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Torres-Montilla, S.

Publications and source records attributed to Torres-Montilla, S..

5 recordsLinked to original sources

A melon (Cucumis melo) homologue of REPRESSOR OF PHOTOSYNTHETIC GENES prevents chloroplast differentiation in the fruit flesh

Fruit flesh color in melon can be orange, green or white, depending on the accumulation of the orange carotenoid {beta}-carotene or / and green chlorophylls. The dominant allele of Green flesh (Gf) causes orange melons, but in the absence of this allele the flesh of ripe melon can be white or green depending on the White flesh (Wf) locus, being white dominant over green. The identity of Wf has remained unclear despite several candidates have been proposed. Here we identified Wf by fine mapping of a segregating population derived from the white-fleshed variety Piel de Sapo (PS, gf gf / Wf Wf) and the orange-fleshed Vedrantais (VED, Gf Gf / wf wf). Wf corresponds to the gene MELO3C003098, herein referred to as CmRPGE1 as it encodes a fruit-specific homologue of REPRESSOR OF PHOTOSYNTHETIC GENES (RPGE) microproteins. Similar to RPGE homologues from other plants, overexpression of the PS allele (CmRPGE1PS) caused a pale green leaf phenotype in Nicotiana benthamiana and Arabidopsis thaliana. By contrast, a 10-nucleotide deletion in the VED allele (CmRPGE1VED) resulted in a loss of RPGE function. The active CmRPGE1PS microprotein interacts with a fruit-localized melon homologue of ARABIDOPSIS PSEUDO-RESPONSE REGULATOR2 (APRR2), a GARP family transcription factor. Binding of CmRPGE1PS retains the melon APRR2 homologue in the cytosol, hence preventing the regulation of target genes involved in chloroplast biogenesis. In green fruit cultivars, the non-functional CmRPGE1VED allele allows APRR2 to perform its function, leading to chloroplast development and consequently a green flesh phenotype. SIGNIFICANT STATEMENTFruit color is a critical quality trait that directly influences consumer preference and market value in melon. In this study, we demonstrate that the White flesh (Wf) gene, a major determinant of melon fruit flesh color, encodes a fruit-specific homologue of REPRESSOR OF PHOTOSYNTHETIC GENES (RPGE) microproteins. The encoded microprotein, CmRPGE1, interacts with melon homologues of ARABIDOPSIS PSEUDO-RESPONSE REGULATOR2 (APRR2), a GARP family transcription factor. In white flesh melons, the CmAPRR2.2 paralog is sequestered in the cytoplasm upon interaction with CmRPGE1, thereby preventing the expression of target genes involved in chlorophyll accumulation. Conversely, the truncated version of CmRPGE1 present in green-fleshed melons fails to interact with CmAPRR2.2 and to prevent its nuclear localization and function, allowing chloroplasts differentiation.

plant biology↗

Conjugation of dn-OPDA with amino acids inhibits its hormonal bioactivity in Marchantia polymorpha

Jasmonates are important phytohormones activating plant tolerance to biotic and abiotic stress, as well as different development processes. A conserved signalling pathway activated by distinct hormones in different plant species mediates these responses: dinor-12-oxo-phytodienoic acid (dn-OPDA) isomers in bryophytes and lycophytes, and JA-Ile in most vascular plants. The final responses depend, in many cases, on the accumulation of specialized metabolites. To identify novel compounds regulated by the dn-OPDA pathway in Marchantia, untargeted metabolomic analyses were carried out in response to dn-OPDA-regulated stress. A novel group of molecules were identified as dn-OPDA-amino acid conjugates (dn-OPDA-aas), and their accumulation after wounding and herbivory confirmed by targeted metabolic profiling in Marchantia and all species in which we previously found dn-iso-OPDA. Mutants in GRETCHEN-HAGEN 3A (MpGH3A) failed to accumulate dn-OPDA-aa conjugates, and showed a constitutive activation of the OPDA pathway and increased resistance to herbivory. Our results show that dn-iso-OPDA bioactivity is reduced by conjugation with amino acids. Therefore, a dichotomous role of jasmonate conjugation in land plants is highlighted: jasmonic acid (JA) conjugation with isoleucine (Ile) produce the bioactive JA-Ile in tracheophytes, whereas conjugation of dn-iso-OPDA with different amino acids disactivate the hormone in bryophytes and lycophytes.

plant biology↗

Novel insights on the contribution of plastoglobules and reactive oxygen species to chromoplast differentiation

Enriching plant tissues in phytonutrients can be done by stimulating their biosynthesis but also by providing appropriate sink structures for their sequestering and storage. Chromoplasts are plastids specialized in the production and accumulation of carotenoids that are naturally formed in non-photosynthetic tissues such as flower petals and ripe fruit. Chromoplasts can also be artificially differentiated from leaf chloroplasts by boosting the production of phytoene (the first committed intermediate of the carotenoid pathway) with the bacterial phytoene synthase crtB. Here we show that crtB-induced leaf chromoplasts develop plastoglobules harboring high levels of carotenoids (mainly phytoene and pro-vitamin A {beta}-carotene) but also other nutritionally-relevant isoprenoids such as tocopherols (vitamin E) and phylloquinone (vitamin K1). Further promoting plastoglobule proliferation by exposure to intense (high) light resulted in a higher accumulation of these health-related metabolites but also an acceleration of the chloroplast-to-chromoplast conversion. We further show that production of reactive oxygen species (ROS) stimulates chromoplastogenesis. Our data suggest that, similar to that already described for decreased photosynthesis and enhanced carotenoid biosynthesis, ROS production is not just a consequence but a promoter of the chromoplast differentiation process.

plant biology↗

Chloroplast protein import determines plant proteostasis and retrograde signaling

Proteins containing polyglutamine (polyQ) repeats are prone to aggregation and can lead to distinct human pathologies. For instance, Huntingtons disease is caused by an abnormal expansion of the polyQ stretch (> Q35) of Huntingtin (HTT) protein. However, plants express hundreds of proteins containing polyQ regions, but no pathologies arising from these factors have been reported to date. Here, we ask how plants maintain the proteostasis of polyQ-containing proteins, which are intrinsically enriched in the plant proteomes. To this end, we overexpressed an aggregation-prone fragment of human HTT (Q69) in plant cells. In contrast to invertebrate and mammalian transgenic models, we find that Arabidopsis thaliana plants suppress Q69 aggregation. This elevated proteostasis ability is mediated through the import and degradation of Q69 in chloroplasts. Conversely, inhibition of chloroplast protein import either genetically or pharmacologically reduces the capacity of plant cells to prevent Q69 aggregation. We find that Q69 interacts with the chloroplast stromal processing peptidase (SPP). Notably, expression of synthetic Arabidopsis SPP is sufficient to suppress aggregation of polyQ-expanded HTT in human cells. Beyond ectopically expressed Q69-HTT, endogenous polyQ-containing proteins also aggregate in Arabidopsis upon inhibition of chloroplast import. Among them, the plastid casein kinase 2 (pCK2), which contains a polyQ region next to the chloroplast targeting sequence motif, can also be localized into the nucleus. Upon inhibition of chloroplast import, pCK2 accumulates at higher levels in the nucleus and forms diamond-shaped amyloid-like fibrils surrounding the chloroplasts. These results indicate that the differential conformation and redistribution of pCK2 to the nucleus depends on chloroplast import efficiency, providing a role of polyQ repeats in chloroplast to nucleus communication (i.e. retrograde signaling). Together, our findings establish chloroplast protein import and proteases as determinants of polyQ proteostasis, with important implications for plant biology that can also lead to therapeutic approaches for human diseases that involve protein aggregation.

plant biology↗

The intrinsic chaperone network of Arabidopsis stem cells confers protection against proteotoxic stress

The biological purpose of plant stem cells is to maintain themselves while providing new pools of differentiated cells that form organs and rejuvenate or replace damaged tissues1-3. Protein homeostasis, or proteostasis, is required for cell function and viability4-7. However, the link between proteostasis and plant stem cell identity remains unknown. In contrast to their differentiated counterparts, we find that root stem cells can prevent the accumulation of aggregated proteins even under proteotoxic stress conditions such as heat stress or proteasome inhibition. Notably, root stem cells exhibit enhanced expression of distinct chaperones that maintain proteome integrity. Particularly, intrinsic high levels of the TRiC/CCT chaperonin determine stem cell maintenance and their remarkable ability to suppress protein aggregation. Overexpression of CCT8, a key activator of TRiC/CCT assembly8, is sufficient to ameliorate protein aggregation in differentiated cells and confer resistance to proteotoxic stress in plants. Taken together, our results indicate that enhanced proteostasis mechanisms in stem cells could be an important requirement for plants to persist under extreme environmental conditions and reach extreme long ages. Thus, proteostasis of stem cells could provide insights to design and breed plants tolerant to environmental challenges caused by the climate change.

plant biology↗