Your browser doesn't support javascript.
loading
Induction of the long noncoding RNA NBR2 from the bidirectional BRCA1 promoter under hypoxic conditions.
Wiedmeier, J Erin; Ohlrich, Anna; Chu, Adrian; Rountree, Michael R; Turker, Mitchell S.
Afiliação
  • Wiedmeier JE; University of Utah School of Medicine, Salt Lake City, UT 84132, United States.
  • Ohlrich A; Oregon Institute of Occupational Health Sciences, Oregon Health & Science University, Portland, OR, 97239, United States.
  • Chu A; University of Utah School of Medicine, Salt Lake City, UT 84132, United States.
  • Rountree MR; Nzumbe Inc., Portland, OR, 97201, United States.
  • Turker MS; Oregon Institute of Occupational Health Sciences, Oregon Health & Science University, Portland, OR, 97239, United States; Department of Molecular and Medical Genetics, Oregon Health & Science University, Portland, OR, 97239, United States. Electronic address: turkerm@ohsu.edu.
Mutat Res ; 796: 13-19, 2017 02.
Article em En | MEDLINE | ID: mdl-28249151
BRCA1 plays an important role in preventing breast cancer and is often silenced or repressed in sporadic cancer. The BRCA1 promoter is bidirectional: it drives transcription of the long non-coding (lnc) NBR2 transcript in the opposite orientation relative to the BRCA1 transcript. Hypoxic conditions repress BRCA1 transcription, but their effect on expression of the NBR2 transcript has not been reported. We used quantitative RT-PCR to measure BRCA1 and NBR2 transcript levels in 0% and 1% oxygen in MCF-7 breast cancer cells and found that NBR2 transcript levels increased as a function of time under hypoxic conditions, whereas BRCA1 mRNA levels were repressed. Hypoxic conditions were ineffective in reducing BRCA1 mRNA in the UACC-3199 breast cancer cell line, which is reported to have an epigenetically silenced BRCA1 promoter, even though appreciable levels of BRCA1 and NBR2 mRNA were detected. Significant recovery back to baseline RNA levels occurred within 48h after the MCF-7 cells were restored to normoxic conditions. We used a construct with the 218bp minimal BRCA1 promoter linked to marker genes to show that this minimal promoter repressed expression bidirectionally under hypoxic conditions, which suggests that the elements necessary for induction of NBR2 are located elsewhere.
Assuntos
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fatores de Transcrição / Neoplasias da Mama / Regulação Neoplásica da Expressão Gênica / Regiões Promotoras Genéticas / Proteína BRCA1 / RNA Longo não Codificante / Proteínas de Neoplasias Limite: Female / Humans Idioma: En Revista: Mutat Res Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fatores de Transcrição / Neoplasias da Mama / Regulação Neoplásica da Expressão Gênica / Regiões Promotoras Genéticas / Proteína BRCA1 / RNA Longo não Codificante / Proteínas de Neoplasias Limite: Female / Humans Idioma: En Revista: Mutat Res Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Estados Unidos