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Volumn 7, Issue 11, 2012, Pages

Initiation of Early Osteoblast Differentiation Events through the Direct Transcriptional Regulation of Msx2 by FOXC1

Author keywords

[No Author keywords available]

Indexed keywords

ALKALINE PHOSPHATASE; TRANSCRIPTION FACTOR FOXC1; TRANSCRIPTION FACTOR MSX2;

EID: 84868675767     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0049095     Document Type: Article
Times cited : (30)

References (35)
  • 3
    • 52949136599 scopus 로고    scopus 로고
    • Transcriptional control of skeletogenesis
    • Karsenty G, (2008) Transcriptional control of skeletogenesis. Annu Rev Genomics Hum Genet 9: 183-196.
    • (2008) Annu Rev Genomics Hum Genet , vol.9 , pp. 183-196
    • Karsenty, G.1
  • 4
    • 0007676001 scopus 로고
    • Genetical studies on the skeleton of the mouse. VII. Congenital hydrocephalus
    • Gruneberg H, (1951) Genetical studies on the skeleton of the mouse. VII. Congenital hydrocephalus. J Genet 45: 327-358.
    • (1951) J Genet , vol.45 , pp. 327-358
    • Gruneberg, H.1
  • 5
    • 0033041178 scopus 로고    scopus 로고
    • Pleiotropic skeletal and ocular phenotypes of the mouse mutation congenital hydrocephalus (ch/Mf1) arise from a winged helix/forkhead transcriptionfactor gene
    • Hong HK, Lass JH, Chakravarti A, (1999) Pleiotropic skeletal and ocular phenotypes of the mouse mutation congenital hydrocephalus (ch/Mf1) arise from a winged helix/forkhead transcriptionfactor gene. Hum Mol Genet 8: 625-637.
    • (1999) Hum Mol Genet , vol.8 , pp. 625-637
    • Hong, H.K.1    Lass, J.H.2    Chakravarti, A.3
  • 6
    • 0032511231 scopus 로고    scopus 로고
    • The forkhead/winged helix gene Mf1 is disrupted in the pleiotropic mouse mutation congenital hydrocephalus
    • Kume T, Deng KY, Winfrey V, Gould DB, Walter MA, et al. (1998) The forkhead/winged helix gene Mf1 is disrupted in the pleiotropic mouse mutation congenital hydrocephalus. Cell 93: 985-996.
    • (1998) Cell , vol.93 , pp. 985-996
    • Kume, T.1    Deng, K.Y.2    Winfrey, V.3    Gould, D.B.4    Walter, M.A.5
  • 7
    • 0141459231 scopus 로고    scopus 로고
    • Progression of calvarial bone development requires Foxc1 regulation of Msx2 and Alx4
    • Rice R, Rice DP, Olsen BR, Thesleff I, (2003) Progression of calvarial bone development requires Foxc1 regulation of Msx2 and Alx4. Dev Biol 262: 75-87.
    • (2003) Dev Biol , vol.262 , pp. 75-87
    • Rice, R.1    Rice, D.P.2    Olsen, B.R.3    Thesleff, I.4
  • 8
    • 0035158663 scopus 로고    scopus 로고
    • Haploinsufficiency of the human homeobox gene ALX4 causes skull ossification defects
    • Mavrogiannis LA, Antonopoulou I, Baxova A, Kutilek S, Kim CA, et al. (2001) Haploinsufficiency of the human homeobox gene ALX4 causes skull ossification defects. Nat Genet 27: 17-18.
    • (2001) Nat Genet , vol.27 , pp. 17-18
    • Mavrogiannis, L.A.1    Antonopoulou, I.2    Baxova, A.3    Kutilek, S.4    Kim, C.A.5
  • 9
    • 0027431005 scopus 로고
    • A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis
    • Jabs EW, Muller U, Li X, Ma L, Luo W, et al. (1993) A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis. Cell 75: 443-450.
    • (1993) Cell , vol.75 , pp. 443-450
    • Jabs, E.W.1    Muller, U.2    Li, X.3    Ma, L.4    Luo, W.5
  • 10
    • 0034192384 scopus 로고    scopus 로고
    • Identification of mutations in the MSX2 homeobox gene in families affected with foramina parietalia permagna
    • Wuyts W, Reardon W, Preis S, Homfray T, Rasore-Quartino A, et al. (2000) Identification of mutations in the MSX2 homeobox gene in families affected with foramina parietalia permagna. Hum Mol Genet 9: 1251-1255.
    • (2000) Hum Mol Genet , vol.9 , pp. 1251-1255
    • Wuyts, W.1    Reardon, W.2    Preis, S.3    Homfray, T.4    Rasore-Quartino, A.5
  • 11
    • 0034074417 scopus 로고    scopus 로고
    • Functional haploinsufficiency of the human homeobox gene MSX2 causes defects in skull ossification
    • Wilkie AO, Tang Z, Elanko N, Walsh S, Twigg SR, et al. (2000) Functional haploinsufficiency of the human homeobox gene MSX2 causes defects in skull ossification. Nat Genet 24: 387-390.
    • (2000) Nat Genet , vol.24 , pp. 387-390
    • Wilkie, A.O.1    Tang, Z.2    Elanko, N.3    Walsh, S.4    Twigg, S.R.5
  • 12
    • 0034029571 scopus 로고    scopus 로고
    • Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation
    • Satokata I, Ma L, Ohshima H, Bei M, Woo I, et al. (2000) Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation. Nat Genet 24: 391-395.
    • (2000) Nat Genet , vol.24 , pp. 391-395
    • Satokata, I.1    Ma, L.2    Ohshima, H.3    Bei, M.4    Woo, I.5
  • 13
    • 0037155912 scopus 로고    scopus 로고
    • FOXC1 transcriptional regulation is mediated by N- and C-terminal activation domains and contains a phosphorylated transcriptional inhibitory domain
    • Berry FB, Saleem RA, Walter MA, (2002) FOXC1 transcriptional regulation is mediated by N- and C-terminal activation domains and contains a phosphorylated transcriptional inhibitory domain. J Biol Chem 277: 10292-10297.
    • (2002) J Biol Chem , vol.277 , pp. 10292-10297
    • Berry, F.B.1    Saleem, R.A.2    Walter, M.A.3
  • 14
    • 0035092384 scopus 로고    scopus 로고
    • Analyses of the effects that disease-causing missense mutations have on the structure and function of the winged-helix protein FOXC1
    • Saleem RA, Banerjee-Basu S, Berry FB, Baxevanis AD, Walter MA, (2001) Analyses of the effects that disease-causing missense mutations have on the structure and function of the winged-helix protein FOXC1. Am J Hum Genet 68: 627-641.
    • (2001) Am J Hum Genet , vol.68 , pp. 627-641
    • Saleem, R.A.1    Banerjee-Basu, S.2    Berry, F.B.3    Baxevanis, A.D.4    Walter, M.A.5
  • 15
    • 85074914953 scopus 로고    scopus 로고
    • A PCR primer bank for quantitative gene expression analysis
    • Wang X, Seed B, (2003) A PCR primer bank for quantitative gene expression analysis. Nucleic Acids Res 31: e154.
    • (2003) Nucleic Acids Res , vol.31
    • Wang, X.1    Seed, B.2
  • 16
    • 38849094466 scopus 로고    scopus 로고
    • FOXC1 is required for cell viability and resistance to oxidative stress in the eye through the transcriptional regulation of FOXO1A
    • Berry FB, Skarie JM, Mirzayans F, Fortin Y, Hudson TJ, et al. (2008) FOXC1 is required for cell viability and resistance to oxidative stress in the eye through the transcriptional regulation of FOXO1A. Hum Mol Genet 17: 490-505.
    • (2008) Hum Mol Genet , vol.17 , pp. 490-505
    • Berry, F.B.1    Skarie, J.M.2    Mirzayans, F.3    Fortin, Y.4    Hudson, T.J.5
  • 17
    • 0028046675 scopus 로고
    • Cloning and characterization of seven human forkhead proteins: binding site specificity and DNA bending
    • Pierrou S, Hellqvist M, Samuelsson L, Enerback S, Carlsson P, (1994) Cloning and characterization of seven human forkhead proteins: binding site specificity and DNA bending. Embo J 13: 5002-5012.
    • (1994) Embo J , vol.13 , pp. 5002-5012
    • Pierrou, S.1    Hellqvist, M.2    Samuelsson, L.3    Enerback, S.4    Carlsson, P.5
  • 18
    • 4043181957 scopus 로고    scopus 로고
    • Reciprocal roles of MSX2 in regulation of osteoblast and adipocyte differentiation
    • Ichida F, Nishimura R, Hata K, Matsubara T, Ikeda F, et al. (2004) Reciprocal roles of MSX2 in regulation of osteoblast and adipocyte differentiation. J Biol Chem 279: 34015-34022.
    • (2004) J Biol Chem , vol.279 , pp. 34015-34022
    • Ichida, F.1    Nishimura, R.2    Hata, K.3    Matsubara, T.4    Ikeda, F.5
  • 19
    • 33645067959 scopus 로고    scopus 로고
    • Compound developmental eye disorders following inactivation of TGFbeta signaling in neural-crest stem cells
    • Ittner LM, Wurdak H, Schwerdtfeger K, Kunz T, Ille F, et al. (2005) Compound developmental eye disorders following inactivation of TGFbeta signaling in neural-crest stem cells. J Biol 4: 11.
    • (2005) J Biol , vol.4 , pp. 11
    • Ittner, L.M.1    Wurdak, H.2    Schwerdtfeger, K.3    Kunz, T.4    Ille, F.5
  • 20
    • 33745099879 scopus 로고    scopus 로고
    • The forkhead transcription factors, Foxc1 and Foxc2, are required for arterial specification and lymphatic sprouting during vascular development
    • Seo S, Fujita H, Nakano A, Kang M, Duarte A, et al. (2006) The forkhead transcription factors, Foxc1 and Foxc2, are required for arterial specification and lymphatic sprouting during vascular development. Dev Biol 294: 458-470.
    • (2006) Dev Biol , vol.294 , pp. 458-470
    • Seo, S.1    Fujita, H.2    Nakano, A.3    Kang, M.4    Duarte, A.5
  • 21
    • 33746926015 scopus 로고    scopus 로고
    • Forkhead transcription factors, Foxc1 and Foxc2, are required for the morphogenesis of the cardiac outflow tract
    • Seo S, Kume T, (2006) Forkhead transcription factors, Foxc1 and Foxc2, are required for the morphogenesis of the cardiac outflow tract. Dev Biol 296: 421-436.
    • (2006) Dev Biol , vol.296 , pp. 421-436
    • Seo, S.1    Kume, T.2
  • 22
    • 33744826811 scopus 로고    scopus 로고
    • Identification of Tgf beta1i4 as a downstream target of Foxc1
    • Sommer P, Napier HR, Hogan BL, Kidson SH, (2006) Identification of Tgf beta1i4 as a downstream target of Foxc1. Dev Growth Differ 48: 297-308.
    • (2006) Dev Growth Differ , vol.48 , pp. 297-308
    • Sommer, P.1    Napier, H.R.2    Hogan, B.L.3    Kidson, S.H.4
  • 23
    • 33750216514 scopus 로고    scopus 로고
    • FGF19 is a target for FOXC1 regulation in ciliary body-derived cells
    • Tamimi Y, Skarie JM, Footz T, Berry FB, Link BA, et al. (2006) FGF19 is a target for FOXC1 regulation in ciliary body-derived cells. Hum Mol Genet 15: 3229-3240.
    • (2006) Hum Mol Genet , vol.15 , pp. 3229-3240
    • Tamimi, Y.1    Skarie, J.M.2    Footz, T.3    Berry, F.B.4    Link, B.A.5
  • 24
    • 0037439240 scopus 로고    scopus 로고
    • Tbx1 is regulated by tissue-specific forkhead proteins through a common Sonic hedgehog-responsive enhancer
    • Yamagishi H, Maeda J, Hu T, McAnally J, Conway SJ, et al. (2003) Tbx1 is regulated by tissue-specific forkhead proteins through a common Sonic hedgehog-responsive enhancer. Genes Dev 17: 269-281.
    • (2003) Genes Dev , vol.17 , pp. 269-281
    • Yamagishi, H.1    Maeda, J.2    Hu, T.3    McAnally, J.4    Conway, S.J.5
  • 25
    • 34547667023 scopus 로고    scopus 로고
    • Cranial suture biology and dental development: genetic and clinical perspectives
    • De Coster PJ, Mortier G, Marks LA, Martens LC, (2007) Cranial suture biology and dental development: genetic and clinical perspectives. J Oral Pathol Med 36: 447-455.
    • (2007) J Oral Pathol Med , vol.36 , pp. 447-455
    • De Coster, P.J.1    Mortier, G.2    Marks, L.A.3    Martens, L.C.4
  • 26
    • 0346252654 scopus 로고    scopus 로고
    • Msx2 and Twist cooperatively control the development of the neural crest-derived skeletogenic mesenchyme of the murine skull vault
    • Ishii M, Merrill AE, Chan YS, Gitelman I, Rice DP, et al. (2003) Msx2 and Twist cooperatively control the development of the neural crest-derived skeletogenic mesenchyme of the murine skull vault. Development 130: 6131-6142.
    • (2003) Development , vol.130 , pp. 6131-6142
    • Ishii, M.1    Merrill, A.E.2    Chan, Y.S.3    Gitelman, I.4    Rice, D.P.5
  • 27
    • 2442484615 scopus 로고    scopus 로고
    • Mechanisms of murine cranial suture patency mediated by a dominant negative transforming growth factor-beta receptor adenovirus
    • Song HM, Fong KD, Nacamuli RP, Warren SM, Fang TD, et al. (2004) Mechanisms of murine cranial suture patency mediated by a dominant negative transforming growth factor-beta receptor adenovirus. Plast Reconstr Surg 113: 1685-1697.
    • (2004) Plast Reconstr Surg , vol.113 , pp. 1685-1697
    • Song, H.M.1    Fong, K.D.2    Nacamuli, R.P.3    Warren, S.M.4    Fang, T.D.5
  • 28
    • 34548853994 scopus 로고    scopus 로고
    • TGF-beta mediated Msx2 expression controls occipital somites-derived caudal region of skull development
    • Hosokawa R, Urata M, Han J, Zehnaly A, Bringas P Jr, et al. (2007) TGF-beta mediated Msx2 expression controls occipital somites-derived caudal region of skull development. Dev Biol 310: 140-153.
    • (2007) Dev Biol , vol.310 , pp. 140-153
    • Hosokawa, R.1    Urata, M.2    Han, J.3    Zehnaly, A.4    Bringas Jr., P.5
  • 29
    • 35348924902 scopus 로고    scopus 로고
    • Cortical dysplasia and skull defects in mice with a Foxc1 allele reveal the role of meningeal differentiation in regulating cortical development
    • Zarbalis K, Siegenthaler JA, Choe Y, May SR, Peterson AS, et al. (2007) Cortical dysplasia and skull defects in mice with a Foxc1 allele reveal the role of meningeal differentiation in regulating cortical development. Proc Natl Acad Sci U S A 104: 14002-14007.
    • (2007) Proc Natl Acad Sci U S A , vol.104 , pp. 14002-14007
    • Zarbalis, K.1    Siegenthaler, J.A.2    Choe, Y.3    May, S.R.4    Peterson, A.S.5
  • 30
    • 45849105979 scopus 로고    scopus 로고
    • Locate, condense, differentiate, grow and confront: developmental mechanisms controlling intramembranous bone and suture formation and function
    • Rice DP, Rice R, (2008) Locate, condense, differentiate, grow and confront: developmental mechanisms controlling intramembranous bone and suture formation and function. Front Oral Biol 12: 22-40.
    • (2008) Front Oral Biol , vol.12 , pp. 22-40
    • Rice, D.P.1    Rice, R.2
  • 31
    • 0032231330 scopus 로고    scopus 로고
    • Mutations of the forkhead/winged-helix gene, FKHL7, in patients with Axenfeld-Rieger anomaly
    • Mears AJ, Jordan T, Mirzayans F, Dubois S, Kume T, et al. (1998) Mutations of the forkhead/winged-helix gene, FKHL7, in patients with Axenfeld-Rieger anomaly. Am J Hum Genet 63: 1316-1328.
    • (1998) Am J Hum Genet , vol.63 , pp. 1316-1328
    • Mears, A.J.1    Jordan, T.2    Mirzayans, F.3    Dubois, S.4    Kume, T.5
  • 32
    • 17344368672 scopus 로고    scopus 로고
    • The forkhead transcription factor gene FKHL7 is responsible for glaucoma phenotypes which map to 6p25
    • Nishimura DY, Swiderski RE, Alward WL, Searby CC, Patil SR, et al. (1998) The forkhead transcription factor gene FKHL7 is responsible for glaucoma phenotypes which map to 6p25. Nat Genet 19: 140-147.
    • (1998) Nat Genet , vol.19 , pp. 140-147
    • Nishimura, D.Y.1    Swiderski, R.E.2    Alward, W.L.3    Searby, C.C.4    Patil, S.R.5
  • 33
    • 11144263725 scopus 로고    scopus 로고
    • Msx2 controls ameloblast terminal differentiation
    • Bei M, Stowell S, Maas R, (2004) Msx2 controls ameloblast terminal differentiation. Dev Dyn 231: 758-765.
    • (2004) Dev Dyn , vol.231 , pp. 758-765
    • Bei, M.1    Stowell, S.2    Maas, R.3
  • 34
    • 0035192040 scopus 로고    scopus 로고
    • Antagonistic regulation of Dlx2 expression by PITX2 and Msx2: implications for tooth development
    • Green PD, Hjalt TA, Kirk DE, Sutherland LB, Thomas BL, et al. (2001) Antagonistic regulation of Dlx2 expression by PITX2 and Msx2: implications for tooth development. Gene Expr 9: 265-281.
    • (2001) Gene Expr , vol.9 , pp. 265-281
    • Green, P.D.1    Hjalt, T.A.2    Kirk, D.E.3    Sutherland, L.B.4    Thomas, B.L.5
  • 35
    • 0027946689 scopus 로고
    • Bone morphogenetic protein-2 converts the differentiation pathway of C2C12 myoblasts into the osteoblast lineage
    • Katagiri T, Yamaguchi A, Komaki M, Abe E, Takahashi N, et al. (1994) Bone morphogenetic protein-2 converts the differentiation pathway of C2C12 myoblasts into the osteoblast lineage. J Cell Biol 127: 1755-1766.
    • (1994) J Cell Biol , vol.127 , pp. 1755-1766
    • Katagiri, T.1    Yamaguchi, A.2    Komaki, M.3    Abe, E.4    Takahashi, N.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.