
A College at Buffalo analysis workforce led by oral biologist Dr. Hyuk-Jae (Edward) Kwon has superior the understanding of genetic problems that weaken tooth enamel by turning off a gene often known as KMT2D in mice.
The research, printed within the Journal of Dental Analysismarks 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 Drugs, and his workforce genetically engineered mice with the KMT2D gene deactivated in enamel-forming cells. The outcome: 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 once they chewed on their chow,” stated Kwon, DDS, PhD.
The KMT2D gene, also referred to as MLL4, encodes an enzyme known as lysine-specific methyltransferase 2D, which performs a job in regulating gene expression in numerous tissues. The workforce found that enamel defects started even earlier than the tooth emerged by the gums.
“We discovered that KMT2D serves as a sort of ‘on swap’ for enamel-building in tooth cells,” Kwon stated. “If this gene is lacking or disrupted, the cells don’t obtain the fitting indicators, and the enamel-producing cells fail to develop correctly.”
The analysis additionally means that focusing on KMT2D with particular medicine might doubtlessly reverse enamel defects and even forestall craniofacial beginning defects.
Learn associated hyperlink: The Actuality of Lacking Enamel
Learn associated hyperlink: U.S. researchers research tooth enamel at atomic degree to know why tooth get brittle as we age
Exploring cleft palate and future therapies
The workforce is now testing candidate medicine in pregnant mice to find out whether or not they can forestall or reverse oral beginning defects throughout mid-gestation. One focus is cleft palatea typical craniofacial anomaly additionally related to Kabuki syndrome.
“When mice are born with a cleft palate, they die 100 per cent of the time,” Kwon stated. “Whereas people can survive and bear surgical procedure, cleft palate generally is a vital burden for sufferers and their households. If we might forestall these problems from occurring, it might be a sport changer.”
Recognition and funding
Kwon was 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 purpose is to know find out how to regenerate organs,” Lee stated. “And to do this, probably the most primary step is figuring out the molecular mechanisms that drive tissue improvement.”
Different contributors to the research embody 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 Drugs and Biomedical Sciences.

