the proto-oncogene lrf is under post-transcriptional control of mir-20a implications for senescence原癌基因的探测器是转录后控制mir-20a对衰老的影响.pdfVIP

the proto-oncogene lrf is under post-transcriptional control of mir-20a implications for senescence原癌基因的探测器是转录后控制mir-20a对衰老的影响.pdf

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the proto-oncogene lrf is under post-transcriptional control of mir-20a implications for senescence原癌基因的探测器是转录后控制mir-20a对衰老的影响

The Proto-Oncogene LRF Is under Post-Transcriptional Control of MiR-20a: Implications for Senescence 1,2,3. 1. 1 1 2,3 1 Laura Poliseno , Letizia Pitto , Marcella Simili , Laura Mariani , Luisa Riccardi , Alessia Ciucci , 1 1 1 2,3 1,4 Milena Rizzo , Monica Evangelista , Alberto Mercatanti , Pier Paolo Pandolfi , Giuseppe Rainaldi * 1 Laboratory of Gene and Molecular Therapy, Institute of Clinical Physiology, CNR, Pisa, Italy, 2 Cancer Genetics Program, Beth Israel Deaconess Cancer Center, Department of Pathology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts, United States of America, 3 Cancer Genetics Program, Beth Israel Deaconess Cancer Center, Department of Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts, United States of America, 4 Istituto Toscano Tumori, Firenze, Italy Abstract MicroRNAs (miRNAs) are short 20–22 nucleotide RNA molecules that act as negative regulators of gene expression via translational repression: they have been shown to play a role in development, proliferation, stress response, and apoptosis. The transcriptional regulator LRF (Leukemia/lymphoma Related Factor) has been shown to prevent p19ARF transcription and consequently to inhibit senescence in mouse embryonic fibroblasts (MEF). Here we report, for the first time, that LRF is post-transcriptionally regulated by miR-20a. Using a gene reporter assay, direct interaction of miR-20a with the LRF 39UTR is demonstrated. To validate the

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