Fate restriction in limb muscle precursor cells precedes high-level expression of MyoD family member genes

QUICK SEARCH:

[advanced]

	Author:		Keyword(s):

Home Help Feedback Subscriptions Archive Search Table of Contents

This Article

	Summary
	Full Text (PDF)
	Alert me when this article is cited
	Alert me if a correction is posted

Services

	Email this article to a friend
	Similar articles in this journal
	Similar articles in PubMed
	Alert me to new issues of the journal
	Download to citation manager


Citing Articles

	Citing Articles via HighWire
	Citing Articles via Google Scholar

Google Scholar

	Articles by Williams, B. A.
	Articles by Ordahl, C. P.
	Search for Related Content

PubMed

	PubMed Citation
	Articles by Williams, B. A.
	Articles by Ordahl, C. P.

Amthor, H., Christ, B. and Patel, K (1999). A molecular mechanism enabling continuous embryonic muscle growth \320 a balance between proliferation and differentiation. Development 126, 1041-1053.[Abstract]

Amthor, H., Christ, B., Weil, M. and Patel, K (1998). The importance of timing differentiation during limb muscle development. Curr. Biol 8, 642-652.[Medline]

Anderson, D. J (1994). Stem cells and transcription factors in the development of the mammalian neural crest. FASEB J 8, 707-713.[Abstract]

Antin, P. B., Karp, G. C. and Ordahl, C. P (1991). Transgene expression in the QM myogenic cell line. Dev. Biol 143, 122-129.[Medline]

Antin, P. B. and Ordahl, C. P (1991). Isolation and characterization of an avian myogenic cell line. Dev. Biol 143, 111-121.[Medline]

Brand, B., Christ, B. and Jacob, H. J (1985). An experimental analysis of the developmental capacities of distal parts of avian leg buds. Amer. J. Anat 173, 321-340.

Brand-Saberi, B., Ebensperger, C., Wilting, J., Balling, R. and Christ, B (1993). The ventralizing effect of the notochord on somite differentiation in chick embryos. Anat. Embryol. (Berl) 188, 239-245.[Medline]

Brand-Saberi, B., Krenn, V. and Christ, B (1989). The control of directed myogenic cell migration in the avian limb bud. Anat. Embryol. (Berl) 180, 555-566.[Medline]

Braun, T., Bober, E., Buschhausen-Denker, G., Kohtz, S., Grzeschik, K. H., Arnold, H. H. and Kotz, S (1989). Differential expression of myogenic determination genes in muscle cells: possible autoactivation by the Myf gene products [published erratum appears in EMBO J 1989 Dec;8(13):4358]. EMBO J 8, 3617-3625.[Medline]

Braun, T., Bober, E., Rudnicki, M. A., Jaenisch, R. and Arnold, H. H (1994). MyoD expression marks the onset of skeletal myogenesis in Myf-5 mutant mice. Development 120, 3083-3092.[Abstract]

Braun, T., Buschhausen-Denker, G., Bober, E., Tannich, E. and Arnold, H. H (1989). A novel human muscle factor related to but distinct from MyoD1 induces myogenic conversion in 10T1/2 fibroblasts. EMBO J 8, 701-709.[Medline]

Braun, T., Rudnicki, M. A., Arnold, H. H. and Jaenisch, R (1992). Targeted inactivation of the muscle regulatory gene Myf-5 results in abnormal rib development and perinatal death. Cell 71, 369-382.[Medline]

Bronner-Fraser, M (1995). Origins and developmental potential of the neural crest. Exp. Cell Res 218, 405-417.[Medline]

Capdevila, J. and Johnson, R. L (1998). Endogenous and ectopic expression of noggin suggests a conserved mechanism for regulation of BMP function during limb and somite patterning. Dev. Biol 197, 205-217.[Medline]

Chevallier, A., Kieny, M. and Mauger, A (1977). Limb-somite relationship: origin of the limb musculature. J. Embryol. Exp. Morph 41, 245-258.[Medline]

Chevallier, A., Pautou, M. P., Harris, A. J. and Kieny, M (1986). On the non-equivalence of skeletal muscle satellite cells and embryonic myoblasts. Arch. Anat. Microsc. Morph. Exp 75, 161-166.[Medline]

Choi, J., Costa, M. L., Mermelstein, C. S., Chagas, C., Holtzer, S. and Holtzer, H (1990). MyoD converts primary dermal fibroblasts, chondroblasts, smooth muscle, and retinal pigmented epithelial cells into striated mononucleated myoblasts and multinucleated myotubes. Proc. Natl Acad. Sci. USA 87, 7988-7992.[Abstract/Free Full Text]

Christ, B., Jacob, H. J. and Jacob, M (1974). [Origin of wing musculature. Experimental studies on quail and chick embryos]. Experientia 30, 1446-1449.[Medline]

Christ, B. and Ordahl, C. P (1995). Early stages of chick somite development. Anat. Embryol. (Berl) 191, 381-396.[Medline]

Davis, R. L., Weintraub, H. and Lassar, A. B (1987). Expression of a single transfected cDNA converts fibroblasts to myoblasts. Cell 51, 987-1000.[Medline]

de la Brousse, F. C. and Emerson, C. P., Jr (1990). Localized expression of a myogenic regulatory gene, qmf1, in the somite dermatome of avian embryos. Genes Dev 4, 567-581.[Abstract/Free Full Text]

Denetclaw, W. F., Jr., Christ, B. and Ordahl, C. P (1997). Location and growth of epaxial myotome precursor cells. Development 124, 1601-1610.[Abstract]

Denetclaw, W. F. and Ordahl, C. P (2000). The growth of the dermomyotome and formation of early myotome lineages in thoraco-lumbar somites of chicken embryos. Development 127, 893-905.[Abstract]

Dockter, J. L. and Ordahl, C. P (1998). Determination of sclerotome to the cartilage fate. Development 125, 2113-2124.[Abstract]

Duprez, D., Fournier-Thibault, C. and Le Douarin, N (1998). Sonic Hedgehog induces proliferation of committed skeletal muscle cells in the chick limb. Development 125, 495-505.[Abstract]

Eichmann, A., Marcelle, C., Breant, C. and Le Douarin, N. M (1993). Two molecules related to the VEGF receptor are expressed in early endothelial cells during avian embryonic development. Mech. Dev 42, 33-48.[Medline]

Fan, C. M. and Tessier-Lavigne, M (1994). Patterning of mammalian somites bysurface ectoderm and notochord: evidence for sclerotome induction by a hedgehog homolog. Cell 79, 1175-1186.[Medline]

Floss, T., Arnold, H. H. and Braun, T (1997). A role for FGF-6 in skeletal muscle regeneration. Genes Dev 11, 2040-2051.[Abstract/Free Full Text]

Gage, F. H., Ray, J. and Fisher, L. J (1995). Isolation, characterization, and use of stem cells from the CNS. Annu. Rev. Neurosci 18, 159-192.[Medline]

Gamel, A. J., Brand-Saberi, B. and Christ, B (1995). Halves of epithelial somites and segmental plate show distinct muscle differentiation behavior in vitro compared to entire somites and segmental plate. Dev. Biol 172, 625-639.[Medline]

Golden, J. A. and Cepko, C. L (1996). Clones in the chick diencephalon contain multiple cell types and siblings are widely dispersed. Development 122, 65-78.[Abstract]

Goldhamer, D. J., Brunk, B. P., Faerman, A., King, A., Shani, M. and Emerson, C. P., Jr (1995). Embryonic activation of the myoD gene is regulated by a highly conserved distal control element. Development 121, 637-649.[Abstract]

Grass, S., Arnold, H. H. and Braun, T (1996). Alterations in somite patterning of Myf-5-deficient mice: a possible role for FGF-4 and FGF-6. Development 122, 141-150.[Abstract]

Gurdon, J. B (1988). A community effect in animal development. Nature 336, 772-774.[Medline]

Gussoni, E., Pavlath, G. K., Lanctot, A. M., Sharma, K. R., Miller, R. G., Steinman, L. and Blau, H. M (1992). Normal dystrophin transcripts detected in Duchenne muscular dystrophy patients after myoblast transplantation. Nature 356, 435-438.[Medline]

Hamburger, V. and Hamilton, H (1951). A series of normal stages in the development of the chick embryo. J. Morph 88, 49-92.

Hannon, K., Smith, C. K. d., Bales, K. R. and Santerre, R. F (1992). Temporal and quantitative analysis of myogenic regulatory and growth factor gene expression in the developing mouse embryo. Dev. Biol 151, 137-144.[Medline]

Hasty, P., Bradley, A., Morris, J. H., Edmondson, D. G., Venuti, J. M., Olson, E. N. and Klein, W. H (1993). Muscle deficiency and neonatal death in mice with a targeted mutation in the myogenin gene [see comments]. Nature 364, 501-506.[Medline]

Hopwood, N. D., Pluck, A. and Gurdon, J. B (1991). Xenopus Myf-5 marks early muscle cells and can activate muscle genes ectopically in early embryos. Development 111, 551-560.[Abstract]

Johnson, R. L., Laufer, E., Riddle, R. D. and Tabin, C (1994). Ectopic expression of Sonic hedgehog alters dorsal-ventral patterning of somites. Cell 79, 1165-1173.[Medline]

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.[Medline]

Kablar, B. and Rudnicki, M. A (1999). Development in the absence of skeletal muscle results in the sequential ablation of motor neurons from the spinal cord to the brain. Dev. Biol 208, 93-109.[Medline]

Kaehn, K., Jacob, H. J., Christ, B., Hinrichsen, K. and Poelmann, R. E (1988). The onset of myotome formation in the chick. Anat. Embryol. (Berl) 177, 191-201.[Medline]

Katagiri, T., Yamaguchi, A., Komaki, M., Abe, E., Takahashi, N., Ikeda, T., Rosen, V., Wozney, J. M., Fujisawa-Sehara, A. and Suda, T (1994). Bone morphogenetic protein-2 converts the differentiation pathway of C2C12 myoblasts into the osteoblast lineage [published erratum appears in J Cell Biol 1995 Feb;128(4):following 713]. J. Cell Biol 127, 1755-1766.[Abstract/Free Full Text]

Kato, N. and Aoyama, H (1998). Dermomyotomal origin of the ribs as revealed by extirpation and transplantation experiments in chick and quail embryos. Development 125, 3437-3443.[Abstract]

Kieny, M., Pautou, M. P. and Chevallier, A (1981). On the stability of the myogenic cell line in avian limb bud development. Arch. Anat. Microsc. Morphol. Exp 70, 81-90.[Medline]

Krenn, V., Gorka, P., Wachtler, F., Christ, B. and Jacob, H. J (1988). On the origin of cells determined to form skeletal muscle in avian embryos. Anat. Embryol. (Berl) 179, 49-54.[Medline]

Lash, J., Holtzer, S. and Holtzer, H (1957). An experimental analysis of the development of the spinal column. Exp. Cell Res 13, 292-303.

Lassar, A. B., Buskin, J. N., Lockshon, D., Davis, R. L., Apone, S., Hauschka, S. D. and Weintraub, H (1989). MyoD is a sequence-specific DNA binding protein requiring a region of myc homology to bind to the muscle creatine kinase enhancer. Cell 58, 823-831.[Medline]

Lassar, A. B., Paterson, B. M. and Weintraub, H (1986). Transfection of a DNA locus that mediates the conversion of 10T1/2 fibroblasts to myoblasts. Cell 47, 649-656.[Medline]

Lin-Jones, J. and Hauschka, S. D (1996). Myogenic determination factor expression in the developing avian limb bud: an RT-PCR analysis. Dev. Biol 174, 407-422.[Medline]

Lin-Jones, J. and Hauschka, S. D (1997). Skeletal and cardiac alpha-actin isoforms exhibit unanticipated temporal and tissue-specific gene expression patterns in developing avian limbs and embryos. Dev. Biol 189, 322-334.[Medline]

Mauger, A., Kieny, M. and Chevallier, A (1980). Limb-somite relationship: myogenic potentialities of somatopleural mesoderm. Arch. Anat. Microsc. Morphol. Exp 69, 175-195.[Medline]

Miner, J. H. and Wold, B (1990). Herculin, a fourth member of the MyoD family of myogenic regulatory genes. Proc. Natl Acad. Sci. USA 87, 1089-1093.[Abstract/Free Full Text]

Munsterberg, A. E. and Lassar, A. B (1995). Combinatorial signals from the neural tube, floor plate and notochord induce myogenic bHLH gene expression in the somite. Development 121, 651-660.[Abstract]

Nabeshima, Y., Hanaoka, K., Hayasaka, M., Esumi, E., Li, S. and Nonaka, I (1993). Myogenin gene disruption results in perinatal lethality because of severe muscle defect [see comments]. Nature 364, 532-535.[Medline]

Ordahl, C. P. and Le Douarin, N. M (1992). Two myogenic lineages within the developing somite. Development 114, 339-353.[Abstract]

Ott, M. O., Bober, E., Lyons, G., Arnold, H. and Buckingham, M (1991). Early expression of the myogenic regulatory gene, myf-5, in precursor cells of skeletal muscle in the mouse embryo. Development 111, 1097-1107.[Abstract/Free Full Text]

Pardanaud, L. and Dieterlen-Lievre, F (1995). Does the paraxial mesoderm of the avian embryo have hemangioblastic capacity?. Anat. Embryol. (Berl) 192, 301-308.[Medline]

Pinney, D. F., Pearson-White, S. H., Konieczny, S. F., Latham, K. E. and Emerson, C. P., Jr (1988). Myogenic lineage determination and differentiation: evidence for a regulatory gene pathway. Cell 53, 781-793.[Medline]

Pourquie, O., Coltey, M., Teillet, M. A., Ordahl, C. and Le Douarin, N. M (1993). Control of dorsoventral patterning of somitic derivatives by notochord and floor plate. Proc. Natl Acad. Sci. USA 90, 5242-5246.[Abstract/Free Full Text]

Reshef, R., Maroto, M. and Lassar, A. B (1998). Regulation of dorsal somitic cell fates: BMPs and Noggin control the timing and pattern of myogenic regulator expression. Genes Dev 12, 290-303.[Abstract/Free Full Text]

Rhodes, S. J. and Konieczny, S. F (1989). Identification of MRF4: a new member of the muscle regulatory factor gene family. Genes Dev 3, 2050-2061.[Abstract/Free Full Text]

Rong, P. M., Teillet, M. A., Ziller, C. and Le Douarin, N. M (1992). The neural tube/notochord complex is necessary for vertebral but not limb and body wall striated muscle differentiation. Development 115, 657-672.[Abstract]

Rudnicki, M. A., Schnegelsberg, P. N., 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.[Medline]

Rutz, R., Haney, C. and Hauschka, S (1982). Spatial analysis of limb bud myogenesis: a proximodistal gradient of muscle colony-forming cells in chick embryo leg buds. Dev. Biol 90, 399-411.[Medline]

Sassoon, D., Lyons, G., Wright, W. E., Lin, V., Lassar, A., Weintraub, H. andBuckingham, M (1989). Expression of two myogenic regulatory factors myogenin and MyoD1 during mouse embryogenesis. Nature 341, 303-307.[Medline]

Schramm, C. and Solursh, M (1990). The formation of premuscle masses during chick wing bud development. Anat. Embryol. (Berl) 182, 235-247.[Medline]

Seed, J. and Hauschka, S. D (1984). Temporal separation of the migration of distinct myogenic precursor populations into the developing chick wing bud. Dev. Biol 106, 389-393.[Medline]

Solursh, M., Drake, C. and Meier, S (1987). The migration of myogenic cellsfrom the somites at the wing level in avian embryos. Dev. Biol 121, 389-396.[Medline]

Sopper, M. M., Hauschka, S. D., Hoffman, E. and Ontell, M (1994). Gene complementation using myoblast transfer into fetal muscle. Gene Ther 1, 108-113.[Medline]

Tajbakhsh, S. and Buckingham, M. E (1994). Mouse limb muscle is determined in the absence of the earliest myogenic factor myf-5. Proc. Natl Acad. Sci. USA 91, 747-751.[Abstract/Free Full Text]

Tajbakhsh, S. and Buckingham, M. E (1995). Lineage restriction of the myogenic conversion factor myf-5 in the brain. Development 121, 4077-4083.[Abstract]

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.[Medline]

Tajbakhsh, S., Vivarelli, E., Cusella-De Angelis, G., Rocancourt, D., Buckingham, M. and Cossu, G (1994). A population of myogenic cells derived from the mouse neural tube. Neuron 13, 813-821.[Medline]

Tapscott, S. J., Lassar, A. B., Davis, R. L. and Weintraub, H (1989). 5-bromo-2-deoxyuridine blocks myogenesis by extinguishing expression of MyoD1. Science 245, 532-536.[Abstract/Free Full Text]

Thayer, M. J., Tapscott, S. J., Davis, R. L., Wright, W. E., Lassar, A. B. and Weintraub, H (1989). Positive autoregulation of the myogenic determination gene MyoD1. Cell 58, 241-248.[Medline]

von Kirschhofer, K., Grim, M., Christ, B. and Wachtler, F (1994). Emergence of myogenic and endothelial cell lineages in avian embryos. Dev. Biol 163, 270-278.[Medline]

Wachtler, F., Christ, B. and Jacob, H. J (1981). On the determination of mesodermal tissues in the avian embryonic wing bud. Anat. Embryol. (Berl) 161, 283-289.[Medline]

Wachtler, F., Christ, B. and Jacob, H. J (1982). Grafting experiments on determination and migratory behaviour of presomitic, somitic and somatopleural cells in avian embryos. Anat. Embryol. (Berl) 164, 369-378.[Medline]

Weintraub, H (1993). The MyoD family and myogenesis: redundancy, networks, and thresholds. Cell 75, 1241-1244.[Medline]

Weintraub, H., Davis, R., Tapscott, S., Thayer, M., Krause, M., Benezra, R., Blackwell, T. K., Turner, D., Rupp, R., Hollenberg, S (1991). The myoD gene family: nodal point during specification of the muscle cell lineage. Science 251, 761-766.[Abstract/Free Full Text]

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.[Abstract/Free Full Text]

Williams, B. A. and Ordahl, C. P (1994). Pax-3 expression in segmental mesoderm marks early stages in myogenic cell specification. Development 120, 785-796.[Abstract]

Williams, B. A. and Ordahl, C. P (1996). Manipulation of the avian segmental plate in vivo. Methods Cell Biol 51, 81-92.[Medline]

Williams, B. A. and Ordahl, C. P (1997). Emergence of determined myotome precursor cells in the somite. Development 124, 4983-4997.[Abstract]

Wilting, J., Brand-Saberi, B., Huang, R., Zhi, Q., Kontges, G., Ordahl, C. P. and Christ, B (1995). Angiogenic potential of the avian somite. Dev. Dyn 202, 165-171.[Medline]

Wright, W. E., Sassoon, D. A. and Lin, V. K (1989). Myogenin, a factor regulating myogenesis, has a domain homologous to MyoD. Cell 56, 607-617.[Medline]

This article has been cited by other articles:

J. Gerhart, C. Neely, J. Elder, J. Pfautz, J. Perlman, L. Narciso, K. K. Linask, K. Knudsen, and M. George-Weinstein
Cells that express MyoD mRNA in the epiblast are stably committed to the skeletal muscle lineage
J. Cell Biol., August 9, 2007; 178(4): 649 - 660.
[Abstract] [Full Text] [PDF]

J. E. Anderson
The satellite cell as a companion in skeletal muscle plasticity: currency, conveyance, clue, connector and colander
J. Exp. Biol., June 15, 2006; 209(12): 2276 - 2292.
[Abstract] [Full Text] [PDF]

X. Borue and D. M. Noden
Normal and aberrant craniofacial myogenesis by grafted trunk somitic and segmental plate mesoderm
Development, August 15, 2004; 131(16): 3967 - 3980.
[Abstract] [Full Text] [PDF]

S. J. Venters and C. P. Ordahl
Persistent myogenic capacity of the dermomyotome dorsomedial lip and restriction of myogenic competence
Development, March 10, 2003; 129(16): 3873 - 3885.
[Abstract] [Full Text] [PDF]

C. Ordahl, E Berdougo, S. Venters, and W. Denetclaw
The dermomyotome dorsomedial lip drives growth and morphogenesis of both the primary myotome and dermomyotome epithelium
Development, January 5, 2001; 128(10): 1731 - 1744.
[Abstract] [PDF]

This Article

Summary

Full Text (PDF)

Alert me when this article is cited

Alert me if a correction is posted

Services

Email this article to a friend

Similar articles in this journal

Similar articles in PubMed

Alert me to new issues of the journal

Download to citation manager

Citing Articles

Citing Articles via HighWire

Citing Articles via Google Scholar

Google Scholar

Articles by Williams, B. A.

Articles by Ordahl, C. P.

Search for Related Content

PubMed

PubMed Citation

Articles by Williams, B. A.

Articles by Ordahl, C. P.

				J. E. Anderson The satellite cell as a companion in skeletal muscle plasticity: currency, conveyance, clue, connector and colander J. Exp. Biol., June 15, 2006; 209(12): 2276 - 2292. [Abstract] [Full Text] [PDF]

				X. Borue and D. M. Noden Normal and aberrant craniofacial myogenesis by grafted trunk somitic and segmental plate mesoderm Development, August 15, 2004; 131(16): 3967 - 3980. [Abstract] [Full Text] [PDF]

				S. J. Venters and C. P. Ordahl Persistent myogenic capacity of the dermomyotome dorsomedial lip and restriction of myogenic competence Development, March 10, 2003; 129(16): 3873 - 3885. [Abstract] [Full Text] [PDF]

				C. Ordahl, E Berdougo, S. Venters, and W. Denetclaw The dermomyotome dorsomedial lip drives growth and morphogenesis of both the primary myotome and dermomyotome epithelium Development, January 5, 2001; 128(10): 1731 - 1744. [Abstract] [PDF]