Department of Biological Sciences, Bose Institute, EN-80 Sector V, Salt Lake, Unified Campus, Kolkata 700091, India.
Institut für Biochemie, Universität Greifswald, Felix-Hausdorff-Str. 4, D-17489 Greifswald, Germany.
Cell Calcium. 2024 Nov;123:102944. doi: 10.1016/j.ceca.2024.102944. Epub 2024 Aug 12.
ORAI1 is an intrinsic component of store-operated calcium entry (SOCE) that strictly regulates Ca influx in most non-excitable cells. ORAI1 is overexpressed in a wide variety of cancers, and its signal transduction has been associated with chemotherapy resistance. There is extensive proteomic interaction of ORAI1 with other channels and effectors, resulting in various altered phenotypes. However, the transcription regulation of ORAI1 is not well understood. We have found a putative G-quadruplex (G4) motif, ORAI1-Pu, in the upstream promoter region of the gene, having regulatory functions. High-resolution 3-D NMR structure elucidation suggests that ORAI1-Pu is a stable parallel-stranded G4, having a long 8-nt loop imparting dynamics without affecting the structural stability. The protruded loop further houses an E-box motif that provides a docking site for transcription factors like Zeb1. The G4 structure was also endogenously observed using Chromatin Immunoprecipitation (ChIP) with anti-G4 antibody (BG4) in the MDA-MB-231 cell line overexpressing ORAI1. Ligand-mediated stabilization suggested that the stabilized G4 represses transcription in cancer cell line MDA-MB-231. Downregulation of transcription further led to decreased Ca entry by the SOCE pathway, as observed by live-cell Fura-2 Ca imaging.
ORAI1 是一种内在的钙库操纵性钙内流(SOCE)的组成部分,它严格调节大多数非兴奋细胞中的 Ca 内流。ORAI1 在多种癌症中过表达,其信号转导与化疗耐药性有关。ORAI1 与其他通道和效应器有广泛的蛋白质组相互作用,导致各种表型改变。然而,ORAI1 的转录调控还不是很清楚。我们在基因的上游启动子区域发现了一个假定的 G-四联体(G4)基序 ORAI1-Pu,它具有调节功能。高分辨率的 3D NMR 结构阐明表明,ORAI1-Pu 是一种稳定的平行链 G4,具有长 8nt 的环,赋予了动力学而不影响结构稳定性。伸出的环进一步容纳了一个 E 盒基序,为转录因子(如 Zeb1)提供了一个附着位点。在用抗 G4 抗体(BG4)进行染色质免疫沉淀(ChIP)时,也在过表达 ORAI1 的 MDA-MB-231 细胞系中观察到了内源性的 G4 结构。配体介导的稳定化表明,稳定的 G4 抑制了 MDA-MB-231 癌细胞系的转录。转录的下调进一步导致 SOCE 途径的 Ca 内流减少,这可以通过活细胞 Fura-2 Ca 成像观察到。