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胶质母细胞瘤细胞中的新型通读融合转录本 Bcl2l2-Pabpn1。

Novel read-through fusion transcript Bcl2l2-Pabpn1 in glioblastoma cells.

机构信息

Department of Neurobiology and Anatomy, Xuzhou Key Laboratory of Neurobiology, Xuzhou Medical University, Xuzhou, China.

School of Nursing, Xuzhou Medical University, Xuzhou, China.

出版信息

J Cell Mol Med. 2022 Sep;26(17):4686-4697. doi: 10.1111/jcmm.17481. Epub 2022 Jul 27.

DOI:10.1111/jcmm.17481
PMID:35894779
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9443946/
Abstract

Read-through fusion transcripts have recently been identified as chimeric RNAs and have since been linked to tumour growth in some cases. Many fusion genes generated by chromosomal rearrangements have been described in glioblastoma. However, read-through fusion transcripts between neighbouring genes in glioblastoma remain unexplored. We performed paired-end RNA-seq of rat C6 glioma cells and normal cells and discovered a read-through fusion transcript Bcl2l2-Pabpn1 in which exon 3 of Bcl-2-like protein 2 (Bcl2l2) fused to exon 2 of Polyadenylate-binding protein 1 (Pabpn1). This fusion transcript was found in both human glioblastoma and normal cells. Unlike other fusions reported in glioblastoma, Bcl2l2-Pabpn1 appeared to result from RNA processing rather than genomic rearrangement. Bcl2l2-Pabpn1 fusion transcript encoded a fusion protein with BH4, BCL and RRM domains. Functionally, Bcl2l2-Pabpn1 knockdown by targeting its fusion junction decreased its expression, and suppressed cell proliferation, migration and invasion in vitro. Mechanistically, Bcl2l2-Pabpn1 blocked Bax activity and activated PI3K/AKT pathway to promote glioblastoma progression. Together, our work characterized a glioblastoma-associated Bcl2l2-Pabpn1 fusion transcript shared by humans and rats.

摘要

通读融合转录本最近被鉴定为嵌合 RNA,并且在某些情况下与肿瘤生长有关。在神经胶质瘤中已经描述了许多由染色体重排产生的融合基因。然而,神经胶质瘤中相邻基因之间的通读融合转录本仍未被探索。我们对大鼠 C6 神经胶质瘤细胞和正常细胞进行了配对末端 RNA-seq 分析,发现了一种 Bcl2l2-Pabpn1 通读融合转录本,其中 Bcl-2 样蛋白 2 (Bcl2l2) 的外显子 3 融合到多聚腺苷酸结合蛋白 1 (Pabpn1) 的外显子 2。该融合转录本在人神经胶质瘤和正常细胞中均有发现。与神经胶质瘤中报道的其他融合不同,Bcl2l2-Pabpn1 似乎是由 RNA 加工而不是基因组重排引起的。Bcl2l2-Pabpn1 融合转录本编码具有 BH4、BCL 和 RRM 结构域的融合蛋白。功能上,通过靶向其融合接头敲低 Bcl2l2-Pabpn1 会降低其表达,并抑制体外细胞增殖、迁移和侵袭。在机制上,Bcl2l2-Pabpn1 阻断 Bax 活性并激活 PI3K/AKT 通路,促进神经胶质瘤的进展。总之,我们的工作描述了一种在人类和大鼠中均存在的与神经胶质瘤相关的 Bcl2l2-Pabpn1 融合转录本。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b48/9443946/886d6e51099c/JCMM-26-4686-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b48/9443946/17b6e992ef52/JCMM-26-4686-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b48/9443946/789b8c320cfa/JCMM-26-4686-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b48/9443946/0ebdda31f2bb/JCMM-26-4686-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b48/9443946/23f27cdba96f/JCMM-26-4686-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b48/9443946/886d6e51099c/JCMM-26-4686-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b48/9443946/17b6e992ef52/JCMM-26-4686-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b48/9443946/789b8c320cfa/JCMM-26-4686-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b48/9443946/0ebdda31f2bb/JCMM-26-4686-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b48/9443946/23f27cdba96f/JCMM-26-4686-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b48/9443946/886d6e51099c/JCMM-26-4686-g005.jpg

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