4.4 Article

Cellular microRNAs up-regulate transcription via interaction with promoter TATA-box motifs

Journal

RNA
Volume 20, Issue 12, Pages 1878-1889

Publisher

COLD SPRING HARBOR LAB PRESS, PUBLICATIONS DEPT
DOI: 10.1261/rna.045633.114

Keywords

microRNAs; TATA-box motif; core transcription machinery; transcription activation

Funding

  1. Introduction of Innovative R&D Team Program of Guangdong Province [2009010058]
  2. National Special Research Program for Important Infectious Diseases [2013ZX10001004]
  3. National Basic Research Program of China (973 Program) [2010CB912202]
  4. National Natural Science Foundation of China [30972620, 81301431]
  5. Natural Science Foundation of Guangdong [9251008901000022]
  6. Research Fund for the Doctoral Program of Higher Education of China [20090171110083]
  7. China Postdoctoral Science Foundation [2012M511866, 2013T60824]

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The TATA box represents one of the most prevalent core promoters where the pre-initiation complexes (PICs) for gene transcription are assembled. This assembly is crucial for transcription initiation and well regulated. Here we show that some cellular microRNAs (miRNAs) are associated with RNA polymerase II (Pol II) and TATA box-binding protein (TBP) in human peripheral blood mononuclear cells (PBMCs). Among them, let-7i sequence specifically binds to the TATA-box motif of interleukin-2 (IL-2) gene and elevates IL-2 mRNA and protein production in CD4(+) T-lymphocytes in vitro and in vivo. Through direct interaction with the TATA-box motif, let-7i facilitates the PIC assembly and transcription initiation of IL-2 promoter. Several other cellular miRNAs, such as mir-138, mir-92a or mir-181d, also enhance the promoter activities via binding to the TATA-box motifs of insulin, calcitonin or c-myc, respectively. In agreement with the finding that an HIV-1-encoded miRNA could enhance viral replication through targeting the viral promoter TATA-box motif, our data demonstrate that the interaction with core transcription machinery is a novel mechanism for miRNAs to regulate gene expression.

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