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Rapid sequence evolution is associated with genetic incompatibilities in the plastid Clp complex
Key message Replacing the native clpP1 gene in the Nicotiana plastid genome with homologs from different donor species showed that the extent of genetic incompatibilities depended on the rate of sequence evolution. The plastid caseinolytic protease (Clp) complex plays essential roles in maintaining...
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Published in: | Plant molecular biology 2022-02, Vol.108 (3), p.277-287 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Key message
Replacing the native
clpP1
gene in the Nicotiana plastid genome with homologs from different donor species showed that the extent of genetic incompatibilities depended on the rate of sequence evolution.
The plastid caseinolytic protease (Clp) complex plays essential roles in maintaining protein homeostasis and comprises both plastid-encoded and nuclear-encoded subunits. Despite the Clp complex being retained across green plants with highly conserved protein sequences in most species, examples of extremely accelerated amino acid substitution rates have been identified in numerous angiosperms. The causes of these accelerations have been the subject of extensive speculation but still remain unclear. To distinguish among prevailing hypotheses and begin to understand the functional consequences of rapid sequence divergence in Clp subunits, we used plastome transformation to replace the native
clpP1
gene in tobacco (
Nicotiana tabacum
) with counterparts from another angiosperm genus (
Silene
) that exhibits a wide range in rates of Clp protein sequence evolution. We found that antibiotic-mediated selection could drive a transgenic
clpP1
replacement from a slowly evolving donor species (
S. latifolia
) to homoplasmy but that
clpP1
copies from
Silene
species with accelerated evolutionary rates remained heteroplasmic, meaning that they could not functionally replace the essential tobacco
clpP1
gene. These results suggest that observed cases of rapid Clp sequence evolution are a source of epistatic incompatibilities that must be ameliorated by coevolutionary responses between plastid and nuclear subunits. |
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ISSN: | 0167-4412 1573-5028 |
DOI: | 10.1007/s11103-022-01241-4 |