XB-ART-50801
Front Aging Neurosci
2015 May 19;7:62. doi: 10.3389/fnagi.2015.00062.
Show Gene links
Show Anatomy links
The emergence of Pax7-expressing muscle stem cells during vertebrate head muscle development.
Nogueira JM
,
Hawrot K
,
Sharpe C
,
Noble A
,
Wood WM
,
Jorge EC
,
Goldhamer DJ
,
Kardon G
,
Dietrich S
.
???displayArticle.abstract???
Pax7 expressing muscle stem cells accompany all skeletal muscles in the body and in healthy individuals, efficiently repair muscle after injury. Currently, the in vitro manipulation and culture of these cells is still in its infancy, yet muscle stem cells may be the most promising route toward the therapy of muscle diseases such as muscular dystrophies. It is often overlooked that muscular dystrophies affect head and body skeletal muscle differently. Moreover, these muscles develop differently. Specifically, head muscle and its stem cells develop from the non-somitic head mesoderm which also has cardiac competence. To which extent head muscle stem cells retain properties of the early head mesoderm and might even be able to switch between a skeletal muscle and cardiac fate is not known. This is due to the fact that the timing and mechanisms underlying head muscle stem cell development are still obscure. Consequently, it is not clear at which time point one should compare the properties of head mesodermal cells and head muscle stem cells. To shed light on this, we traced the emergence of head muscle stem cells in the key vertebrate models for myogenesis, chicken, mouse, frog and zebrafish, using Pax7 as key marker. Our study reveals a common theme of head muscle stem cell development that is quite different from the trunk. Unlike trunk muscle stem cells, head muscle stem cells do not have a previous history of Pax7 expression, instead Pax7 expression emerges de-novo. The cells develop late, and well after the head mesoderm has committed to myogenesis. We propose that this unique mechanism of muscle stem cell development is a legacy of the evolutionary history of the chordate head mesoderm.
???displayArticle.pubmedLink??? 26042028
???displayArticle.pmcLink??? PMC4436886
???displayArticle.link??? Front Aging Neurosci
???displayArticle.grants??? [+]
Species referenced: Xenopus
Genes referenced: acta4 actl6a adm alx4 des des.2 eya1 isl1 msc myf5 myf6 myh1 myod1 myog myrf npb pam pax3 pax7 ptp4a2 rpsa six1 slc12a3 tbx1 tcf15 tcf21 tcf3 tnni1 tsc1
???displayArticle.antibodies??? Myh1 Ab1
Lines/Strains:
???attribute.lit??? ???displayArticles.show???
![]() |
Figure 10. Time course of pax7 mRNA expression in Xenopus laevis. Lateral views, anterior to the left. Embryonic stages are indicated at the top. Inset in (D): pharyngeal arches and head mesenchyme were dissected away from the left side to reveal the brain. Up to stage 36, Pax7 expression is confined to the central nervous system including the ventral diencephalon (arrowhead), the hypophysis (hp), and the frontonasal neural crest cells. Weak expression is also seen in the somites. From stage 39 onwards, weak expression can be detected in craniofacial muscle anlagen. Abbreviations as before and: cg, cement gland; hp, hypophysis; ht, heart; first arch derived muscle: im, m. intermandibularis anlage; lm, m. levatores mandibulae anlage; second arch derived muscle: ih, m. interhyoideus anlage; oh, m. orbitohyoideus anlage; qh, m. quadrato-hyoangularis anlage; q/oh, common oh and qh precursor. |
![]() |
Figure 11. Time course of head mesoderm and muscle gene expression in Xenopus laevis. Same stages, views, and abbreviations as in Figure 11; markers are indicated on the left. Note that msc, myf5, myod, myog, and desmin are expressed before, mrf4 concomitant with the onset of pax7 expression. |
![]() |
Figure 12. Sarcomeric myosin (A,C,E,G,I) and pax7 protein expression (B,D,F,H,J) in st26 Xenopus laevis control embryos and in craniofacial muscle anlagen embryos at st40. (KâM) GFP expression and pax7 protein expression in a st40 cardiac actin; GFP embryo. (A,B,C,D,G,H,K,L) lateral views, rostral to the left, dorsal; to the top; (E,F,I,J) ventral views, rostral to the left. In (AâF) a HRP-coupled secondary antibody was used, in (GâJ) a secondary antibody coupled to Alexa fluor 594. In (KâM), Alexa fluor 488 and 594 coupled secondary antibodies were used to detect anti GFP and pax7 primaries, respectively. The staining at st26 recapitulates the known myosin and pax7 expression patterns. At st40, the strong expression of sarcomeric myosin and the activity of the cardiac actin promoter indicate that in particular in muscle anlagen associated with the first (mandibular) and second (hyoid) pharyngeal arch, muscle differentiation is well under way. In these muscle anlagen, a faint expression is visible for pax7. The pattern is punctuate, as expected for a nuclear localisation of the pax7 protein. Abbreviations as in Figures 1, 10, 11 and: somite derived muscle: gh, m. geniohyoideus anlage. |
![]() |
Figure 1. Time course of Pax7 expression in the chicken embryo; stages of development are indicated at the top of the panel. (AâL) Expression of Pax7 mRNA with (A-Ci) dorsal views, anterior to the top, (DâM) lateral views of the right side of embryos, anterior to the top, dorsal to the left. In (G), cranial ganglia are revealed by Isl1 expression (red staining). In (L), the eye was removed after staining. (M) Expression of Pax7 protein; lateral view of the left side of an embryo, anterior to the top, dorsal to the right, the eye has been removed before staining. The onset of Pax7 expression in craniofacial muscle anlagen is demarcated by green frames to the respective image. Throughout the first 5 days of development, Pax7 is well detectable in the central nervous system, cranial neural crest cells and the somites and somite-derived muscle precursors/embryonic muscle stem cells. In muscle anlagen derived from the paraxial head mesoderm, expression is first seen at stage HH18 in the lateral rectus eye muscle anlage, the only head muscle to express some trunk markers. In the other head mesoderm derived muscles, Pax7 mRNA can be detected in strongly stained specimen at stage 22; expression becomes more robust at stages 23â24 and is followed by protein expression at HH25. Abbreviations: cns, central nervous system; do, dorsal oblique eye muscle anlage; dr, dorsal rectus eye muscle anlage; hg/hb, hypoglossal/hypobranchial muscle anlage; lr, lateral rectus eye muscle anlage; ma, mandibular arch muscle anlage (jaw closure muscles); mr, medial rectus eye muscle anlage; ncc, neural crest cells; npb, neural plate border; nt, neural tube; ps, primitive streak; s/s1, somite/ somite 1; vo, ventral oblique eye muscle anlage; vr, ventral rectus eye muscle anlage; V, 5th cranial ganglion (trigeminal ganglion). |
![]() |
Figure 2. Series of frontal (BâJ) and cross (KâM) sections of a HH22 chicken head, stained for the expression of Pax7 mRNA, the plane and order of sections in indicated in (A). (BâJ) anterior to the top, lateral to the right; (KâM) dorsal to the top. Abbreviations as in Figure 1. The position of the Pax7 signals beneath the trigeminal ganglion, beneath the eye and in the core of the mandibular arch confirms that these are expression domains associated with developing head muscles. |
![]() |
Figure 3. Time course for the mRNA expression of head mesoderm markers in chicken embryos at HH10 (dorsal views) and HH13/14-E4 (lateral views); in (D), cranial nerves are revealed with the RMO270 antibody (brown staining). Gene names are displayed on the left of the panel; developmental stages are indicated at the top. The onset of marker gene expression is demarcated by a green frame, for genes being expressed earlier than HH10, frames are displayed in magenta. Abbreviations as in Figure 1 and: a/hm, anterior head mesoderm; ect, surface ectoderm; eom, extraocular muscle anlagen; end, endoderm; lam, lateral mesoderm; ht, heart; ov, otic vesicle; pam, pharyngeal arch muscle anlagen; p/hm, posterior head mesoderm. The open arrowhead in (H,J) points at Alx4 expression in the mandibular arch ectoderm and in (VâY) at Tbx1 expression in the posterior ectoderm of the hyoid (2nd pharyngeal) arch. Note that all head mesoderm markers begin their expression well before Pax7. With the exception of Alx4 which from HH13/14 onwards mainly labels cranial neural crest cells and Tcf21/Capsulin which throughout has lower expression levels than its paralog MSc/MyoR, all head mesoderm markers continue to strongly label the myogenic head mesoderm. Their expression domains are wider than that of Pax7, whose expression domain is nested in the expression domain of the head mesoderm genes (compare Figures 1, 4). |
![]() |
Figure 4. Time course for the mRNA expression of Mrf transcriptions factors in chicken embryos from HH10-E4; orientation of specimen and frames indicating the onset of expression as in Figure 3. Gene names and developmental stages are displayed as in Figure 3, Abbreviations as in Figures 1, 3 and: hy, hyoid arch. Myf5 and MyoD indicate the myogenic commitment of precursor cells and are expressed in developing craniofacial muscle anlagen from HH13/14 (Myf5) and HH16 (MyoD) onwards, i.e., significantly before the onset of Pax7. Expression of Myogenin (MyoG/Mgn) indicates the entry of cells into muscle differentiation and commences at E3.5-4, i.e., about the same time as Pax7 (compare with Figure 1). |
![]() |
Figure 5. Time course in chicken embryos from HH10-E4 for markers indicating the cohesion of muscle anlagen (Cadherin 4âmRNA expression) and terminal differentiation [Troponin I 1 (Tnni1)âmRNA expression; sarcomeric MyosinâMF20 antibody staining]. Orientation of specimen and frames indicating the onset of expression as in Figures 3, 4; abbreviations as in Figures 1, 3, 4. The time course of Cadherin 4 expression resembles that of MyoD, and Tnni1 expression commences in many craniofacial muscle anlagen E3, i.e., both are expressed before or at the onset of Pax7 expression. Sarcomeric Myosins can be detected at E3.5-4, simultaneous to the onset of Pax7. |
![]() |
Figure 6. Time course for the mRNA expression of trunk pre-myogenic genes; embryos are displayed and annotated as in Figures 3â5. Abbreviations as before and: na, nasal pit. (AâE) Pax3 labels the central nervous system, the frontonasal neural crest, the trigeminal ganglion, the somites and the somite-derived hypobranchial and limb muscle precursors, but remains absent from genuine craniofacial muscle anlagen. (FâJ) Paraxis expression overlaps with that of Pax3 and 7 in the somite-derived muscle precursors and in the frontonasal crest. Similar to Pax7, Paraxis is also expressed in the lateral rectus eye muscle, but is absent from all other craniofacial muscles. Six1 (KâO) and Eya1 (PâT) are expressed in the head mesoderm before and at HH10. From that stage onwards mesoderm expression becomes somewhat obscured by the overlying expression in neural crest cells. However, Six1 (but not Eya1) remains detectable in craniofacial muscle anlagen. |
![]() |
Figure 7. Time course of Pax7 expression in the mouse. (AâD) Pax7 mRNA expression from E9.5-E12.5 of development; lateral views of the right side of embryos, anterior to the top. Expression is readily detectable in the developing central nervous system, emigrating neural crest cells (prolonged expression in the frontonasal neural crest) and the somites. Head muscle anlagen show expression first at E10.5. (E) Serial cross sections of the mandibular arch at E12.5, dorsal to the top; (F,G) higher magnifications of the areas indicated by the boxes in (E) and stained for Dapi and MyoD protein (Fi,ii) or Dapi and Pax7 protein (Gi,ii). Note that MyoD and Pax7 domains overlap. (H,I) Serial frontal sections of the mandible at birth (P0), dorsal to the top, lateral to the left. (H) Sirius Red staining showing muscle fibers in yellow and bone and connective tissue in red. (I) Dapi staining of the same region, with (Ii) showing a magnification of the cheek and the floor of the mouth as indicated in (I). Skeletal muscle fibers are shown in red. (J) Subsequent section stained for Pax7 protein in red. Note the punctate, nuclear staining for Pax7, associated with the Myosin-positive muscle fibers. (KâQ) Lineage tracing of Pax7 expressing cells, revealed by beta galactosidase staining; lateral views of the right side of embryos, dorsal to the top. With a delay of 1 day, cells with a history of Pax7 expression can be detected in the central nervous system, the trigeminal ganglion, the frontonasal neural crest and the somites. In craniofacial muscle anlagen, cells with a history of Pax7 expression can be detected between E11.5 and E12.5, with a more robust staining appearing at E13.5. Eventually, all craniofacial muscles are stained and the staining is found in muscle fibers, indicating that, similar to the trunk, Pax7-positive cells contribute to fetal and perinatal muscle growth. Abbreviations as in Figures 1, 3, 4 and: fl, forelimb; ISH, in situ hybridisation; ms, masseter; te, temporalis muscle; wt, wildtype. |
![]() |
Figure 8. mRNA Expression of mouse head mesoderm markers and markers for myogenic commitment before and at the onset of Pax7 expression. Lateral views, dorsal to the top. Stages of development are indicated at the top of the panel, gene names on the left. (A,B) Musculin expression commences before E9.5 (not shown); at E9.5-10.5, the gene is widely expressed in the myogenic head mesoderm. Myf5 (C,D) and MyoD (E,F) expression commences at E9.5, i.e., before the onset of Pax7. (G,H) Myogenin expression is not yet detectable at these stages and commences slightly later at E11.5 (not shown). |
![]() |
Figure 9. Lineage tracing of MyoD expressing cells in MyoDiCre/+ R26NG embryos, revealed by anti-GFP antibody (green) staining. (AâD) Lateral views of the right side of E10.5-E13.5 embryos; the dotted line indicates the sectional plane in (FâI). (Ei-iii) Lateral views of the left side of an E11.5 embryo, stained for Pax7 mRNA (blue) and GFP protein (green); dorsal to the top. (F) Frontal section of an E13.5 embryo, stained for Pax7 protein (red), GFP (green), and Dapi (blue). (G) Detail of the ventral rectus eye muscle, (H) detail of the tongue, (I) detail of the masseter as indicated in (D,F). The widely distributed bright green (F) or yellow cells (GâI) are autofluorescing blood cells. Cells with a history of MyoD expression can readily be detected at E10.5 and 11.5, first in the mandibular and hyoid arch, then in the developing extraocular muscles. In head-mesoderm-derived muscles, Pax7 mRNA and subsequent protein expression colocalises with that of MyoD-Cre driven GFP, and Pax7 containing nuclei reside in GFP expressing cells. In contrast, in the somite-derived tongue muscle, most Pax7-positive nuclei are not located in GFP expressing cells. Abbreviations as in Figures 1, 4, 5 and: eom, developing extraocular muscles. |
![]() |
Figure 13. pax7a mRNA, myod mRNA, and sarcomeric myosin expression (MF20 antibody staining) in 72 hpf zebrafish larvae, lateral views, anterior to the left; markers are indicated on the left of the panel. While myogenic markers show robust expression in craniofacial muscle anlagen, pax7 mRNA is barely detectable (arrowheads). Abbreviations as before and: am, adductor mandibulae; hh, hyohyoideus; hpf, hours post fertilization; ih, interhyoideus; im/a, intermandibularis anterior muscle; im/p, intermandibularis posterior muscle; m, mouth; pf, pectoral fin; sh, sternohyoideus. |
![]() |
Figure 14. Proposed model for the emergence of craniofacial muscle stem cells: the bi-potential head mesodermal cells commit to myogenesis before adapting a muscle stem cell state, and then a lateral inhibition mechanism initiated by the differentiating cells controls the simultaneous production of functional muscle and the maintenance of the stem cell pool. |
![]() |
msc (musculin) gene expression in Xenopus laevis embryo, assayed via in situ hybridization, NF stage 33, lateral view, anterior left, dorsal up. Key: hy= hyoid arch; ov= otic vesicle. |
![]() |
msc (musculin) gene expression in Xenopus laevis embryo, assayed via in situ hybridization, NF stage 39, lateral view, anterior left, dorsal up. |
![]() |
Figure 11 A- D. Time course of msc (musculin) gene expression in Xenopus laevis, lateral views, anterior left, dorsal up. Key: pam: pharygeagel arch musculature; hp= hypophysis; ht= heart; hy = hyoid arch; im= m. intermandibularis primordium; lm= m. levatores mandibulae primordium; ih=m. interhyoideus primordium; oh= m. orbitohyoideus primordium; qh= m. quadrato-hyoangularis primordium; q/oh=common oh and qh precursor; ov= otic vesicle |
![]() |
Figure 11 E- H'. Time course of myl5 () gene expression in Xenopus laevis, lateral views, anterior left, dorsal up. Key: pam: pharygeagel arch musculature; hp= hypophysis; ht= heart; hy = hyoid arch; im= m. intermandibularis primordium; lm= m. levatores mandibulae primordium; ih=m. interhyoideus primordium; oh= m. orbitohyoideus primordium; qh= m. quadrato-hyoangularis primordium; q/oh=common oh and qh precursor; ov= otic vesicle |
![]() |
|
![]() |
|
![]() |
|
![]() |
References [+] :
Ahmed,
Establishment of the epaxial-hypaxial boundary in the avian myotome.
2006, Pubmed
Ahmed, Establishment of the epaxial-hypaxial boundary in the avian myotome. 2006, Pubmed
Alvares, Intrinsic, Hox-dependent cues determine the fate of skeletal muscle precursors. 2003, Pubmed
Baker, A Xenopus c-kit-related receptor tyrosine kinase expressed in migrating stem cells of the lateral line system. 1995, Pubmed , Xenbase
Bandín, Regional expression of Pax7 in the brain of Xenopus laevis during embryonic and larval development. 2013, Pubmed , Xenbase
Biressi, Myf5 expression during fetal myogenesis defines the developmental progenitors of adult satellite cells. 2013, Pubmed
Bothe, Dynamic control of head mesoderm patterning. 2011, Pubmed
Bothe, The molecular setup of the avian head mesoderm and its implication for craniofacial myogenesis. 2006, Pubmed
Braun, Differential expression of myogenic determination genes in muscle cells: possible autoactivation by the Myf gene products. 1989, Pubmed
Bryson-Richardson, The genetics of vertebrate myogenesis. 2008, Pubmed
Buckingham, Distinct and dynamic myogenic populations in the vertebrate embryo. 2009, Pubmed
Camp, Fate mapping identifies the origin of SHF/AHF progenitors in the chick primitive streak. 2012, Pubmed
Castellanos, Mammalian TBX1 preferentially binds and regulates downstream targets via a tandem T-site repeat. 2014, Pubmed
Christophorou, Activation of Six1 target genes is required for sensory placode formation. 2009, Pubmed
Collins, Integrated functions of Pax3 and Pax7 in the regulation of proliferation, cell size and myogenic differentiation. 2009, Pubmed
Couly, The developmental fate of the cephalic mesoderm in quail-chick chimeras. 1992, Pubmed
Czajkowski, Divergent and conserved roles of Dll1 signaling in development of craniofacial and trunk muscle. 2014, Pubmed
Daughters, Origin of muscle satellite cells in the Xenopus embryo. 2011, Pubmed , Xenbase
Della Gaspera, Myogenic waves and myogenic programs during Xenopus embryonic myogenesis. 2012, Pubmed , Xenbase
Diao, Pax3/7BP is a Pax7- and Pax3-binding protein that regulates the proliferation of muscle precursor cells by an epigenetic mechanism. 2012, Pubmed
Diehl, Extraocular muscle morphogenesis and gene expression are regulated by Pitx2 gene dose. 2006, Pubmed
Dietrich, Control of dorsoventral pattern in the chick paraxial mesoderm. 1997, Pubmed
Dietrich, Specification of the hypaxial musculature. 1998, Pubmed
Dietrich, The role of SF/HGF and c-Met in the development of skeletal muscle. 1999, Pubmed
Dong, Pitx2 promotes development of splanchnic mesoderm-derived branchiomeric muscle. 2006, Pubmed
Emery, The muscular dystrophies. 2002, Pubmed
Evans, Genome evolution and speciation genetics of clawed frogs (Xenopus and Silurana). 2008, Pubmed , Xenbase
Evans, A mitochondrial DNA phylogeny of African clawed frogs: phylogeography and implications for polyploid evolution. 2004, Pubmed , Xenbase
Gans, Neural crest and the origin of vertebrates: a new head. 1983, Pubmed
Garbern, Cardiac stem cell therapy and the promise of heart regeneration. 2013, Pubmed
Garg, Tbx1, a DiGeorge syndrome candidate gene, is regulated by sonic hedgehog during pharyngeal arch development. 2001, Pubmed
Gianakopoulos, MyoD directly up-regulates premyogenic mesoderm factors during induction of skeletal myogenesis in stem cells. 2011, Pubmed
Gillis, A stem-deuterostome origin of the vertebrate pharyngeal transcriptional network. 2012, Pubmed
Goulding, Signals from the notochord and floor plate regulate the region-specific expression of two Pax genes in the developing spinal cord. 1993, Pubmed
Grifone, Eya1 and Eya2 proteins are required for hypaxial somitic myogenesis in the mouse embryo. 2007, Pubmed
Grifone, Six1 and Six4 homeoproteins are required for Pax3 and Mrf expression during myogenesis in the mouse embryo. 2005, Pubmed
Gros, A common somitic origin for embryonic muscle progenitors and satellite cells. 2005, Pubmed
Guille, Microinjection into Xenopus oocytes and embryos. 1999, Pubmed , Xenbase
Gurdon, Methods for nuclear transplantation in amphibia. 1977, Pubmed
HAMBURGER, A series of normal stages in the development of the chick embryo. 1951, Pubmed
Hammond, Signals and myogenic regulatory factors restrict pax3 and pax7 expression to dermomyotome-like tissue in zebrafish. 2007, Pubmed
Harel, Distinct origins and genetic programs of head muscle satellite cells. 2009, Pubmed
Harland, In situ hybridization: an improved whole-mount method for Xenopus embryos. 1991, Pubmed , Xenbase
Heanue, Synergistic regulation of vertebrate muscle development by Dach2, Eya2, and Six1, homologs of genes required for Drosophila eye formation. 1999, Pubmed
Hebert, The role of Pitx2 in maintaining the phenotype of myogenic precursor cells in the extraocular muscles. 2013, Pubmed
Hinits, Differential requirements for myogenic regulatory factors distinguish medial and lateral somitic, cranial and fin muscle fibre populations. 2009, Pubmed
Holland, Gene duplications and the origins of vertebrate development. 1994, Pubmed
Holland, AmphiPax3/7, an amphioxus paired box gene: insights into chordate myogenesis, neurogenesis, and the possible evolutionary precursor of definitive vertebrate neural crest. 1999, Pubmed
Hughes, Evolution of duplicate genes in a tetraploid animal, Xenopus laevis. 1993, Pubmed , Xenbase
Hutcheson, Embryonic and fetal limb myogenic cells are derived from developmentally distinct progenitors and have different requirements for beta-catenin. 2009, Pubmed
Jostes, The murine paired box gene, Pax7, is expressed specifically during the development of the nervous and muscular system. 1990, Pubmed , Xenbase
Kanisicak, Progenitors of skeletal muscle satellite cells express the muscle determination gene, MyoD. 2009, Pubmed
Kassar-Duchossoy, Pax3/Pax7 mark a novel population of primitive myogenic cells during development. 2005, Pubmed
Kawabe, Carm1 regulates Pax7 transcriptional activity through MLL1/2 recruitment during asymmetric satellite stem cell divisions. 2012, Pubmed
Kelly, The del22q11.2 candidate gene Tbx1 regulates branchiomeric myogenesis. 2004, Pubmed
Kimmel, Stages of embryonic development of the zebrafish. 1995, Pubmed , Xenbase
Kitamura, Mouse Pitx2 deficiency leads to anomalies of the ventral body wall, heart, extra- and periocular mesoderm and right pulmonary isomerism. 1999, Pubmed
Kragl, Cells keep a memory of their tissue origin during axolotl limb regeneration. 2009, Pubmed
Kusakabe, Expression and interaction of muscle-related genes in the lamprey imply the evolutionary scenario for vertebrate skeletal muscle, in association with the acquisition of the neck and fins. 2011, Pubmed
Lepper, Adult satellite cells and embryonic muscle progenitors have distinct genetic requirements. 2009, Pubmed
Lin, Myogenic regulatory factors Myf5 and Myod function distinctly during craniofacial myogenesis of zebrafish. 2006, Pubmed
Lours, The dissociation of the Fgf-feedback loop controls the limbless state of the neck. 2005, Pubmed
Lu, Control of facial muscle development by MyoR and capsulin. 2002, Pubmed
Maczkowiak, The Pax3 and Pax7 paralogs cooperate in neural and neural crest patterning using distinct molecular mechanisms, in Xenopus laevis embryos. 2010, Pubmed , Xenbase
Mahadevan, Developmental expression of the amphioxus Tbx1/ 10 gene illuminates the evolution of vertebrate branchial arches and sclerotome. 2004, Pubmed
Moncaut, Musculin and TCF21 coordinate the maintenance of myogenic regulatory factor expression levels during mouse craniofacial development. 2012, Pubmed
Mootoosamy, Distinct regulatory cascades for head and trunk myogenesis. 2002, Pubmed
Mourikis, Distinct contextual roles for Notch signalling in skeletal muscle stem cells. 2014, Pubmed
Mourikis, Cell-autonomous Notch activity maintains the temporal specification potential of skeletal muscle stem cells. 2012, Pubmed
Müller, Evolutionary aspects of developmentally regulated helix-loop-helix transcription factors in striated muscle of jellyfish. 2003, Pubmed
Noden, Differentiation of avian craniofacial muscles: I. Patterns of early regulatory gene expression and myosin heavy chain synthesis. 1999, Pubmed
Noden, The embryonic origins of avian cephalic and cervical muscles and associated connective tissues. 1983, Pubmed
Noden, The differentiation and morphogenesis of craniofacial muscles. 2006, Pubmed
Ohno, Evolution from fish to mammals by gene duplication. 1968, Pubmed
Ono, Muscle satellite cells are a functionally heterogeneous population in both somite-derived and branchiomeric muscles. 2010, Pubmed
Pajcini, Transient inactivation of Rb and ARF yields regenerative cells from postmitotic mammalian muscle. 2010, Pubmed
Penn, A MyoD-generated feed-forward circuit temporally patterns gene expression during skeletal muscle differentiation. 2004, Pubmed
Postlethwait, The zebrafish genome in context: ohnologs gone missing. 2007, Pubmed
Razy-Krajka, Collier/OLF/EBF-dependent transcriptional dynamics control pharyngeal muscle specification from primed cardiopharyngeal progenitors. 2014, Pubmed
Relaix, Satellite cells are essential for skeletal muscle regeneration: the cell on the edge returns centre stage. 2012, Pubmed
Relaix, Six homeoproteins directly activate Myod expression in the gene regulatory networks that control early myogenesis. 2013, Pubmed
Relaix, A Pax3/Pax7-dependent population of skeletal muscle progenitor cells. 2005, Pubmed
Relaix, Pax3 and Pax7 have distinct and overlapping functions in adult muscle progenitor cells. 2006, Pubmed
Rosenberg, A potential role of R-cadherin in striated muscle formation. 1997, Pubmed
Sambasivan, Embryonic founders of adult muscle stem cells are primed by the determination gene Mrf4. 2013, Pubmed
Sambasivan, An eye on the head: the development and evolution of craniofacial muscles. 2011, Pubmed
Sambasivan, Distinct regulatory cascades govern extraocular and pharyngeal arch muscle progenitor cell fates. 2009, Pubmed
Schienda, Somitic origin of limb muscle satellite and side population cells. 2006, Pubmed
Schilling, Musculoskeletal patterning in the pharyngeal segments of the zebrafish embryo. 1997, Pubmed
Schmidt, Cranial muscles in amphibians: development, novelties and the role of cranial neural crest cells. 2013, Pubmed , Xenbase
Schuster-Gossler, Premature myogenic differentiation and depletion of progenitor cells cause severe muscle hypotrophy in Delta1 mutants. 2007, Pubmed
Seale, Pax7 is required for the specification of myogenic satellite cells. 2000, Pubmed
Seo, The zebrafish Pax3 and Pax7 homologues are highly conserved, encode multiple isoforms and show dynamic segment-like expression in the developing brain. 1998, Pubmed
Shimizu, Peduncle of Hydra and the heart of higher organisms share a common ancestral origin. 2003, Pubmed
Somorjai, Vertebrate-like regeneration in the invertebrate chordate amphioxus. 2012, Pubmed
Šošić, Regulation of paraxis expression and somite formation by ectoderm- and neural tube-derived signals. 1997, Pubmed
Steinmetz, Independent evolution of striated muscles in cnidarians and bilaterians. 2012, Pubmed
Stolfi, Early chordate origins of the vertebrate second heart field. 2010, Pubmed , Xenbase
Summerbell, Expression of the myogenic regulatory factor Mrf4 precedes or is contemporaneous with that of Myf5 in the somitic bud. 2002, Pubmed
Takahashi, The role of Alx-4 in the establishment of anteroposterior polarity during vertebrate limb development. 1998, Pubmed , Xenbase
Thisse, High-resolution in situ hybridization to whole-mount zebrafish embryos. 2008, Pubmed
Troy, Coordination of satellite cell activation and self-renewal by Par-complex-dependent asymmetric activation of p38α/β MAPK. 2012, Pubmed
Vasyutina, RBP-J (Rbpsuh) is essential to maintain muscle progenitor cells and to generate satellite cells. 2007, Pubmed
von Maltzahn, Pax7 is critical for the normal function of satellite cells in adult skeletal muscle. 2013, Pubmed
von Scheven, Protein and genomic organisation of vertebrate MyoR and Capsulin genes and their expression during avian development. 2006, Pubmed
Wang, NK4 antagonizes Tbx1/10 to promote cardiac versus pharyngeal muscle fate in the ascidian second heart field. 2013, Pubmed
Weintraub, Activation of muscle-specific genes in pigment, nerve, fat, liver, and fibroblast cell lines by forced expression of MyoD. 1989, Pubmed
Wilson-Rawls, Differential regulation of epaxial and hypaxial muscle development by paraxis. 1999, Pubmed
Wood, MyoD-expressing progenitors are essential for skeletal myogenesis and satellite cell development. 2013, Pubmed
Yamamoto, A multifunctional reporter mouse line for Cre- and FLP-dependent lineage analysis. 2009, Pubmed
Yoshida, Cell heterogeneity upon myogenic differentiation: down-regulation of MyoD and Myf-5 generates 'reserve cells'. 1998, Pubmed
Yoshioka, Pitx2, a bicoid-type homeobox gene, is involved in a lefty-signaling pathway in determination of left-right asymmetry. 1998, Pubmed
Zacharias, Pitx2 is an upstream activator of extraocular myogenesis and survival. 2011, Pubmed
Ziermann, Patterns of spatial and temporal cranial muscle development in the African clawed frog, Xenopus laevis (Anura: Pipidae). 2007, Pubmed , Xenbase