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the 4th international edition and 13th Iranian Conference on Bioinformatics
international edition and Iranian Conference on Bioinformatics
صفحه اصلی
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4th international edition and 13th Iranian Conference on Bioinformatics
Dissecting the genetic causes of inflammatory bowel disease based on whole exome sequencing
نویسندگان :
Amir Shahbazi
1
Mehdi Totonchi
2
1- Department of Molecular Genetics, Faculty of Biological Sciences, Tarbiat Modares University, Tehran, Iran
2- Medical Genetics and Molecular Biology Research Hub, Royan TuCAGene Ltd., Tehran, Iran.
کلمات کلیدی :
Inflammatory Bowel Disease (IBD)،Whole-Exome Sequencing (WES)،Gene Variant،Novel Mutation
چکیده :
Introduction IBD refers to the chronic inflammatory diseases of the gastrointestinal tract and mainly encompasses Crohn's disease (CD) and ulcerative colitis (UC). While genetic susceptibility is a major factor in the pathogenesis of IBD, the identification of casual gene variants remains challenging because the disease is heterogeneous. Whole-exome sequencing is an effective approach for identifying rare and novel variants in coding regions ,providing critical insights into the genetic architecture of complex diseases like IBD. Methods This study aimed to identify new genetic variants associated with IBD using WES in one family with familial IBD. We analyzed 5 person,3 was affected and 2 person was healthy, using high-throughput WES technology, Data processing involved quality control and trimming , alignment to the reference genome (GRCh37) using hisat2 , and for variant calling using GATK toolkit. Results We identified a novel frame shift variant in FCGBP Gene (NM_003890.2:chr19-40399459 TG>T, p.His2079Ilefs*20) . gene implicated May be involved in the maintenance of the mucosal structure as a gel-like component of the mucosa. This variant exhibited in one of patient in family of under study that show strong connection with IBD and was absent in healthy controls. Conclusion These findings demonstrate the use of WES in identifying the genetic causes of IBD and emphasize the role of GeneFCGBP in the development of IBD. This discovery opens up new possibilities for the identification of the mechanisms of disease, the development of new therapies and the advancement of precision medicine in the treatment of IBD patients.
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بیشتر
ثمین همایش، سامانه مدیریت کنفرانس ها و جشنواره ها - نگارش 44.5.0