Col1a1-GFP transgene expression in developing incisors

被引:23
作者
Braut, A
Kalajzic, I
Kalajzic, Z
Rowe, DW
Kollar, EJ
Mina, M [1 ]
机构
[1] Univ Connecticut, Ctr Hlth, Dept Pediat Dent, Farmington, CT 06030 USA
[2] Univ Connecticut, Ctr Hlth, Dept Genet & Dev Biol, Farmington, CT USA
[3] Univ Connecticut, Ctr Hlth, Dept Biostruct & Funct, Farmington, CT 06032 USA
关键词
dentinogenesis; green fluorescent protein; type I collagen;
D O I
10.1080/03008200290001078
中图分类号
Q2 [细胞生物学];
学科分类号
071009 [细胞生物学]; 090102 [作物遗传育种];
摘要
Previous studies have shown that terminal differentiation of odontoblasts is accompanied by dramatic increases in type I collagen synthesis. Recently transgenic mice in which green fluorescent protein (GFP) expression is under the control of the rat 3.6 (pOBCol3.6GFPtpz) and 2.3 (pOBCol2.3GFPemd) Col1a1 promoter fragments were generated. Our analysis of these GFP-expressing transgenic mice shows that the 2.3-kb promoter fragment directs strong expression of GFP only to bones and teeth, whereas the 3.6-kb fragment of promoter directs strong expression of GFP in bone and tooth, as well as in other type I collagen producing tissues. Our observations of incisors in these transgenic mice show high levels of GFP expression in functional odontoblasts and in differentiated osteoblasts. These observations show that expression of GFP reporter genes closely follow the patterns of expression of alpha1(I) collagen in various tissues including odontoblasts.
引用
收藏
页码:216 / 219
页数:4
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