Department of Biochemistry and Molecular Biology, National and Kapodistrian University of Athens, 15701, Athens, Greece.
Apoptosis. 2022 Dec;27(11-12):869-882. doi: 10.1007/s10495-022-01753-w. Epub 2022 Jul 25.
BCL2 antagonist/killer (BAK) is a multidomain pro-apoptotic effector protein, encoded by the human BAK1 gene, which has emerged as a key checkpoint in the apoptotic machinery. Disassembly of BAK's tertiary structure, such as the truncation of the α1 helix, leads to deregulation of the pro-apoptotic functions and reduction of the protein's stability, thus being implicated in human malignancies. Although many studies have already clarified the vital role of BAK in cellular mechanisms, its pre-mRNA maturation process under cancerous and physiological human cells is neglected. In the present work, we developed and employed a custom multiplexed nanopore sequencing approach that enabled the identification and structural characterization of previously undescribed BAK1 mRNA transcripts (BAK1 v.2-v.11). The described novel mRNAs are derived from multiple types of alternative splicing events, including exon skipping and intron retentions. The implemented multiplexed long-read sequencing approach provided the detailed expression profile of the novel mRNAs in a wide panel of human malignancies and at the same time allowed their relative quantification as compared to the annotated BAK1 v.1. The validation of each novel transcript was carried out with qPCR-based assays. Our results strongly support that most of the novel BAK1 mRNAs harbor open reading frames with conserved BH domains that provide new insights into the correlated mechanisms of apoptosis suppression and cancer. The current study highlights for the first time the hidden aspects of BAK1's transcriptional landscape in both physiological and cancerous human cells and distinguishes the amino acid sequence of the putative BAK isoforms that may possess key apoptosis-related functions not only in diseases, but also under normal cellular conditions.
BCL2 拮抗剂/杀伤(BAK)是一种具有多个结构域的促凋亡效应蛋白,由人类 BAK1 基因编码,它已成为凋亡机制中的一个关键检查点。BAK 三级结构的解体,如α1 螺旋的截断,导致促凋亡功能失调和蛋白质稳定性降低,从而与人类恶性肿瘤有关。尽管许多研究已经阐明了 BAK 在细胞机制中的重要作用,但在癌症和生理人类细胞中,其前体 mRNA 的成熟过程仍未被重视。在本工作中,我们开发并采用了一种定制的多重纳米孔测序方法,该方法能够识别和结构表征以前未描述的 BAK1 mRNA 转录本(BAK1 v.2-v.11)。所描述的新 mRNA 来源于多种类型的选择性剪接事件,包括外显子跳跃和内含子保留。所实施的多重长读测序方法提供了广泛的人类恶性肿瘤中新型 mRNA 的详细表达谱,同时允许与注释的 BAK1 v.1 相比对其进行相对定量。每个新转录本的验证均通过基于 qPCR 的测定法进行。我们的结果强烈支持大多数新型 BAK1 mRNA 具有开放阅读框,包含保守的 BH 结构域,这为凋亡抑制和癌症相关机制提供了新的见解。本研究首次强调了生理和癌症人类细胞中 BAK1 转录谱的隐藏方面,并区分了假定的 BAK 同工型的氨基酸序列,这些同工型可能不仅在疾病中,而且在正常细胞条件下具有关键的凋亡相关功能。