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Investigation of the Molecular Evolution of Treg Suppression Mechanisms Indicates a Convergent Origin.
- Source :
-
Current issues in molecular biology [Curr Issues Mol Biol] 2023 Jan 09; Vol. 45 (1), pp. 628-648. Date of Electronic Publication: 2023 Jan 09. - Publication Year :
- 2023
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Abstract
- Regulatory T cell (Treg) suppression of conventional T cells is a central mechanism that ensures immune system homeostasis. The exact time point of Treg emergence is still disputed. Furthermore, the time of Treg-mediated suppression mechanisms’ emergence has not been identified. It is not yet known whether Treg suppression mechanisms diverged from a single pathway or converged from several sources. We investigated the evolutionary history of Treg suppression pathways using various phylogenetic analysis tools. To ensure the conservation of function for investigated proteins, we augmented our study using nonhomology-based methods to predict protein functions among various investigated species and mined the literature for experimental evidence of functional convergence. Our results indicate that a minority of Treg suppressor mechanisms could be homologs of ancient conserved pathways. For example, CD73, an enzymatic pathway known to play an essential role in invertebrates, is highly conserved between invertebrates and vertebrates, with no evidence of positive selection (w = 0.48, p-value < 0.00001). Our findings indicate that Tregs utilize homologs of proteins that diverged in early vertebrates. However, our findings do not exclude the possibility of a more evolutionary pattern following the duplication degeneration−complementation (DDC) model. Ancestral sequence reconstruction showed that Treg suppression mechanism proteins do not belong to one family; rather, their emergence seems to follow a convergent evolutionary pattern.
Details
- Language :
- English
- ISSN :
- 1467-3045
- Volume :
- 45
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Current issues in molecular biology
- Publication Type :
- Academic Journal
- Accession number :
- 36661528
- Full Text :
- https://doi.org/10.3390/cimb45010042