一个希腊家庭中与晶格状角膜营养不良变异相关的新型TGFBI突变的临床和结构特征。

IF 4.1 1区 医学 Q1 OPHTHALMOLOGY
Margarita Zacharogianni , Nikos C. Papandreou , Nikolaos M. Marinakis , Faidon-Nikolaos Tilemis , Joanne Traeger-Synodinos , Sotiria Palioura
{"title":"一个希腊家庭中与晶格状角膜营养不良变异相关的新型TGFBI突变的临床和结构特征。","authors":"Margarita Zacharogianni ,&nbsp;Nikos C. Papandreou ,&nbsp;Nikolaos M. Marinakis ,&nbsp;Faidon-Nikolaos Tilemis ,&nbsp;Joanne Traeger-Synodinos ,&nbsp;Sotiria Palioura","doi":"10.1016/j.ajo.2025.03.003","DOIUrl":null,"url":null,"abstract":"<div><h3>Purpose</h3><div>To describe a novel pathogenic <em>TGFBI</em> variant identified in a Greek family and investigate its structural impact on the TGFBI protein, focusing on clinical significance and genotype-phenotype correlations.</div></div><div><h3>Design</h3><div>Single-family case-control study with computational structural analysis.</div></div><div><h3>Methods</h3><div>Three generations of a Greek family, including the proband, her brother, and their mother were clinically evaluated using slit-lamp examination and anterior segment optical coherence tomography. Whole exome sequencing was performed on the proband, followed by targeted sequencing of family members. Bioinformatics tools, including DynaMut2, PROVEAN, and AlphaFold2, were used to predict the mutation's impact on protein structure and stability.</div></div><div><h3>Results</h3><div>A novel heterozygous variant, c.1517_1518insCCCCCCCAAGGG, was identified. This 12-nucleotide insertion replaces methionine at position 506 with isoleucine, proline, proline, lysine, and glycine (p.M506delinsIPPKG). Clinically, this mutation was associated with geographic subepithelial and anterior stromal opacities without discernible lattice lines and presented as recurrent corneal erosions in the second decade. Structural analysis revealed disruption of the first α-helix of the FAS1-4 domain, destabilizing the protein and potentially exposing amyloidogenic regions. Previously reported mutations within this α-helix consistently produce a phenotype of geographic subepithelial opacities and a similar age of onset.</div></div><div><h3>Conclusions</h3><div>M506delinsIPPKG represents a novel pathogenic <em>TGFBI</em> variant associated with an autosomal dominant lattice corneal dystrophies variant. The structural disruption of the FAS1-4 domain's α-helix likely underlies the disease mechanism and links structural changes to specific phenotypic traits. These findings contribute to our understanding of genotype-phenotype correlations in <em>TGFBI</em>-related corneal dystrophies and highlight the importance of structural analysis in such cases.</div></div>","PeriodicalId":7568,"journal":{"name":"American Journal of Ophthalmology","volume":"274 ","pages":"Pages 112-121"},"PeriodicalIF":4.1000,"publicationDate":"2025-03-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Clinical and Structural Characterization of a Novel TGFBI Mutation Linked to a Lattice Corneal Dystrophy Variant in a Greek Family\",\"authors\":\"Margarita Zacharogianni ,&nbsp;Nikos C. Papandreou ,&nbsp;Nikolaos M. Marinakis ,&nbsp;Faidon-Nikolaos Tilemis ,&nbsp;Joanne Traeger-Synodinos ,&nbsp;Sotiria Palioura\",\"doi\":\"10.1016/j.ajo.2025.03.003\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Purpose</h3><div>To describe a novel pathogenic <em>TGFBI</em> variant identified in a Greek family and investigate its structural impact on the TGFBI protein, focusing on clinical significance and genotype-phenotype correlations.</div></div><div><h3>Design</h3><div>Single-family case-control study with computational structural analysis.</div></div><div><h3>Methods</h3><div>Three generations of a Greek family, including the proband, her brother, and their mother were clinically evaluated using slit-lamp examination and anterior segment optical coherence tomography. Whole exome sequencing was performed on the proband, followed by targeted sequencing of family members. Bioinformatics tools, including DynaMut2, PROVEAN, and AlphaFold2, were used to predict the mutation's impact on protein structure and stability.</div></div><div><h3>Results</h3><div>A novel heterozygous variant, c.1517_1518insCCCCCCCAAGGG, was identified. This 12-nucleotide insertion replaces methionine at position 506 with isoleucine, proline, proline, lysine, and glycine (p.M506delinsIPPKG). Clinically, this mutation was associated with geographic subepithelial and anterior stromal opacities without discernible lattice lines and presented as recurrent corneal erosions in the second decade. Structural analysis revealed disruption of the first α-helix of the FAS1-4 domain, destabilizing the protein and potentially exposing amyloidogenic regions. Previously reported mutations within this α-helix consistently produce a phenotype of geographic subepithelial opacities and a similar age of onset.</div></div><div><h3>Conclusions</h3><div>M506delinsIPPKG represents a novel pathogenic <em>TGFBI</em> variant associated with an autosomal dominant lattice corneal dystrophies variant. The structural disruption of the FAS1-4 domain's α-helix likely underlies the disease mechanism and links structural changes to specific phenotypic traits. These findings contribute to our understanding of genotype-phenotype correlations in <em>TGFBI</em>-related corneal dystrophies and highlight the importance of structural analysis in such cases.</div></div>\",\"PeriodicalId\":7568,\"journal\":{\"name\":\"American Journal of Ophthalmology\",\"volume\":\"274 \",\"pages\":\"Pages 112-121\"},\"PeriodicalIF\":4.1000,\"publicationDate\":\"2025-03-04\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"American Journal of Ophthalmology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S000293942500114X\",\"RegionNum\":1,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"OPHTHALMOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"American Journal of Ophthalmology","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S000293942500114X","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"OPHTHALMOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

目的:描述在一个希腊家族中发现的一种新的致病TGFBI变异,并研究其对TGFBI蛋白的结构影响,重点研究其临床意义和基因型-表型相关性。设计:单家庭病例对照研究与计算结构分析。方法:采用裂隙灯检查和前段光学相干断层扫描对一个希腊家庭三代,包括先证者及其兄弟及其母亲进行临床评估。先证者进行全外显子组测序,然后对家庭成员进行靶向测序。使用生物信息学工具,包括DynaMut2、PROVEAN和AlphaFold2来预测突变对蛋白质结构和稳定性的影响。结果:鉴定出一种新的杂合变异体c.1517_1518insCCCCCCCAAGGG。这个12个核苷酸的插入用异亮氨酸、脯氨酸、脯氨酸、赖氨酸和甘氨酸取代了506位的蛋氨酸(p.m 506delinsppkg)。临床上,这种突变与地理上皮下和前间质混浊有关,没有明显的晶格线,并在第二个十年中表现为复发性角膜糜烂。结构分析显示FAS1-4结构域的第一个α-螺旋断裂,使蛋白质不稳定,并可能暴露淀粉样蛋白区。先前报道的α-螺旋内的突变一致产生地理上皮下混浊的表型和相似的发病年龄。结论:m506delinsppkg代表了一种与常染色体显性LCD变异相关的新型致病性TGFBI变异。FAS1-4结构域α-螺旋的结构破坏可能是疾病机制的基础,并将结构变化与特定表型性状联系起来。这些发现有助于我们理解tgfbi相关角膜营养不良症的基因型-表型相关性,并强调了在此类病例中进行结构分析的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Clinical and Structural Characterization of a Novel TGFBI Mutation Linked to a Lattice Corneal Dystrophy Variant in a Greek Family

Purpose

To describe a novel pathogenic TGFBI variant identified in a Greek family and investigate its structural impact on the TGFBI protein, focusing on clinical significance and genotype-phenotype correlations.

Design

Single-family case-control study with computational structural analysis.

Methods

Three generations of a Greek family, including the proband, her brother, and their mother were clinically evaluated using slit-lamp examination and anterior segment optical coherence tomography. Whole exome sequencing was performed on the proband, followed by targeted sequencing of family members. Bioinformatics tools, including DynaMut2, PROVEAN, and AlphaFold2, were used to predict the mutation's impact on protein structure and stability.

Results

A novel heterozygous variant, c.1517_1518insCCCCCCCAAGGG, was identified. This 12-nucleotide insertion replaces methionine at position 506 with isoleucine, proline, proline, lysine, and glycine (p.M506delinsIPPKG). Clinically, this mutation was associated with geographic subepithelial and anterior stromal opacities without discernible lattice lines and presented as recurrent corneal erosions in the second decade. Structural analysis revealed disruption of the first α-helix of the FAS1-4 domain, destabilizing the protein and potentially exposing amyloidogenic regions. Previously reported mutations within this α-helix consistently produce a phenotype of geographic subepithelial opacities and a similar age of onset.

Conclusions

M506delinsIPPKG represents a novel pathogenic TGFBI variant associated with an autosomal dominant lattice corneal dystrophies variant. The structural disruption of the FAS1-4 domain's α-helix likely underlies the disease mechanism and links structural changes to specific phenotypic traits. These findings contribute to our understanding of genotype-phenotype correlations in TGFBI-related corneal dystrophies and highlight the importance of structural analysis in such cases.
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
CiteScore
9.20
自引率
7.10%
发文量
406
审稿时长
36 days
期刊介绍: The American Journal of Ophthalmology is a peer-reviewed, scientific publication that welcomes the submission of original, previously unpublished manuscripts directed to ophthalmologists and visual science specialists describing clinical investigations, clinical observations, and clinically relevant laboratory investigations. Published monthly since 1884, the full text of the American Journal of Ophthalmology and supplementary material are also presented online at www.AJO.com and on ScienceDirect. The American Journal of Ophthalmology publishes Full-Length Articles, Perspectives, Editorials, Correspondences, Books Reports and Announcements. Brief Reports and Case Reports are no longer published. We recommend submitting Brief Reports and Case Reports to our companion publication, the American Journal of Ophthalmology Case Reports. Manuscripts are accepted with the understanding that they have not been and will not be published elsewhere substantially in any format, and that there are no ethical problems with the content or data collection. Authors may be requested to produce the data upon which the manuscript is based and to answer expeditiously any questions about the manuscript or its authors.
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信