Academic Journal

H-Ras is degraded by Wnt/{beta}-catenin signaling via {beta}-TrCP-mediated polyubiquitylation

التفاصيل البيبلوغرافية
العنوان: H-Ras is degraded by Wnt/{beta}-catenin signaling via {beta}-TrCP-mediated polyubiquitylation
المؤلفون: Kim, Sung-Eun, Yoon, Ju-Yong, Jeong, Woo-Jeong, Jeon, Soung-Hoo, Park, Yoon, Yoon, Jong-Bok, Park, Young Nyun, Kim, Hoguen, Choi, Kang-Yell
بيانات النشر: Company of Biologists
سنة النشر: 2009
المجموعة: HighWire Press (Stanford University)
مصطلحات موضوعية: Research Article
الوصف: Ras is an important proto-protein that is regulated primarily by GDP/GTP exchange. Here, we report a novel regulatory mechanism whereby turnover of both endogenous and overexpressed H-Ras protein is controlled by β-TrCP-mediated ubiquitylation, proteasomal degradation and the Wnt/β-catenin signaling pathway. The interaction of H-Ras with the WD40 domain of β-TrCP targeted H-Ras for polyubiquitylation and degradation. This process was stimulated by Axin or adenomatous polyposis coli (Apc), and was inhibited by Wnt3a. Ras-mediated cellular transformation was also inhibited by the expression of β-TrCP and/or Axin. In vivo regulation of Ras stability by Wnt/β-catenin signaling was determined via measurements of the status of Ras in the intestines of mice stimulated with recombinant Wnt3a by intravenous tail vein injection. The regulation of Ras stability by Wnt/β-catenin signaling provides a mechanical basis for crosstalk between the Wnt/β-catenin and the Ras-ERK pathways involved in transformation.
نوع الوثيقة: text
وصف الملف: text/html
اللغة: English
Relation: http://jcs.biologists.org/cgi/content/short/jcs.040493v1; http://dx.doi.org/10.1242/jcs.040493
DOI: 10.1242/jcs.040493
الاتاحة: http://jcs.biologists.org/cgi/content/short/jcs.040493v1
https://doi.org/10.1242/jcs.040493
Rights: Copyright (C) 2009, Company of Biologists
رقم الانضمام: edsbas.5D4AE56F
قاعدة البيانات: BASE