Rare variant burden analysis from exomes of three consanguineous families reveals LILRB1 and PRSS3 as potential key proteins in inflammatory bowel disease pathogenesis

• Published in: Frontiers in medicine Vol. 10; p. 1164305
• Main Authors: Jan, Rana Mohammed, Al-Numan, Huda Husain, Al-Twaty, Nada Hassan, Alrayes, Nuha, Alsufyani, Hadeel A, Alaifan, Meshari A, Alhussaini, Bakr H, Shaik, Noor Ahmad, Awan, Zuhier, Qari, Yousef, Saadah, Omar I, Banaganapalli, Babajan, Mosli, Mahmoud Hisham, Elango, Ramu
• Format: Journal Article
• Language: English
• Published: Switzerland Frontiers Media S.A 05-05-2023
• Subjects: Crohn’s disease; gastrointestinal tract; inflammatory bowel disease; Medicine; missense mutation; protein modeling; gastrointestinal tract; protein modeling; inflammatory bowel disease; missense mutation; Crohn’s disease
• ISSN: 2296-858X; 2296-858X
• DOI: 10.3389/fmed.2023.1164305

Inflammatory bowel disease (IBD) is a chronic autoimmune disorder characterized by severe inflammation and mucosal destruction of the intestine. The specific, complex molecular processes underlying IBD pathogenesis are not well understood. Therefore, this study is aimed at identifying and uncovering the role of key genetic factors in IBD.
The whole exome sequences (WESs) of three consanguineous Saudi families having many siblings with IBD were analyzed to discover the causal genetic defect. Then, we used a combination of artificial intelligence approaches, such as functional enrichment analysis using immune pathways and a set of computational functional validation tools for gene expression, immune cell expression analyses, phenotype aggregation, and the system biology of innate immunity, to highlight potential IBD genes that play an important role in its pathobiology.
Our findings have shown a causal group of extremely rare variants in the
(Q53L, Y99N, W351G, D365A, and Q376H) and
(F4L and V25I) genes in IBD-affected siblings. Findings from amino acids in conserved domains, tertiary-level structural deviations, and stability analysis have confirmed that these variants have a negative impact on structural features in the corresponding proteins. Intensive computational structural analysis shows that both genes have very high expression in the gastrointestinal tract and immune organs and are involved in a variety of innate immune system pathways. Since the innate immune system detects microbial infections, any defect in this system could lead to immune functional impairment contributing to IBD.
The present study proposes a novel strategy for unraveling the complex genetic architecture of IBD by integrating WES data of familial cases, with computational analysis.