Regulation of Gli1 transcriptional activity in the nucleus by Dyrk1

被引:154
作者
Mao, JH
Maye, P
Kogerman, P
Tejedor, FJ
Toftgard, R
Xie, W
Wu, GQ
Wu, DQ
机构
[1] Univ Connecticut, Ctr Hlth, Dept Genet & Dev Biol, Farmington, CT 06030 USA
[2] Karolinska Inst, Dept Biosci, SE-14157 Huddinge, Sweden
[3] Novum, Ctr Nutr & Toxicol, SE-14157 Huddinge, Sweden
[4] Tallinn Univ Technol, NICPB, EE-200108 Tallinn, Estonia
[5] Tallinn Univ Technol, Ctr Gene Technol, EE-200108 Tallinn, Estonia
[6] Univ Miguel Hernandezy, CSIC, Inst Neurociencias, Unidad Neurobiol Desarrollo, Alicante 03550, Spain
[7] Univ Rochester, Dept Pharmacol, Rochester, NY 14642 USA
[8] SE Univ, Sch Med, Dept Genet, Nanjing 210018, Peoples R China
[9] Vanderbilt Univ, Dept Med Med Genet, Nashville, TN 37232 USA
关键词
D O I
10.1074/jbc.M206743200
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
To investigate the cellular role of dual specificity Yak1-related kinase (Dyrk) 1, a nuclear localized dual specificity protein kinase, we examined its effect on transcriptional regulation using reporter gene assays. We found that Dyrk1 can substantially enhance Gli1-dependent, but not LEF-1-, c-Jun-, or Elk-dependent, gene transcription. In part, Dyrk1 does this through retaining Gli1 in the nucleus. However, we also demonstrate that Dyrk1 can enhance the transcriptional activity of Gli1-AHA, a nuclear export mutant, suggesting that Dyrk1 may be more directly involved in regulating the transcriptional activity of Gli1. In addition, Dyrk1 acted synergistically with Sonic hedgehog (Shh) to induce gene transcription and differentiation in mouse C3H10T1/2 cells. The failure of Shh to stimulate Dyrk1 kinase activity suggests that Dyrk1 may not be directly regulated by the Shh signaling pathway but functionally interacts with it. Thus, Gli1 transcriptional activity may be subjected to further regulation in the cell nucleus by a pathway distinct from Shh signaling, one mediated by Dyrk1.
引用
收藏
页码:35156 / 35161
页数:6
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