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The HMGN3 gene is located on chromosome 6 at the position 6q14.1 . The gene produces multiple transcript variants encoding different isoforms of the HMGN3 protein . The protein itself is characterized by its ability to bind to nucleosomes, which are the fundamental units of chromatin. This binding is facilitated by the nucleosomal binding domain present in the protein.
HMGN3 is known to interact with the thyroid hormone receptor beta in the presence of thyroid hormone . This interaction is significant because it influences the compactness of chromatin fibers. By reducing the compactness, HMGN3 enhances transcription from chromatin templates . This means that HMGN3 plays a vital role in regulating gene expression by modulating chromatin structure.
Additionally, HMGN3 has been implicated in the regulation of insulin and glucagon levels. It modulates the expression of pancreatic genes involved in insulin secretion . Specifically, HMGN3 regulates the expression of the glucose transporter SLC2A2 by binding to its promoter region and recruiting transcription factors such as PDX1 . This regulation is crucial for maintaining glucose homeostasis in the body.
The biological significance of HMGN3 extends to various physiological processes. For instance, it is involved in the regulation of glycine concentration in synaptic junctions in the central nervous system by regulating the expression of the glycine transporter SLC6A9 . This function is essential for proper neurotransmission and synaptic function.
Moreover, HMGN3 may play a role in ocular development and astrocyte function . These diverse roles highlight the importance of HMGN3 in maintaining normal physiological functions across different tissues and organs.
Research on HMGN3 has provided insights into its potential clinical implications. Given its role in regulating insulin secretion, HMGN3 could be a target for therapeutic interventions in diabetes and other metabolic disorders. Additionally, its involvement in chromatin remodeling and gene expression regulation makes it a potential target for cancer therapy, where dysregulation of these processes is often observed.