Reprogramming the translatome during daily light transitions as affected by cytosolic glyceraldehyde-3-phosphate dehydrogenases GAPC1/C2

© The Author(s) 2023. Published by Oxford University Press on behalf of the Society for Experimental Biology. All rights reserved. For permissions, please email: journals.permissionsoup.com.

Bibliographische Detailangaben
Veröffentlicht in:Journal of experimental botany. - 1985. - 75(2024), 8 vom: 15. Apr., Seite 2494-2509
1. Verfasser: Wegener, Melanie (VerfasserIn)
Weitere Verfasser: Persicke, Marcus, Dietz, Karl-Josef
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2024
Zugriff auf das übergeordnete Werk:Journal of experimental botany
Schlagworte:Journal Article GAPC1/C2 RNA binding glyceraldehyde-3-phosphate dehydrogenase metabolite profiling moonlighting function night–dark transition polysome (un)loading translatome Arabidopsis Proteins mehr... Glyceraldehyde-3-Phosphate Dehydrogenases EC 1.2.1.- RNA 63231-63-0
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520 |a © The Author(s) 2023. Published by Oxford University Press on behalf of the Society for Experimental Biology. All rights reserved. For permissions, please email: journals.permissionsoup.com. 
520 |a Dark-light and light-dark transitions during the day are switching points of leaf metabolism that strongly affect the regulatory state of the cells, and this change is hypothesized to affect the translatome. The cytosolic glyceraldehyde-3-phosphate dehydrogenases GAPC1 and GAPC2 function in glycolysis, and carbohydrate and energy metabolism, but GAPC1/C2 also shows moonlighting functions in gene expression and post-transcriptional regulation. In this study we examined the rapid reprogramming of the translatome that occurs within 10 min at the end of the night and the end of the day in wild-type (WT) Arabidopsis and a gapc1/c2 double-knockdown mutant. Metabolite profiling compared to the WT showed that gapc1/c2 knockdown led to increases in a set of metabolites at the start of day, particularly intermediates of the citric acid cycle and linked pathways. Differences in metabolite changes were also detected at the end of the day. Only small sets of transcripts changed in the total RNA pool; however, RNA-sequencing revealed major alterations in polysome-associated transcripts at the light-transition points. The most pronounced difference between the WT and gapc1/c2 was seen in the reorganization of the translatome at the start of the night. Our results are in line with the proposed hypothesis that GAPC1/C2 play a role in the control of the translatome during light/dark transitions 
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650 4 |a RNA binding 
650 4 |a glyceraldehyde-3-phosphate dehydrogenase 
650 4 |a metabolite profiling 
650 4 |a moonlighting function 
650 4 |a night–dark transition 
650 4 |a polysome (un)loading 
650 4 |a translatome 
650 7 |a Arabidopsis Proteins  |2 NLM 
650 7 |a Glyceraldehyde-3-Phosphate Dehydrogenases  |2 NLM 
650 7 |a EC 1.2.1.-  |2 NLM 
650 7 |a RNA  |2 NLM 
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700 1 |a Persicke, Marcus  |e verfasserin  |4 aut 
700 1 |a Dietz, Karl-Josef  |e verfasserin  |4 aut 
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