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Comparative study of primates' transcortin: immunoreactivity and steroid-binding activity
Endocrinologia Japonica
|April 1, 1986
Summary
This study explored primate transcortin (corticosteroid-binding globulin) evolution using antibody reactions. Highly evolved primates like humans and apes showed immunoreactivity, suggesting evolutionary changes in transcortin structure.
Area of Science:
- Primate evolutionary biology
- Biochemistry
- Immunology
Background:
- Transcortin (corticosteroid-binding globulin, CBG) plays a crucial role in regulating corticosteroid levels.
- Understanding the evolutionary trajectory of CBG provides insights into primate adaptation and speciation.
- Previous studies have established the importance of CBG in various mammalian species.
Purpose of the Study:
- To investigate the phylogenetic distribution and evolutionary aspects of transcortin (CBG) in primates.
- To examine the immunoreactivity of primate transcortin with anti-human transcortin antibodies.
- To assess the cortisol-binding activity of transcortin across different primate groups.
Main Methods:
- Utilized radioimmunoassay techniques with 125I-labelled human transcortin and anti-human transcortin antiserum.
- Tested plasma samples from various primate groups including Catarrhini, Platyrrhini, and Prosimiae.
- Assessed cortisol-binding activity in primate plasma samples.
Main Results:
- Transcortin immunoreactivity was detected in Catarrhini (Old World monkeys and apes) but not in Platyrrhini (New World monkeys) or Prosimiae.
- Cortisol-binding activity was present in most primates, with notable exceptions in certain Platyrrhini species.
- Thyroxine-binding globulin (TBG) immunoreactivity was observed only in plasma from Pan (chimpanzee).
Conclusions:
- The presence of immunoreactive transcortin and TBG in highly evolved apes aligns with primate cladogenetic classifications.
- Evolutionary modifications in transcortin structure may have occurred without compromising its cortisol-binding function.
- Specific Platyrrhini species may have unique adaptations related to cortisol regulation due to absent or altered transcortin function.