Department of Genomics, Institute of Hematology and Blood Transfusion, Prague, Czech Republic.
Department of Genetics and Microbiology, Faculty of Science, Charles University, Prague, Czech Republic.
Mol Oncol. 2023 Dec;17(12):2565-2583. doi: 10.1002/1878-0261.13486. Epub 2023 Jul 17.
Mutations in the splicing factor 3b subunit 1 (SF3B1) gene are frequent in myelodysplastic neoplasms (MDS). Because the splicing process is involved in the production of circular RNAs (circRNAs), we investigated the impact of SF3B1 mutations on circRNA processing. Using RNA sequencing, we measured circRNA expression in CD34+ bone marrow MDS cells. We defined circRNAs deregulated in a heterogeneous group of MDS patients and described increased circRNA formation in higher-risk MDS. We showed that the presence of SF3B1 mutations did not affect the global production of circRNAs; however, deregulation of specific circRNAs was observed. Particularly, we demonstrated that strong upregulation of circRNAs processed from the zinc finger E-box binding homeobox 1 (ZEB1) transcription factor; this upregulation was exclusive to SF3B1-mutated patients and was not observed in those with mutations in other splicing factors or other recurrently mutated genes, or with other clinical variables. Furthermore, we focused on the most upregulated ZEB1-circRNA, hsa_circ_0000228, and, by its knockdown, we demonstrated that its expression is related to mitochondrial activity. Using microRNA analyses, we proposed miR-1248 as a direct target of hsa_circ_0000228. To conclude, we demonstrated that mutated SF3B1 leads to deregulation of ZEB1-circRNAs, potentially contributing to the defects in mitochondrial metabolism observed in SF3B1-mutated MDS.
剪接因子 3b 亚基 1(SF3B1)基因中的突变在骨髓增生异常肿瘤(MDS)中很常见。由于剪接过程涉及环状 RNA(circRNA)的产生,我们研究了 SF3B1 突变对 circRNA 加工的影响。我们使用 RNA 测序测量了 CD34+骨髓 MDS 细胞中的 circRNA 表达。我们定义了在一组异质 MDS 患者中失调的 circRNAs,并描述了高危 MDS 中 circRNA 形成增加。我们表明 SF3B1 突变的存在不会影响 circRNA 的整体产生;然而,观察到特定 circRNA 的失调。特别是,我们证明了锌指 E 盒结合同源盒 1(ZEB1)转录因子的 circRNA 的强烈上调;这种上调仅存在于 SF3B1 突变患者中,而在其他剪接因子或其他反复突变基因或其他临床变量的患者中未观察到。此外,我们专注于上调最明显的 ZEB1-circRNA,hsa_circ_0000228,并通过其敲低,我们证明其表达与线粒体活性有关。通过 microRNA 分析,我们提出 miR-1248 是 hsa_circ_0000228 的直接靶标。总之,我们证明了突变的 SF3B1 导致 ZEB1-circRNA 的失调,可能导致 SF3B1 突变 MDS 中观察到的线粒体代谢缺陷。