Thakur Ram Krishna, Kumar Praveen, Halder Kangkan, Verma Anjali, Kar Anirban, Parent Jean-Luc, Basundra Richa, Kumar Akinchan, Chowdhury Shantanu
Proteomics and Structural Biology Unit, Institute of Genomics and Integrative Biology, CSIR, Delhi, India.
Nucleic Acids Res. 2009 Jan;37(1):172-83. doi: 10.1093/nar/gkn919. Epub 2008 Nov 25.
Regulatory influence of the G-quadruplex or G4 motif present within the nuclease hypersensitive element (NHE) in the promoter of c-MYC has been noted. On the other hand, association of NM23-H2 to the NHE leads to c-MYC activation. Therefore, NM23-H2 interaction with the G4 motif within the c-MYC NHE presents an interesting mechanistic possibility. Herein, using luciferase reporter assay and chromatin immunoprecipitation we show NM23-H2 mediated c-MYC activation involves NM23-H2-G4 motif binding within the c-MYC NHE. G4 motif complex formation with recombinant NM23-H2 was independently confirmed using fluorescence energy transfer, which also indicated that the G4 motif was resolved to an unfolded state within the protein-bound complex. Taken together, this supports transcriptional role of NM23-H2 via a G4 motif.
c-MYC启动子中核酸酶超敏元件(NHE)内存在的G-四链体或G4基序的调控作用已被关注。另一方面,NM23-H2与NHE的结合会导致c-MYC激活。因此,NM23-H2与c-MYC NHE内的G4基序相互作用呈现出一种有趣的机制可能性。在此,我们利用荧光素酶报告基因检测和染色质免疫沉淀表明,NM23-H2介导的c-MYC激活涉及NM23-H2与c-MYC NHE内G4基序的结合。利用荧光能量转移独立证实了重组NM23-H2与G4基序复合物的形成,这也表明G4基序在蛋白质结合复合物中转变为未折叠状态。综上所述,这支持了NM23-H2通过G4基序发挥转录作用。