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在阿贝尔逊鼠白血病病毒诱导前B细胞转化过程中,p19Arf定位的变化伴随着凋亡危机。

Changes in p19Arf localization accompany apoptotic crisis during pre-B-cell transformation by Abelson murine leukemia virus.

作者信息

Zimmerman Rebekah Stackpole, Rosenberg Naomi

机构信息

Department of Pathology, Genetics Graduate Program, Sackler School of Graduate Biomedical Sciences, Tufts University School of Medicine, Boston, Massachusetts 02111, USA.

出版信息

J Virol. 2008 Sep;82(17):8383-91. doi: 10.1128/JVI.00348-08. Epub 2008 Jun 25.

Abstract

Transformation by Abelson murine leukemia virus (Ab-MLV) is a multistep process in which growth-stimulatory signals from the v-Abl oncoprotein and growth-suppressive signals from the p19(Arf)-p53 tumor suppressor pathway oppose each other and influence the outcome of infection. The process involves a proliferative phase during which highly viable primary transformants expand, followed by a period of marked apoptosis (called "crisis") that is dependent on the presence of p19(Arf) and p53; rare cells that survive this phase emerge as fully transformed and malignant. To understand the way in which v-Abl expression affects p19(Arf) expression, we examined changes in expression of Arf during all stages of Ab-MLV transformation process. As is consistent with the ability of v-Abl to stimulate Myc, a transcription factor known to induce p19(Arf), Myc and Arf are induced soon after infection and p19(Arf) is expressed. At these early time points, the infected cells remain highly viable. The onset of crisis is marked by an increase in p19(Arf) expression and a change in localization of the protein from the nucleoplasm to the nucleolus. These data together suggest that the localization and expression levels of p19(Arf) modulate the effects of the protein during oncogenesis and reveal that the p19(Arf)-mediated response is subject to multiple layers of regulation that influence its function during Ab-MLV-mediated transformation.

摘要

阿贝尔森鼠白血病病毒(Ab-MLV)介导的细胞转化是一个多步骤过程,其中来自v-Abl癌蛋白的生长刺激信号与来自p19(Arf)-p53肿瘤抑制途径的生长抑制信号相互拮抗,并影响感染的结果。该过程包括一个增殖阶段,在此期间高度存活的初级转化细胞得以扩增,随后是一段明显的凋亡期(称为“危机”),这依赖于p19(Arf)和p53的存在;在这个阶段存活下来的罕见细胞会发展成为完全转化的恶性细胞。为了了解v-Abl表达影响p19(Arf)表达的方式,我们研究了Ab-MLV转化过程各个阶段中Arf表达的变化。与v-Abl刺激Myc的能力一致,Myc是一种已知可诱导p19(Arf)的转录因子,感染后Myc和Arf很快被诱导,p19(Arf)得以表达。在这些早期时间点,被感染的细胞保持高度存活。危机的开始以p19(Arf)表达的增加以及该蛋白从核质向核仁的定位变化为标志。这些数据共同表明,p19(Arf)的定位和表达水平在肿瘤发生过程中调节该蛋白的作用,并揭示p19(Arf)介导的反应受到多层调控的影响,这些调控在Ab-MLV介导的转化过程中影响其功能。

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