Explaining tomato fruit growth by a multi-scale model on regulation of cell division, cell growth and carbohydrate dynamics

A multi-scale approach to model tomato fruit growth is proposed, in order to account for the interaction between gene functioning and growth conditions, and, ultimately, to explain the fruit phenotype of various genotypes in diverse growth environments. There is particular focus on: (I) cell division regulated by cell cycle genes, (II) cell expansion as influenced by polyploidy resulting from endoreduplication and carbohydrate and water dynamics. The growth processes at gene, cell and tissue, fruit and plant scale have been identified and included in the model. Sub-populations of cells differing in age are considered to act as sinks competing for carbohydrates. The key cell cycle genes of tomato were incorporated into an existing model of the gene regulatory network of the cell cycle. This model was modified to simulate endoreduplication. Moreover, the modelled cell cycle process was made sensitive to temperature and assimilate supply. The multi-scale approach required that a simulation could only proceed if a calculation task at a neighbouring scale had been performed. Preliminary model results indicate that cell number and ploidy level were very important in determining fruit growth. Subsequently, in the cell expansion phase, growth rate was limited by assimilate supply which in the end determined the realized fruit size. Observations at gene, cell and tissue scale are in progress in order to calibrate and validate the model, to enable reliable prediction of cell division and expansion of cells in tomato fruit tissues at contrasting conditions of temperature and carbohydrate supply

Anemia prevalence in women of reproductive age in low- and middle-income countries between 2000 and 2018

Anemia is a globally widespread condition in women and is associated with reduced economic productivity and increased mortality worldwide. Here we map annual 2000–2018 geospatial estimates of anemia prevalence in women of reproductive age (15–49 years) across 82 low- and middle-income countries (LMICs), stratify anemia by severity and aggregate results to policy-relevant administrative and national levels. Additionally, we provide subnational disparity analyses to provide a comprehensive overview of anemia prevalence inequalities within these countries and predict progress toward the World Health Organization’s Global Nutrition Target (WHO GNT) to reduce anemia by half by 2030. Our results demonstrate widespread moderate improvements in overall anemia prevalence but identify only three LMICs with a high probability of achieving the WHO GNT by 2030 at a national scale, and no LMIC is expected to achieve the target in all their subnational administrative units. Our maps show where large within-country disparities occur, as well as areas likely to fall short of the WHO GNT, offering precision public health tools so that adequate resource allocation and subsequent interventions can be targeted to the most vulnerable populations.Peer reviewe

What drives fruit growth?

Cell division, endoreduplication (an increase in nuclear DNA content without cell division) and cell expansion are important processes for growth. It is debatable whether organ growth is driven by all three cellular processes. Alternatively, all could be part of a dominant extracellular growth regulatory mechanism. Cell level processes have been studied extensively and a positive correlation between cell number and fruit size is commonly reported, although few positive correlations between cell size or ploidy level and fruit size have been found. Here, we discuss cell-level growth dynamics in fruits and ask what drives fruit growth and during which development stages. We argue that (1) the widely accepted positive correlation between cell number and fruit size does not imply a causal relationship; (2) fruit growth is regulated by both cell autonomous and noncell autonomous mechanisms as well as a global coordinator, the target of rapamycin; and (3) increases in fruit size follow the neocellular theory of growth

Light mediated regulation of cell division, endoreduplication and cell expansion

Cell division, endoreduplication and cell expansion are key processes for plant growth and development. Light is the main source of energy for plants and as such has a strong effect on plant growth and development. Insight into the role of light in cellular processes is important for our understanding of plant responses to light. Recent advances in artificial plant lighting, cell imaging techniques and molecular biology have provided opportunities to study light responses of plants at the cell and gene level. Regulatory networks for cellular processes have also been unravelled and many transcription factors identified. In this review, we highlight key transcription factors and photoreceptors involved in the regulation of cell division, endoreduplication and cell expansion by light. We suggest that light responses result from either degradation of transcription factors or inhibitory competition between transcription factors for promoter regions of target genes. We also suggest that light stimulates cell division irrespective of the organ under consideration, while endoreduplication and cell expansion responses to light vary from organ to organ

Fruit illumination stimulates cell division but has no detectable effect on fruit size in tomato (Solanum lycopersicum)

Light affects plant growth through assimilate availability and signals regulating development. The effects of light on growth of tomato fruit were studied using cuvettes with light-emitting diodes providing white, red or blue light to individual tomato trusses for different periods during daytime. Hypotheses tested were as follows: (1) light-grown fruits have stronger assimilate sinks than dark-grown fruits, and (2) responses depend on light treatment provided, and fruit development stage. Seven light treatments [dark, 12-h white, 24-h white, 24-h red and 24-h blue light, dark in the first 24 days after anthesis (DAA) followed by 24-h white light until breaker stage, and its reverse] were applied. Observations were made between anthesis and breaker stage at fruit, cell and gene levels. Fruit size and carbohydrate content did not respond to light treatments while cell division was strongly stimulated at the expense of cell expansion by light. The effects of light on cell number and volume were independent of the combination of light color and intensity. Increased cell division and decreased cell volume when fruits were grown in the presence of light were not clearly corroborated by the expression pattern of promoters and inhibitors of cell division and expansion analyzed in this study, implying a strong effect of posttranscriptional regulation. Results suggest the existence of a complex homeostatic regulatory system for fruit growth in which reduced cell division is compensated by enhanced cell expansion

A multilevel analysis of fruit growth of two tomato cultivars in response to fruit temperature

Fruit phenotype is a resultant of inherent genetic potential in interaction with impact of environment experienced during crop and fruit growth. The aim of this study was to analyze the genetic and physiological basis for the difference in fruit size between a small (‘Brioso’) and intermediate (‘Cappricia’) sized tomato cultivar exposed to different fruit temperatures. It was hypothesized that fruit heating enhances expression of cell cycle and expansion genes, rates of carbon import, cell division and expansion, and shortens growth duration, whereas increase in cell number intensifies competition for assimilates among cells. Unlike previous studies in which whole-plant and fruit responses cannot be separated, we investigated the temperature response by varying fruit temperature using climate-controlled cuvettes, while keeping plant temperature the same. Fruit phenotype was assessed at different levels of aggregation (whole fruit, cell and gene) between anthesis and breaker stage. We showed that: (1) final fruit fresh weight was larger in ‘Cappricia’ owing to more and larger pericarp cells, (2) heated fruits were smaller because their mesocarp cells were smaller than those of control fruits and (3) no significant differences in pericarp carbohydrate concentration were detected between heated and control fruits nor between cultivars at breaker stage. At the gene level, expression of cell division promoters (CDKB2, CycA1 and E2Fe-like) was higher while that of the inhibitory fw2.2 was lower in ‘Cappricia’. Fruit heating increased expression of fw2.2 and three cell division promoters (CDKB1, CDKB2 and CycA1). Expression of cell expansion genes did not corroborate cell size observations

A multilevel analysis of fruit growth of two tomato cultivars in response to fruit temperature

Fruit phenotype is a resultant of inherent genetic potential in interaction with impact of environment experienced during crop and fruit growth. The aim of this study was to analyze the genetic and physiological basis for the difference in fruit size between a small (‘Brioso’) and intermediate (‘Cappricia’) sized tomato cultivar exposed to different fruit temperatures. It was hypothesized that fruit heating enhances expression of cell cycle and expansion genes, rates of carbon import, cell division and expansion, and shortens growth duration, whereas increase in cell number intensifies competition for assimilates among cells. Unlike previous studies in which whole-plant and fruit responses cannot be separated, we investigated the temperature response by varying fruit temperature using climate-controlled cuvettes, while keeping plant temperature the same. Fruit phenotype was assessed at different levels of aggregation (whole fruit, cell and gene) between anthesis and breaker stage. We showed that: (1) final fruit fresh weight was larger in ‘Cappricia’ owing to more and larger pericarp cells, (2) heated fruits were smaller because their mesocarp cells were smaller than those of control fruits and (3) no significant differences in pericarp carbohydrate concentration were detected between heated and control fruits nor between cultivars at breaker stage. At the gene level, expression of cell division promoters (CDKB2, CycA1 and E2Fe-like) was higher while that of the inhibitory fw2.2 was lower in ‘Cappricia’. Fruit heating increased expression of fw2.2 and three cell division promoters (CDKB1, CDKB2 and CycA1). Expression of cell expansion genes did not corroborate cell size observations