Transdifferentiation of esophageal smooth to skeletal muscle is myogenic bHLH factor-dependent

Development

Volumn 127, Issue 8, 2000, Pages 1627-1639

  Kablar, Boris ^a   Tajbakhsh, Shahragim ^b   Rudnicki, Michael A ^a  

^a MCMASTER UNIVERSITY   (Canada)

^b INSTITUT PASTEUR   (France)

Author keywords

Esophagus; Myf5; MyoD; Skeletal muscle; Transdifferentiation

Indexed keywords

MYOGENIC FACTOR;

ANIMAL CELL; ANIMAL TISSUE; ARTICLE; CELL PROLIFERATION; EMBRYO; ESOPHAGUS MUSCLE; MOUSE; MUSCLE DEVELOPMENT; NONHUMAN; PRIORITY JOURNAL; SKELETAL MUSCLE; SMOOTH MUSCLE; STEM CELL; TISSUE DIFFERENTIATION;

ANIMALS; CELL DIFFERENTIATION; CELL DIVISION; DNA-BINDING PROTEINS; ESOPHAGUS; MICE; MICE, TRANSGENIC; MUSCLE PROTEINS; MUSCLE, SKELETAL; MUSCLE, SMOOTH; MYOD PROTEIN; MYOGENIC REGULATORY FACTOR 5; MYOGENIN; TRANS-ACTIVATORS;

ANIMALIA;

EID: 0343183280     PISSN: 09501991     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (57)

1. Anderson, D. J. (1989). Cellular 'neoteny': a possible developmental basis for chromaffin cell plasticity. Trends Genet 5, 174-178.
2. Asakura, A., Lyons, G. E. and Tapscott, S. J. (1995). The regulation of MyoD gene expression: conserved elements mediate expression in embryonic axial muscle. Dev. Biol. 171, 386-398.
3. Bader, D., Masaki, T. and Fischmann, D. A. (1982). Immunochemical analysis of myosin heavy chain during avian myogenesis in vivo and in vitro. J. Cell Biol. 95, 763-770.
4. Beresford, W. A. (1990). Direct transdifferentiation: can cells change their pnenotype without dividing? Cell Diff. Dev. 29, 81-93.
5. Blau, H. M. (1992). Differentiation requires continuous active control. Annu. Rev. Biochem. 61, 1213-1230.
6. Braun, T., Rudnicki, M. A., Arnold, H.-H. and Jaenisch, R. (1992). Targeted inactivation of the mouse regulatory gene Myf5 results in abnormal distal rib development and early postnatal death in homozygous mouse mutants. Cell 71, 369-382.
7. Brockes, J. P. (1994). New approaches to amphibian limb regeneration. Trends Genet. 10, 169-173.
8. Cheng, T.-C., Wallace, M. C., Merlie, J. P. and Olson, E. N. (1993). Separable regulatory elements governing myogenin transcription in mouse embryogenesis. Science 261, 215-218.
9. Choi, J., Costa, M. L., Mermelstein, C. S., Chagas, C., Holtzer, S. and Holtzer, H. (1990). MyoD converts primary dermal fibroblasts, chondroblasts, smooth muscles and retinal pigmented epithelial cells into striated mononucleated myoblasts and multinucleated myotubes. Proc. Natl. Acad. Sci. USA 87, 7988-7992.
10. Christ, B. and Ordahl, C. P. (1995). Early stages of chick somite development. Anal. Embroyl. 191, 381-396.
11. Epstein, M. L., Mikawa, T., Brown, A. M. C. and McFarlin, D. R. (1994). Mapping the origin of the avian enteric nervous system with a retroviral marker. Dev. Dyn. 201, 236-244.
12. Gavrieli, Y., Sherman, Y. and Ben-Sasson, S. A. (1992). Identification of programmed cell death in situ via specific labeling of nuclear DNA fragmentation. J. Cell Biol. 119, 493-501.
13. Gershon, M. D., Sherman, D. and Gintzler, A. R. (1981). An ultrastructural analysis of the developing enteric nervous system of the guinea pig small intestine. J. Neurocytol. 10, 271-296.
14. Goldhamer, D. J., Brunk, B. P., Faerman, A., King, A., Shani, M. and Emerson, C. P. (1995). Embryonic activation of the MyoD gene is regulated by a highly conserved distal control element. Development 121, 637-649.
15. Hasty, P., Bradley, A., Morris, J. H., Edmondson, D. G., Venuti, J., Olson, E. N. and Klein, W. H. (1993). Muscle deficiency and neonatal death in mice with targeted mutation in the myogenin gene. Nature 364, 501-506.
16. Hauschka, S. D. (1994). The Embryonic Origin of Muscle. In Myology, 2nd edition (ed. A. G. Engel and C. Franzini-Armstrong), pp. 3-73. New York: McGraw-Hill.
17. Hitchcock, P. F. and Raymond, P. A. (1992). Retinal regeneration. Trends Neurosci. 15, 103-108.
18. Holtzer, H., Rubinstein, N., Fellini, S., Yeoh, G., Chi, J., Birnbaum, J. and Okayawa, M. (1975). Lineages, quantal cell cycles, and the generation of cell diversity. Q. Rev. Biophys. 8, 523-557.
19. Juric-Lekic, G., Bulic-Jakus, F., Kablar, B. and Svajger, A. (1991). The ability of the epithelium of diencephalic origin to differentiate into cells of the ocular lens. Int. J. Dev. Biol. 35, 231-237.
20. Kablar, B. (1995). Structural study on the appearance of innervation in the stomach of mouse and rat embryos. Tissue Cell 21, 309-315.
21. Kablar, B., Krastel, K., Ying, C., Asakura, A., Tapscott, S. J. and Rudnicki, M. A. (1997). MyoD and Myf-5 differentially regulate the development of limb versus trunk skeletal muscle. Development 124, 4729-4738.
22. Kablar, B., Asakura A., Krastel, K., Ying, C., May, L. L., Goldhamer, D. J. and Rudnicki, M. A. (1998). MyoD and Myf-5 define the specification of musculature of distinct embryonic origin. Biochem. Cell Biol. 76, 1-13.
23. Kablar, B., Krastel, K., Ying, C., Tapscott, S. J., Goldhamer, D. J. and Rudnicki, M. A. (1999). Myogenic determination occurs independently in somites and limb buds. Dev. Biol. 206, 219-231.
24. Laird, P. W., Zijderveld, A., Linders, K., Rudnicki, M. A., Jaenisch, R. and Berns, A. (1991). Simplified mammalian DNA isolation procedure. Nucl. Acids Res. 19, 4293.
25. Landis, S. C. (1990). Target regulation of neurotransmitter phenotype. Trends Neurosci. 13, 344-350.
26. Link, B. A. and Nishi, R. (1998). Development of the avian iris and ciliary body: mechanisms of cellular differentiation during the smooth-to-striated muscle transition. Dev. Biol. 203, 163-176.
27. Litingtung, Y., Lei, L., Westphal, H. and Chiang, C. (1998). Sonic hedgehog is essential to foregut development. Nature Genet. 20, 58-61.
28. Megeney, L. A. and Rudnicki, M. A. (1995). Determination versus differentiation and the MyoD-family of transcription factors. Biochem. Cell Biol. 73, 723-732.
29. Miner, J. H., Miller, J. B. and Wold, B. J. (1992). Skeletal muscle phenotypes initiated by ectopic MyoD in transgenic mouse heart. Development 114, 853-860.
30. Minoo, P., Su, G., Drum, H., Bringas, P. and Kimura, S. (1999). Defects in tracheoesophageal and lung morphogenesis in Nkx2.1(-/-) mouse embryos. Dev. Biol. 209, 60-71.
31. Motoyama, J., Liu, J., Mo, R., Ding, Q., Post, M. and Hui, C. (1998). Essential function of Gli2 and Gli3 in the formation of lung, trachea and oesophagus. Nature Genet. 20, 54-57.
32. Naheshima, Y., Hanaoka, K., Hayasaka, M., Esumi, E., Li, S., Nonaka, I. and Nabeshima, Y. (1993). Myogenin gene disruption results in perinatal lethality because of severe muscle defect. Nature 364, 532-535.
33. Nakano, K. E. and Nakamura, H. (1985). Origin of the irideal striated muscle in birds. J. Embryol. Exp. Morph. 88, 1-13.
34. Okada, T. S. (1991). Transdifferentiation: Flexibility in Cell Differentiation. Oxford: Clarendon Press.
35. Ordahl, C. P. and Williams, B. A. (1988). Knowing chops from chuck: roasting MyoD redundancy. BioEssay 20, 357-362.
36. Ordahl, C. P. and Le Douarin, N. (1992). Two myogenic cell lineages within the developing somite. Development 114, 339-353.
37. Patapoutian, A., Yoon, J. K., Miner, J. H., Wang, S., Stark, K. and Wold, B. (1995a). Disruption of the mouse MRF4 gene identities multiple waves of myogenesis in the myotome. Development 121, 3347-3358.
38. Patapoutian, A., Wold, B. J. and Wagner, R. A. (1995b). Evidence for developmentally programmed transdifferentiation in mouse esophageal muscle. Science 270, 1818-1821.
39. Patterson, P. H. (1990). Control of cell fate in a vertebrate neurogenic lineage. Cell 62, 1035-1038.
40. Pritchard, D. J. (1981). Transdifferentiation of chicken embryonic neural retina into pigment epithelium: indications of its biochemical basis. J. Embryol. Exp. Morph. 72, 457-462.
41. Rudnicki, M. A., Braun, T., Hinuma, S. and Jaenisch, R. (1992). Inactivation of MyoD in mice leads to upregulation of the myogenic HLH gene Myf5 and results in apparently normal muscle development. Cell 71, 383-390.
42. Rudnicki, M. A., Schnegelsberg, P. N. J., Stead, R. H., Braun, T., Arnold, H.-H. and Jaenisch, R. (1993). MyoD or Myf-5 is required for the formation of skeletal muscle. Cell 75, 1351-1359.
43. Rudnicki, M. A. and Jaenisch, R. (1995). The MyoD family of transcription factors and skeletal myogenesis. BioEssay 17, 203-209.
44. Samarasinghe, D. D. (1972). Some observations on the innervation of the striated muscle in the mouse esophagus-an electron microscope study. J. Anat. 112, 173-184.
45. Sambrook, J., Fritsch, E. F. and Maniatis, T. (1989). Molecular Cloning: A Laboratory Manual. Cold Spring Harbor, Cold Spring Harbor Laboratory Press
46. Sang, Q. and Young, H. M. (1997). Development of nicotinic receptor clusters and innervation accompanying the change in muscle phenotype in the mouse esophagus. J. Comp. Neurol. 386, 119-136.
47. Sang, Q. and Young, H. M. (1998). The origin and development of the vagal and spinal innervation of the external muscle of the mouse esophagus. Brain Res. 809, 253-268.
48. Tajbakhsh, S., Rocancourt, D. and Buckingham M. (1996). Muscle progenitor cells failing to respond to positional cues adopt non-myogenic fates in myf-5 null mice. Nature 384, 266-270
49. Tajhakhsh, S., Rocancourt, D., Cossu, G. and Buckingham, M. (1997). Redefining the genetic hierarchies controlling skeletal myogenesis: Pax-3 and myf-5 act upstream of myoD. Cell 89, 127-138.
50. Tajbakhsh, S. and Spörle, R. (1998). Somite development: constructing the vertebrate body. Cell 92, 9-16.
51. Tapscott, S. J., Lassar, A. B. and Weintrauh, H. (1992). A novel myoblast enhancer element mediates MyoD transcription. Mol. Cell. Biol. 12, 4994-5003.
52. Volpe, P., Biral, D., Pizzo, P., Salviati, G. and Margreth, A. (1993). Ontogenesis of chick iris intrinsic muscle: evidence for a smooth-to-striated muscle transition. Dev. Biol. 159, 441-449.
53. Wang, Y., Schnegelsberg, P. N. J., Dausman, J. and Jaenish, R. (1996) Functional redundancy of the muscle-specific transcription factors Myf5 and myogenin. Nature 379, 823-825.
54. Weintraub, H., Tapscott, S. J., Davis, R. L., Thayer, M. J., Adam, M. A., Lassar, A. B. and Miller, A. D. (1989). Activation of muscle-specific genes in pigment, nerve, fat, liver, and fibroblast cell lines by forced expression of MyoD. Proc. Natl. Acad. Sci. USA 86, 5434-5438.
55. Weintraub, H., Davis, R., Tapscott, S., Thayer, M., Krause, M., Benezra, B., Blackwell, T. K., Turner, D., Rupp, R., Hollenberg, S., Zhuang, Y. and Lassar, A. (1991). The MyoD gene family: Nodal point during specification of the muscle cell lineage. Science 251, 761-766.
56. Yamashita, T. and Sohal, G. S. (1987). Embryonic origin of skeletal muscle in the iris of the duck and quail. Cell Tissue Res. 224, 121-131.
57. Zhang, W., Behringer, R. R. and Olson, E. N. (1995). Inactivation of the myogenic bHLH gene MRF4 results in upregulation of myogenin and rib anomalies. Genes Dev. 9, 1388-1399.