• 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

多瘤病毒早期功能对体外肌源性分化的抑制作用。

Inhibition of in vitro myogenic differentiation by a polyomavirus early function.

作者信息

Maione R, Fimia G M, Amati P

机构信息

Dipartimento di Biopatologia Umana, Università di Roma La Sapienza, Italy.

出版信息

Oncogene. 1992 Jan;7(1):85-93.

PMID:1311065
Abstract

In the present work we report on the role of a polyomavirus (Py) early function in interfering with both morphological and biochemical differentiation of the myogenic C2 cell line. The analysis of cell clones stably transfected with a plasmid carrying an ORI- Py genome showed that in the presence of the whole viral early region myogenesis is blocked and a transformed phenotype is evident. By using a plasmid that only encodes large-T function, the involvement of this individual early viral gene product was determined. Inhibition of myogenic differentiation by Py large T is proportional to the level of its expression. This inhibition does not appear to require alteration of cell growth properties. The analysis of muscle-specific functions expressed at different steps in the myogenic pathway showed that Py large T blocks the expression of terminal differentiation markers without altering the expression of the regulatory gene MyoD.

摘要

在本研究中,我们报告了一种多瘤病毒(Py)早期功能在干扰成肌C2细胞系的形态和生化分化方面的作用。对稳定转染携带ORI-Py基因组质粒的细胞克隆进行分析表明,在整个病毒早期区域存在的情况下,肌生成被阻断,转化表型明显。通过使用仅编码大T功能的质粒,确定了这种单个早期病毒基因产物的作用。Py大T对成肌分化的抑制作用与其表达水平成正比。这种抑制作用似乎不需要改变细胞生长特性。对成肌途径不同步骤表达的肌肉特异性功能进行分析表明,Py大T阻断终末分化标志物的表达,而不改变调节基因MyoD的表达。

相似文献

1
Inhibition of in vitro myogenic differentiation by a polyomavirus early function.多瘤病毒早期功能对体外肌源性分化的抑制作用。
Oncogene. 1992 Jan;7(1):85-93.
2
Inhibition of in vitro muscle differentiation by the immortalizing oncogene py LT-ag.永生化癌基因py LT-ag对体外肌肉分化的抑制作用
Symp Soc Exp Biol. 1992;46:53-71.
3
SV40 T antigen inhibits expression of MyoD and myogenin, up-regulates Myf-5, but does not affect early expression of desmin or alpha 7 integrin during muscle development.SV40大T抗原在肌肉发育过程中抑制MyoD和肌细胞生成素的表达,上调Myf-5,但不影响结蛋白或α7整合素的早期表达。
Exp Cell Res. 1994 Feb;210(2):278-86. doi: 10.1006/excr.1994.1040.
4
Adenovirus 5 E1A represses muscle-specific enhancers and inhibits expression of the myogenic regulatory factor genes, MyoD1 and myogenin.腺病毒5型E1A抑制肌肉特异性增强子,并抑制成肌调节因子基因MyoD1和肌细胞生成素的表达。
Cell Growth Differ. 1990 Aug;1(8):375-82.
5
Expression of two myogenic regulatory factors myogenin and MyoD1 during mouse embryogenesis.
Nature. 1989 Sep 28;341(6240):303-7. doi: 10.1038/341303a0.
6
Interleukin 1 alpha mediated inhibition of myogenic terminal differentiation: increased sensitivity of Ha-ras transformed cultures.
Cell Growth Differ. 1992 Apr;3(4):241-8.
7
Expression of Hox-7.1 in myoblasts inhibits terminal differentiation and induces cell transformation.
Nature. 1992 Dec 3;360(6403):477-81. doi: 10.1038/360477a0.
8
Conditional conversion of ES cells to skeletal muscle by an exogenous MyoD1 gene.通过外源性MyoD1基因将胚胎干细胞条件性转化为骨骼肌。
New Biol. 1992 Mar;4(3):217-24.
9
Bone morphogenetic protein-2 inhibits terminal differentiation of myogenic cells by suppressing the transcriptional activity of MyoD and myogenin.骨形态发生蛋白-2通过抑制MyoD和肌细胞生成素的转录活性来抑制成肌细胞的终末分化。
Exp Cell Res. 1997 Feb 1;230(2):342-51. doi: 10.1006/excr.1996.3432.
10
Involvement of myogenic regulator factors during fusion in the cell line C2C12.成肌调节因子在C2C12细胞系融合过程中的作用
Int J Dev Biol. 2002 Mar;46(2):235-41.

引用本文的文献

1
Activation of CREB/ATF sites by polyomavirus large T antigen.多瘤病毒大T抗原对CREB/ATF位点的激活。
J Virol. 2005 Apr;79(7):4180-90. doi: 10.1128/JVI.79.7.4180-4190.2005.
2
J domain-independent regulation of the Rb family by polyomavirus large T antigen.多瘤病毒大T抗原对Rb家族的J结构域非依赖性调控。
J Virol. 2000 Jun;74(11):5280-90. doi: 10.1128/jvi.74.11.5280-5290.2000.
3
Polyomavirus large T antigen induces alterations in cytoplasmic signalling pathways involving Shc activation.多瘤病毒大T抗原诱导涉及Shc激活的细胞质信号通路改变。
J Virol. 1999 Feb;73(2):1427-37. doi: 10.1128/JVI.73.2.1427-1437.1999.
4
The activity of differentiation factors induces apoptosis in polyomavirus large T-expressing myoblasts.分化因子的活性可诱导表达多瘤病毒大T抗原的成肌细胞发生凋亡。
Mol Biol Cell. 1998 Jun;9(6):1449-63. doi: 10.1091/mbc.9.6.1449.
5
Phosphorylation sites in polyomavirus large T antigen that regulate its function in viral, but not cellular, DNA synthesis.多瘤病毒大T抗原中调节其在病毒而非细胞DNA合成中功能的磷酸化位点。
J Virol. 1997 Sep;71(9):6472-8. doi: 10.1128/JVI.71.9.6472-6478.1997.
6
A natural hepatocyte growth factor/scatter factor autocrine loop in myoblast cells and the effect of the constitutive Met kinase activation on myogenic differentiation.成肌细胞中天然肝细胞生长因子/分散因子自分泌环及组成型Met激酶激活对成肌分化的影响。
J Cell Biol. 1997 Jun 2;137(5):1057-68. doi: 10.1083/jcb.137.5.1057.
7
Induction of cyclins E and A in response to mitogen removal: a basic alteration associated with the arrest of differentiation of C2 myoblasts transformed by simian virus 40 large T antigen.响应有丝分裂原去除而诱导细胞周期蛋白E和A:与猿猴病毒40大T抗原转化的C2成肌细胞分化停滞相关的一种基本改变。
J Virol. 1997 Mar;71(3):2217-24. doi: 10.1128/JVI.71.3.2217-2224.1997.
8
Characterization of siamycin I, a human immunodeficiency virus fusion inhibitor.西阿霉素I(一种人类免疫缺陷病毒融合抑制剂)的特性研究
Antimicrob Agents Chemother. 1996 Jan;40(1):133-8. doi: 10.1128/AAC.40.1.133.
9
Genetic analysis of polyomavirus large T nuclear localization: nuclear localization is required for productive association with pRb family members.多瘤病毒大T抗原核定位的遗传分析:与视网膜母细胞瘤蛋白(pRb)家族成员有效结合需要核定位。
J Virol. 1996 Jun;70(6):3581-8. doi: 10.1128/JVI.70.6.3581-3588.1996.
10
Characterization of an immortalizing N-terminal domain of polyomavirus large T antigen.多瘤病毒大T抗原N端永生化结构域的特性分析
J Virol. 1994 Feb;68(2):668-73. doi: 10.1128/JVI.68.2.668-673.1994.