Medizinische Klinik und Poliklinik IV, Campus Innenstadt, Klinikum der Universität München, Munich, Germany.
MGZ - Medizinisch Genetisches Zentrum, Munich, Germany.
Eur J Hum Genet. 2022 Sep;30(9):1051-1059. doi: 10.1038/s41431-022-01106-w. Epub 2022 Jun 9.
Over 20% of the DNA mismatch repair (MMR) germline variants in suspected Lynch syndrome patients are classified as variants of uncertain significance (VUS). Well-established functional assays are pivotal for assessing the biological impact of these variants and provide relevant evidence for clinical classification. In our collaborative European Mismatch Repair Working Group (EMMR-WG) we compared three different experimental approaches for evaluating the effect of seven variants on mRNA splicing in MMR genes: (i) RT-PCR of full-length transcripts (FLT), (ii) RT-PCR of targeted transcript sections (TTS), both from patient biological samples and (iii) minigene splicing assays. An overall good concordance was observed between splicing patterns in TTS, FLT and minigene analyses for all variants. The FLT analysis depicted a higher number of different isoforms and mitigated PCR-bias towards shorter isoforms. TTS analyses may miss aberrant isoforms and minigene assays may under/overestimate the severity of certain splicing defects. The interpretation of the experimental findings must be cautious to adequately discriminate abnormal events from physiological complex alternative splicing patterns. A consensus strategy for investigating the impact of MMR variants on splicing was defined. First, RNA should be obtained from patient's cell cultures (such as fresh lymphocyte cultures) incubated with/without a nonsense-mediated decay inhibitor. Second, FLT RT-PCR analysis is recommended to oversee all generated isoforms. Third, TTS analysis and minigene assays are useful independent approaches for verifying and clarifying FLT results. The use of several methodologies is likely to increase the strength of the experimental evidence which contributes to improve variant interpretation.
在疑似林奇综合征患者的 DNA 错配修复 (MMR) 种系变异中,超过 20% 被归类为意义不明的变异 (VUS)。经过充分验证的功能检测对于评估这些变异的生物学影响至关重要,并且为临床分类提供了相关证据。在我们合作的欧洲错配修复工作组 (EMMR-WG) 中,我们比较了三种不同的实验方法来评估七个变异对 MMR 基因中 mRNA 剪接的影响:(i) 来自患者生物样本的全长转录本 (FLT) 的 RT-PCR,(ii) 靶向转录本部分 (TTS) 的 RT-PCR,以及 (iii) 小基因剪接测定。所有变体的 TTS、FLT 和小基因分析中的剪接模式均观察到良好的一致性。FLT 分析显示出更多不同的异构体,并减轻了对较短异构体的 PCR 偏倚。TTS 分析可能会错过异常异构体,而小基因测定可能会低估/高估某些剪接缺陷的严重程度。必须谨慎解释实验结果,以充分区分异常事件与生理复杂的替代剪接模式。确定了一种用于研究 MMR 变异对剪接影响的共识策略。首先,应从患者的细胞培养物(如新鲜淋巴细胞培养物)中获得 RNA,这些细胞培养物用/不用无义介导的衰变抑制剂孵育。其次,建议进行 FLT RT-PCR 分析以全面观察所有产生的异构体。第三,TTS 分析和小基因测定是验证和澄清 FLT 结果的有用独立方法。使用多种方法学可能会增加实验证据的强度,从而有助于改善变异解释。