The molecular mechanism of amelogenin exon4 alternative splicing and its association to amelogenesis imperfecta

NIH RePORTER · NIH · F31 · $48,003 · view on reporter.nih.gov ↗

Abstract

PROJECT SUMMARY/ABSTRACT Enamel, the protective outer layer of our teeth, is crucial for maintaining dental health. A gene called amelogenin plays a vital role in enamel formation, and it uses a process called alternative splicing to create different versions of itself for various functions. When mutations occur in the amelogenin gene, it can lead to hereditary enamel defects known as X-linked Amelogenesis Imperfecta (X-AI). Many mutations that cause hereditary diseases affect the alternative splicing of the gene, in place of changing the amino acid within the final protein. Instead, they alter the way the gene is spliced. However, X-AI and its causing mutations in amelogenin have not been studied in association with alternative splicing until recently. Previous research has shown that a significant number of X-AI-causing mutations are found in specific parts of the amelogenin gene called exons 4 and 5. Research has demonstrated that these mutations can disrupt the alternative splicing of exon4 in laboratory experiments, suggesting a direct link between these mutations, alternative splicing of exon4, and the development of enamel defects. However, there is not a full understanding of how this process works in the body or how these mutations impact enamel formation by the change of alternative splicing in amelogenin. This current study aims to get answers to these scientific questions by investigating how specific proteins called Ser/Arg rich splicing factors (SRSFs) influence the splicing of amelogenin exon4. Additionally, the proposal explores how an X-AI-causing mutation affects splicing patterns and contributes to enamel defects as teeth develop. By examining these questions, the goal is to better understand the genetic factors behind X-AI and other related conditions. Patients with X-AI have hypoplastic, hypo mineralized, and/or hypocalcified enamel, resulting in a reduced quality of life due to discomfort caused by pain, increased chance of pulpal infections, and compromised appearance. Ultimately, this knowledge could pave the way for improved treatments to enhance the quality of life for patients affected by enamel defects.

Key facts

NIH application ID
11071014
Project number
1F31DE034641-01
Recipient
UNIVERSITY OF CALIFORNIA, SAN FRANCISCO
Principal Investigator
Rozana Shemirani
Activity code
F31
Funding institute
NIH
Fiscal year
2024
Award amount
$48,003
Award type
1
Project period
2024-09-27 → 2027-07-26