Chen Lan, Liu Tianyu, Tu Yunhua, Rong Dongyun, Cao Yu
Department of Dermatology, The Affiliated Hospital of Guiyang Medical University, Guiyang, Guizhou 550004, P.R. China.
Oncol Rep. 2016 Feb;35(2):1049-56. doi: 10.3892/or.2015.4442. Epub 2015 Nov 23.
Cullin1 (Cul1) serves as a rigid scaffold in the SCF (Skp1/Cullin/Rbx1/F-box protein) E3 ubiquitin ligase complex and has been found to be overexpressed in melanoma and to enhance melanoma cell proliferation by promoting G1-S phase transition. However, the underlying mechanisms involved in the regulation of melanoma cell proliferation by Cul1 remain poorly understood. In the present study, we found that Cul1 promoted mTORC1 activity and cap-dependent translation by enhancing the ubiquitination and degradation of DEPTOR. We further showed that suppression of the eIF4F complex assembly profoundly inhibited the promoting effect of Cul1 on melanoma cell proliferation, while enhancement of the eIF4F complex activity reversed the inhibitory effect of Cul1 depletion on melanoma cell proliferation, indicating that Cul1 contributes to melanoma cell proliferation by activating cap‑dependent translation. These data elucidate the role of Cul1 in cap-dependent translation and improves our understanding of the underlying mechanisms involved in the regulation of melanoma cell proliferation by Cul1.
Cullin1(Cul1)在SCF(Skp1/Cullin/Rbx1/F-box蛋白)E3泛素连接酶复合物中作为一个刚性支架,并且已发现在黑色素瘤中过表达,并通过促进G1-S期转变来增强黑色素瘤细胞增殖。然而,Cul1调控黑色素瘤细胞增殖所涉及的潜在机制仍知之甚少。在本研究中,我们发现Cul1通过增强DEPTOR的泛素化和降解来促进mTORC1活性和帽依赖性翻译。我们进一步表明,抑制eIF4F复合物组装可显著抑制Cul1对黑色素瘤细胞增殖的促进作用,而增强eIF4F复合物活性可逆转Cul1缺失对黑色素瘤细胞增殖的抑制作用,这表明Cul1通过激活帽依赖性翻译促进黑色素瘤细胞增殖。这些数据阐明了Cul1在帽依赖性翻译中的作用,并增进了我们对Cul1调控黑色素瘤细胞增殖所涉及的潜在机制的理解。