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A Novel Long Non-Coding RNA in the hTERT Promoter Region Regulates hTERT Expression

机译:hTERT启动子区域中的新型长非编码RNA调节hTERT表达。

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摘要

A novel antisense transcript was identified in the human telomerase reverse transcriptase (hTERT) promoter region, suggesting that the hTERT promoter is bidirectional. This transcript, named hTERT antisense promoter-associated (hTAPAS) RNA, is a 1.6 kb long non-coding RNA. hTAPAS transcription is initiated 167 nucleotides upstream of the hTERT transcription start site and is present in both the nucleus and the cytoplasm. Surprisingly, we observed that a large fraction of the hTERT polyadenylated RNA is localized in the nucleus, suggesting this might be an additional means of regulating the cellular abundance of hTERT protein. Both hTAPAS and hTERT are expressed in immortalized B-cells and human embryonic stem cells but are not detected in normal somatic cells. hTAPAS expression inversely correlates with hTERT expression in different types of cancer samples. Moreover, hTAPAS expression is not promoted by an hTERT promoter mutation (-124 C>T). Antisense-oligonucleotide mediated knockdown of hTAPAS results in an increase in hTERT expression. Conversely, ectopic overexpression of hTAPAS down regulates hTERT expression, suggesting a negative role in hTERT gene regulation. These observations provide insights into hTAPAS as a novel player that negatively regulates hTERT expression and may be involved in telomere length homeostasis.
机译:在人类端粒酶逆转录酶(hTERT)启动子区域中发现了一种新型的反义转录物,表明hTERT启动子是双向的。该转录本名为hTERT反义启动子相关(hTAPAS)RNA,是一个1.6 kb长的非编码RNA。 hTAPAS转录起始于hTERT转录起始位点上游167个核苷酸,并同时存在于细胞核和细胞质中。出人意料的是,我们观察到hTERT多腺苷酸化RNA的大部分位于细胞核中,这表明这可能是调节hTERT蛋白细胞丰度的另一种手段。 hTAPAS和hTERT均在永生化B细胞和人类胚胎干细胞中表达,但在正常体细胞中未检测到。在不同类型的癌症样本中,hTAPAS表达与hTERT表达成反比。此外,hTERT启动子突变(-124 C> T)不能促进hTAPAS表达。反义寡核苷酸介导的hTAPAS的敲低导致hTERT表达的增加。相反,hTAPAS的异位过表达下调了 hTERT 的表达,暗示了在 hTERT 基因调控中的负作用。这些观察结果提供了对 hTAPAS 的新发现,它是负调控 hTERT 表达的新型参与者,可能参与了端粒长度的稳态。

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