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Published on: July 16, 2017
ADAR Family Proteins: A Structural Review
Carolyn N Ashley1, Emmanuel Broni1, Whelton A Miller1,2
1Department of Medicine, Loyola University Medical Center, Loyola University Chicago, Maywood, IL 60153, USA.
Adenosine deaminases acting on RNA (ADAR) proteins are key to genetic information diversity and neuronal complexity. Their structures and functions are vital for understanding RNA editing and developing new therapeutics.
Area of Science:
- Molecular Biology
- Neuroscience
- Genetics
Background:
- ADAR proteins play critical roles in RNA editing, influencing genetic diversity and neuronal network sophistication.
- These proteins possess distinct structural features, including double-stranded RNA binding domains (dsRBD) and catalytic deaminase domains (CDD).
- ADARs exhibit diverse functions beyond RNA editing, impacting immunity, RNA interference, and disease modulation.
Purpose of the Study:
- To review the structures of ADAR proteins and their link to function.
- To explore the therapeutic potential of targeting ADAR proteins.
- To examine the roles of ADAR1, ADAR2, and ADAR3, including their isoforms and tissue-specific regulation.
Main Methods:
- Literature review focusing on structural biology of ADAR proteins.
- Analysis of published data on ADAR functions in RNA editing and other biological processes.
- Examination of ADARs' involvement in immunity, RNA interference, and disease.
Main Results:
- ADAR protein structures, including dsRBD and CDD, are crucial for their RNA editing functions.
- Distinct isoforms of ADAR1, ADAR2, and ADAR3 contribute to functional variability and tissue-specific regulation.
- ADARs have a dual role in disease, potentially promoting or inhibiting disease progression.
Conclusions:
- Understanding ADAR protein structures is essential for elucidating their complex functions.
- Targeting ADAR proteins presents a promising avenue for therapeutic development.
- Further research into ADARs' biological mechanisms and health implications is warranted.
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