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GLB1基因中加工后的假基因插入通过改变内含子剪接调控格局导致莫尔基奥B病。

Processed pseudogene insertion in GLB1 causes Morquio B disease by altering intronic splicing regulatory landscape.

作者信息

Bychkov Igor, Kuznetsova Antonina, Baydakova Galina, Gorobets Leonid, Kenis Vladimir, Dimitrieva Alena, Filatova Alexandra, Tabakov Vyacheslav, Skoblov Mikhail, Zakharova Ekaterina

机构信息

Research Centre for Medical Genetics, Moscow, Russia.

Clinical and Diagnostic Center "Zdorovoe detstvo", Rostov-on-Don, Russia.

出版信息

NPJ Genom Med. 2022 Jul 26;7(1):44. doi: 10.1038/s41525-022-00315-y.

Abstract

Morquio B disease (MBD) is an ultra-rare lysosomal storage disease, which represents the relatively mild form of GLB1-associated disorders. In this article, we present the unique case of "pure" MBD associated with an insertion of the mobile genetic element from the class of retrotransposons. Using whole-genome sequencing (WGS), we identified an integration of the processed pseudogene NPM1 deep in the intron 5 of GLB1. The patient's mRNA analysis and the detailed functional analysis revealed the underlying molecular genetic mechanism of pathogenesis, which is an alteration of the GLB1 normal splicing. By co-expression of minigenes and antisense splice-modulating oligonucleotides (ASMOs), we demonstrated that pseudogene-derived splicing regulatory motifs contributed to an activation of the cryptic exon located 36 bp upstream of the integration site. Blocking the cryptic exon with ASMOs incorporated in the modified U7 small nuclear RNA (modU7snRNA) almost completely restored the wild-type splicing in the model cell line, that could be further extended toward the personalized genetic therapy. To our knowledge, this is the second reported case of the processed pseudogene insertion for monogenic disorders. Our data emphasizes the unique role of WGS in identification of such rare and probably underrepresented in literature types of disease-associated genetic variants.

摘要

莫尔基奥B病(MBD)是一种极其罕见的溶酶体贮积病,是GLB1相关疾病中相对较轻的一种形式。在本文中,我们报告了一例独特的“纯”MBD病例,该病例与逆转录转座子类移动遗传元件的插入有关。通过全基因组测序(WGS),我们在GLB1基因的第5内含子深处鉴定到了加工假基因NPM1的整合。对患者的mRNA分析和详细的功能分析揭示了发病机制的潜在分子遗传机制,即GLB1正常剪接的改变。通过共表达小基因和反义剪接调节寡核苷酸(ASMO),我们证明假基因衍生的剪接调节基序促成了位于整合位点上游36 bp处的隐蔽外显子的激活。将ASMO掺入修饰的U7小核RNA(modU7snRNA)中阻断隐蔽外显子,几乎完全恢复了模型细胞系中的野生型剪接,这可能会进一步扩展到个性化基因治疗。据我们所知,这是第二例报道的单基因疾病中加工假基因插入的病例。我们的数据强调了WGS在识别此类罕见且可能在文献中报道不足的疾病相关遗传变异类型方面的独特作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cefc/9325892/81cc4bd2c548/41525_2022_315_Fig1_HTML.jpg

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