Suppr超能文献

Siah-1b是p53的直接转录靶点:siah-1b启动子中功能性p53反应元件的鉴定。

Siah-1b is a direct transcriptional target of p53: identification of the functional p53 responsive element in the siah-1b promoter.

作者信息

Fiucci Giusy, Beaucourt Séverine, Duflaut Dominique, Lespagnol Alexandra, Stumptner-Cuvelette Pamela, Géant Anne, Buchwalter Gilles, Tuynder Marcel, Susini Laurent, Lassalle Jean-Michel, Wasylyk Christine, Wasylyk Bohdan, Oren Moshe, Amson Robert, Telerman Adam

机构信息

Molecular Engines Laboratories, 20 Rue Bouvier, 75011 Paris, France.

出版信息

Proc Natl Acad Sci U S A. 2004 Mar 9;101(10):3510-5. doi: 10.1073/pnas.0400177101. Epub 2004 Feb 25.

Abstract

Siah proteins are E3 ubiquitin ligases. They are homologues of the Drosophila seven in absentia (Sina), a protein required for the R7 photoreceptor development. We have previously found that the expression of human siah-1 and its mouse homologue siah-1b are induced by p53 during apoptosis and tumor reversion. So far, no evidence that the siah-1b gene is a direct transcriptional target of p53 has been provided. In the present study we investigate this issue. Northern blot analysis with a specific probe demonstrates an increase in siah-1b transcription on activation of endogenous and inducible exogenous p53. To explore whether this effect is directly mediated by p53 we analyzed 20 kb of chromosome X DNA, containing the siah-1b locus. A p53-binding site was identified in the siah-1b promoter, located at nucleotides -2155/-2103 relative to the translational start site. This site is composed of two half-sites, conforming to the p53-binding consensus sequence but separated by a nonclassical 33-bp spacer. In luciferase assays, p53 induces a substantial increase in siah-1b promoter activity. Gel shift and DNase-I-footprinting studies, combined with mutational analysis and chromatin immunoprecipitation, indicate that p53 effectively binds the siah-1b promoter in vitro and in vivo. Thus, the siah-1b gene is a direct transcriptional target of p53.

摘要

Siah蛋白是E3泛素连接酶。它们是果蝇中无七(Sina)蛋白的同源物,Sina是R7光感受器发育所必需的一种蛋白质。我们之前发现,在细胞凋亡和肿瘤逆转过程中,人类siah-1及其小鼠同源物siah-1b的表达由p53诱导。到目前为止,尚未有证据表明siah-1b基因是p53的直接转录靶点。在本研究中,我们对这一问题进行了调查。用特异性探针进行的Northern印迹分析表明,内源性和可诱导的外源性p53激活后,siah-1b转录增加。为了探究这种效应是否直接由p53介导,我们分析了包含siah-1b基因座的20 kb X染色体DNA。在siah-1b启动子中鉴定出一个p53结合位点,相对于翻译起始位点位于核苷酸-2155/-2103处。该位点由两个半位点组成,符合p53结合共有序列,但被一个非经典的33 bp间隔区隔开。在荧光素酶测定中,p53可使siah-1b启动子活性大幅增加。凝胶迁移和DNase-I足迹研究,结合突变分析和染色质免疫沉淀,表明p53在体外和体内均能有效结合siah-1b启动子。因此,siah-1b基因是p53的直接转录靶点。

相似文献

1
Siah-1b is a direct transcriptional target of p53: identification of the functional p53 responsive element in the siah-1b promoter.
Proc Natl Acad Sci U S A. 2004 Mar 9;101(10):3510-5. doi: 10.1073/pnas.0400177101. Epub 2004 Feb 25.
3
The characterization of the human Siah-1 promoter(1).
FEBS Lett. 2002 Feb 13;512(1-3):223-6. doi: 10.1016/s0014-5793(02)02265-2.
4
Phylogenetic analysis of the SINA/SIAH ubiquitin E3 ligase family in Metazoa.
BMC Evol Biol. 2017 Aug 7;17(1):182. doi: 10.1186/s12862-017-1024-x.
7
Hepatitis B virus X protein activates E3 ubiquitin ligase Siah-1 to control virus propagation via a negative feedback loop.
J Gen Virol. 2017 Jul;98(7):1774-1784. doi: 10.1099/jgv.0.000856. Epub 2017 Jul 17.
9
A novel retinoic acid-responsive element regulates retinoic acid-induced BLR1 expression.
Mol Cell Biol. 2004 Mar;24(6):2423-43. doi: 10.1128/MCB.24.6.2423-2443.2004.
10
Mediation of Af4 protein function in the cerebellum by Siah proteins.
Proc Natl Acad Sci U S A. 2004 Oct 12;101(41):14901-6. doi: 10.1073/pnas.0406196101. Epub 2004 Sep 30.

引用本文的文献

3
Mutant p53 Gain-of-Function: Role in Cancer Development, Progression, and Therapeutic Approaches.
Front Cell Dev Biol. 2021 Feb 11;8:607670. doi: 10.3389/fcell.2020.607670. eCollection 2020.
6
An investigation of the correlation between the S-glutathionylated GAPDH levels in blood and Alzheimer's disease progression.
PLoS One. 2020 May 29;15(5):e0233289. doi: 10.1371/journal.pone.0233289. eCollection 2020.
7
Reactive Oxygen Species, Metabolic Plasticity, and Drug Resistance in Cancer.
Int J Mol Sci. 2020 May 12;21(10):3412. doi: 10.3390/ijms21103412.
8
S-Nitrosylation: An Emerging Paradigm of Redox Signaling.
Antioxidants (Basel). 2019 Sep 17;8(9):404. doi: 10.3390/antiox8090404.
9
Plakoglobin restores tumor suppressor activity of p53 mutant by sequestering the oncogenic potential of β-catenin.
Cancer Sci. 2018 Jun;109(6):1876-1888. doi: 10.1111/cas.13612. Epub 2018 May 23.
10
Seven in Absentia E3 Ubiquitin Ligases: Central Regulators of Neural Cell Fate and Neuronal Polarity.
Front Cell Neurosci. 2017 Oct 13;11:322. doi: 10.3389/fncel.2017.00322. eCollection 2017.

本文引用的文献

1
Siah-1 facilitates ubiquitination and degradation of synphilin-1.
J Biol Chem. 2003 Dec 19;278(51):51504-14. doi: 10.1074/jbc.M306347200. Epub 2003 Sep 23.
2
The p53-inducible TSAP6 gene product regulates apoptosis and the cell cycle and interacts with Nix and the Myt1 kinase.
Proc Natl Acad Sci U S A. 2003 Mar 4;100(5):2284-9. doi: 10.1073/pnas.0530298100. Epub 2003 Feb 26.
5
Structural analysis of Siah1 and its interactions with Siah-interacting protein (SIP).
J Biol Chem. 2003 Jan 17;278(3):1837-40. doi: 10.1074/jbc.M210263200. Epub 2002 Nov 5.
6
Normal p53 function in primary cells deficient for Siah genes.
Mol Cell Biol. 2002 Dec;22(23):8155-64. doi: 10.1128/MCB.22.23.8155-8164.2002.
7
Stress-induced decrease in TRAF2 stability is mediated by Siah2.
EMBO J. 2002 Nov 1;21(21):5756-65. doi: 10.1093/emboj/cdf576.
8
Biological models and genes of tumor reversion: cellular reprogramming through tpt1/TCTP and SIAH-1.
Proc Natl Acad Sci U S A. 2002 Nov 12;99(23):14976-81. doi: 10.1073/pnas.222470799. Epub 2002 Oct 24.
10
The p53MH algorithm and its application in detecting p53-responsive genes.
Proc Natl Acad Sci U S A. 2002 Jun 25;99(13):8467-72. doi: 10.1073/pnas.132268899. Epub 2002 Jun 19.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验