Skeletal defects in Osterix-Cre transgenic mice

被引:62
作者
Huang, Wei [1 ]
Olsen, Bjorn R. [1 ]
机构
[1] Harvard Univ, Sch Dent Med, Dept Dev Biol, Boston, MA 02115 USA
基金
美国国家卫生研究院;
关键词
Osterix-Cre; Skeletal defects; Mouse; Transgenic; BONE-FORMATION; OSTEOBLAST DIFFERENTIATION; MOUSE; EXPRESSION; RECEPTOR; GENES;
D O I
10.1007/s11248-014-9828-6
中图分类号
Q5 [生物化学];
学科分类号
070307 [化学生物学];
摘要
Cre/loxP recombination is a powerful strategy widely used for in vivo conditional gene targeting. This technique has made possible many important discoveries of gene function in normal and disease biology. However, due to the transgenic nature of most Cre mouse strains undesired phenotypes occasionally occur in Cre mice. Here we report skeletal defects in Osterix-Cre (Osx-Cre) transgenic mice including delayed calvarial ossification and fracture calluses at multiple skeletal sites. These data suggest that Osx-Cre containing controls should be used for both in vivo and in vitro skeletal analyses of conditional knockout mice generated with this Osx-Cre mouse strain.
引用
收藏
页码:167 / 172
页数:6
相关论文
共 19 条
[1]
Chen JQ, 2014, PLOS ONE, V9, DOI [10.1371/journal.pone.0085161, 10.1371/journal.pone.0101277]
[2]
Decreased body weight in young Osterix-Cre transgenic mice results in delayed cortical bone expansion and accrual [J].
Davey, Rachel A. ;
Clarke, Michele V. ;
Sastra, Stephen ;
Skinner, Jarrod P. ;
Chiang, Cherie ;
Anderson, Paul H. ;
Zajac, Jeffrey D. .
TRANSGENIC RESEARCH, 2012, 21 (04) :885-893
[3]
The p38 MAPK pathway is essential for skeletogenesis and bone homeostasis in mice [J].
Greenblatt, Matthew B. ;
Shim, Jae-Hyuck ;
Zou, Weiguo ;
Sitara, Despina ;
Schweitzer, Michelle ;
Hu, Dorothy ;
Lotinun, Sutada ;
Sano, Yasuyo ;
Baron, Roland ;
Park, Jin Mo ;
Arthur, Simon ;
Xie, Min ;
Schneider, Michael D. ;
Zhai, Bo ;
Gygi, Steven ;
Davis, Roger ;
Glimcher, Laurie H. .
JOURNAL OF CLINICAL INVESTIGATION, 2010, 120 (07) :2457-2473
[4]
BMP signaling negatively regulates bone mass through sclerostin by inhibiting the canonical Wnt pathway [J].
Kamiya, Nobuhiro ;
Ye, Ling ;
Kobayashi, Tatsuya ;
Mochida, Yoshiyuki ;
Yamauchi, Mitsuo ;
Kronenberg, Henry M. ;
Feng, Jian Q. ;
Mishina, Yuji .
DEVELOPMENT, 2008, 135 (22) :3801-3811
[5]
Targeted disruption of Cbfa1 results in a complete lack of bone formation owing to maturational arrest of osteoblasts [J].
Komori, T ;
Yagi, H ;
Nomura, S ;
Yamaguchi, A ;
Sasaki, K ;
Deguchi, K ;
Shimizu, Y ;
Bronson, RT ;
Gao, YH ;
Inada, M ;
Sato, M ;
Okamoto, R ;
Kitamura, Y ;
Yoshiki, S ;
Kishimoto, T .
CELL, 1997, 89 (05) :755-764
[6]
Kuhn Ralf, 2002, Methods Mol Biol, V180, P175
[7]
Genetic and Pathologic Aspects of Retinoic Acid-Induced Limb Malformations in the Mouse [J].
Lee, Grace S. ;
Liao, Xiaoyan ;
Shimizu, Hirohito ;
Collins, Michael D. .
BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY, 2010, 88 (10) :863-882
[8]
[9]
The novel zinc finger-containing transcription factor Osterix is required for osteoblast differentiation and bone formation [J].
Nakashima, K ;
Zhou, X ;
Kunkel, G ;
Zhang, ZP ;
Deng, JM ;
Behringer, RR ;
de Crombrugghe, B .
CELL, 2002, 108 (01) :17-29
[10]
Gαq Signal in Osteoblasts Is Inhibitory to the Osteoanabolic Action of Parathyroid Hormone [J].
Ogata, Naoshi ;
Shinoda, Yusuke ;
Wettschureck, Nina ;
Offermanns, Stefan ;
Takeda, Shu ;
Nakamura, Kozo ;
Segre, Gino V. ;
Chung, Ung-il ;
Kawaguchi, Hiroshi .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2011, 286 (15) :13733-13740