Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloro- form extraction. Anal. Biochem. 162:156–159.
  • Christy, B. A., L. K. Sanders, L. F. Lau, N. G. Çopeland, N. A. Jenkins, and D. Nathans. 1991. An Id-related helix-loop-helix protein encoded by a growth factor inducible gene. Proc. Natl. Acad. Sci. USA 88:1815–1819.
  • Cubas, P., J. F. de Celis, S. Campuzano, and J. Modelell. 1991. Proneural clusters of achaete-scute expression and the generation of sensory organs in the Drosophila imaginai wing disc. Genes Dev. 5:996–1008.
  • Danielson, P. E., S. Forss-Petter, Μ. A. Brow, L. Calavetta, J. Douglass, R. J. Milner, and J. G. Sutcliffe. 1988. P1B15: a cDNA clone of the rat mRNA encoding cyclophilin. DNA 7:261–267.
  • Davis, R. L., P. Cheng, A. B. Lassar, and H. Weintraub. 1990. The MyoD DNA binding domain contains a recognition code for muscle-specific gene activation. Cell 60:733–746.
  • Doupe, A. J., S. C. Landis, and P. H. Patterson. 1985. Environmental influences in the development of neural crest derivatives: glucocorticoids, growth factors, and chromaffin cell plasticity. J. Neurosci. 5:2119–2142.
  • Ellis, H. Μ., D. R. Spann, and J. W. Posakony. 1990. extramacrochaetae, a negative regulator of sensory organ development in Drosophila, defines a new class of helix-loop-helix proteins. Cell 61:27–38.
  • Evan, G. L, A. H. Wyllie, C. S. Gilbert, T. D. Littlewood, H. Land, Μ. Brooks, C. Μ. Waters, L. Z. Penn, and D. C. Hancock. 1992. Induction of apoptosis in fibroblasts by c-myc protein. Cell 69:119–128.
  • Feder, J. N., C. J. Guidos, B. Kusler, C. Carswell, D. Lewis, and R. T. Schimke. 1990. A cell cycle analysis of growth-related genes expressed during T lymphocyte maturation. J. Cell Biol. 111:2693–2701.
  • Feder, J. N., L. Y. Jan, and Y.-N. Jan. Unpublished data.
  • Freytag, S. O., and T. J. Geddes. 1992. Reciprocal regulation of adipogenesis by Myc and C/EBPα. Science 256:379–382.
  • Garrell, J., and J. Modolell. 1990. The Drosophila extramacrochaetae locus, an antagonist of proneural genes that, like these genes, encodes a helix-loop-helix DNA binding protein. Cell 61:39–48.
  • Ghysen, A., and C. Dambly-Chaudiere. 1989. Genesis of the Drosophila peripheral nervous system. Trends Genet 5:251–255.
  • Goelet, P., V. F. Castellucci, S. Schacher, and E. R. Kandel. 1986. The long and the short of long-term memory—a molecular framework. Nature (London) 322:419–422.
  • Greenberg, Μ. E., and E∙ B. Ziff. 1984. Stimulation of 3T3 cells induces transcription of the c-fos proto-oncogene. Nature (London) 311:433–438.
  • Greene, L. A., and A. S. Tischler. 1976. Establishment of a noradrenergic clonal line of rat adrenal pheochromocytoma cells which respond to nerve growth factor. Proc. Natl. Acad. Sci. USA 73:2424–2428.
  • Ito, E., J. L. Sonnenberg, and R. Narayanan. 1989. Nerve growth factor-induced differentiation in PC12 cells is blocked by fos oncogene. Oncogene 4:1193–1199.
  • Ito, E., L. A. Sweterlitsch, P. B. Tran, F. J. Rauscher III, and R. Narayanan. 1990. Inhibition of PC12 cell differentiation by the immediate early gene fra-1. Oncogene 5:1755–1760.
  • Jan, Y. N., and L. Y. Jan. 1990. Genes required for specifying cell fates in Drosophila embryonic sensory nervous system. Trends Neurosci. 13:493–498.
  • Jessell, T. Μ., and D. A. Melton. 1992. Diffusible factors in vertebrate embryonic induction. Cell 68:257–270.
  • Johnson, J. E., S. J. Birren, and D. J. Anderson. 1990. Two rat homologues of Drosophila achaete-scute specifically expressed in neuronal precursors. Nature (London) 346:858–861.
  • Johnson, J. E., K. Zimmerman, T. Saito, and D. J. Anderson. 1992. Induction and repression of mammalian achaete-scute homologue (MASH) gene expression during neuronal differentiation of P1, embryonal carcinoma cells. Development 114:75–87.
  • Klambt, C., E. Knust, K. Tietze, and J. A. Campos-Ortega. 1989. Closely related transcripts encoded by the neurogenic gene complex enhancer of split of Drosophila melanogaster. EMBO J. 8:203–210.
  • Knust, E., U. Dietrich, U. Tepass, K. A. Bremer, D. Weigel, H. Vaessin, and J. A. Campos-Ortega. 1987. EGF homologous sequences encoded in the genome of Drosophila melanogaster, and their relation to neurogenic genes. EMBO J. 6:761–766.
  • Landis, S. C., and P. H. Patterson. 1981. Neural crest lineages. Trends Neurosci. 4:172–175.
  • Lo, L., J. E. Johnson, C. W. Wuenschell, T. Saito, and D. J. Anderson. 1991. Mammalian achaete-scute homolog 1 is transiently expressed by spatially restricted subsets of early neuroepithelial and neural crest cells. Genes Dev. 5:1524–1537.
  • McGinnis, W., and R. Krumlauf. 1992. Homeobox genes and axial patterning. Cell 68:283–302.
  • Michelson, A. Μ., S. Μ. Abmayr, Μ. Bate, A. Arias, and T. Maniatis. 1990. Expression of a MyoD family member prefigures muscle pattern in Drosophila embryos. Genes Dev. 4:2086–2097.
  • Moscoso del Prado, J., and A. Garica-Bellido. 1984. Genetic regulation of the achaete-scute complex of Drosophila melanogaster. Roux’s Arch. Dev. Biol. 193:246–251.
  • Murre, C., P. S. McCaw, and D. Baltimore. 1989. A new DNA binding and dimerization motif in immunoglobulin enhancer binding, daughterless, MyoD, and myc proteins. Cell 56:777–783.
  • Murre, C., P. S. McCaw, H. Vaessin, Μ. Caudy, L. Y. Jan, Y. N. Jan, C. Cabrera, J. N. Buskin, S. D. Hauschka, A. B. Lassar, H. Weintraub, and D. Baltimore. 1989. Interactions between heterologous helix-loop-helix proteins generate complexes that bind specifically to a common DNA sequence. Cell 58:537–544.
  • Nepveu, A., and K. B. Marcu. 1986. Intragenic pausing and anti-sense transcription within the murine c-myc locus. EMBO J. 5:2859–2865.
  • Padgett, R. W., R. D. St. Johnston, and W. Μ. Gelbart. 1987. A transcript from a Drosophila pattern gene predicts a protein homologous to the transforming growth factor-β family. Nature (London) 325:81–84.
  • Romani, S., S. Campuzano, E. Macagno, and J. Modolell. 1989. Expression of achaete and scute genes in Drosophila imaginal discs and their function in sensory organ development. Genes Dev. 3:997–1007.
  • Romani, S., S. Campuzano, and J. Modelell. 1987. The achaetescute complex is expressed in neurogenic regions of Drosophila embryos. EMBO J. 6:2085–2092.
  • Rushlow, C. A., A. Hogan, S. Μ. Pinchin, K. Μ. Howe, Μ. Lardelli, and D. Ish-Horowicz. 1989. The Drosophila hairy protein acts in both segmentation and bristle patterning and shows homology to N-myc. EMBO J. 8:3095–3103.
  • Rutledge, B. J., K. Zhang, E. Bier, Y. N. Jan, and N. Perrimon. The Drosophila spitz gene encodes a putative EGF-like growth factor involved in dorsal-ventral axis formation and neurogenesis. Genes Dev., in press.
  • Rydel, R. E., and L. A. Greene. 1987. Acidic and basic fibroblast growth factors promote stable neurite outgrowth and neuronal differentiation in cultures of PC12 cells. J. Neurosci. 7:3639–3653.
  • Sheng, Μ., and Μ. E. Greenberg. 1990. The regulation and function of c-fos and other immediate early genes in the nervous system. Neuron 4:477–485.
  • Shepherd, S., H. Vaessin, E. Beir, L. Y. Jan, and Y. N. Jan. deadpan, an essential pan-neural gene encoding an HLH protein, acts as a denominator in Drosophila sex determination. Cell 70:911–922.
  • Skeath, J. B., and S. B. Carroll. 1991. Regulation of achaetescute gene expression and sensory organ pattern formation in the Drosophila wing. Genes Dev. 5:984–995.
  • Spencer, F. A., F. M. Hoffman, and W. Μ. Gelbart. 1982. Decapentaplegic: a gene complex affecting morphogenesis in Drosophila melanogaster. Cell 28:451–461.
  • Stein, R., S. Orit, and D. J. Anderson. 1988. The induction of a neural-specific gene, SCG10, by nerve growth factor in PC12 cells is transcriptional, protein synthesis dependent, and glucocorticoid inhibitable. Dev. Biol. 127:316–325.
  • Togari, A., G. Dickens, H. Kuzuya, and G. Guroff. 1985. The effect of fibroblast growth factor of PC12 cells. J. Neurosci. 5:307–316.
  • Unsicker, K., B. Krish, J. Otten, and H. Thoenen. 1978. Nerve growth factor-induced fiber outgrowth from isolated rat adrenal chromaffin cell cultures. Proc. Natl. Acad. Sci. USA 75:3498–3502.
  • Vaessin, H. Personal communication.
  • Vaessin, H., Μ. Caudy, E. Bier, L. Y. Jan, and Y. N. Jan. 1990. Role of helix-loop-helix proteins in Drosophila neurogenesis. Cold Spring Harbor Symp. Quant. Biol. 55:239–245.
  • van den Heuvel, Μ., R. Nusse, P. Johnston, and P. A. Lawrence. 1989. Distribution of the wingless gene product in Drosophila embryos: a protein involved in cell-cell communication. Cell 59:739–749.
  • Van Doren, Μ., H. Μ. Ellis, and J. W. Posakony. 1991. The Drosophila extramacrochaetae protein anatagonizes sequencespecific DNA binding by daughterless/achaetescute protein complexes. Development 113:245–255.
  • Villares, R., and C. V. Cabrera. 1987. The achaetescute gene complex of D. melanogaster: conserved domains in a subset of genes required for neurogenesis and their homology to myc. Cell 5:415–424.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.