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Pri-Or, A.

Publications and source records attributed to Pri-Or, A..

2 recordsLinked to original sources

Two opposing redox signals mediated by 2-Cys peroxiredoxin shape the redox proteome during photosynthetic induction

Photosynthetic induction, characterized by the lag in CO2 assimilation rates typically observed upon plant transition from darkness to light, has traditionally been attributed to Rubisco activase activity and stomatal opening. Yet, the faster induction of photosynthesis in the 2-Cys peroxiredoxins (Prxs) mutant (2cpab) highlighted the critical role of chloroplast redox state in regulating photosynthetic rates during this phase. Since 2-Cys Prxs are involved in transmission of oxidative signals to target enzymes, it was hypothesized that it slows down photosynthesis during the induction phase. SPEAR, a redox proteomics approach for simultaneous protein expression and redox analysis, was used to systematically map redox changes occurring at the proteome level during photosynthesis induction and to unravel the role of 2-Cys Prxs in shaping these redox alterations. No significant difference was observed in protein expression levels between WT and 2cpab plants, suggesting that protein abundance does not account for the 2cpab phenotype. During the transition from dark to low light, 82 and 54 cysteine-containing peptides were reduced or oxidized, respectively, in WT plants. Most redox-regulated cysteines in photosynthetic proteins were found oxidized in the dark and became reduced in response to light, including ATP synthase gamma chain 1 (ATPC1) and glyceraldehyde-3-phosphate dehydrogenase (GAPB). A reverse pattern was observed among redox-regulated cysteines in proteins involved in starch degradation and chloroplast glycolysis, which shifted from a reduced to an oxidized state in response to light. These findings demonstrate the initiation of two opposing redox responses, affecting distinct sets of metabolic proteins during the induction phase. Remarkably, a significantly lower number of cysteines were reduced or oxidized in 2cpab plants, highlighting the crucial role 2-Cys Prxs play in shaping both signals. Taken together, rotational shifts between metabolic pathways during the photosynthesis induction phase are regulated by two opposing redox signals mediated by 2-Cys Prx activity.

plant biology↗

The molecular and cellular interplay between the osteopetrosis-associated proteins SNX10, OSTM1, and CLC-7 during osteoclastogenesis

Bone-resorbing osteoclasts (OCLs) are large, multi-nucleated cells that are formed through well-regulated differentiation and cell fusion of monocyte-macrophage precursors. Disruption of OCL-mediated bone resorption perturbs bone formation, remodeling, and homeostasis that, in turn, can lead to severe illnesses, such as autosomal recessive osteopetrosis (ARO). Mutations in the intracellular trafficking-associated protein sorting nexin 10 (SNX10) lead to "OCL-rich" ARO, in which OCLs are produced but are inactive. Furthermore, OCL fusion is deregulated in SNX10-knockout (SKO) mice: mature mutant OCLs fuse continuously to generate gigantic cells, in vitro and in vivo, unlike wild-type OCLs that stop fusing with each other upon maturation. Mutations in CLC-7, the lysosomal voltage-gated Cl-/H+ exchanger, and OSTM1, the beta-chain of the exchanger, also induce ARO in humans and in mouse models, and are associated with the presence of large OCLs. This study explored the molecular interplay between SNX10, CLC-7 and OSTM1 by directly comparing the phenotypes of cultured OCLs lacking one of these proteins. We show that loss of SNX10, OSTM1, or CLC-7 leads to the formation of similarly-gigantic OCLs in culture, due to deregulated fusion between mature OCLs that proceeds with similar kinetics. All three proteins are associated with LAMP1-positive lysosomes, localized in both perinuclear and peripheral regions of mature wild-type OCLs. Co-immunoprecipitation studies indicated that SNX10 physically interacts with CLC-7. Notably, SNX10-KO OCLs exhibited a significant reduction in peripheral lysosomes containing CLC-7 and OSTM1, suggesting that SNX10 is required for their transport to the cell periphery. Taken together, these findings indicate that SNX10 regulates the subcellular distribution of lysosomes containing CLC-7 and OSTM1, thereby controlling both the fusion and functionality of mature OCLs.

cell biology↗