DAOA-AS1

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DAOA-AS1 is a non-coding RNA that is part of the G72/G30 gene complex, which has been implicated in the neurobiology of several psychiatric disorders, including schizophrenia and bipolar disorder. The acronym DAOA stands for D-amino acid oxidase activator, and AS1 indicates that it is an antisense RNA 1. This RNA molecule is involved in the regulation of the DAOA gene, which plays a role in the modulation of neurotransmitter systems in the brain, particularly those involving glutamate, a key neurotransmitter in the central nervous system.

Function[edit | edit source]

DAOA-AS1, through its interaction with the DAOA gene, is thought to influence glutamatergic neurotransmission. Glutamate is the most abundant excitatory neurotransmitter in the vertebrate nervous system and is involved in most aspects of normal brain function, including cognition, memory, and learning. Dysregulation of glutamate signaling has been linked to the pathophysiology of several psychiatric conditions, suggesting that DAOA-AS1 might play a role in these disorders by affecting glutamate neurotransmission.

Clinical Significance[edit | edit source]

Research has identified associations between polymorphisms in the G72/G30 gene complex and increased risk of psychiatric disorders such as schizophrenia and bipolar disorder. These findings suggest that DAOA-AS1 could be involved in the development of these conditions, possibly through its regulatory effects on the DAOA gene and, consequently, on glutamate neurotransmission. Understanding the exact role of DAOA-AS1 in these disorders could lead to new therapeutic targets for their treatment.

Genetic Studies[edit | edit source]

Genetic studies have focused on the association between variations in the DAOA-AS1 gene and susceptibility to psychiatric disorders. These studies aim to identify specific polymorphisms that are more prevalent in individuals with these conditions compared to the general population. Such associations provide clues about the biological pathways that may be disrupted in psychiatric disorders and offer potential targets for drug development.

Future Directions[edit | edit source]

Further research is needed to elucidate the precise mechanisms by which DAOA-AS1 influences the DAOA gene and glutamate neurotransmission. Additionally, studies exploring the potential therapeutic implications of targeting DAOA-AS1 in psychiatric disorders are warranted. Understanding the role of non-coding RNAs like DAOA-AS1 in the brain could open up new avenues for the treatment of psychiatric conditions.


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Contributors: Prab R. Tumpati, MD