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首页> 外文期刊>Mutation research-Fundamental and Molecular Mechanisms of Mutagenesis >Induction of the long noncoding RNA NBR2 from the bidirectional BRCA1 promoter under hypoxic conditions
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Induction of the long noncoding RNA NBR2 from the bidirectional BRCA1 promoter under hypoxic conditions

机译:在缺氧条件下诱导双向BRCA1启动子的长度非划分RNA NBR2

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摘要

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 (Inc) 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 BRCAI 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 BRCAI promoter, even though appreciable levels of BRCA1 and NBR2 mRNA were detected. Significant recovery back to baseline RNA levels occurred within 48 h after the MCF-7 cells were restored to normoxic conditions. We used a construct with the 218 bp 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. (C) 2017 Published by Elsevier B.V.
机译:BRCA1在预防乳腺癌中起着重要作用,并且通常在散发性癌症中沉默或压抑。 BRCA1启动子是双向的:它驱动相对于BRCA1转录物相对取向的长非编码(Inc)NBR2转录物的转录。缺氧条件抑制BRCA1转录,但它们尚未报告它们对NBR2转录物的表达的影响。我们使用定量RT-PCR在MCF-7乳腺癌细胞中测量0%和1%氧中的BRCA1和NBR2转录水平,发现NBR2转录水平随缺氧条件下的时间函数而增加,而BRCAI mRNA水平被压抑。在UACC-3199乳腺癌细胞系中还原BRCA1 mRNA的BRCA1 mRNA缺氧条件是无效的,据报道,据报道,即使检测到明显的BRCA1和NBR2 mRNA的明显水平。在将MCF-7细胞恢复到常氧条件下,在48小时内发生重大恢复恢复到基线RNA水平。我们使用与标记基因有关的218bp最小BRCA1启动子的构建体,表明该最小启动子在缺氧条件下双向相互双向的表达,这表明诱导NBR2所需的元素位于其他地方。 (c)2017年由Elsevier B.V发布。

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