Transcription factor Sp3 is essential for post-natal survival and late tooth development

被引:170
作者
Bouwman, P
Göllner, H
Elsässer, HP
Eckhoff, G
Karis, A
Grosveld, F
Philipsen, S
Suske, G
机构
[1] Univ Marburg, Inst Mol Biol & Tumorforsch, D-35037 Marburg, Germany
[2] Univ Marburg, Inst Zytobiol & Zytopathol, D-35037 Marburg, Germany
[3] Erasmus Univ, Dept Cell Biol, NL-3000 DR Rotterdam, Netherlands
关键词
knockout; post-natal death; Sp1; Sp3; tooth development;
D O I
10.1093/emboj/19.4.655
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Sp3 is a ubiquitously expressed transcription factor closely related to Sp1 (specificity protein 1). We have disrupted the mouse Sp3 gene by homologous recombination, Sp3-deficient embryos are growth retarded and invariably die at birth of respiratory failure. The cause for the observed breathing defect remains obscure since only minor morphological alterations were observed in the lung, and surfactant protein expression is indistinguishable from that in wild-type mice. Histological examinations of individual organs in Sp3(-/-) mice show a pronounced defect in late tooth formation. In Sp3 null mice, the dentin/enamel layer of the developing teeth is impaired due to the lack of ameloblast-specific gene products, Comparison of the Sp1 and Sp3 knockout phenotype shows that Sp1 and Sp3 have distinct functions in vivo, but also suggests a degree of functional redundancy.
引用
收藏
页码:655 / 661
页数:7
相关论文
共 35 条
[1]   A RAPID MICROPREPARATION TECHNIQUE FOR EXTRACTION OF DNA-BINDING PROTEINS FROM LIMITING NUMBERS OF MAMMALIAN-CELLS [J].
ANDREWS, NC ;
FALLER, DV .
NUCLEIC ACIDS RESEARCH, 1991, 19 (09) :2499-2499
[2]   Combinatorial action of HNF3 and Sp family transcription factors in the activation of the rabbit uteroglobin/CC10 promoter [J].
Braun, H ;
Suske, G .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (16) :9821-9828
[3]   Comparison of upstream regions of X- and Y-chromosomal amelogenin genes [J].
Chen, E ;
Yuan, ZA ;
Collier, PM ;
Greene, SR ;
Abrams, WR ;
Gibson, CW .
GENE, 1998, 216 (01) :131-137
[4]   EARLY DETERMINATION AND PERMISSIVE EXPRESSION OF AMELOGENIN TRANSCRIPTION DURING MOUSE MANDIBULAR FIRST MOLAR DEVELOPMENT [J].
COUWENHOVEN, RI ;
SNEAD, ML .
DEVELOPMENTAL BIOLOGY, 1994, 164 (01) :290-299
[5]   An inhibitor domain in Sp3 regulates its glutamine-rich activation domains [J].
Dennig, J ;
Beato, M ;
Suske, G .
EMBO JOURNAL, 1996, 15 (20) :5659-5667
[6]   MEMBERS OF THE SP TRANSCRIPTION FACTOR FAMILY CONTROL TRANSCRIPTION FROM THE UTEROGLOBIN PROMOTER [J].
DENNIG, J ;
HAGEN, G ;
BEATO, M ;
SUSKE, G .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (21) :12737-12744
[7]   Cloning and characterization of the murine ameloblastin promoter [J].
Dhamija, S ;
Liu, Y ;
Yamada, Y ;
Snead, ML ;
Krebsbach, PH .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (29) :20738-20743
[8]   Immunohistochemical similarities and differences between amelogenin and tuftelin gene products during tooth development [J].
Diekwisch, TGH ;
Ware, J ;
Fincham, AG ;
ZeichnerDavid, M .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 1997, 45 (06) :859-866
[9]   TISSUE-SPECIFIC INVITRO TRANSCRIPTION FROM THE MOUSE ALBUMIN PROMOTER [J].
GORSKI, K ;
CARNEIRO, M ;
SCHIBLER, U .
CELL, 1986, 47 (05) :767-776
[10]   CLONING BY RECOGNITION SITE SCREENING OF 2 NOVEL GT BOX BINDING-PROTEINS - A FAMILY OF SP1 RELATED GENES [J].
HAGEN, G ;
MULLER, S ;
BEATO, M ;
SUSKE, G .
NUCLEIC ACIDS RESEARCH, 1992, 20 (21) :5519-5525