Neurogenesis in an annelid: Characterization of brain neural precursors in the polychaete Capitella sp. I

Developmental Biology

Volumn 335, Issue 1, 2009, Pages 237-252

  Meyer, Néva P ^a   Seaver, Elaine C ^a  

^a UNIVERSITY OF HAWAII   (United States)

Author keywords

Achaete scute; Annelid; Brain; Capitella sp. I; elav; Ingression; Lophotrochozoan; Neurogenesis; Polychaete; Proneural

Indexed keywords

BROXURIDINE;

ANIMAL CELL; ANIMAL TISSUE; ANNELID WORM; ARTICLE; BRAIN DEVELOPMENT; CAPITELLA; CELL DIVISION; CONTROLLED STUDY; ECTODERM; EPITHELIUM; GENE EXPRESSION; GENE ISOLATION; IMMUNOHISTOCHEMISTRY; IN SITU HYBRIDIZATION; MICROSCOPY; MITOSIS SPINDLE; NERVOUS SYSTEM DEVELOPMENT; NEURAL STEM CELL; NEUROBLAST; NONHUMAN; POLYCHAETA; PRIORITY JOURNAL;

ANNELIDA; ARTHROPODA; CAPITELLA; HEXAPODA; LOPHOTROCHOZOA; POLYCHAETA; VERTEBRATA;

EID: 70349972018     PISSN: 00121606     EISSN: 1095564X     Source Type: Journal    
DOI: 10.1016/j.ydbio.2009.06.017     Document Type: Article

References (61)

1. Ackermann C., Dorresteijn A., and Fischer A. Clonal domains in postlarval Platynereis dumerilii (Annelida: Polychaeta). J. Morphol. 266 (2005) 258-280
2. Akai J., Halley P.A., and Storey K.G. FGF-dependent Notch signaling maintains the spinal cord stem zone. Genes Dev. 19 (2005) 2877-2887
3. Berger C., Renner S., Luer K., and Technau G.M. The commonly used marker ELAV is transiently expressed in neuroblasts and glial cells in the Drosophila embryonic CNS. Dev. Dyn. 236 (2007) 3562-3568
4. Bertrand N., Castro D.S., and Guillemot F. Proneural genes and the specification of neural cell types. Nat. Rev. Neurosci. 3 (2002) 517-530
5. Birgbauer E., and Fraser S.E. Violation of cell lineage restriction compartments in the chick hindbrain. Development 120 (1994) 1347-1356
6. Birney E., Kumar S., and Krainer A.R. Analysis of the RNA-recognition motif and RS and RGG domains: conservation in metazoan pre-mRNA splicing factors. Nucleic Acids Res. 21 (1993) 5803-5816
7. Cabrera C.V., Martinez-Arias A., and Bate M. The expression of three members of the achaete-scute gene complex correlates with neuroblast segregation in Drosophila. Cell 50 (1987) 425-433
8. Casarosa S., Fode C., and Guillemot F. Mash1 regulates neurogenesis in the ventral telencephalon. Development 126 (1999) 525-534
9. Chipman A.D., and Stollewerk A. Specification of neural precursor identity in the geophilomorph centipede Strigamia maritima. Dev. Biol. 290 (2006) 337-350
10. Chitnis A., and Kintner C. Sensitivity of proneural genes to lateral inhibition affects the pattern of primary neurons in Xenopus embryos. Development 122 (1996) 2295-2301
11. Denes A.S., Jekely G., Steinmetz P.R., Raible F., Snyman H., Prud'homme B., Ferrier D.E., Balavoine G., and Arendt D. Molecular architecture of annelid nerve cord supports common origin of nervous system centralization in bilateria. Cell 129 (2007) 277-288
12. Diez del Corral R., Breitkreuz D.N., and Storey K.G. Onset of neuronal differentiation is regulated by paraxial mesoderm and requires attenuation of FGF signalling. Development 129 (2002) 1681-1691
13. Doe C.Q. Molecular markers for identified neuroblasts and ganglion mother cells in the Drosophila central nervous system. Development 116 (1992) 855-863
14. Doe C.Q., and Goodman C.S. Early events in insect neurogenesis. I. Development and segmental differences in the pattern of neuronal precursor cells. Dev. Biol. 111 (1985) 193-205
15. Doe C.Q., and Goodman C.S. Early events in insect neurogenesis. II. The role of cell interactions and cell lineage in the determination of neuronal precursor cells. Dev. Biol. 111 (1985) 206-219
16. Doe C.Q., Fuerstenberg S., and Peng C.Y. Neural stem cells: from fly to vertebrates. J. Neurobiol. 36 (1998) 111-127
17. Doherty D., Feger G., Younger-Shepherd S., Jan L.Y., and Jan Y.N. Delta is a ventral to dorsal signal complementary to Serrate, another Notch ligand, in Drosophila wing formation. Genes Dev. 10 (1996) 421-434
18. Dove H., and Stollewerk A. Comparative analysis of neurogenesis in the myriapod Glomeris marginata (Diplopoda) suggests more similarities to chelicerates than to insects. Development 130 (2003) 2161-2171
19. Farah M.H., Olson J.M., Sucic H.B., Hume R.I., Tapscott S.J., and Turner D.L. Generation of neurons by transient expression of neural bHLH proteins in mammalian cells. Development 127 (2000) 693-702
20. Frobius A.C., and Seaver E.C. Capitella sp. I homeobrain-like, the first lophotrochozoan member of a novel paired-like homeobox gene family. Gene Expr. Patterns 6 (2006) 985-991
21. Frobius A.C., and Seaver E.C. ParaHox gene expression in the polychaete annelid Capitella sp. I. Dev. Genes Evol. 216 (2006) 81-88
22. Goto H., Tomono Y., Ajiro K., Kosako H., Fujita M., Sakurai M., Okawa K., Iwamatsu A., Okigaki T., Takahashi T., and Inagaki M. Identification of a novel phosphorylation site on histone H3 coupled with mitotic chromosome condensation. J. Biol. Chem. 274 (1999) 25543-25549
23. Hammerle B., and Tejedor F.J. A novel function of DELTA-NOTCH signalling mediates the transition from proliferation to neurogenesis in neural progenitor cells. PLoS ONE 2 (2007) e1169
24. Hartenstein V., and Campos-Ortega J.A. Early neurogenesis in wild-type Drosophila melanogaster. Roux's Archives of Developmental Biology 193 (1984) 308-325
25. Heitzler P., and Simpson P. The choice of cell fate in the epidermis of Drosophila. Cell 64 (1991) 1083-1092
26. Henry J.J.a.M.Q.M. Conservation and innovation in spiralian development. Hydrobiologia 402 (1999) 255-265
27. Jacob M.H. Neurogenesis in Aplysia californica resembles nervous system formation in vertebrates. J. Neurosci. 4 (1984) 1225-1239
28. Jacobson M., and Rao M.S. Developmental Neurobiology (2005), Kluwer Academic/Plenum, New York
29. Kadner D., and Stollewerk A. Neurogenesis in the chilopod Lithobius forficatus suggests more similarities to chelicerates than to insects. Dev. Genes Evol. 214 (2004) 367-379
30. Kramer A.P., and Weisblat D.A. Developmental neural kinship groups in the leech. J. Neurosci. 5 (1985) 388-407
31. Kunisch M., Haenlin M., and Campos-Ortega J.A. Lateral inhibition mediated by the Drosophila neurogenic gene delta is enhanced by proneural proteins. Proc. Natl. Acad. Sci. U. S. A. 91 (1994) 10139-10143
32. Martin-Bermudo M.D., Martinez C., Rodriguez A., and Jimenez F. Distribution and function of the lethal of scute gene product during early neurogenesis in Drosophila. Development 113 (1991) 445-454
33. Mathis L., Kulesa P.M., and Fraser S.E. FGF receptor signalling is required to maintain neural progenitors during Hensen's node progression. Nat. Cell Biol. 3 (2001) 559-566
34. Merkle F.T., and Alvarez-Buylla A. Neural stem cells in mammalian development. Curr. Opin. Cell. Biol. 18 (2006) 704-709
35. Nielsen C. Trochophora larvae: cell-lineages, ciliary bands, and body regions. 1. Annelida and Mollusca. J. Exp. Zoolog. B Mol. Dev. Evol. 302 (2004) 35-68
36. Nieto M., Schuurmans C., Britz O., and Guillemot F. Neural bHLH genes control the neuronal versus glial fate decision in cortical progenitors. Neuron 29 (2001) 401-413
37. Pascale A., Amadio M., and Quattrone A. Defining a neuron: neuronal ELAV proteins. Cell Mol. Life Sci. 65 (2008) 128-140
38. Pearson B.J., and Doe C.Q. Specification of temporal identity in the developing nervous system. Annu. Rev. Cell. Dev. Biol. 20 (2004) 619-647
39. Robinow S., and White K. Characterization and spatial distribution of the ELAV protein during Drosophila melanogaster development. J. Neurobiol. 22 (1991) 443-461
40. Samson M.L. Rapid functional diversification in the structurally conserved ELAV family of neuronal RNA binding proteins. BMC Genomics 9 392 (2008)
41. Seaver E.C., and Kaneshige L.M. Expression of 'segmentation' genes during larval and juvenile development in the polychaetes Capitella sp. I and H. elegans. Dev. Biol. 289 (2006) 179-194
42. Seaver E.C., Paulson D.A., Irvine S.Q., and Martindale M.Q. The spatial and temporal expression of Ch-en, the engrailed gene in the polychaete Chaetopterus, does not support a role in body axis segmentation. Dev. Biol. 236 (2001) 195-209
43. Seaver E.C., Thamm K., and Hill S.D. Growth patterns during segmentation in the two polychaete annelids, Capitella sp. I and Hydroides elegans: comparisons at distinct life history stages. Evol. Dev. 7 (2005) 312-326
44. Shankland M. Formation and specification of neurons during the development of the leech central nervous system. J. Neurobiol. 27 (1995) 294-309
45. Shook D., and Keller R. Mechanisms, mechanics and function of epithelial-mesenchymal transitions in early development. Mech. Dev. 120 (2003) 1351-1383
46. Simionato E., Kerner P., Dray N., Le Gouar M., Ledent V., Arendt D., and Vervoort M. atonal- and achaete-scute-related genes in the annelid Platynereis dumerilii: insights into the evolution of neural basic-Helix-Loop-Helix genes. BMC Evol. Biol. 8 (2008) 170
47. Skeath J.B. At the nexus between pattern formation and cell-type specification: the generation of individual neuroblast fates in the Drosophila embryonic central nervous system. Bioessays 21 (1999) 922-931
48. Skeath J.B., and Carroll S.B. Regulation of proneural gene expression and cell fate during neuroblast segregation in the Drosophila embryo. Development 114 (1992) 939-946
49. Skeath J.B., and Thor S. Genetic control of Drosophila nerve cord development. Curr. Opin. Neurobiol. 13 (2003) 8-15
50. Stollewerk A. Recruitment of cell groups through Delta/Notch signalling during spider neurogenesis. Development 129 (2002) 5339-5348
51. Stollewerk A., and Simpson P. Evolution of early development of the nervous system: a comparison between arthropods. Bioessays 27 (2005) 874-883
52. Stollewerk A., Weller M., and Tautz D. Neurogenesis in the spider Cupiennius salei. Development 128 (2001) 2673-2688
53. Thamm K., and Seaver E.C. Notch signaling during larval and juvenile development in the polychaete annelid Capitella sp. I. Dev. Biol. 320 (2008) 304-318
54. Tomita K., Moriyoshi K., Nakanishi S., Guillemot F., and Kageyama R. Mammalian achaete-scute and atonal homologs regulate neuronal versus glial fate determination in the central nervous system. EMBO J. 19 (2000) 5460-5472
55. Torrence S.A., and Stuart D.K. Gangliogenesis in leech embryos: migration of neural precursor cells. J. Neurosci. 6 (1986) 2736-2746
56. Turner D.L., and Weintraub H. Expression of achaete-scute homolog 3 in Xenopus embryos converts ectodermal cells to a neural fate. Genes Dev. 8 (1994) 1434-1447
57. Urbach R., Schnabel R., and Technau G.M. The pattern of neuroblast formation, mitotic domains and proneural gene expression during early brain development in Drosophila. Development 130 (2003) 3589-3606
58. Wakamatsu Y., and Weston J.A. Sequential expression and role of Hu RNA-binding proteins during neurogenesis. Development 124 (1997) 3449-3460
59. Yim S.J., Lee Y.S., Lee J.A., Chang D.J., Han J.H., Kim H., Park H., Jun H., Kim V.N., and Kaang B.K. Regulation of ApC/EBP mRNA by the Aplysia AU-rich element-binding protein, ApELAV, and its effects on 5-hydroxytryptamine-induced long-term facilitation. J. Neurochem. 98 (2006) 420-429
60. Yoon K., and Gaiano N. Notch signaling in the mammalian central nervous system: insights from mouse mutants. Nat. Neurosci. 8 (2005) 709-715
61. Younossi-Hartenstein A., Nassif C., Green P., and Hartenstein V. Early neurogenesis of the Drosophila brain. J. Comp. Neurol. 370 (1996) 313-329