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Mutation Scanning of D1705 and D1709 in the RNAse IIIb Domain of MicroRNA Processing Enzyme Dicer in Cutaneous Melanoma

机译:皮肤黑色素瘤中MicroRNA加工酶切子酶RNAse IIIb结构域中D1705和D1709的突变扫描

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摘要

Since the discovery of microRNAs (miRNAs) there have been performed several studies showing perturbations in the expression of miRNAs and the miRNA expression machinery in cutaneous melanoma. Dicer, a pivotal cytosolic enzyme of miRNA maturation has shown to be affected by both somatic and germline mutations in a variety of cancers. Recent studies have shown that recurrent somatic mutations of Dicer frequently affect the metal-ion-binding sites D1709 and D1705 of its RNase IIIb domain, therefore called hot spot mutations. The present study investigates metal-ion-binding sites D1709 and D1705 of the Dicer RNase IIIb domain in cutaneous melanomas and melanoma metastasis by Sanger sequencing. All investigated samples showed wildtype sequence and no single mutation was detected. The miRNA processing enzyme Dicer of melanoma and melanoma metastasis does not appear to be affected by mutation in the metal-ion-binding sites D1709 and D1705 of its RNase IIIb domain.
机译:自从发现microRNA(miRNA)以来,已经进行了数项研究,这些研究表明皮肤黑色素瘤中miRNA的表达和miRNA表达机制受到干扰。 Dicer是miRNA成熟的关键细胞溶质酶,已被多种癌症的体细胞和种系突变所影响。最近的研究表明,Dicer的复发性体细胞突变经常影响其RNase IIIb结构域的金属离子结合位点D1709和D1705,因此称为热点突变。本研究通过Sanger测序研究了皮肤黑色素瘤和黑色素瘤转移中Dicer RNase IIIb结构域的金属离子结合位点D1709和D1705。所有调查的样品均显示野生型序列,未检测到单个突变。黑色素瘤和黑色素瘤转移的miRNA处理酶Dicer似乎不受其RNase IIIb结构域的金属离子结合位点D1709和D1705突变的影响。

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