Koch Heike B, Zhang Ru, Verdoodt Berlinda, Bailey Aaron, Zhang Chang-Dong, Yates John R, Menssen Antje, Hermeking Heiko
Molecular Oncology, Independent Max-Planck-Research Group, Max-Planck-Institute of Biochemistry, Martinsried, Germany.
Cell Cycle. 2007 Jan 15;6(2):205-17. doi: 10.4161/cc.6.2.3742. Epub 2007 Jan 20.
The c-MYC oncogene encodes a transcription factor, which is sufficient and necessary for the induction of cellular proliferation. However, the c-MYC protein is a relatively weak transactivator suggesting that it may have other functions. To identify protein interactors which may reveal new functions or represent regulators of c-MYC we systematically identified proteins associated with c-MYC in vivo using a proteomic approach. We combined tandem affinity purification (TAP) with the mass spectral multidimensional protein identification technology (MudPIT). Thereby, 221 c-MYC-associated proteins were identified. Among them were 17 previously known c-MYC-interactors. Selected new c-MYC-associated proteins (DBC-1, FBX29, KU70, MCM7, Mi2-beta/CHD4, RNA Pol II, RFC2, RFC3, SV40 Large T Antigen, TCP1alpha, U5-116kD, ZNF281) were confirmed independently. For association with MCM7, SV40 Large T Antigen and DBC-1 the functionally important MYC-box II region was required, whereas FBX29 and Mi2-beta interacted via MYC-box II and the BR-HLH-LZ motif. In addition, regulators of c-MYC activity were identified: ectopic expression of FBX29, an E3 ubiquitin ligase, decreased c-MYC protein levels and inhibited c-MYC transactivation, whereas knock-down of FBX29 elevated the concentration of c-MYC. Furthermore, sucrose gradient analysis demonstrated that c-MYC is present in numerous complexes with varying size and composition, which may accommodate the large number of new c-MYC-associated proteins identified here and mediate the diverse functions of c-MYC. Our results suggest that c-MYC, besides acting as a mitogenic transcription factor, regulates cellular proliferation by direct association with protein complexes involved in multiple synthetic processes required for cell division, as for example DNA-replication/repair and RNA-processing. Furthermore, this first comprehensive description of the c-MYC-associated sub-proteome will facilitate further studies aimed to elucidate the biology of c-MYC.
c-MYC癌基因编码一种转录因子,它对于诱导细胞增殖而言是充分且必要的。然而,c-MYC蛋白是一种相对较弱的反式激活因子,这表明它可能具有其他功能。为了鉴定可能揭示新功能或代表c-MYC调节因子的蛋白相互作用分子,我们使用蛋白质组学方法在体内系统地鉴定了与c-MYC相关的蛋白。我们将串联亲和纯化(TAP)与质谱多维蛋白质鉴定技术(MudPIT)相结合。由此,鉴定出了221种与c-MYC相关的蛋白。其中有17种是先前已知的c-MYC相互作用分子。所选的新的与c-MYC相关的蛋白(DBC-1、FBX29、KU70、MCM7、Mi2-β/CHD4、RNA聚合酶II、RFC2、RFC3、SV40大T抗原、TCP1α、U5-116kD、ZNF281)得到了独立验证。与MCM7、SV40大T抗原和DBC-1的结合需要功能重要的MYC-box II区域,而FBX29和Mi2-β则通过MYC-box II和BR-HLH-LZ基序相互作用。此外,还鉴定出了c-MYC活性的调节因子:E3泛素连接酶FBX29的异位表达降低了c-MYC蛋白水平并抑制了c-MYC的反式激活,而敲低FBX29则提高了c-MYC的浓度。此外,蔗糖密度梯度分析表明,c-MYC存在于许多大小和组成各异的复合物中,这可能容纳此处鉴定出的大量新的与c-MYC相关的蛋白,并介导c-MYC的多种功能。我们的结果表明,c-MYC除了作为促有丝分裂转录因子发挥作用外,还通过与参与细胞分裂所需的多个合成过程(例如DNA复制/修复和RNA加工)的蛋白复合物直接结合来调节细胞增殖。此外,对与c-MYC相关的亚蛋白质组的这首次全面描述将有助于旨在阐明c-MYC生物学特性的进一步研究。