Programming neural Hoxd10: In vivo evidence that early node-associated signals predominate over paraxial mesoderm signals at posterior spinal levels

Developmental Biology

Volumn 261, Issue 1, 2003, Pages 99-115

  Omelchenko, Natalia ^a   Lance Jones, Cynthia ^a  

^a UNIVERSITY OF PITTSBURGH SCHOOL OF MEDICINE   (United States)

Author keywords

Axial patterning; Chick embryo; Hensen's node; Hox genes; Paraxial mesoderm; Spinal cord; Tailbud

Indexed keywords

ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; CONTROLLED STUDY; DEVELOPMENTAL STAGE; DNA TRANSPOSITION; EMBRYO; EMBRYONAL TISSUE; EMBRYONIC STRUCTURES; FOWL; GENE EXPRESSION; GENETIC ANALYSIS; HOX GENE; HOXD10 GENE; IN VIVO STUDY; ISOLATION PROCEDURE; LUMBOSACRAL SPINE; MESODERM; NEURAL TUBE; NEUROECTODERM; NONHUMAN; PRIORITY JOURNAL; SPINAL CORD; TAIL;

AVES;

EID: 0041661955     PISSN: 00121606     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0012-1606(03)00280-X     Document Type: Article

References (51)

1. Akam M. The molecular basis for metameric pattern in the Drosophila embryo. Development. 101:1987;1-22.
2. Bell E., Wingate R.J., Lumsden A. Homeotic transformation of rhombomere identity after localized Hoxb1 misexpression. Science. 284:1999;2168-2171.
3. Belting H.G., Shashikant C.S., Ruddle F.H. Multiple phases of expression and regulation of mouse Hoxc8 during early embryogenesis. J. Exp. Zool. 282:1998;196-222.
4. Berggren K., McCaffery P., Drager U., Forehand C.J. Differential distribution of retinoic acid synthesis in the chicken embryo as determined by immunolocalization of the retinoic acid synthetic enzyme, RALDH-2. Dev. Biol. 210:1999;288-304.
5. Burke A.C., Nelson C.E., Morgan B.A., Tabin C. Hox genes and the evolution of vertebrate axial morphology. Development. 121:1995;333-346.
6. Capecchi M.R. Hox genes and mammalian development. Cold Spring Harbor Symp. Quant. Biol. 62:1997;273-281.
7. Carpenter E.M. Hox genes and spinal cord development. Dev. Neurosci. 24:2002;24-34.
8. Carpenter E.M., Goddard J.M., Davis A.P., Nguyen T.P., Capecchi M.R. Targeted disruption of Hoxd-10 affects mouse hindlimb development. Development. 124:1997;4505-4514.
9. Catala M., Teillet M.A., De Robertis E.M., Le Douarin M.L. A spinal cord fate map in the avian embryo while regressing, Hensen's node lays down the notochord and floor plate thus joining the spinal cord lateral walls . Development. 122:1996;2599-2610.
10. Catala M., Teillet M.A., Le Douarin N.M. Organization and development of the tail bud analyzed with the quail-chick chimaera system. Mech. Dev. 51:1995;51-65.
11. Chevallier A., Kieny M., Mauger A., Sengel P. Developmental fate of the somitic mesoderm in the chick embryo. Ede D.A., Hinchliffe J.R., Balls M. Vertebrate Limb and Somite Morphogenesis. 1977;421-432 Cambridge University Press, London.
12. Christ B., Jacob H.J., Jacob M. Differentiating abilities of avian somatopleural mesoderm. Experientia. 35:1979;1376-1378.
13. Colas J.F., Schoenwolf G.C. Towards a cellular and molecular understanding of neurulation. Dev. Dyn. 221:2001;117-145.
14. Dias M.S., Schoenwolf G.C. Formation of ectopic neurepithelium in chick blastoderms age-related capacities for induction and self-differentiation following transplantation of quail Hensen's nodes . Anat. Rec. 228:1990;437-448.
15. Ensini M., Tsuchida T.N., Belting H.G., Jessell T.M. The control of rostrocaudal pattern in the developing spinal cord specification of motor neuron subtype identity is initiated by signals from paraxial mesoderm . Development. 125:1998;969-982.
16. Garcia-Martinez V., Schoenwolf G.C. Positional control of mesoderm movement and fate during avian gastrulation and neurulation. Dev. Dyn. 193:1992;249-256.
17. Gaunt S.J. Conservation in the Hox code during morphological evolution. Int. J. Dev. Biol. 38:1994;549-552.
18. Gaunt S.J., Strachan L. Forward spreading in the establishment of a vertebrate Hox expression boundry the expression domain separates Into anterior and posterior zones, and the spread occurs across implanted glass barriers . Dev. Dyn. 199:1994;229-240.
19. Goldstein R.S., Kalcheim C. Determination of epithelial half-somites in skeletal morphogenesis. Development. 116:1992;441-445.
20. Grapin-Botton A., Bonnin M.A., Le Douarin N.M. Hox gene induction in the neural tube depends on three parameters competence, signal supply and paralogue group . Development. 124:1997;849-859.
21. Grapin-Botton A., Bonnin M.A., McNaughton L.A., Krumlauf R., Le Douarin N.M. Plasticity of transposed rhombomeres Hox gene induction is correlated with phenotypic modifications . Development. 121:1995;2707-2721.
22. Guthrie S., Muchamore I., Kuroiwa A., Marshall H., Krumlauf R., Lumsden A. Neuroectodermal autonomy of Hox-2.9 expression revealed by rhombomere transpositions. Nature. 356:1992;157-159.
23. Hamburger V., Hamilton H.L. A series of normal stages in the development of the chick embryo. J. Morphol. 88:1951;49-92.
24. Inagaki T., Schoenwolf G.C. Axis development in avian embryos the ability of Hensen's node to self-differentiate, as analyzed with heterochronic grafting experiments . Anat. Embryol. 188:1993;1-11.
25. Itasaki N., Sharpe J., Morrison A., Krumlauf R. Reprogramming Hox expression in the vertebrate hindbrain influence of paraxial mesoderm and rhombomere transposition . Neuron. 16:1996;487-500.
26. Jungbluth S., Bell E., Lumsden A. Specification of distinct motor neuron identities by the singular activities of individual Hox genes. Development. 126:1999;2751-2758.
27. Kant R., Goldstein R.S. Plasticity of axial identity among somites cranial somites can generate vertebrate without expressing Hox genes appropriate to the trunk . Dev. Biol. 216:1999;507-520.
28. Kelly W.L., Bryden M.M. A modified differential stain for cartilage and bone in whole mount preparations of mammalian fetuses and small vertebrates. Stain Technol. 58:1983;131-134.
29. Kieny M., Mauger A., Sengel P. Early regionalization of the somitic mesoderm as studied by the development of the axial skeleton of the chick embryo. Dev. Biol. 28:1972;142-161.
30. Knezevic V., De Santo R., Mackem S. Continuing organizer function during chick tail development. Development. 125:1998;1791-1801.
31. Krumlauf R. Hox genes in vertebrate development. Cell. 78:1994;191-201.
32. Kuratani S.C., Eichele G. Rhombomere transplantation repatterns the segmental organization of cranial nerves and reveals cell-autonomous expression of a homeodomain protein. Development. 117:1993;105-117.
33. Lance-Jones C., Omelchenko N., Bailis A., Lynch S., Sharma K. Hoxd10 induction and regionalization in the developing lumbosacral spinal cord. Development. 128:2001;2255-2268.
34. Liu J.P., Laufer E., Jessell T.M. Assigning the positional identity of spinal motor neurons, rostrocaudal patterning of Hox-c expression by FGFs, Gdf11, and Retinoids. Neuron. 32:2001;997-1012.
35. Lumsden A., Keynes R. Segmental patterns of neuronal development in the chick hindbrain. Nature. 337:1989;424-428.
36. Maden M., Sonneveld E., van der Saag P.T., Gale E. The distribution of endogenous retinoic acid in the chick embryo implications for developmental mechanisms . Development. 125:1998;4133-4144.
37. Matise M.P., Lance-Jones C. A critical period for the specification of motor pools in the chick lumbosacral spinal cord. Development. 122:1996;659-669.
38. McGinnis W., Krumlauf R. Homeobox genes and axial patterning. Cell. 68:1992;283-302.
39. Nieto M.A., Patel K., Wilkinson D.G. In situ hybridization analysis of chick embryos in whole mount and tissue sections. Methods Cell Biol. 51:1996;219-235.
40. Nowicki J.L., Burke A.C. Hox genes and morphological identity axial versus lateral patterning in the vertebrate mesoderm . Development. 127:2000;4265-4275.
41. Omelchenko N., Lance-Jones C. Stage-dependent influence of Hensen's node on Hoxd-10 expression in the developing spinal cord. Soc. Neurosci. Abstr. 26:2000;50.
42. Rijli F.M., Gavalas A., Chambon P. Segmentation and specification in the branchial region of the head the role of the Hox selector genes . Int. J. Dev. Biol. 42:1998;393-401.
43. Schaeren-Wiemers N., 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 digoxygenin- labelled cRNA probes . Histochemistry. 100:1993;431-440.
44. Schoenwolf G.C. Tail (end) bud contributions to the posterior region of the chick embryo. J. Exp. Zool. 201:1977;227-246.
45. Schoenwolf G.C. Effects of complete tail bud extirpation on early development of the posterior region of the chick embryo. Anat. Rec. 192:1978;289-295.
46. Schoenwolf G.C. Shaping and bending of the avian neuroepithelium morphometric analyses . Dev. Biol. 109:1985;127-139.
47. Schoenwolf G.C., Sheard P. Fate mapping the avian epiblast with focal injections of a fluorescent-histochemical marker ectodermal derivatives . J. Exp. Zool. 255:1990;323-339.
48. Selleck M.A., Stern C.D. Fate mapping and cell lineage analysis of Hensen's node in the chick embryo. Development. 112:1991;615-626.
49. Simon H., Hornbruch A., Lumsden A. Independent assignment of antero-posterior and dorso-ventral positional values in the developing chick hindbrain. Curr. Biol. 5:1995;205-214.
50. Swindell E.C., Thaller C., Sockanathan S., Petkovich M., Jessell T.M., Eichele G. Complementary domains of retinoic acid production and degradation in the early chick embryo. Dev. Biol. 216:1999;282-296.
51. Trainor P., Krumlauf R. Plasticity in mouse neural crest cells reveals a new patterning role for cranial mesoderm. Nat. Cell Biol. 2:2000;96-102.