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C/EBPß mediates RNA polymerase III-driven transcription of oncomiR-138 in malignant gliomas.
Di Pascale, Federica; Nama, Srikanth; Muhuri, Manish; Quah, Shan; Ismail, Hisyam M; Chan, Xin Hui Derryn; Sundaram, Gopinath M; Ramalingam, Rajkumar; Burke, Brian; Sampath, Prabha.
Afiliação
  • Di Pascale F; Institute of Medical Biology, Agency for Science Technology & Research (A*STAR), Singapore 138648, Singapore.
  • Nama S; Department of Biochemistry, Yong Loo Lin School of Medicine, National University of Singapore, Singapore.
  • Muhuri M; Institute of Medical Biology, Agency for Science Technology & Research (A*STAR), Singapore 138648, Singapore.
  • Quah S; Institute of Medical Biology, Agency for Science Technology & Research (A*STAR), Singapore 138648, Singapore.
  • Ismail HM; Institute of Medical Biology, Agency for Science Technology & Research (A*STAR), Singapore 138648, Singapore.
  • Chan XHD; Institute of Medical Biology, Agency for Science Technology & Research (A*STAR), Singapore 138648, Singapore.
  • Sundaram GM; Institute of Medical Biology, Agency for Science Technology & Research (A*STAR), Singapore 138648, Singapore.
  • Ramalingam R; Institute of Medical Biology, Agency for Science Technology & Research (A*STAR), Singapore 138648, Singapore.
  • Burke B; Institute of Medical Biology, Agency for Science Technology & Research (A*STAR), Singapore 138648, Singapore.
  • Sampath P; Institute of Medical Biology, Agency for Science Technology & Research (A*STAR), Singapore 138648, Singapore.
Nucleic Acids Res ; 46(1): 336-349, 2018 01 09.
Article em En | MEDLINE | ID: mdl-29136251
MicroRNA-138 (miR-138) is a pro-survival oncomiR for glioma stem cells. In malignant gliomas, dysregulated expression of microRNAs, such as miR-138, promotes Tumour initiation and progression. Here, we identify the ancillary role of the CCAAT/enhancer binding protein ß (C/EBPß) as a transcriptional activator of miR-138. We demonstrate that a short 158 bp DNA sequence encoding the precursor of miR-138-2 is essential and sufficient for transcription of miR-138. This short sequence includes the A-box and B-box elements characteristic of RNA Polymerase III (Pol III) promoters, and is also directly bound by C/EBPß via an embedded 'C/EBPß responsive element' (CRE). CRE and the Pol III B-box element overlap, suggesting that C/EBPß and transcription factor 3C (TFIIIC) interact at the miR-138-2 locus. We propose that this interaction is essential for the recruitment of the RNA Pol III initiation complex and associated transcription of the oncomiR, miR-138 in malignant gliomas.
Assuntos

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Transcrição Gênica / RNA Polimerase III / Proteína beta Intensificadora de Ligação a CCAAT / MicroRNAs / Glioma Tipo de estudo: Prognostic_studies Limite: Animals / Humans Idioma: En Revista: Nucleic Acids Res Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Singapura

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Transcrição Gênica / RNA Polimerase III / Proteína beta Intensificadora de Ligação a CCAAT / MicroRNAs / Glioma Tipo de estudo: Prognostic_studies Limite: Animals / Humans Idioma: En Revista: Nucleic Acids Res Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Singapura