• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

人P51/TAP63(一种P53同源物)蛋白质稳定性的调控结构域。

Regulatory domain of protein stability of human P51/TAP63, a P53 homologue.

作者信息

Osada M, Inaba R, Shinohara H, Hagiwara M, Nakamura M, Ikawa Y

机构信息

Human Gene Sciences Center, Medical Research Institute, Tokyo Medical and Dental University, Yushima 1-5-45, Tokyo, Bunkyo-ku, 113-8510, Japan.

出版信息

Biochem Biophys Res Commun. 2001 May 25;283(5):1135-41. doi: 10.1006/bbrc.2001.4905.

DOI:10.1006/bbrc.2001.4905
PMID:11355891
Abstract

The amino terminal of human P51/TAp63, a P53 homologue, possesses a transactivation domain involved in the activation of its target genes by binding to DNA elements responsive to the p53 protein family. Using a series of amino terminal deletions, the transactivation domain was mapped between amino acid residues 50 to 69. This domain also regulates protein stability in a proteasome-dependent manner, and Ser51 and Ser68 were found to be essential for this stability. Our results suggest that P51 activity is greatly affected by protein stability.

摘要

人P51/TAp63是一种P53同源物,其氨基末端拥有一个反式激活结构域,该结构域通过与对p53蛋白家族有反应的DNA元件结合来激活其靶基因。通过一系列氨基末端缺失实验,反式激活结构域被定位在氨基酸残基50至69之间。该结构域还以蛋白酶体依赖性方式调节蛋白质稳定性,并且发现Ser51和Ser68对于这种稳定性至关重要。我们的结果表明,P51活性受蛋白质稳定性的极大影响。

相似文献

1
Regulatory domain of protein stability of human P51/TAP63, a P53 homologue.人P51/TAP63(一种P53同源物)蛋白质稳定性的调控结构域。
Biochem Biophys Res Commun. 2001 May 25;283(5):1135-41. doi: 10.1006/bbrc.2001.4905.
2
Effects of p51/p63 missense mutations on transcriptional activities of p53 downstream gene promoters.p51/p63错义突变对p53下游基因启动子转录活性的影响。
Cancer Res. 1999 Dec 1;59(23):5908-11.
3
deltaNp63alpha functions as both a positive and a negative transcriptional regulator and blocks in vitro differentiation of murine keratinocytes.δNp63α作为一种正负转录调节因子发挥作用,并阻断小鼠角质形成细胞的体外分化。
Oncogene. 2003 Jun 5;22(23):3635-44. doi: 10.1038/sj.onc.1206536.
4
The N terminus of the murine p53 tumour suppressor is an independent regulatory domain affecting activation and thermostability.小鼠p53肿瘤抑制蛋白的N端是一个影响激活和热稳定性的独立调节结构域。
J Mol Biol. 1998 Jan 30;275(4):575-88. doi: 10.1006/jmbi.1997.1507.
5
Distance constraints and stereospecific alignment requirements characteristic of p53 DNA-binding consensus sequence homologies.p53 DNA 结合共有序列同源性的距离限制和立体特异性比对要求。
Oncogene. 1995 Aug 17;11(4):723-33.
6
Proteasome-mediated degradation of transcriptional activators correlates with activation domain potency in vivo.蛋白酶体介导的转录激活因子降解与体内激活域效力相关。
EMBO J. 1999 Nov 15;18(22):6439-47. doi: 10.1093/emboj/18.22.6439.
7
The neurogene BTG2TIS21/PC3 is transactivated by DeltaNp73alpha via p53 specifically in neuroblastoma cells.神经基因BTG2TIS21/PC3在神经母细胞瘤细胞中通过DeltaNp73alpha经p53特异性反式激活。
J Cell Sci. 2005 Mar 15;118(Pt 6):1245-53. doi: 10.1242/jcs.01704. Epub 2005 Mar 1.
8
Role of an ING1 growth regulator in transcriptional activation and targeted histone acetylation by the NuA4 complex.ING1生长调节因子在NuA4复合物介导的转录激活和靶向组蛋白乙酰化中的作用。
Mol Cell Biol. 2001 Nov;21(22):7629-40. doi: 10.1128/MCB.21.22.7629-7640.2001.
9
Differential recognition of response elements determines target gene specificity for p53 and p63.反应元件的差异识别决定了p53和p63的靶基因特异性。
Mol Cell Biol. 2005 Jul;25(14):6077-89. doi: 10.1128/MCB.25.14.6077-6089.2005.
10
Characterization of transcriptional activation and DNA-binding functions in the hinge region of the vitamin D receptor.维生素D受体铰链区转录激活和DNA结合功能的表征
Biochemistry. 2005 Feb 22;44(7):2678-85. doi: 10.1021/bi0477182.

引用本文的文献

1
TP63 gain-of-function mutations cause premature ovarian insufficiency by inducing oocyte apoptosis.TP63 功能获得性突变通过诱导卵母细胞凋亡导致卵巢早衰。
J Clin Invest. 2023 Mar 1;133(5):e162315. doi: 10.1172/JCI162315.
2
Tmub1 Suppresses Hepatocellular Carcinoma by Promoting the Ubiquitination of ΔNp63 Isoforms.Tmub1通过促进ΔNp63亚型的泛素化来抑制肝细胞癌。
Mol Ther Oncolytics. 2020 Jun 4;18:126-136. doi: 10.1016/j.omto.2020.06.005. eCollection 2020 Sep 25.
3
C-terminal α Domain of p63 Binds to p300 to Coactivate β-Catenin.
p63 蛋白 C 端 α 结构域与 p300 结合,共同激活 β-连环蛋白。
Neoplasia. 2019 May;21(5):494-503. doi: 10.1016/j.neo.2019.03.010. Epub 2019 Apr 12.
4
UBE4B: a promising regulatory molecule in neuronal death and survival.UBE4B:神经元死亡与存活中一个有前景的调控分子。
Int J Mol Sci. 2012 Dec 10;13(12):16865-79. doi: 10.3390/ijms131216865.
5
The human papillomavirus E6 oncogene represses a cell adhesion pathway and disrupts focal adhesion through degradation of TAp63β upon transformation.人乳头瘤病毒 E6 癌基因通过转化过程中 TAp63β 的降解来抑制细胞黏附途径并破坏黏着斑。
PLoS Pathog. 2011 Sep;7(9):e1002256. doi: 10.1371/journal.ppat.1002256. Epub 2011 Sep 29.
6
The role of p63 in cancer, stem cells and cancer stem cells.p63 在癌症、干细胞和癌症干细胞中的作用。
Cell Mol Biol Lett. 2011 Jun;16(2):296-327. doi: 10.2478/s11658-011-0009-9. Epub 2011 Mar 20.
7
U-box-type ubiquitin E4 ligase, UFD2a attenuates cisplatin mediated degradation of DeltaNp63alpha.U-box型泛素E4连接酶UFD2a减弱顺铂介导的DeltaNp63alpha降解。
Cell Cycle. 2008 May 1;7(9):1231-7. doi: 10.4161/cc.7.9.5795. Epub 2008 Feb 19.
8
Differential recognition of response elements determines target gene specificity for p53 and p63.反应元件的差异识别决定了p53和p63的靶基因特异性。
Mol Cell Biol. 2005 Jul;25(14):6077-89. doi: 10.1128/MCB.25.14.6077-6089.2005.
9
A C-terminal inhibitory domain controls the activity of p63 by an intramolecular mechanism.一个C末端抑制结构域通过分子内机制控制p63的活性。
Mol Cell Biol. 2002 Dec;22(24):8601-11. doi: 10.1128/MCB.22.24.8601-8611.2002.