“New findings could lead way towards treatments for intellectual disability in Down syndrome.”

The late Professor Kyung-Tai Min and his research team in the School of Life Sciences at S. Korea’s Ulsan National Institute of Science and Technology (UNIST) have identified for the first time that the Down syndrome critical region 1 (DSCR 1) protein contributes to intellectual disability found in Down syndrome. This research, which was conducted during the lifetime of Professor Min may pave the way for advances in diagnosis and treatment for cognitive deficits. The findings of this research have been featured in the 2020 edition of Asia Research News Magazine, and also appeared on the cover page.

Learning and memory impairments in a Down syndrome mouse model were reversed by correcting expression of a gene that influences the generation of new neurons in the brain. The finding could pave the way to treat the cognitive impairment associated with the syndrome in humans.

Adult neurogenesis is the process of generating new neurons in the adult brain. Defects in this process have been observed in various animal models of neurological disorders including schizophrenia, depression, Parkinson’s disease, Alzheimer’s disease, and neurodevelopmental disorders, such as Down syndrome. But the precise cellular and molecular mechanisms underlying adult neurogenesis and their links to neurological disorders are not well understood.


Figure 1. Correcting DSCR 1 dosage prevents impaired adult neurogenesis and learning and memory found in Ts65Dn mouse.

Molecular neurobiologist Kyung-Tai Min and his colleagues at UNIST found that interactions between a gene called the Down syndrome critical region 1 (DSCR1) and two other molecules, TET1 and miRNA-124, were necessary for adult neurogenesis and were important in learning and memory.

DSCR1 is known for its involvement in learning and memory and is overexpressed in Down syndrome. TET1, which is an enzyme, and miRNA-124, which is a micro-RNA, are known for having roles in adult neurogenesis, but the details were not clear. Min and his team have now found how the three molecules work together to regulate adult neurogenesis.

They showed that DSCR1 binds to a non-coding section of TET1 RNA, subsequently controlling expression of TET1 proteins, which then regulate miRNA-124 expression levels. This process is required for adult neurogenesis and for maintaining learning and memory abilities.


Figure 2. Researchers has unveiled that DSCR 1 knockout and transgenic brains show defective hippocampal adult neurogenesis.

Knocking out DSCR1 in mice led to increased TET1 levels, and ultimately increased miRNA-124 expression. Correcting TET1 levels in these mice prevented defective adult neurogenesis. Also, adult neurogenesis, and learning and memory impairments improved in a mouse model of Down syndrome when the scientists restored DSCR1 levels.

The findings reveal that precise regulation of DSCR1 and the interplay between TET1 and miRNA-124 are crucial for normal adult neurogenesis.

“Our findings not only provide a basic understanding of the mechanisms regulating adult neurogenesis, but will also contribute to the development of a novel therapy for the cognitive deficits manifested in Down syndrome patients,” says Min.

ResearchSEA Magazine Down Syndrome cover page

The findings of this research have been featured in the 2020 edition of Asia Research News Magazine, and also appeared on the cover page.

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