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1.
Plant J ; 118(6): 2202-2218, 2024 Jun.
Article in English | MEDLINE | ID: mdl-38578875

ABSTRACT

Alternative splicing (AS) is a complex process that generates transcript variants from a single pre-mRNA and is involved in numerous biological functions. Many RNA-binding proteins are known to regulate AS; however, little is known about the underlying mechanisms, especially outside the mammalian clade. Here, we show that polypyrimidine tract binding proteins (PTBs) from Arabidopsis thaliana regulate AS of cassette exons via pyrimidine (Py)-rich motifs close to the alternative splice sites. Mutational studies on three PTB-dependent cassette exon events revealed that only some of the Py motifs in this region are critical for AS. Moreover, in vitro binding of PTBs did not reflect a motif's impact on AS in vivo. Our mutational studies and bioinformatic investigation of all known PTB-regulated cassette exons from A. thaliana and human suggested that the binding position of PTBs relative to a cassette exon defines whether its inclusion or skipping is induced. Accordingly, exon skipping is associated with a higher frequency of Py stretches within the cassette exon, and in human also upstream of it, whereas exon inclusion is characterized by increased Py motif occurrence downstream of said exon. Enrichment of Py motifs downstream of PTB-activated 5' splice sites is also seen for PTB-dependent intron removal and alternative 5' splice site events from A. thaliana, suggesting this is a common step of exon definition. In conclusion, the position-dependent AS regulatory mechanism by PTB homologs has been conserved during the separate evolution of plants and mammals, while other critical features, in particular intron length, have considerably changed.


Subject(s)
Alternative Splicing , Arabidopsis Proteins , Arabidopsis , Exons , Polypyrimidine Tract-Binding Protein , Arabidopsis/genetics , Arabidopsis/metabolism , Exons/genetics , Polypyrimidine Tract-Binding Protein/genetics , Polypyrimidine Tract-Binding Protein/metabolism , Arabidopsis Proteins/genetics , Arabidopsis Proteins/metabolism , Pyrimidines , Humans
2.
Plant J ; 104(4): 1038-1053, 2020 11.
Article in English | MEDLINE | ID: mdl-32890447

ABSTRACT

Phytochromes are red/far-red light receptors in plants involved in the regulation of growth and development. Phytochromes can sense the light environment and contribute to measuring day length; thereby, they allow plants to respond and adapt to changes in the ambient environment. Two well-characterized signalling pathways act downstream of phytochromes and link light perception to the regulation of gene expression. The CONSTITUTIVELY PHOTOMORPHOGENIC 1/SUPPRESSOR OF PHYA-105 (COP1/SPA) E3 ubiquitin ligase complex and the PHYTOCHROME INTERACTING FACTORs (PIFs) are key components of these pathways and repress light responses in the dark. In light-grown seedlings, phytochromes inhibit COP1/SPA and PIF activity and thereby promote light signalling. In a yeast-two-hybrid screen for proteins binding to light-activated phytochromes, we identified COLD-REGULATED GENE 27 (COR27). COR27 and its homologue COR28 bind to phyA and phyB, the two primary phytochromes in seed plants. COR27 and COR28 have been described previously with regard to a function in the regulation of freezing tolerance, flowering and the circadian clock. Here, we show that COR27 and COR28 repress early seedling development in blue, far-red and in particular red light. COR27 and COR28 contain a conserved Val-Pro (VP)-peptide motif, which mediates binding to the COP1/SPA complex. COR27 and COR28 are targeted for degradation by COP1/SPA and mutant versions with a VP to AA amino acid substitution in the VP-peptide motif are stabilized. Overall, our data suggest that COR27 and COR28 accumulate in light but act as negative regulators of light signalling during early seedling development, thereby preventing an exaggerated response to light.


Subject(s)
Arabidopsis Proteins/metabolism , Arabidopsis/genetics , Light Signal Transduction , Phytochrome B/metabolism , Repressor Proteins/metabolism , Ubiquitin-Protein Ligases/metabolism , Arabidopsis/growth & development , Arabidopsis/physiology , Arabidopsis/radiation effects , Arabidopsis Proteins/genetics , Cell Cycle Proteins/genetics , Cell Cycle Proteins/metabolism , Circadian Clocks , Mutation , Proteasome Endopeptidase Complex , Proteolysis , Repressor Proteins/genetics , Seedlings/genetics , Seedlings/growth & development , Seedlings/physiology , Ubiquitin-Protein Ligases/genetics
3.
New Phytol ; 225(4): 1635-1650, 2020 02.
Article in English | MEDLINE | ID: mdl-31596952

ABSTRACT

Phytochrome B (phyB) is an excellent light quality and quantity sensor that can detect subtle changes in the light environment. The relative amounts of the biologically active photoreceptor (phyB Pfr) are determined by the light conditions and light independent thermal relaxation of Pfr into the inactive phyB Pr, termed thermal reversion. Little is known about the regulation of thermal reversion and how it affects plants' light sensitivity. In this study we identified several serine/threonine residues on the N-terminal extension (NTE) of Arabidopsis thaliana phyB that are differentially phosphorylated in response to light and temperature, and examined transgenic plants expressing nonphosphorylatable and phosphomimic phyB mutants. The NTE of phyB is essential for thermal stability of the Pfr form, and phosphorylation of S86 particularly enhances the thermal reversion rate of the phyB Pfr-Pr heterodimer in vivo. We demonstrate that S86 phosphorylation is especially critical for phyB signaling compared with phosphorylation of the more N-terminal residues. Interestingly, S86 phosphorylation is reduced in light, paralleled by a progressive Pfr stabilization under prolonged irradiation. By investigating other phytochromes (phyD and phyE) we provide evidence that acceleration of thermal reversion by phosphorylation represents a general mechanism for attenuating phytochrome signaling.


Subject(s)
Arabidopsis/metabolism , Phytochrome B/metabolism , Amino Acid Sequence , Apoproteins/genetics , Apoproteins/metabolism , Arabidopsis/genetics , Arabidopsis Proteins/genetics , Arabidopsis Proteins/metabolism , Phosphorylation , Phytochrome/genetics , Phytochrome/metabolism , Phytochrome B/genetics , Plants, Genetically Modified , Signal Transduction
4.
AIDS Behav ; 21(12): 3630-3635, 2017 Dec.
Article in English | MEDLINE | ID: mdl-28028652

ABSTRACT

Geophagy, or the ingestion of earth or clay, is widespread among women of Sub-Saharan African, Caribbean or French Guiana origin. Little is known about this practice among HIV patients native of these countries and who are followed-up in France. The aims of this study were to determine (i) the prevalence and factors associated with geophagy among HIV patients native of these countries, (ii) patients' knowledge about the harmful effects of geophagy, and (iii) the association of geophagy with iron deficiency, or a history of anemia or constipation. Among the 119 included patients, current geophagy and previous geophagy were present in 11/119 (9%) and 47/119 (40%) patients, respectively. Female gender was the only factor associated with consumption (OR 5.37; 95% CI 2.07-15.92 p = 0.001). Awareness about the risk of iron-deficient anemia was low (24%). Preventive education should be integrated into the care of HIV adults from countries in which geophagy is a culture and widely accepted practice.


Subject(s)
Anemia, Iron-Deficiency/complications , HIV Infections/complications , Health Knowledge, Attitudes, Practice , Pica/complications , Soil , Adult , Africa South of the Sahara/ethnology , Anemia, Iron-Deficiency/epidemiology , Caribbean Region/ethnology , Ethnicity , Feeding and Eating Disorders , Female , France/epidemiology , French Guiana/ethnology , Humans , Male , Prevalence
6.
AIDS ; 29(2): 241-3, 2015 Jan 14.
Article in English | MEDLINE | ID: mdl-25486416

ABSTRACT

We investigated measles humoral immunity levels in a cohort of HIV-infected adult patients in France and attempted to identify risk factors for antimeasles antibodies seronegativity. Being born after 1983 [odds ratio (OR) 4.40; 95% confidence interval (95% CI) 1.26-14.09; P = 0.0013] and a nadir CD4⁺ cell count below 100 cells/µl (OR 4.79; 95% CI 1.61-14.82; P = 0.0048) were the two factors independently associated with measles seronegativity. Systematic measles antibody screening should be performed in HIV-infected individuals born in the era of measles vaccination (after 1983 in France).


Subject(s)
Antibodies, Viral/blood , HIV Infections/epidemiology , Measles/epidemiology , Vaccination/statistics & numerical data , Adult , CD4 Lymphocyte Count , Female , France/epidemiology , HIV-1 , Humans , Immunity, Humoral , Male , Middle Aged , Odds Ratio , Prevalence , Risk Factors
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