Altered neuronal lineages in the facial ganglia of Hoxa2 mutant mice

Developmental Biology

Volumn 314, Issue 1, 2008, Pages 171-188

  Yang, Xiu ^a   Zhou, Yuefang ^b   Barcarse, Erin A ^a   O'Gorman, Stephen ^a  

^a CASE WESTERN RESERVE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b SAINT LOUIS UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

Cranial ganglia; Hox genes; Hoxa2; Lineage marking; Meis; Neural crest; Neurogenesis; P19 cells; Pbx

Indexed keywords

HOX PROTEIN; MEIS PROTEIN; PBX PROTEIN; UNCLASSIFIED DRUG;

ANIMAL CELL; ANIMAL EXPERIMENT; ARTICLE; CARCINOMA CELL; CELL CULTURE; CELL DIFFERENTIATION; CELL LINEAGE; CELL TRANSFORMATION; CHICK; CONTROLLED STUDY; EMBRYO; GANGLION; GENE; GENE EXPRESSION; GENE FUNCTION; GENE OVEREXPRESSION; HOXA2 GENE; MOUSE; NERVE CELL; NERVOUS SYSTEM DEVELOPMENT; NONHUMAN; PRIORITY JOURNAL;

MUS;

EID: 38349086949     PISSN: 00121606     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ydbio.2007.11.032     Document Type: Article

References (90)

1. Altman J., and Bayer S.A. Development of the cranial nerve ganglia and related nuclei in the rat. Adv. Anat. Embryol. Cell Biol. 74 (1982) 1-90
2. Anderson D.J. Cellular and molecular biology of neural crest cell lineage determination. Trends Genet. 13 (1997) 276-280
3. Arenkiel B.R., et al. Hoxb1 neural crest preferentially form glia of the PNS. Dev. Dyn. 227 (2003) 379-386
4. Aubin J., et al. Transcriptional interferences at the Hoxa4/Hoxa5 locus: importance of correct Hoxa5 expression for the proper specification of the axial skeleton. Dev. Dyn. 212 (1998) 141-156
5. Ayer-LeLievre C.S., and LeDouarin N.M. The early development of cranial sensory ganglia and the potentialities of their component cells studied in quail-chick chimeras. Dev. Biol. 94 (1982) 291-310
6. Baker C.V., et al. Early- and late-migrating cranial neural crest cell populations have equivalent developmental potential in vivo. Development 124 (1997) 3077-3087
7. Barrow J.R., and Capecchi M.R. Targeted disruption of the Hoxb-2 locus in mice interferes with expression of Hoxb-1 and Hoxb-4. Development 122 (1996) 3817-3828
8. Bettenhausen B., et al. Transient and restricted expression during mouse embryogenesis of Dll1, a murine gene closely related to Drosophila Delta. Development 121 (1995) 2407-2418
9. Boudreau N., et al. Induction of the angiogenic phenotype by Hox D3. J. Cell Biol. 139 (1997) 257-264
10. Conlon R.A., et al. Notch1 is required for the coordinate segmentation of somites. Development 121 (1995) 1533-1545
11. Conover J.C., et al. Neuronal deficits, not involving motor neurons, in mice lacking BDNF and/or NT4. Nature 375 (1995) 235-238
12. Couly G., et al. The regeneration of the cephalic neural crest, a problem revisited: the regenerating cells originate from the contralateral or from the anterior and posterior neural fold. Development 122 (1996) 3393-3407
13. Couly G., et al. Determination of the identity of the derivatives of the cephalic neural crest: incompatibility between Hox gene expression and lower jaw development. Development 125 (1998) 3445-3459
14. Couly G., et al. Interactions between Hox-negative cephalic neural crest cells and the foregut endoderm in patterning the facial skeleton in the vertebrate head. Development 129 (2002) 1061-1073
15. Creuzet S., et al. Negative effect of Hox gene expression on the development of the neural crest-derived facial skeleton. Development 129 (2002) 4301-4313
16. d'Amico-Martel A., and Noden D.M. An autoradiographic analysis of the development of the chick trigeminal ganglion. J. Embryol. Exp. Morphol. 55 (1980) 167-182
17. d'Amico-Martel A., and Noden D.M. Contributions of placodal and neural crest cells to avian cranial peripheral ganglia. J. Comp. Neurol. 166 (1983) 445-468
18. Davenne M., et al. Hoxa2 and Hoxb2 control dorsoventral patterns of neuronal development in the rostral hindbrain. Neuron 22 (1999) 677-691
19. Dong Z., et al. Neu differentiation factor is a neuron-glia signal and regulates survival, proliferation, and maturation of rat Schwann cell precursors. Neuron 15 (1995) 585-596
20. Duboule D. Patterning in the vertebrate limb. Curr. Opin. Genet. Dev. 1 (1991) 211-216
21. Duboule D., and Morata G. Colinearity and functional hierarchy among genes of the homeotic complexes. Trends Genet. 10 (1994) 358-364
22. Dunwoodie S.L., et al. Mouse Dll3: a novel divergent Delta gene which may complement the function of other Delta homologues during early pattern formation in the mouse embryo. Development 124 (1997) 3065-3076
23. Ericson J., et al. Early stages of motor neuron differentiation revealed by expression of homeobox gene Islet-1. Science 256 (1992) 1555-1560
24. Featherstone M.S., et al. Hox-5.1 defines a homeobox-containing gene locus on mouse chromosome 2. Proc. Natl. Acad. Sci. U. S. A. 85 (1988) 4760-4764
25. Fode C., et al. The bHLH protein Neurogenin 2 is a determination factor for epibranchial placode-derived sensory neurons. Neuron 20 (1998) 483-494
26. Frohman M.A., et al. Isolation of the mouse Hox-2.9 gene; analysis of embryonic expression suggests that positional information along the anterior-posterior axis is specified by mesoderm. Development 110 (1990) 589-607
27. Gendron-Maguire M., et al. Hoxa-2 mutant mice exhibit homeotic transformation of skeletal elements derived from cranial neural crest. Cell 75 (1993) 1317-1331
28. Goddard J.M., et al. Mice with targeted disruption of Hoxb-1 fail to form the motor nucleus of the VIIth nerve. Development 122 (1996) 3217-3228
29. Gonzalez-Reyes A., and Morata G. The developmental effect of overexpressing a Ubx product in Drosophila embryos is dependent on its interactions with other homeotic products. Cell 61 (1990) 515-522
30. Gonzalez-Reyes A., et al. Are cross-regulatory interactions between homeotic genes functionally significant. Nature 344 (1990) 78-80
31. Gorski J.A., and Jones K.R. Efficient bicistronic expression of cre in mammalian cells. Nucleic Acids Res. 27 (1999) 2059-2061
32. Grammatopoulos G.A., et al. Homeotic transformation of branchial arch identity after Hoxa2 overexpression. Development 127 (2000) 5355-5365
33. Harrison T.A., et al. Compensatory responses and development of the nodose ganglion following ablation of placodal precursors in the embryonic chick (Gallus domesticus). Cell Tissue Res. 281 (1995) 379-385
34. Hirsch M.R., et al. Control of noradrenergic differentiation and Phox2a expression by MASH1 in the central and peripheral nervous system. Development 125 (1998) 599-608
35. Huang E.J., and Reichardt L.F. Neurotrophins: roles in neuronal development and function. Annu. Rev. Neurosci. 24 (2001) 677-736
36. Huang E.J., and Reichardt L.F. TRK receptors: roles in neuronal signal transduction. Annu. Rev. Biochem. 72 (2003) 609-642
37. Jones K.R., et al. Targeted disruption of the BDNF gene perturbs brain and sensory neuron development but not motor neuron development. Cell 76 (1994) 989-999
38. Jones-Villeneuve E.M., et al. Retinoic acid induces embryonal carcinoma cells to differentiate into neurons and glial cells. J. Cell Biol. 94 (1982) 253-262
39. Knoepfler P.S., and Kamps M.P. The pentapeptide motif of Hox proteins is required for cooperative DNA binding with Pbx1, physically contacts Pbx1, and enhances DNA binding by Pbx1. Mol. Cell. Biol. 15 (1995) 5811-5819
40. Knoepfler P.S., and Kamps M.P. The Pbx family of proteins is strongly upregulated by a post-transcriptional mechanism during retinoic acid-induced differentiation of P19 embryonal carcinoma cells. Mech. Dev. 63 (1997) 5-14
41. Knoepfler P.S., et al. A conserved motif N-terminal to the DNA-binding domains of myogenic bHLH transcription factors mediates cooperative DNA binding with pbx-Meis1/Prep1. Nucleic Acids Res. 27 (1999) 3752-3761
42. Kuhlbrodt K., et al. Sox10, a novel transcriptional modulator in glial cells. J. Neurosci. 18 (1998) 237-250
43. Le Douarin N. The Neural Crest (1983), Cambridge Univ. Press, Cambridge
44. Le Douarin N., and Smith J. Development o the peripheral nervous system from the neural crest. Annu. Rev. Cell Biol. 4 (1988) 375-404
45. Lee M.K., et al. The expression and posttranslational modification of a neuron-specific beta-tubulin isotype during chick embryogenesis. Cell Motil. Cytoskeleton 17 (1990) 118-132
46. Lindsell C.E., et al. 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
47. Liu X., and Jaenisch R. Severe peripheral sensory neuron loss and modest motor neuron reduction in mice with combined deficiency of brain-derived neurotrophic factor, neurotrophin 3 and neurotrophin 4/5. Dev. Dyn. 218 (2000) 94-101
48. Lo L., et al. 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
49. Lo L., et al. Comparison of the generic neuronal differentiation and neuron subtype specification functions of mammalian achaete-scute and atonal homologs in cultured neural progenitor cells. Development 129 (2002) 1553-1567
50. Lumsden A., et al. Segmental origin and migration of neural crest cells in the hindbrain region of the chick embryo. Development 113 (1991) 1281-1291
51. Ma Q., et al. Identification of neurogenin, a vertebrate neuronal determination gene. Cell 87 (1996) 43-52
52. Ma Q., et al. Neurogenin1 is essential for the determination of neuronal precursors for proximal cranial sensory ganglia. Neuron 20 (1998) 469-482
53. Ma Q., et al. Neurogenin1 and Neurogenin2 control two distinct waves of neurogenesis in developing dorsal root ganglia. Genes Dev. 13 (1999) 1717-1728
54. Manley N.R., and Capecchi M.R. Hox group 3 paralogous genes act synergistically in the formation of somitic and neural crest-derived structures. Dev. Biol. 192 (1997) 274-288
55. Matsumoto I., et al. A comparative study of three cranial sensory ganglia projecting into the oral cavity: in situ hybridization analyses of neurotrophin receptors and thermosensitive cation channels. Brain Res. Mol. Brain Res. 93 (2001) 105-112
56. McGonnell I.M., and Graham A. Trunk neural crest has skeletogenic potential. Curr. Biol. 12 (2002) 767-771
57. Moens C.B., and Selleri L. Hox cofactors in vertebrate development. Dev. Biol. 291 (2006) 193-206
58. Morin X., et al. Defects in sensory and autonomic ganglia and absence of locus coeruleus in mice deficient for the homeobox gene Phox2a. Neuron 18 (1997) 411-423
59. Murphy P., and Hill R.E. Expression of the mouse labial-like homeobox-containing genes, Hox 2.9 and Hox 1.6, during segmentation of the hindbrain. Development 111 (1991) 61-74
60. Murphy P., et al. Segment-specific expression of a homoeobox-containing gene in the mouse hindbrain. Nature 341 (1989) 156-159
61. Myat A., et al. A chick homologue of Serrate and its relationship with Notch and Delta homologues during central neurogenesis. Dev. Biol. 174 (1996) 233-247
62. Neuteboom S.T., et al. The hexapeptide LFPWMR in Hoxb-8 is required for cooperative DNA binding with Pbx1 and Pbx2 proteins. Proc. Natl. Acad. Sci. U. S. A. 92 (1995) 9166-9170
63. Nichols D.H. Formation and distribution of neural crest mesenchyme to the first pharyngeal arch region of the mouse embryo. Am. J. Anat. 176 (1986) 221-231
64. Noden D.M. The role of the neural crest in patterning of avian cranial skeletal, connective, and muscle tissues. Dev. Biol. 96 (1983) 144-165
65. O'Gorman S., et al. Recombinase-mediated gene activation and site-specific integration in mammalian cells. Science 251 (1991) 1351-1355
66. O'Gorman S., et al. Protamine-Cre recombinase transgenes efficiently recombine target sequences in the male germline of mice, but not in embryonic stem cells. Proc. Natl. Acad. Sci. U. S. A. 94 (1997) 14602-14607
67. Popperl H., and Featherstone M.S. Identification of a retinoic acid response element upstream of the murine Hox-4.2 gene. Mol. Cell. Biol. 13 (1993) 257-265
68. Popperl H., et al. Segmental expression of Hoxb-1 is controlled by a highly conserved autoregulatory loop dependent upon exd/pbx. Cell 81 (1995) 1031-1042
69. Pratt M.A., et al. Retinoic acid fails to induce expression of Hox genes in differentiation-defective murine embryonal carcinoma cells carrying a mutant gene for alpha retinoic acid receptor. Differentiation 53 (1993) 105-113
70. Prince V., and Lumsden A. Hoxa-2 expression in normal and transposed rhombomeres: independent regulation in the neural tube and neural crest. Development 120 (1994) 911-923
71. Qin P., et al. Retinoic acid regulates the expression of PBX1, PBX2, and PBX3 in P19 cells both transcriptionally and post-translationally. J. Cell. Biochem. 92 (2004) 147-163
72. Qin P., et al. Pre-B cell leukemia transcription factor (PBX) proteins are important mediators for retinoic acid-dependent endodermal and neuronal differentiation of mouse embryonal carcinoma P19 cells. J. Biol. Chem. 279 (2004) 16263-16271
73. Raible D.W., and Eisen J.S. Regulative interactions in zebrafish neural crest. Development 122 (1996) 501-507
74. Ren S.Y., et al. Targeted insertion results in a rhombomere 2-specific Hoxa2 knockdown and ectopic activation of Hoxa1 expression. Dev. Dyn. 225 (2002) 305-315
75. Rijli F.M., et al. A homeotic transformation is generated in the rostral branchial region of the head by disruption of Hoxa-2, which acts as a selector gene. Cell 75 (1993) 1333-1349
76. Rijli F.M., et al. Insertion of a targeting construct in a Hoxd-10 allele can influence the control of Hoxd-9 expression. Dev. Dyn. 201 (1994) 366-377
77. Robertson E.J., et al. Germline transmission of genes introduced into cultured pluripotential cells by retroviral vector. Nature 323 (1986) 445-448
78. Rudniki M.A., and McBurney M.W. Cell culture methods and induction of differentiation of embryonal carcinom cell lines. In: Robertson E.J. (Ed). Teratocarcinomas and Embryonic Stem Cells, A Practical Approach (1987), IRL Press, Oxford 19-49
79. Saleh M., et al. Cell signaling switches HOX-PBX complexes from repressors to activators of transcription mediated by histone deacetylases and histone acetyltransferases. Mol. Cell. Biol. 20 (2000) 8623-8633
80. Schaeren-Wiemers N., and Gerfin-Moser A. A single protocol to detect transcripts of various types and expression levels in neural tissue and cultured cells: in situ hybridization using digoxigenin-labelled cRNA probes. Histochemistry 100 (1993) 431-440
81. Sechrist J., et al. Segmental migration of the hindbrain neural crest does not arise from its segmental generation. Development 118 (1993) 691-703
82. Serbedzija G.N., et al. Vital dye analysis of cranial neural crest cell migration in the mouse embryo. Development 116 (1992) 297-307
83. Simeone A., et al. Sequential activation of HOX2 homeobox genes by retinoic acid in human embryonal carcinoma cells. Nature 346 (1990) 763-766
84. Soriano P. Generalized lacZ expression with the ROSA26 Cre reporter strain. Nat. Genet. 21 (1999) 70-71
85. Studer M., et al. Altered segmental identity and abnormal migration of motor neurons in mice lacking Hoxb-1. Nature 384 (1996) 630-634
86. Thomas K.R., and Capecchi M.R. Site-directed mutagenesis by gene targeting in mouse embryo-derived stem cells. Cell 51 (1987) 503-512
87. Trainor P.A., et al. Role of the isthmus and FGFs in resolving the paradox of neural crest plasticity and prepatterning. Science 295 (2002) 1288-1291
88. Tybulewicz V.L., et al. Neonatal lethality and lymphopenia in mice with a homozygous disruption of the c-abl proto-oncogene. Cell 65 (1991) 1153-1163
89. Wakamatsu Y., et al. Fate determination of neural crest cells by NOTCH-mediated lateral inhibition and asymmetrical cell division during gangliogenesis. Development 127 (2000) 2811-2821
90. Wilkinson K.D., et al. The neuron-specific protein PGP 9.5 is a ubiquitin carboxyl-terminal hydrolase. Science 246 (1989) 670-673