Role of serine/threonine protein kinase STN7 in the formation of two distinct photosystem I supercomplexes in Physcomitrium patens

dc.contributor.authorGerotto Caterina
dc.contributor.authorTrotta Andrea
dc.contributor.authorBajwa Azfar Ali
dc.contributor.authorMorosinotto Tomas
dc.contributor.authorAro Eva-Mari
dc.contributor.organizationfi=molekulaarinen kasvibiologia|en=Molecular Plant Biology|
dc.contributor.organization-code1.2.246.10.2458963.20.50535969575
dc.contributor.organization-code2610104
dc.converis.publication-id175902498
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/175902498
dc.date.accessioned2022-10-27T12:11:18Z
dc.date.available2022-10-27T12:11:18Z
dc.description.abstractPhosphorylation-dependent formation of photosystem I supercomplexes provides both short- and long-term acclimation of moss photosynthetic apparatus to changing environmental cues.Reversible thylakoid protein phosphorylation provides most flowering plants with dynamic acclimation to short-term changes in environmental light conditions. Here, through generating Serine/Threonine protein kinase 7 (STN7)-depleted mutants in the moss Physcomitrella (Physcomitrium patens), we identified phosphorylation targets of STN7 kinase and their roles in short- and long-term acclimation of the moss to changing light conditions. Biochemical and mass spectrometry analyses revealed STN7-dependent phosphorylation of N-terminal Thr in specific Light-Harvesting Complex II (LHCII) trimer subunits (LHCBM2 and LHCBM4/8) and provided evidence that phospho-LHCBM accumulation is responsible for the assembly of two distinct Photosystem I (PSI) supercomplexes (SCs), both of which are largely absent in STN7-depleted mutants. Besides the canonical state transition complex (PSI-LHCI-LHCII), we isolated the larger moss-specific PSI-Large (PSI-LHCI-LHCB9-LHCII) from stroma-exposed thylakoids. Unlike PSI-LHCI-LHCII, PSI-Large did not demonstrate short-term dynamics for balancing the distribution of excitation energy between PSII and PSI. Instead, PSI-Large contributed to a more stable increase in PSI antenna size in Physcomitrella, except under prolonged high irradiance. Additionally, the STN7-depleted mutants revealed altered light-dependent phosphorylation of a monomeric antenna protein, LHCB6, whose phosphorylation displayed a complex regulation by multiple kinases. Collectively, the unique phosphorylation plasticity and dynamics of Physcomitrella monomeric LHCB6 and trimeric LHCBM isoforms, together with the presence of PSI SCs with different antenna sizes and responsiveness to light changes, reflect the evolutionary position of mosses between green algae and vascular plants, yet with clear moss-specific features emphasizing their adaptation to terrestrial low-light environments.
dc.identifier.eissn1532-2548
dc.identifier.jour-issn0032-0889
dc.identifier.olddbid173775
dc.identifier.oldhandle10024/156869
dc.identifier.urihttps://www.utupub.fi/handle/11111/33013
dc.identifier.urlhttps://academic.oup.com/plphys/advance-article/doi/10.1093/plphys/kiac294/6613940
dc.identifier.urnURN:NBN:fi-fe2022081153792
dc.language.isoen
dc.okm.affiliatedauthorTrotta, Andrea
dc.okm.affiliatedauthorBajwa, Azfar
dc.okm.affiliatedauthorAro, Eva-Mari
dc.okm.discipline1183 Plant biology, microbiology, virologyen_GB
dc.okm.discipline1183 Kasvibiologia, mikrobiologia, virologiafi_FI
dc.okm.internationalcopublicationinternational co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA1 ScientificArticle
dc.publisherOXFORD UNIV PRESS INC
dc.publisher.countryUnited Statesen_GB
dc.publisher.countryYhdysvallat (USA)fi_FI
dc.publisher.country-codeUS
dc.relation.doi10.1093/plphys/kiac294
dc.relation.ispartofjournalPlant Physiology
dc.source.identifierhttps://www.utupub.fi/handle/10024/156869
dc.titleRole of serine/threonine protein kinase STN7 in the formation of two distinct photosystem I supercomplexes in Physcomitrium patens
dc.year.issued2022

Tiedostot

Näytetään 1 - 1 / 1
Ladataan...
Name:
kiac294.pdf
Size:
1.81 MB
Format:
Adobe Portable Document Format