2012
DOI: 10.1016/j.tplants.2012.06.005
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Molecular regulation of seed and fruit set

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Cited by 340 publications
(273 citation statements)
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“…In tomato, photosynthesis in developing fruit can contribute up to 20% of the fruit photosynthate, and light-harvesting electron transfer and CO 2 fixation proteins are conserved in the active state in fruit tissue (Blanke and Lenz, 1989;Hetherington et al, 1998;Carrara et al, 2001;Matas et al, 2011). Yet, the prevailing idea is that fruit growth and metabolism are predominantly supported by photoassimilate supply from the source (Ruan et al, 2012), and in this regard, our data cannot rule out that the higher sugar content observed in the transgenic lines could also arise from a more efficient import of photoassimilate into fruit. Indeed, altering auxin sensitivity via down-regulation of tomato IAA9 has been reported to promote the development of vascular bundles (Wang et al, 2005), which may enhance sink strength and sugar supply to the fruit.…”
Section: Discussioncontrasting
confidence: 58%
“…In tomato, photosynthesis in developing fruit can contribute up to 20% of the fruit photosynthate, and light-harvesting electron transfer and CO 2 fixation proteins are conserved in the active state in fruit tissue (Blanke and Lenz, 1989;Hetherington et al, 1998;Carrara et al, 2001;Matas et al, 2011). Yet, the prevailing idea is that fruit growth and metabolism are predominantly supported by photoassimilate supply from the source (Ruan et al, 2012), and in this regard, our data cannot rule out that the higher sugar content observed in the transgenic lines could also arise from a more efficient import of photoassimilate into fruit. Indeed, altering auxin sensitivity via down-regulation of tomato IAA9 has been reported to promote the development of vascular bundles (Wang et al, 2005), which may enhance sink strength and sugar supply to the fruit.…”
Section: Discussioncontrasting
confidence: 58%
“…Furthermore, while LMHS decreased the expression of YUCCA-like auxin biosynthesis genes ToFZY1 in 2-dbp ovaries and ToFZY6 in 2-dap fruits in the wild type, their transcript levels were sustained in the CWINelevated transgenic plants (Fig. 10, C and D), implying a more steady homeostasis of auxin, a major hormone known to stimulate fruit set directly or indirectly (Dorcey et al, 2009;Ruan et al, 2012). Given the altered mRNA levels of the auxin responsive gene, IAA9 and YUCCA-like auxin synthesis genes ToFZY1 and ToFZY6 as discussed above, and the role of auxin in cell division (Wang and Ruan, 2013), it was somehow surprising that no difference was observed in cell number or size in ovaries and fruits between the two genotypes (Supplemental Fig.…”
Section: Elevated Cwin Activity Enhances Tomato Fruit Set Under Lmhsmentioning
confidence: 96%
“…At 28/ 14 C, the High WSC lines had the abovementioned generally lower (not always significant) levels of expression of sucrose hydrolysis and fructosyl transferases, which may have assisted in the movement of sucrose to the spike. Effectively, the genotypic avenue leading to higher growth, soluble sugars in reproductive organs and floret number seems to differ from previous models, where heightened invertase expression in ovaries are behind increased glucose levels and seed set (Boyer and McLaughlin 2007;Ruan et al 2012). It should be noted that in addition to studying a small number of genes involved in sucrose production, transport and utilisation, this study has only assessed mRNA expression levels and not enzyme activity per se.…”
Section: Links Between Genotypic Variation In Floret Fertility Sugarmentioning
confidence: 97%