A College at Buffalo analysis workforce led by oral biologist Dr. Hyuk-Jae (Edward) Kwon has superior the understanding of genetic issues that weaken tooth enamel by turning off a gene generally known as KMT2D in mice.
The research, printed within the Journal of Dental Analysis, marks the primary in-depth investigation figuring out KMT2D as a key regulator in enamel formation
Kwon, an affiliate professor within the Division of Oral Biology at UB’s College of Dental Medication, and his workforce genetically engineered mice with the KMT2D gene deactivated in enamel-forming cells. The consequence: the mice developed tooth that have been tough, chalky and thinner than regular—carefully resembling the dental anomalies seen in sufferers with Kabuki syndrome, a uncommon genetic dysfunction.
“What we began to see is that these mice developed tooth that have been very fragile and would break after they chewed on their chow,” mentioned Kwon, DDS, PhD.
The KMT2D gene, often known as MLL4, encodes an enzyme referred to as lysine-specific methyltransferase 2D, which performs a task in regulating gene expression in numerous tissues. The workforce found that enamel defects started even earlier than the tooth emerged by means of the gums.
“We discovered that KMT2D serves as a sort of ‘on change’ for enamel-building in tooth cells,” Kwon mentioned. “If this gene is lacking or disrupted, the cells don’t obtain the suitable indicators, and the enamel-producing cells fail to develop correctly.”
The analysis additionally means that concentrating on KMT2D with particular medication may doubtlessly reverse enamel defects and even stop craniofacial delivery defects.
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Exploring cleft palate and future therapies
The workforce is now testing candidate medication in pregnant mice to find out whether or not they can stop or reverse oral delivery defects throughout mid-gestation. One focus is cleft palate, a standard craniofacial anomaly additionally related to Kabuki syndrome.
“When mice are born with a cleft palate, they die 100 per cent of the time,” Kwon mentioned. “Whereas people can survive and endure surgical procedure, cleft palate could be a important burden for sufferers and their households. If we may stop these issues from occurring, it might be a sport changer.”
Recognition and funding
Kwon was just lately awarded second place within the IADR Joseph Lister Award for New Investigators on the 2025 Worldwide Affiliation for Dental, Oral and Craniofacial Analysis (IADR) Pan European Area Normal Session in Barcelona, Spain.
His colleague, Dr. Jung-Mi Lee, a analysis scientist in UB’s Division of Oral Biology, performed a key function within the research by eradicating the gene within the oral epithelium. Lee has since acquired a two-year, $320,000 grant from the U.S. Nationwide Institute of Dental and Craniofacial Analysis to additional examine the gene’s regulatory mechanisms in dental regeneration.
“Our long-term objective is to grasp how one can regenerate organs,” Lee mentioned. “And to do this, essentially the most fundamental step is figuring out the molecular mechanisms that drive tissue improvement.”
Different contributors to the research embrace Drs. Soo-Kyung Lee and Jae W. Lee, professors in UB’s Division of Organic Sciences and co-directors of the FOXGI Analysis Heart, and Dr. Yungki Park, affiliate professor of biochemistry on the Jacobs College of Medication and Biomedical Sciences.
