• 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

The evolutionary conserved gene C16orf35 encodes a nucleo-cytoplasmic protein that interacts with p73.

作者信息

Lunardi Andrea, Chiacchiera Fulvio, D'Este Elisa, Carotti Marcello, Dal Ferro Marco, Di Minin Giulio, Del Sal Giannino, Collavin Licio

机构信息

Laboratorio Nazionale CIB (LNCIB), AREA Science Park, Padriciano 99, 34149 Trieste, Italy.

出版信息

Biochem Biophys Res Commun. 2009 Oct 16;388(2):428-33. doi: 10.1016/j.bbrc.2009.08.027. Epub 2009 Aug 8.

DOI:10.1016/j.bbrc.2009.08.027
PMID:19666006
Abstract

C16orf35 is a highly conserved gene positioned upstream of the alpha-globins in humans and other vertebrates. The deduced protein is also highly conserved, it has no defined structural features or domains, and its function is currently unknown. Here we show that the C16orf35 protein has nuclear and cytosolic distribution, and can localize to PML nuclear bodies. The C16orf35 protein was detected in several human transformed cells lines, and studies of transient and stable overexpression indicate that increased levels of C16orf35 inhibit cell proliferation. We also find that C16orf35 interacts with human p73, and represses transcription by TAp73gamma but not by TAp73alpha. This selectivity is not due to differential interaction, since C16orf35 binds both p73 variants. Our data suggest that C16orf35 can modulate differentially the specific activities of selected p73 isoforms.

摘要

相似文献

1
The evolutionary conserved gene C16orf35 encodes a nucleo-cytoplasmic protein that interacts with p73.
Biochem Biophys Res Commun. 2009 Oct 16;388(2):428-33. doi: 10.1016/j.bbrc.2009.08.027. Epub 2009 Aug 8.
2
Sp1 binds to the external promoter of the p73 gene and induces the expression of TAp73gamma in lung cancer.Sp1 结合到 p73 基因的外部启动子上,并诱导肺癌中 TAp73gamma 的表达。
FEBS J. 2010 Jul;277(14):3014-27. doi: 10.1111/j.1742-4658.2010.07710.x. Epub 2010 Jun 7.
3
Differential response of p53 target genes to p73 overexpression in SH-SY5Y neuroblastoma cell line.p53靶基因对SH-SY5Y神经母细胞瘤细胞系中p73过表达的差异反应。
J Cell Sci. 2004 Jan 15;117(Pt 2):293-301. doi: 10.1242/jcs.00834.
4
Identification of Daxx interacting with p73, one of the p53 family, and its regulation of p53 activity by competitive interaction with PML.鉴定与p53家族成员之一p73相互作用的Daxx及其通过与PML竞争性相互作用对p53活性的调节。
Nucleic Acids Res. 2003 Sep 15;31(18):5356-67. doi: 10.1093/nar/gkg741.
5
p73 supports cellular growth through c-Jun-dependent AP-1 transactivation.p73通过依赖c-Jun的AP-1反式激活来支持细胞生长。
Nat Cell Biol. 2007 Jun;9(6):698-705. doi: 10.1038/ncb1598. Epub 2007 May 13.
6
Two new p73 splice variants, gamma and delta, with different transcriptional activity.两种具有不同转录活性的新型p73剪接变体,γ和δ。
J Exp Med. 1998 Nov 2;188(9):1763-8. doi: 10.1084/jem.188.9.1763.
7
Regulation of p73 by Hck through kinase-dependent and independent mechanisms.Hck通过激酶依赖性和非依赖性机制对p73进行调控。
BMC Mol Biol. 2007 May 30;8:45. doi: 10.1186/1471-2199-8-45.
8
The transcriptional repressor ZEB regulates p73 expression at the crossroad between proliferation and differentiation.转录抑制因子ZEB在增殖与分化的交叉点调控p73的表达。
Mol Cell Biol. 2001 Dec;21(24):8461-70. doi: 10.1128/MCB.21.24.8461-8470.2001.
9
p73 and p63 sustain cellular growth by transcriptional activation of cell cycle progression genes.p73和p63通过细胞周期进程基因的转录激活来维持细胞生长。
Cancer Res. 2009 Nov 15;69(22):8563-71. doi: 10.1158/0008-5472.CAN-09-0259. Epub 2009 Oct 27.
10
P53 and p73 differ in their ability to inhibit glucocorticoid receptor (GR) transcriptional activity.P53和p73在抑制糖皮质激素受体(GR)转录活性的能力上存在差异。
Mol Cancer. 2006 Dec 6;5:68. doi: 10.1186/1476-4598-5-68.

引用本文的文献

1
Internal ribosome entry sites enhance translation in trans in antisense non-coding SINEUP and circular RNAs.内部核糖体进入位点增强反义非编码SINEUP和环状RNA中的反式翻译。
Nucleic Acids Res. 2025 Aug 11;53(15). doi: 10.1093/nar/gkaf788.
2
On the Prevalence and Roles of Proteins Undergoing Liquid-Liquid Phase Separation in the Biogenesis of PML-Bodies.在 PML 体生成中经历液-液相分离的蛋白质的流行和作用。
Biomolecules. 2023 Dec 18;13(12):1805. doi: 10.3390/biom13121805.
3
p53-Related Transcription Targets of TAp73 in Cancer Cells-Bona Fide or Distorted Reality?
TAp73 与 p53 相关的转录靶标在癌细胞中的真实写照?
Int J Mol Sci. 2020 Feb 17;21(4):1346. doi: 10.3390/ijms21041346.
4
Tumor suppressor NPRL2 induces ROS production and DNA damage response.抑癌基因 NPRL2 诱导活性氧产生和 DNA 损伤反应。
Sci Rep. 2017 Nov 10;7(1):15311. doi: 10.1038/s41598-017-15497-0.
5
SINEUPs are modular antisense long non-coding RNAs that increase synthesis of target proteins in cells.SINEUPs是模块化反义长链非编码RNA,可增加细胞中靶蛋白的合成。
Front Cell Neurosci. 2015 May 13;9:174. doi: 10.3389/fncel.2015.00174. eCollection 2015.
6
SEA you later alli-GATOR--a dynamic regulator of the TORC1 stress response pathway.待会儿见,短尾鳄——TORC1应激反应途径的动态调节因子。
J Cell Sci. 2015 Jun 15;128(12):2219-28. doi: 10.1242/jcs.168922. Epub 2015 May 1.
7
Nprl3 is required for normal development of the cardiovascular system.Nprl3 对于心血管系统的正常发育是必需的。
Mamm Genome. 2012 Aug;23(7-8):404-15. doi: 10.1007/s00335-012-9398-y. Epub 2012 Apr 27.