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本文引用的文献

1
An active role of the DeltaN isoform of p63 in regulating basal keratin genes K5 and K14 and directing epidermal cell fate.p63的DeltaN亚型在调节基础角蛋白基因K5和K14以及指导表皮细胞命运中发挥积极作用。
PLoS One. 2009 May 20;4(5):e5623. doi: 10.1371/journal.pone.0005623.
2
BMP type I receptor inhibition reduces heterotopic [corrected] ossification.骨形态发生蛋白I型受体抑制可减少异位骨化。 (注:原文中“heterotopic [corrected] ossification”可能有误,推测应为“heterotopic ossification”,即异位骨化,这里按照推测后的正确内容进行了翻译)
Nat Med. 2008 Dec;14(12):1363-9. doi: 10.1038/nm.1888. Epub 2008 Nov 30.
3
Holding their own: the noncanonical roles of Smad proteins.坚守自身:Smad蛋白的非经典作用
Sci Signal. 2008 Nov 18;1(46):pe48. doi: 10.1126/scisignal.146pe48.
4
Direct targets of the TRP63 transcription factor revealed by a combination of gene expression profiling and reverse engineering.通过基因表达谱分析与逆向工程相结合揭示的TRP63转录因子的直接靶标
Genome Res. 2008 Jun;18(6):939-48. doi: 10.1101/gr.073601.107. Epub 2008 Apr 25.
5
Cripto-1 alters keratinocyte differentiation via blockade of transforming growth factor-beta1 signaling: role in skin carcinogenesis.Cripto-1通过阻断转化生长因子-β1信号通路改变角质形成细胞分化:在皮肤癌发生中的作用
Mol Cancer Res. 2008 Mar;6(3):509-16. doi: 10.1158/1541-7786.MCR-07-0396.
6
Tprg, a gene predominantly expressed in skin, is a direct target of the transcription factor p63.Tprg是一种主要在皮肤中表达的基因,是转录因子p63的直接靶标。
J Invest Dermatol. 2008 Jul;128(7):1676-85. doi: 10.1038/jid.2008.12. Epub 2008 Feb 7.
7
A novel bone morphogenetic protein signaling in heterotypic cell interactions in prostate cancer.一种在前列腺癌异型细胞相互作用中的新型骨形态发生蛋白信号传导。
Cancer Res. 2008 Jan 1;68(1):198-205. doi: 10.1158/0008-5472.CAN-07-5074.
8
Targeted repression of bone morphogenetic protein 7, a novel target of the p53 family, triggers proliferative defect in p53-deficient breast cancer cells.靶向抑制骨形态发生蛋白7(p53家族的一个新靶点)会引发p53缺陷型乳腺癌细胞的增殖缺陷。
Cancer Res. 2007 Oct 1;67(19):9117-24. doi: 10.1158/0008-5472.CAN-07-0996.
9
Abnormal urethra formation in mouse models of split-hand/split-foot malformation type 1 and type 4.1型和4型裂手/裂足畸形小鼠模型中的异常尿道形成
Eur J Hum Genet. 2008 Jan;16(1):36-44. doi: 10.1038/sj.ejhg.5201925. Epub 2007 Sep 19.
10
BMP7 is a podocyte survival factor and rescues podocytes from diabetic injury.骨形态发生蛋白7是一种足细胞存活因子,可挽救足细胞免受糖尿病损伤。
Am J Physiol Renal Physiol. 2007 Nov;293(5):F1641-8. doi: 10.1152/ajprenal.00179.2007. Epub 2007 Sep 5.

p63通过抑制Smad7以骨形态发生蛋白依赖性方式抑制非表皮谱系标志物。

p63 Suppresses non-epidermal lineage markers in a bone morphogenetic protein-dependent manner via repression of Smad7.

作者信息

De Rosa Laura, Antonini Dario, Ferone Giustina, Russo Monia T, Yu Paul B, Han Rong, Missero Caterina

机构信息

CEINGE Biotecnologie Avanzate, via Comunale Margherita 482, 80145 Napoli, Italy.

出版信息

J Biol Chem. 2009 Oct 30;284(44):30574-82. doi: 10.1074/jbc.M109.049619. Epub 2009 Aug 28.

DOI:10.1074/jbc.M109.049619
PMID:19717565
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2781612/
Abstract

p63, a p53 family member, plays an essential role in epidermal development by regulating its transcriptional program. Here we report a previously uncovered role of p63 in controlling bone morphogenetic protein (BMP) signaling, which is required for maintaining low expression levels of several non-epidermal genes. p63 represses transcription of the inhibitory Smad7 and activates Bmp7, thereby sustaining BMP signaling. In the absence of p63, compromised BMP signaling leads to inappropriate non-epidermal gene expression in postnatal mouse keratinocytes and in embryonic epidermis. Reactivation of BMP signaling by Smad7 knockdown and/or, to a lesser extent, by BMP treatment suppresses expression of non-epidermal genes in the absence of p63. Canonical BMP/Smad signaling is essential for control of non-epidermal genes as use of a specific inhibitor, or simultaneous knockdown of Smad1 and Smad5 counteract suppression of non-epidermal genes. Our data indicate that p63 prevents ectopic expression of non-epidermal genes by a mechanism involving Smad7 repression and, to a lesser extent, Bmp7 induction, with consequent enhancement of BMP/Smad signaling.

摘要

p63是一种p53家族成员,通过调节其转录程序在表皮发育中发挥重要作用。在此,我们报告了p63在控制骨形态发生蛋白(BMP)信号传导方面一个先前未被发现的作用,该信号传导对于维持几个非表皮基因的低表达水平是必需的。p63抑制抑制性Smad7的转录并激活Bmp7,从而维持BMP信号传导。在缺乏p63的情况下,受损的BMP信号传导导致出生后小鼠角质形成细胞和胚胎表皮中出现不适当的非表皮基因表达。通过敲低Smad7和/或在较小程度上通过BMP处理来重新激活BMP信号传导,可在缺乏p63的情况下抑制非表皮基因的表达。经典的BMP/Smad信号传导对于控制非表皮基因至关重要,因为使用特异性抑制剂或同时敲低Smad1和Smad5会抵消对非表皮基因的抑制作用。我们的数据表明,p63通过一种涉及抑制Smad7以及在较小程度上诱导Bmp7的机制来防止非表皮基因的异位表达,从而增强BMP/Smad信号传导。