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Frequent deletions and down-regulation of micro-RNA genes miR15 and miR16 at 13q14 in chronic lymphocytic leukemia

机译:慢性淋巴细胞白血病中13q14的微小RNA基因miR15和miR16的频繁缺失和下调

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摘要

Micro-RNAs (miR genes) are a large family of highly conserved noncoding genes thought to be involved in temporal and tissue-specific gene regulation. MiRs are transcribed as short hairpin precursors (≈70 nt) and are processed into active 21- to 22-nt RNAs by Dicer, a ribonuclease that recognizes target mRNAs via base-pairing interactions. Here we show that miR15 and miR16 are located at chromosome 13q14, a region deleted in more than half of B cell chronic lymphocytic leukemias (B-CLL). Detailed deletion and expression analysis shows that miR15 and miR16 are located within a 30-kb region of loss in CLL, and that both genes are deleted or down-regulated in the majority (≈68%) of CLL cases.
机译:微小RNA(miR基因)是一个高度保守的非编码基因家族,被认为与时间和组织特异性基因调控有关。 MiR被转录为短发夹前体(约70 nt),并被Dicer(一种通过碱基配对相互作用识别靶mRNA的核糖核酸酶)加工成活性的21至22 nt RNA。在这里,我们显示miR15和miR16位于13q14号染色体上,该区域在超过一半的B细胞慢性淋巴细胞性白血病(B-CLL)中缺失。详细的删除和表达分析表明,miR15和miR16位于CLL丢失的30 kb区域内,并且在大多数(约68%)CLL病例中,这两个基因均被删除或下调。

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