结节性硬化综合征患者 TSC1 和 TSC2 的分子和功能评估

IF 2.8 3区 生物学 Q2 GENETICS & HEREDITY Genes Pub Date : 2024-11-03 DOI:10.3390/genes15111432
Luiz Gustavo Dufner-Almeida, Laís F M Cardozo, Mariana R Schwind, Danielly Carvalho, Juliana Paula G Almeida, Andrea Maria Cappellano, Thiago G P Alegria, Santoesha Nanhoe, Mark Nellist, Maria Rita Passos-Bueno, Silvana Chiavegatto, Nasjla S Silva, Sérgio Rosemberg, Ana Paula A Pereira, Sérgio Antônio Antoniuk, Luciana A Haddad
{"title":"结节性硬化综合征患者 TSC1 和 TSC2 的分子和功能评估","authors":"Luiz Gustavo Dufner-Almeida, Laís F M Cardozo, Mariana R Schwind, Danielly Carvalho, Juliana Paula G Almeida, Andrea Maria Cappellano, Thiago G P Alegria, Santoesha Nanhoe, Mark Nellist, Maria Rita Passos-Bueno, Silvana Chiavegatto, Nasjla S Silva, Sérgio Rosemberg, Ana Paula A Pereira, Sérgio Antônio Antoniuk, Luciana A Haddad","doi":"10.3390/genes15111432","DOIUrl":null,"url":null,"abstract":"<p><p>Tuberous sclerosis complex (TSC) is an autosomal dominant neurodevelopmental disorder and multisystem disease caused by pathogenic DNA alterations in the <i>TSC1</i> and <i>TSC2</i> tumor suppressor genes. A molecular genetic diagnosis of TSC confirms the clinical diagnosis, facilitating the implementation of appropriate care and surveillance. <i>TSC1</i> and <i>TSC2</i> encode the core components of the TSC1/2 complex (TSC1/2), a negative regulator of the mechanistic target of rapamycin (MTOR) complex 1 (TORC1). Functional analysis of the effects of <i>TSC1</i> and <i>TSC2</i> variants on TORC1 activity can help establish variant pathogenicity. We searched for pathogenic alterations to <i>TSC1</i> and <i>TSC2</i> in DNA isolated from 116 individuals with a definite clinical diagnosis of TSC. Missense variants and in-frame deletions were functionally assessed. Pathogenic DNA alterations were identified in 106 cases (91%); 18 (17%) in <i>TSC1</i> and 88 (83%) in <i>TSC2</i>. Of these, 35 were novel. Disruption of TSC1/2 activity was demonstrated for seven <i>TSC2</i> variants. Molecular diagnostics confirms the clinical diagnosis of TSC in a large proportion of cases. Functional assessment can help establish variant pathogenicity and is a useful adjunct to DNA analysis.</p>","PeriodicalId":12688,"journal":{"name":"Genes","volume":"15 11","pages":""},"PeriodicalIF":2.8000,"publicationDate":"2024-11-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11593644/pdf/","citationCount":"0","resultStr":"{\"title\":\"Molecular and Functional Assessment of <i>TSC1</i> and <i>TSC2</i> in Individuals with Tuberous Sclerosis Complex.\",\"authors\":\"Luiz Gustavo Dufner-Almeida, Laís F M Cardozo, Mariana R Schwind, Danielly Carvalho, Juliana Paula G Almeida, Andrea Maria Cappellano, Thiago G P Alegria, Santoesha Nanhoe, Mark Nellist, Maria Rita Passos-Bueno, Silvana Chiavegatto, Nasjla S Silva, Sérgio Rosemberg, Ana Paula A Pereira, Sérgio Antônio Antoniuk, Luciana A Haddad\",\"doi\":\"10.3390/genes15111432\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Tuberous sclerosis complex (TSC) is an autosomal dominant neurodevelopmental disorder and multisystem disease caused by pathogenic DNA alterations in the <i>TSC1</i> and <i>TSC2</i> tumor suppressor genes. A molecular genetic diagnosis of TSC confirms the clinical diagnosis, facilitating the implementation of appropriate care and surveillance. <i>TSC1</i> and <i>TSC2</i> encode the core components of the TSC1/2 complex (TSC1/2), a negative regulator of the mechanistic target of rapamycin (MTOR) complex 1 (TORC1). Functional analysis of the effects of <i>TSC1</i> and <i>TSC2</i> variants on TORC1 activity can help establish variant pathogenicity. We searched for pathogenic alterations to <i>TSC1</i> and <i>TSC2</i> in DNA isolated from 116 individuals with a definite clinical diagnosis of TSC. Missense variants and in-frame deletions were functionally assessed. Pathogenic DNA alterations were identified in 106 cases (91%); 18 (17%) in <i>TSC1</i> and 88 (83%) in <i>TSC2</i>. Of these, 35 were novel. Disruption of TSC1/2 activity was demonstrated for seven <i>TSC2</i> variants. Molecular diagnostics confirms the clinical diagnosis of TSC in a large proportion of cases. Functional assessment can help establish variant pathogenicity and is a useful adjunct to DNA analysis.</p>\",\"PeriodicalId\":12688,\"journal\":{\"name\":\"Genes\",\"volume\":\"15 11\",\"pages\":\"\"},\"PeriodicalIF\":2.8000,\"publicationDate\":\"2024-11-03\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11593644/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Genes\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.3390/genes15111432\",\"RegionNum\":3,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"GENETICS & HEREDITY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Genes","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.3390/genes15111432","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"GENETICS & HEREDITY","Score":null,"Total":0}
引用次数: 0

摘要

结节性硬化综合征(TSC)是一种常染色体显性神经发育障碍和多系统疾病,由 TSC1 和 TSC2 肿瘤抑制基因的 DNA 致病性改变引起。TSC的分子遗传学诊断证实了临床诊断,有助于实施适当的护理和监测。TSC1和TSC2编码TSC1/2复合体(TSC1/2)的核心成分,TSC1/2是雷帕霉素机制靶标(MTOR)复合体1(TORC1)的负调控因子。对 TSC1 和 TSC2 变体对 TORC1 活性的影响进行功能分析有助于确定变体的致病性。我们从 116 名临床诊断明确的 TSC 患者分离的 DNA 中寻找 TSC1 和 TSC2 的致病性变异。对错义变异和框架内缺失进行了功能评估。在106个病例(91%)中发现了致病性DNA改变;TSC1和TSC2中分别有18个和88个致病性DNA改变(分别占17%和83%)。其中 35 例为新病变。7个TSC2变异基因被证实破坏了TSC1/2的活性。分子诊断证实了大部分 TSC 病例的临床诊断。功能评估有助于确定变异的致病性,是 DNA 分析的有效辅助手段。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Molecular and Functional Assessment of TSC1 and TSC2 in Individuals with Tuberous Sclerosis Complex.

Tuberous sclerosis complex (TSC) is an autosomal dominant neurodevelopmental disorder and multisystem disease caused by pathogenic DNA alterations in the TSC1 and TSC2 tumor suppressor genes. A molecular genetic diagnosis of TSC confirms the clinical diagnosis, facilitating the implementation of appropriate care and surveillance. TSC1 and TSC2 encode the core components of the TSC1/2 complex (TSC1/2), a negative regulator of the mechanistic target of rapamycin (MTOR) complex 1 (TORC1). Functional analysis of the effects of TSC1 and TSC2 variants on TORC1 activity can help establish variant pathogenicity. We searched for pathogenic alterations to TSC1 and TSC2 in DNA isolated from 116 individuals with a definite clinical diagnosis of TSC. Missense variants and in-frame deletions were functionally assessed. Pathogenic DNA alterations were identified in 106 cases (91%); 18 (17%) in TSC1 and 88 (83%) in TSC2. Of these, 35 were novel. Disruption of TSC1/2 activity was demonstrated for seven TSC2 variants. Molecular diagnostics confirms the clinical diagnosis of TSC in a large proportion of cases. Functional assessment can help establish variant pathogenicity and is a useful adjunct to DNA analysis.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Genes
Genes GENETICS & HEREDITY-
CiteScore
5.20
自引率
5.70%
发文量
1975
审稿时长
22.94 days
期刊介绍: Genes (ISSN 2073-4425) is an international, peer-reviewed open access journal which provides an advanced forum for studies related to genes, genetics and genomics. It publishes reviews, research articles, communications and technical notes. There is no restriction on the length of the papers and we encourage scientists to publish their results in as much detail as possible.
期刊最新文献
Characterization and Phylogenetic Analysis of the First Complete Chloroplast Genome of Shizhenia pinguicula (Orchidaceae: Orchideae). An Updated Analysis of Exon-Skipping Applicability for Duchenne Muscular Dystrophy Using the UMD-DMD Database. Application of CRISPR/Cas9 Technology in Rice Germplasm Innovation and Genetic Improvement. MIR27A rs895819 CC Genotype Severely Reduces miR-27a Plasma Expression Levels. Multiple Osteochondritis Dissecans as Main Manifestation of Multiple Epiphyseal Dysplasia Caused by a Novel Cartilage Oligomeric Matrix Protein Pathogenic Variant: A Clinical Report.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1