Department of Biochemistry and Molecular Biology, Wright State University, 3640 Colonel Glenn Hwy, Dayton, OH 45435, USA.
Int J Mol Sci. 2024 Aug 30;25(17):9415. doi: 10.3390/ijms25179415.
MDM4 is upregulated in the majority of melanoma cases and has been described as a "key therapeutic target in cutaneous melanoma". Numerous isoforms of MDM4 exist, with few studies examining their specific expression in human tissues. The changes in splicing of MDM4 during human melanomagenesis are critical to p53 activity and represent potential therapeutic targets. Compounding this, studies relying on short reads lose "connectivity" data, so full transcripts are frequently only inferred from the presence of splice junction reads. To address this problem, long-read nanopore sequencing was utilized to read the entire length of transcripts. Here, MDM4 transcripts, both alternative and canonical, are characterized in a pilot cohort of human melanoma specimens. RT-PCR was first used to identify the presence of novel splice junctions in these specimens. RT-qPCR then quantified the expression of major MDM4 isoforms observed during sequencing. The current study both identifies and quantifies MDM4 isoforms present in melanoma tumor samples. In the current study, we observed high expression levels of MDM4-S, MDM4-FL, MDM4-A, and the previously undescribed Ensembl transcript MDM4-209. A novel transcript lacking both exons 6 and 9 is observed and named MDM4-A/S for its resemblance to both MDM4-A and MDM4-S isoforms.
MDM4 在大多数黑色素瘤病例中上调,并被描述为“皮肤黑色素瘤的关键治疗靶点”。MDM4 存在多种异构体,很少有研究检查它们在人类组织中的特异性表达。MDM4 在人类黑色素瘤发生过程中的剪接变化对 p53 活性至关重要,代表潜在的治疗靶点。更复杂的是,依赖短读的研究会丢失“连接性”数据,因此完整的转录本通常仅根据剪接接头读数的存在来推断。为了解决这个问题,我们利用长读长纳米孔测序来读取转录本的全长。在这里,我们在一个人类黑色素瘤标本的试点队列中对 MDM4 转录本进行了特征分析。首先使用 RT-PCR 来鉴定这些标本中新型剪接接头的存在。然后,RT-qPCR 定量了测序过程中观察到的主要 MDM4 异构体的表达。本研究既鉴定又定量了黑色素瘤肿瘤样本中存在的 MDM4 异构体。在本研究中,我们观察到 MDM4-S、MDM4-FL、MDM4-A 和之前未描述的 Ensembl 转录本 MDM4-209 的高表达水平。观察到一种缺失第 6 和第 9 外显子的新型转录本,并因其与 MDM4-A 和 MDM4-S 异构体的相似性而命名为 MDM4-A/S。