ADAMTS9

From WikiMD's Wellness Encyclopedia


ADAMTS9 is a member of the ADAMTS (A Disintegrin and Metalloproteinase with Thrombospondin Motifs) family of proteins. This family is characterized by a combination of metalloproteinase and disintegrin domains, and is involved in a variety of biological processes, including extracellular matrix (ECM) remodeling, angiogenesis, and cell migration.

Structure[edit | edit source]

ADAMTS9 is a large, multi-domain protein that includes the following domains:

  • Propeptide domain: This domain is involved in the regulation of the enzyme's activity. It is cleaved to activate the enzyme.
  • Metalloproteinase domain: This domain contains the catalytic site responsible for the proteolytic activity of the enzyme. It requires a zinc ion for its activity.
  • Disintegrin-like domain: This domain is thought to mediate interactions with other proteins, particularly those in the ECM.
  • Thrombospondin type 1 repeats (TSR): ADAMTS9 contains multiple TSRs, which are involved in binding to ECM components and modulating cell-matrix interactions.
  • Cysteine-rich domain: This domain may play a role in substrate recognition and binding.
  • Spacer domain: This domain contributes to the overall structure and function of the protein.

Function[edit | edit source]

ADAMTS9 is involved in the processing of various ECM components, including proteoglycans such as aggrecan and versican. It plays a critical role in ECM remodeling, which is essential for normal development and tissue homeostasis. ADAMTS9 is also implicated in the regulation of angiogenesis, the process by which new blood vessels form from pre-existing vessels.

Role in Development[edit | edit source]

During embryonic development, ADAMTS9 is expressed in various tissues and is essential for normal organogenesis. It is particularly important in the development of the cardiovascular system, kidneys, and limbs.

Role in Disease[edit | edit source]

ADAMTS9 has been associated with several pathological conditions, including:

  • Cancer: Altered expression of ADAMTS9 has been observed in various cancers, where it may influence tumor progression and metastasis.
  • Arthritis: Due to its role in ECM degradation, ADAMTS9 may contribute to the breakdown of cartilage in osteoarthritis.
  • Obesity and Metabolic syndrome: Genetic studies have linked variants in the ADAMTS9 gene with susceptibility to obesity and related metabolic disorders.

Genetics[edit | edit source]

The ADAMTS9 gene is located on chromosome 3p14.3. It is composed of multiple exons and encodes a protein of approximately 1,930 amino acids. The expression of ADAMTS9 is regulated at both the transcriptional and post-transcriptional levels.

Clinical Significance[edit | edit source]

Mutations or dysregulation of ADAMTS9 can lead to developmental abnormalities and contribute to the pathogenesis of various diseases. Understanding the precise role of ADAMTS9 in these processes is an area of active research, with potential implications for the development of therapeutic interventions.

Research Directions[edit | edit source]

Current research on ADAMTS9 focuses on elucidating its specific substrates and interaction partners, understanding its regulation, and exploring its potential as a therapeutic target in diseases such as cancer and arthritis.

See Also[edit | edit source]

External Links[edit | edit source]

Template:ADAMTS family

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Contributors: Prab R. Tumpati, MD