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Sfrp2 is a transcriptional target of SREBP-1 in mouse chondrogenic cells.

作者信息

Kim Mi-Jin, Kim Jung-Eun, Lee Wan, Park Seung-Yoon

机构信息

Department of Biochemistry, School of Medicine, Dongguk University, Gyeongju, 780-714, Republic of Korea.

出版信息

Mol Cell Biochem. 2015 Aug;406(1-2):163-71. doi: 10.1007/s11010-015-2434-y. Epub 2015 May 14.

DOI:10.1007/s11010-015-2434-y
PMID:25971371
Abstract

Secreted frizzled-related protein 2 (Sfrp2) is highly expressed in developing limbs and is associated with skeletal malformation such as Brachydactyly and Syndactyly. However, the mechanism by which Sfrp2 gene was transcriptionally regulated in chondrogenic cells is largely unknown. Here, we found that sterol regulatory element binding protein-1 (SREBP-1) regulated transcriptional activation of the Sfrp2 gene in chondrogenic cells. Overexpression of SREBP-1 led to stimulation of Sfrp2 promoter activity and increase of Sfrp2 mRNA in chondrogenic ATDC5 cells. Reporter gene assays using deleted Sfrp2 promoter constructs showed that the position between -1150 and -840 is required for SREBP-1-mediated Sfrp2 promoter activity. Mutagenesis analysis showed that the SREBP-1-binding site at nucleotide -935 to -926 is a functional motif for Sfrp2 transcription. Promoter enzyme immunoassay and chromatin immunoprecipitation assay demonstrated that SREBP-1 binds directly to the SREBP-1-binding motif in the mouse Sfrp2 promoter. Thus, these results demonstrated that SREBP-1 acts as a positive regulator of Sfrp2 transcription in chondrogenic cells.

摘要

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本文引用的文献

1
SREBP-1 transcription factors regulate skeletal muscle cell size by controlling protein synthesis through myogenic regulatory factors.SREBP-1 转录因子通过调节肌生成调节因子来控制蛋白质合成,从而调节骨骼肌细胞大小。
PLoS One. 2012;7(11):e50878. doi: 10.1371/journal.pone.0050878. Epub 2012 Nov 30.
2
A new role for sterol regulatory element binding protein 1 transcription factors in the regulation of muscle mass and muscle cell differentiation.固醇调节元件结合蛋白 1 转录因子在调节肌肉质量和肌肉细胞分化中的新作用。
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Transcription factors RUNX1 and RUNX3 in the induction and suppressive function of Foxp3+ inducible regulatory T cells.
转录因子RUNX1和RUNX3在Foxp3 +诱导性调节性T细胞的诱导和抑制功能中的作用
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Mol Cancer. 2008 Nov 6;7:83. doi: 10.1186/1476-4598-7-83.
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Syndactyly and preaxial synpolydactyly in the single Sfrp2 deleted mutant mice.单基因Sfrp2缺失突变小鼠中的并指畸形和轴前多指(趾)畸形。
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Brachy-syndactyly caused by loss of Sfrp2 function.由Sfrp2功能丧失引起的短指并指畸形。
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7
Inhibition of myoblast differentiation by Sfrp1 and Sfrp2.Sfrp1和Sfrp2对成肌细胞分化的抑制作用。
Cell Tissue Res. 2008 May;332(2):299-306. doi: 10.1007/s00441-008-0574-z. Epub 2008 Mar 6.
8
Depletion of mitochondrial DNA up-regulates the expression of MDR1 gene via an increase in mRNA stability.线粒体DNA的缺失通过增加mRNA稳定性上调MDR1基因的表达。
Exp Mol Med. 2008 Feb 29;40(1):109-17. doi: 10.3858/emm.2008.40.1.109.
9
SFRP2 regulates cardiomyogenic differentiation by inhibiting a positive transcriptional autofeedback loop of Wnt3a.分泌型卷曲相关蛋白2(SFRP2)通过抑制Wnt3a的正向转录自反馈环来调节心肌生成分化。
Stem Cells. 2008 Jan;26(1):35-44. doi: 10.1634/stemcells.2007-0475. Epub 2007 Oct 4.
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Sfrp1 and Sfrp2 regulate anteroposterior axis elongation and somite segmentation during mouse embryogenesis.Sfrp1和Sfrp2在小鼠胚胎发育过程中调节前后轴伸长和体节分割。
Development. 2006 Mar;133(6):989-99. doi: 10.1242/dev.02274. Epub 2006 Feb 8.