Runx2 and dental development

被引:124
作者
Camilleri, Simon [1 ]
McDonald, Fraser [1 ]
机构
[1] Kings Coll London, Inst Dent, Dept Orthodont, London SE1 9RT, England
关键词
bone; odontogenesis; Runx2; tooth eruption;
D O I
10.1111/j.1600-0722.2006.00399.x
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
The Runx2 gene is a master transcription factor of bone and plays a role in all stages of bone formation. It is essential for the initial commitment of mesenchymal cells to the osteoblastic lineage and also controls the proliferation, differentiation, and maintenance of these cells. Control is complex, with involvement of a multitude of factors, thereby regulating the expression and activity of this gene both temporally and spatially. The use of multiple promoters and alternative splicing of exons further extends its diversity of actions. RUNX2 is also essential for the later stages of tooth formation, is intimately involved in the development of calcified tooth tissue, and exerts an influence on proliferation of the dental lamina. Furthermore, RUNX2 regulates the alveolar remodelling process essential for tooth eruption and may play a role in the maintenance of the periodontal ligament. In this article, the structure of Runx2 is described. The control and function of the gene and its product are discussed, with special reference to developing tooth tissues, in an attempt to elucidate the role of this gene in the development of the teeth and supporting structures.
引用
收藏
页码:361 / 373
页数:13
相关论文
共 145 条
[1]   Runx2 mediates FGF signaling from epithelium to mesenchyme during tooth morphogenesis [J].
Åberg, T ;
Wang, XP ;
Kim, JH ;
Yamashiro, T ;
Bei, M ;
Rice, R ;
Ryoo, HM ;
Thesleff, I .
DEVELOPMENTAL BIOLOGY, 2004, 270 (01) :76-93
[2]   Phenotypic changes in dentition of Runx2 homozygote-null mutant mice [J].
Åberg, T ;
Cavender, A ;
Gaikwad, JS ;
Bronckers, ALJJ ;
Wang, XP ;
Waltimo-Sirén, J ;
Thesleff, I ;
D'Souza, RN .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 2004, 52 (01) :131-139
[3]   A molecular pathogenesis for transcription factor associated poly-alanine tract expansions [J].
Albrecht, AN ;
Kornak, U ;
Böddrich, A ;
Süring, K ;
Robinson, PN ;
Stiege, AC ;
Lurz, R ;
Stricker, S ;
Wanker, EE ;
Mundlos, S .
HUMAN MOLECULAR GENETICS, 2004, 13 (20) :2351-2359
[4]   Detection of dentin sialoprotein in rat periodontium [J].
Baba, O ;
Qin, CL ;
Brunn, JC ;
Jones, JE ;
Wygant, JN ;
McIntyre, BW ;
Butler, WT .
EUROPEAN JOURNAL OF ORAL SCIENCES, 2004, 112 (02) :163-170
[5]   Phosphorylation, acetylation and ubiquitination: The molecular basis of RUNX regulation [J].
Bae, SC ;
Lee, YH .
GENE, 2006, 366 (01) :58-66
[6]   Tumor suppressor activity of RUNX3 [J].
Bae, SC ;
Choi, JK .
ONCOGENE, 2004, 23 (24) :4336-4340
[7]   PEBP2-ALPHA-B/MOUSE AML1 CONSISTS OF MULTIPLE ISOFORMS THAT POSSESS DIFFERENTIAL TRANSACTIVATION POTENTIALS [J].
BAE, SC ;
OGAWA, E ;
MARUYAMA, M ;
OKA, H ;
SATAKE, M ;
SHIGESADA, K ;
JENKINS, NA ;
GILBERT, DJ ;
COPELAND, NG ;
ITO, Y .
MOLECULAR AND CELLULAR BIOLOGY, 1994, 14 (05) :3242-3252
[8]   Differential regulation of the two principal Runx2/Cbfa1 N-terminal isoforms in response to bone morphogenetic protein-2 during development of the osteoblast phenotype [J].
Banerjee, C ;
Javed, A ;
Choi, JY ;
Green, J ;
Rosen, V ;
van Wijnen, AJ ;
Stein, JL ;
Lian, JB ;
Stein, GS .
ENDOCRINOLOGY, 2001, 142 (09) :4026-4039
[9]   Cleidocranial dysplasia: Molecular genetic analysis and phenotypic-based description of a middle European patient group [J].
Baumert, U ;
Golan, I ;
Redlich, M ;
Aknin, JJ ;
Muessig, D .
AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2005, 139A (02) :78-85
[10]   Cleidocranial dysplasia .1. General principles of the orthodontic and surgical treatment modality [J].
Becker, A ;
Lustmann, J ;
Shteyer, A .
AMERICAN JOURNAL OF ORTHODONTICS AND DENTOFACIAL ORTHOPEDICS, 1997, 111 (01) :28-33