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Published on: August 15, 2019
Demystifying the ACE polymorphism: from genetics to biology
Raquel Castellon1, Hamdi K Hamdi
1H2RC Corporation, Orange, CA 92867, USA.
Current Pharmaceutical Design
|May 17, 2007
Summary
The angiotensin converting enzyme (ACE) I/D polymorphism is linked to numerous diseases. This review explains its function in cell survival and its broader biological and disease relevance.
Area of Science:
- Genetics
- Molecular Biology
- Physiology
Background:
- The angiotensin converting enzyme (ACE) I/D polymorphism is extensively studied.
- It has been associated with a wide range of diseases, including cardiovascular, metabolic, immune, cancer, aging, neurodegenerative, and psychiatric conditions.
- Despite numerous studies, the precise function and broad disease associations of the ACE polymorphism remain incompletely understood.
Purpose of the Study:
- To review current knowledge on the ACE I/D polymorphism.
- To elucidate the function of the ACE polymorphism in the context of cell survival.
- To propose a model explaining its biological and disease roles at organism and population levels.
Main Methods:
- Literature review of existing studies on ACE polymorphism.
- Analysis of ACE function related to cell survival mechanisms.
- Development of a conceptual model for ACE polymorphism's role in health and disease.
Main Results:
- The ACE I/D polymorphism's association with diverse diseases is a key finding.
- ACE's function is explained in relation to cellular survival pathways.
- A model is presented to integrate ACE polymorphism's effects across biological scales.
Conclusions:
- The ACE I/D polymorphism plays a significant role in cell survival.
- Understanding ACE function provides insights into its widespread disease associations.
- The proposed model aids in comprehending ACE's impact on organismal and population health.
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When crossing pea plants, Mendel noticed that one of the parental traits would sometimes disappear in the first generation of offspring, called the F1 generation, and could reappear in the next generation (F2). He concluded that one of the traits must be dominant over the other, thereby causing masking of one trait in the F1 generation. When he crossed the F1 plants, he found that 75% of the offspring in the F2 generation had the dominant phenotype, while 25% had the recessive phenotype.

