Correct coordination of neuronal differentiation events in ventral forebrain requires the bHLH factor MASH1

Molecular and Cellular Neurosciences

Volumn 14, Issue 4-5, 1999, Pages 355-369

  Horton, Sharon ^a   Meredith, Andrea ^a   Richardson, James A ^b   Johnson, Jane E ^a  

^a UNIVERSITY OF TEXAS SOUTHWESTERN MEDICAL CENTER   (United States)

^b UNIVERSITY OF TEXAS SOUTHWESTERN MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BROXURIDINE; HELIX LOOP HELIX PROTEIN; TRANSCRIPTION FACTOR;

ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; CELL PROLIFERATION; CENTRAL NERVOUS SYSTEM; CONTROLLED STUDY; DIENCEPHALON; EMBRYO; FOREBRAIN; GENE EXPRESSION; MORPHOLOGY; MOUSE; NERVE CELL DIFFERENTIATION; NERVOUS SYSTEM DEVELOPMENT; NONHUMAN; PERIPHERAL NERVOUS SYSTEM; PRIORITY JOURNAL; TELENCEPHALON;

ANIMALIA;

EID: 0032702817     PISSN: 10447431     EISSN: None     Source Type: Journal    
DOI: 10.1006/mcne.1999.0791     Document Type: Article

References (53)

1. opsin-1 in the rat opsin gene. Dev. Brain Res. 90:1995;184-189.
2. Anderson D. J., Jan Y. N. The determination of the neuronal phenotype. Cowan W. M., Jessell T. M., Zipursky S. L. Molecular and Cellular Approaches to Neural Development. 1997;26-63 Oxford Univ. Press, New York.
3. Anderson S. A., Eisenstat D. D., Shi L., Rubenstein J. L. R. Interneuron migration from basal forebrain to neocortex: Dependence on Dlx genes. Science. 278:1997a;474-476.
4. Anderson S. A., Qiu M., Bulfone A., Eisenstat D. D., Meneses J., Pedersen R., Rubenstein J. L. R. Mutations of the homeobox genes Dlx-1 and Dlx-2 disrupt the striatal subventricular zone and differentiation of late born striatal neurons. Neuron. 19:1997b;27-37.
5. Birren S. J., Lo L., Anderson D. J. Sympathetic neuroblasts undergo a developmental switch in trophic dependence. Development. 119:1993;597-610.
6. Borges M. W., Linnoila R. I., van de Velde H. J., Chen H., Nelkin B. D., Mabry M., Baylin S. B., Ball D. W. An achaete-scute homologue essential for neuroendocrine differentiation in the lung. Nature. 386:1997;852-855.
7. Campos-Ortega J. A., Jan Y. N. Genetic and molecular bases of neurogenesis in Drosophila melanogaster. Annu. Rev. Neurosci. 14:1991;399-420.
8. Caric D., Gooday D., Hill R. E., McConnell S. K., Price D. J. Determination of the migratory capacity of embryonic cortical cells lacking the transcription factor Pax-6. Development. 124:1997;5087-5096.
9. Casarosa S., Fode C., Guillemot F. Mash1 regulates neurogenesis in the ventral telencephalon. Development. 126:1999;525-534.
10. Cau E., Gradwohl G., Fode C., Guillemot F. Mash1 activates a cascade of bHLH regulators in olfactory neuron progenitors. Development. 124:1997;1611-1621.
11. Caviness V. S. J., Takahashi T., Nowakowski R. S. Numbers, time and neocortical neurogenesis: a general developmental and evolutionary model. Trends Neurosci. 18:1995;379-383.
12. Chitnis A., Henrique D., Lewis J., Ish-Horowicz D., Kintner C. Primary neurogenesis in Xenopus embryos regulated by a homologue of the Dorsophila neurogenic gene Delta. Nature. 375:1995;761-766.
13. Chitnis A., Kintner C. Sensitivity of proneural genes to lateral inhibition affects the pattern of primary neurons in Xenopus embryos. Development. 122:1996;2295-2301.
14. Deacon T. W., Pakzaban P., Isacson O. The lateral ganglionic eminence is the origin of cells committed to striatal phenotypes: neural transplantation and developmental evidence. Brain Res. 668:1994;211-219.
15. Easter S. S. J., Ross L. S., Frankfurter A. Initial tract formation in the mouse brain. J. Neurosci. 13:1993;285-299.
16. Ferreira A., Caceres A. Expression of the class III beta-tubulin isotype in developing neurons in culture. J. Neurosci. Res. 32:1992;516-529.
17. Ghysen A., Dambly-Chaudiere C., Jan L., Jan Y. N. Cell interactions and gene interactions in peripheral neurogenesis. Genes Dev. 7:1993;723-733.
18. Gordon M. K., Mumm J. S., Davis R. A., Holcomb J. D., Calof A. L. Dynamics of MASH1 expression in vitro and in vivo suggest a non-stem cell site of MASH1 action in the olfactory receptor neuron lineage. Mol. Cell. Neurosci. 6:1995;363-379.
19. Guillemot F., Joyner A. Expression of murine Achaete-Scute and Notch homologues in the developing central nervous system. Mech. Dev. 42:1993;171-185.
20. Guillemot F., Lo L. C., Johnson J. E., Auerbach A., Anderson D. J., Joyner A. L. Mammalian achaete-scute homolog 1 is required for the early development of olfactory and autonomic neurons. Cell. 75:1993;463-476.
21. Halliday A. L., Cepko C. L. Generation and migration of cells in the developing striatum. Neuron. 9:1992;15-26.
22. Henrique D., Hirsinger E., Adam J., Le Roux I., Pourquie O., Ish-Horowicz D., Lewis J. Maintenance of neuroepithelial progenitor cells by Delta-Notch signaling in the embryonic chick retina. Curr. Biol. 7:1997;661-670.
23. Hirsch M.-R., Tiveron M.-C., Guillemot F., Brunet J.-F., Goridis C. Control of noradrenergic differentiation and Phox2a expression by MASH1 in the central and peripheral nervous system. Development. 125:1998;599-608.
24. Jasoni C. L., Reh T. L. Temporal and spatial pattern of MASH-1 expression in the developing rat retina demonstrates progenitor cell heterogeneity. J. Comp. Neurol. 369:1996;319-327.
25. Johnson J. E., Birren S. J., Anderson D. J. Two rat homologues of Drosophila achaete-scute specifically expressed in neuronal precursors. Nature. 346:1990;858-861.
26. Johnson J. E., Zimmerman K., Saito T., Anderson D. J. Induction and repression of mammalian achaete-scute homolog (MASH) gene expression during neuronal differentiation of P19 embryonal carcinoma cells. Development. 114:1992;75-87.
27. Lanigan T. M., DeRaad S. K., Russo A. F. Requirement of the MASH-1 transcription factor for neuroendocrine differentiation of thyroid C cells. J. Neurobiol. 32:1998;126-134.
28. Lee J. E. Basic helix-loop-helix genes in neural development. Curr. Opin. Neurobiol. 7:1997;13-20.
29. Lee M. K., Tuttle J. B., Rebhun L. I., Cleveland D. N., Frankfurter A. The expression and post-translational modification of a neurons-specific β-tubulin isoform during chick embryogenesis. Cell. Motil. Cytoskeleton. 17:1990;118-132.
30. Lendahl U., Zimmerman L. B., McKay R. D. G. CNS stem cells express a new class of intermediate filament protein. Cell. 60:1990;585-595.
31. Lewis J. Neurogenic genes and vertebrate neurogenesis. Curr. Opin. Neurobiol. 6:1996;3-10.
32. Lillien L. Neural progeitors and stem cells: mechanisms of progenitor heterogeneity. Curr. Opin. Neurobiol. 8:1998;37-44.
33. Lindsell C. E., Boulter J., diSibio G., Gossler A., Weinmaster G. Expression patterns of Jagged, Delta1, Notch1, Notch2, and Notch3 genes identify ligand-receptor pairs that may function in neural development. Mol. Cell. Neurosci. 8:1996;14-27.
34. Lo L., Sommer L., Anderson D. J. MASH1 maintains competence for BMP2-induced neuronal differentiation in post-migratory neural crest cells. Curr. Biol. 7:1997;440-450.
35. Lo L., Tiveron M.-C., Anderson D. J. MASH1 activates expression of the paired homeodomain transcription factor Phox2a, and couples pan-neuronal and subtype-specific components of autonomic neuronal identity. Development. 125:1998;609-620.
36. Lo L.-C., Johnson J. E., Wuenschell C. W., Saito T., Anderson D. J. Mammalian achaete-scute homolog 1 is transiently expressed by spatially restricted subsets of early neuroepithelial and neural crest cells. Genes Dev. 5:1991;1524-1537.
37. Luskin M. B., Pearlman A. L., Sanes J. R. Cell lineage in the cerebral cortex of the mouse studied in vivo and in vitro with a recombinant retrovirus. Neuron. 1:1988;635-647.
38. Ma Q., Kintner C., Anderson D. J. Identification of neurogenin, a vertebrate neuronal determination gene. Cell. 87:1996;43-52.
39. Ma Q., Sommer L., Cserjesi P., Anderson D. J. Mash1 and neurogenin1 expression patterns define complementary domains of neuroepithelium in the developing CNS and are correlated with regions expressing notch ligands. J. Neurosci. 17:1997;3644-3652.
40. Menezes J. R., Luskin M. B. Expression of neuron-specific tubulin defines a novel population in the proliferative layers of the developing telencephalon. J. Neurosci. 14:1994;5399-5416.
41. Panganiban G., Sebring A., Nagy L., Carroll S. B. The development of crustacean limbs, and the evolution of arthropods. Science. 270:1995;1363-1366.
42. Porteus M. H., Bulfone A., Liu J.-K., Puelles L., Lo L.-C., Rubenstein J. L. R. DLX-2, MASH-1, and MAP-2 expression and bromodeoxyuridine incorporation define molecularly distinct cell populations in the embryonic mouse forebrain. J. Neurosci. 14:1994;6370-6383.
43. Price J., Thurlow L. Cell lineage in the rat cerebral cortex: A study using retroviral-mediated gene transfer. Development. 104:1988;473-482.
44. Rakic P. Neurons in rhesus monkey visual cortex: Systemic relation between time of origin and eventual disposition. Science. 183:1974;425-427.
45. Simpson P. Notch and the choice of cell fate in Drosophila neuroepithelium. Trends Genet. 6:1990;343-345.
46. Sommer L., Shah N., Rao M., Anderson D. J. The cellular function of MASH1 in autonomic neurogenesis. Neuron. 15:1995;1245-1258.
47. Song D. D., Harlan R. E. The development of enkephalin and substance P neurons in the basal ganglia: Insights into neostriatal compartments and the extended amygdala. Dev. Brain Res. 83:1994;247-261.
48. Tanabe Y., Jessell T. M. Diversity and pattern in the developing spinal cord. Science. 274:1996;1115-1123.
49. Tomita K., Nakanishi S., Guillemot F., Kageyama R. Mash1 promotes neuronal differentiation in the retina. Genes Cell. 1:1996;765-774.
50. Torii M., Matsuzaki F., Osumi N., Kaibuchi K., Nakamura S., Casarosa S., Guillemot F., Nakafuku M. Transcription factors Mash-1 and Prox-1 delineate early steps in differentiation of neural stem cells in the developing central nervous system. Development. 126:1999;443-456.
51. Tuttle R., Nakagawa Y., Johnson J. E., O'Leary D. D. M. Defects in thalamocortical axon pathfinding correlate with altered cell domains in embryonic MASH1 deficient mice. Development. 126:1999;1903-1916.
52. van Doren M., Powell P. A., Pasternak D., Singson A., Posakony J. W. Spatial regulation of proneural gene activity: Auto- and cross-activation of achaete is antagonized by extramacrochaetae. Genes Dev. 6:1992;2592-2605.
53. Wettstein D. A., Turner D. L., Kintner C. The Xenopus homolog of Drosophila Suppressor of Hairless mediates Notch signaling during primary neurogenesis. Development. 124:1997;693-702.