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Association, mutual stabilization, and transcriptional activity of the STRA13 and MSP58 proteins

机译:STRA13和MSP58蛋白的缔合,相互稳定和转录活性

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STRA13 is a hypoxia-inducible bHLH transcription factor implicated in the pVHL/HIF, TGF-beta, and Jak/STAT pathways. To further characterize the STRA13 protein-interacting network and mechanisms of STRA13-dependent transcription, we utilized yeast two-hybrid screening. Here we report on STRA13 interaction with the cell cycle-associated transcription factor MSP58. We demonstrated that the basic domain of STRA13 and the FHA domain of MSP58 are essential for this association. We performed phospho-peptide mapping of both MSP58 and STRA13 and showed that their association was modulated by the STRA13 phosphorylation status. STRA13/MSP58 complex formation protected both proteins from the proteasome-mediated degradation, extending their half-lives considerably. STRA13 and MSP58 synergistically co-operated in the STRA13 promoter-driven transcription repression. Both proteins were co-localized in the nucleus and showed transcript accumulation during the S phase of the cell cycle. Thus, we characterize a novel STRA13-associated transcription repression complex and provide a link between cell cycle regulation and STRA13 activity.
机译:STRA13是缺氧诱导的bHLH转录因子,与pVHL / HIF,TGF-beta和Jak / STAT途径有关。为了进一步表征STRA13蛋白质相互作用网络和STRA13依赖性转录机制,我们利用了酵母双杂交筛选技术。在这里,我们报告STRA13与细胞周期相关转录因子MSP58的相互作用。我们证明了STRA13的基本域和MSP58的FHA域对于此关联至关重要。我们对MSP58和STRA13进行了磷酸肽图分析,结果表明它们的缔合受到STRA13磷酸化状态的调节。 STRA13 / MSP58复合物的形成保护了这两种蛋白质免受蛋白酶体介导的降解,大大延长了其半衰期。 STRA13和MSP58在STRA13启动子驱动的转录抑制中协同合作。两种蛋白质都共定位在细胞核中,并在细胞周期的S期显示转录本积累。因此,我们表征新型STRA13相关的转录抑制复合物,并提供细胞周期调控和STRA13活性之间的联系。

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