在巴西患者中将 PMS2CL 假基因的一个频繁变异错误地归类为 PMS2 功能缺失变异。

IF 1.8 4区 医学 Q3 GENETICS & HEREDITY
Familial Cancer Pub Date : 2024-11-01 Epub Date: 2024-06-20 DOI:10.1007/s10689-024-00411-1
Anthony Vladimir Campos Segura, Sara Iolanda Oliveira da Silva, Karina Miranda Santiago, Rafael Canfield Brianese, Dirce Maria Carraro, Giovana Tardin Torrezan
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引用次数: 0

摘要

PMS2 是林奇综合征的一个基因,由于存在多个假基因,给基因检测带来了挑战。本研究旨在描述一系列携带 PMS2CL 伪基因变异的病例,该变异被不同的命名法错误地归入 PMS2。我们回顾了在一个中心接受多基因基因检测的 647 名巴西患者的数据,以确定那些携带 PMS2 V1:c.2186_2187delTC 或 V2:c.2182_2184delACTinsG 变异的患者,这些变异据称位于 PMS2 第 13 外显子。进行了基因特异性 PCR 和转录本测序。在 647 人中,1.8%(12 人)携带所调查的变异,变异等位基因频率在 15% 到 34% 之间。通过目测比对,我们确认 V1 和 V2 代表同一个变异体,并通过基因特异性 PCR 和 PMS2 转录本分析,证明 V1/V2 实际上位于 PMS2CL 假基因中。基因组数据库(ExAC 和 gnomAD)报告称,这种变异在非洲人群中的发生率为 2.5 - 5.3%。目前,在 ClinVar 中,V1 被归类为 "意义不确定",V2 被归类为 "冲突",有几个实验室将其归类为 "致病"。我们在巴西人群中发现了一种频繁出现的非洲 PMS2CL 变异,它被错误地归类为 PMS2 变异。在一些手稿和临床实验室中,V1/V2 很可能被错误地归入 PMS2,这凸显了一个由差异引起的问题。考虑到短读 NGS 区分 PMS2 和 PMS2CL 某些区域的局限性,使用互补方法提供准确诊断势在必行。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Misclassification of a frequent variant from PMS2CL pseudogene as a PMS2 loss of function variant in Brazilian patients.

Misclassification of a frequent variant from PMS2CL pseudogene as a PMS2 loss of function variant in Brazilian patients.

PMS2, a Lynch Syndrome gene, presents challenges in genetic testing due to the existence of multiple pseudogenes. This study aims to describe a series of cases harboring a variant in the PMS2CL pseudogene that has been incorrectly assigned to PMS2 with different nomenclatures. We reviewed data from 647 Brazilian patients who underwent multigene genetic testing at a single center to identify those harboring the PMS2 V1:c.2186_2187delTC or V2:c.2182_2184delACTinsG variants, allegedly located at PMS2 exon 13. Gene-specific PCR and transcript sequencing was performed. Among the 647 individuals, 1.8% (12) carried the investigated variants, with variant allele frequencies ranging from 15 to 34%. By visually inspecting the alignments, we confirmed that both V1 and V2 represented the same variant and through gene-specific PCR and PMS2 transcript analysis, we demonstrated that V1/V2 is actually located in the PMS2CL pseudogene. Genomic databases (ExAC and gnomAD) report an incidence of 2.5 - 5.3% of this variant in the African population. Currently, V1 is classified as "uncertain significance" and V2 as "conflicting" in ClinVar, with several laboratories classifying them as "pathogenic". We identified a frequent African PMS2CL variant in the Brazilian population that is misclassified as a PMS2 variant. It is likely that V1/V2 have been erroneously assigned to PMS2 in several manuscripts and by clinical laboratories, underscoring a disparity-induced matter. Considering the limitations of short-read NGS differentiating between certain regions of PMS2 and PMS2CL, using complementary methodologies is imperative to provide an accurate diagnosis.

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来源期刊
Familial Cancer
Familial Cancer 医学-遗传学
CiteScore
4.10
自引率
4.50%
发文量
36
审稿时长
6-12 weeks
期刊介绍: In recent years clinical cancer genetics has become increasingly important. Several events, in particular the developments in DNA-based technology, have contributed to this evolution. Clinical cancer genetics has now matured to a medical discipline which is truly multidisciplinary in which clinical and molecular geneticists work together with clinical and medical oncologists as well as with psycho-social workers. Due to the multidisciplinary nature of clinical cancer genetics most papers are currently being published in a wide variety of journals on epidemiology, oncology and genetics. Familial Cancer provides a forum bringing these topics together focusing on the interests and needs of the clinician. The journal mainly concentrates on clinical cancer genetics. Most major areas in the field shall be included, such as epidemiology of familial cancer, molecular analysis and diagnosis, clinical expression, treatment and prevention, counselling and the health economics of familial cancer.
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