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Mutations in the chloroplast inner envelope protein TIC100 impair and repair chloroplast protein import and impact retrograde signaling

Abstract:
Chloroplast biogenesis requires synthesis of proteins in the nucleocytoplasm and the chloroplast itself. Nucleus-encoded chloroplast proteins are imported via multiprotein translocons in the organelle’s envelope membranes. Controversy exists around whether a 1-MDa complex comprising TIC20, TIC100, and other proteins constitutes the inner membrane TIC translocon. The Arabidopsis thaliana cue8 virescent mutant is broadly defective in plastid development. We identify CUE8 as TIC100. The tic100cue8 mutant accumulates reduced levels of 1-MDa complex components and exhibits reduced import of two nucleus-encoded chloroplast proteins of different import profiles. A search for suppressors of tic100cue8 identified a second mutation within the same gene, tic100soh1, which rescues the visible, 1 MDa complex-subunit abundance, and chloroplast protein import phenotypes. tic100soh1 retains but rapidly exits virescence and rescues the synthetic lethality of tic100cue8 when retrograde signaling is impaired by a mutation in the GENOMES UNCOUPLED 1 gene. Alongside the strong virescence, changes in RNA editing and the presence of unimported precursor proteins show that a strong signaling response is triggered when TIC100 function is altered. Our results are consistent with a role for TIC100, and by extension the 1-MDa complex, in the chloroplast import of photosynthetic and nonphotosynthetic proteins, a process which initiates retrograde signaling.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1093/plcell/koac153

Authors



More from this funder
Funding agency for:
Maffei, DPF
Bedard, J
Mohd Ali, S
Loudya, N
Grant:
BB/N006372/1
BB/K018442/1
BB/J009369/2
BB/R009333/1
BB/R016984/1


Publisher:
Oxford University Press
Journal:
The Plant Cell More from this journal
Volume:
34
Issue:
8
Pages:
3028-3046
Publication date:
2022-05-30
Acceptance date:
2022-05-19
DOI:
EISSN:
1532-298X
ISSN:
1040-4651


Language:
English
Keywords:
Pubs id:
1260683
Local pid:
pubs:1260683
Deposit date:
2022-05-24

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