4.6 Article

The dark matter of the human genome and its role in human cancers

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GENE
卷 811, 期 -, 页码 -

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ELSEVIER
DOI: 10.1016/j.gene.2021.146084

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Cancer; Long non-coding RNAs; miRNAs; Non-coding RNAs; Transcribed ultra-conserved regions; T-UCR; Ultraconserved regions; UCR

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T-UCRs are a novel family of non-coding RNAs which are completely conserved across human, mouse, and rat genomes. They are believed to be potential predisposing biomarkers for cancer development and may play a role in the malignant transformation of human tumors. Further research is needed to fully understand the functions and fate of T-UCRs in human cancers.
The transcribed ultra-conserved regions (T-UCRs) are a novel family of non-coding RNAs which are absolutely conserved (100%) across orthologous regions of the human, mouse, and rat genomes. T-UCRs represent a small portion of the human genome that is likely to be functional but does not code for proteins and is referred to as the dark matter of the human genome. Although T-UCRs are ubiquitously expressed, tissue- and disease-specific expression of T-UCRs have also been observed. Accumulating evidence suggests that T-UCRs are differentially expressed and involved in the malignant transformation of human tumors through various genetic and epigenetic regulatory mechanisms. Therefore, T-UCRs are novel candidate predisposing biomarkers for cancer development. T-UCRs have shown to drive malignant transformation of human cancers through regulating non-coding RNAs and/or protein coding genes. However, the functions and fate of most T-UCRs remain mysterious. Here, we review and highlight the current knowledge on these ultra-conserved elements in the formation and progression of human cancers.

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