Temporal and spatial expression of hexose transporters in developing tomato (Lycopersicon esculentum) fruit

2005 ◽  
Vol 32 (9) ◽  
pp. 777 ◽  
Author(s):  
Stephen J. Dibley ◽  
Michael L. Gear ◽  
Xiao Yang ◽  
Elke G. Rosche ◽  
Christina E. Offler ◽  
...  

Correlative physiological evidence suggests that membrane transport into storage parenchyma cells is a key step in determining hexose levels accumulated in tomato (Lycopersicon esculentum Mill.) fruit (Ruan et al. 1997). Expression of three previously identified hexose transporter genes (LeHT1, 2 and 3) demonstrated that LeHT3, and to a lesser extent LeHT1, are the predominant transporters expressed in young fruit (10 d after anthesis; DAA). Expression of both transporters dropped sharply until 24 DAA, after which only LeHT3 expression remained at detectable levels through to fruit ripening. LeHT2 was not expressed substantially until the onset of fruit ripening. For fruit at both 10 and 30 DAA, LeHT3 transcripts were detected in storage parenchyma cells of the outer pericarp tissue, but not in vascular bundles or the first layer of parenchyma cells surrounding these bundles. In contrast to LeHT gene expression, hexose transporter protein levels were maximal between 20 and 30 DAA, which corresponded to the period of highest hexose accumulation. The delayed appearance of transporter protein is consistent with some form of post-transcriptional regulation. Based on these analyses, LeHT3 appears to be responsible for the rapid hexose accumulation in developing tomato fruit.

2015 ◽  
Vol 42 (10) ◽  
pp. 957 ◽  
Author(s):  
Ricky J. Milne ◽  
Christina E. Offler ◽  
John W. Patrick ◽  
Christopher P. L. Grof

Cellular pathways of phloem loading in source leaves and phloem unloading in stems of sweet Sorghum bicolor (L.) Moench were deduced from histochemical determinations of cell wall composition and from the relative radial mobilities of fluorescent tracer dyes exiting vascular pipelines. The cell walls of small vascular bundles in source leaves, the predicted site of phloem loading, contained minimal quantities of lignin and suberin. A phloem-loaded symplasmic tracer, carboxyfluorescein, was retained within the collection phloem, indicating symplasmic isolation. Together, these findings suggested that phloem loading in source leaves occurs apoplasmically. Lignin was restricted to the walls of protoxylem elements located in meristematic, elongating and recently elongated regions of the stem. The apoplasmic tracer, 8-hydroxypyrene-1,3,6-trisulfonic acid, moved radially from the transpiration stream, consistent with phloem and storage parenchyma cells being interconnected by an apoplasmic pathway. The major phase of sucrose accumulation in mature stems coincided with heavy lignification and suberisation of sclerenchyma sheath cell walls restricting apoplasmic tracer movement from the phloem to storage parenchyma apoplasms. Phloem unloading at this stage of stem development followed a symplasmic route linking sieve elements and storage parenchyma cells, as confirmed by the phloem-delivered symplasmic tracer, 8-hydroxypyrene-1,3,6-trisulfonic acid, moving radially from the stem phloem.


1999 ◽  
Vol 22 (1) ◽  
pp. 101-104 ◽  
Author(s):  
Elizanilda R. do Rêgo ◽  
Fernando L. Finger ◽  
Vicente W.D. Casali ◽  
Antônio A. Cardoso

A naturally occurring yellow tomato fruit mutant cv. Santa Clara was reciprocally crossed with the red wild type, after which F1 plants were self pollinated or backcrossed with both parents. Plants from F1 generations produced all fruits with a homogeneous deep red color when ripe. F2 plants showed a 3:1 red:yellow segregation of fruit color, and 100% red when backcrossed with red wild type or 1:1 red:yellow segregation in backcrosses with the yellow mutant; hence, yellow fruit color was determined by a recessive allele. Based on reciprocal crosses, fruit color is unlikely to be determined by maternal genes. Accumulation of lycopene dropped by 99.3% and<FONT FACE="Symbol"> b</font>-carotene by 77% in ripe yellow fruits, compared to the red wild type. Leaf and flower chlorophyll and total carotenoid concentrations were not affected by the yellow mutation. However, the mutant fruit had a higher rate of chlorophyll degradation during fruit ripening, whilst fruit from the F1 generation showed lower rates of degradation, similar to that observed in red wild type fruits.


1996 ◽  
Vol 121 (3) ◽  
pp. 520-524 ◽  
Author(s):  
Jerry D. Cohen

An in vitro system was used for the production of tomato (Lycopersicon esculentum) fruit in culture starting from immature flowers. This system produced small parthenocarpic (seedless) fruit in response to 10-4m indole-3-acetic acid (IAA) supplied in the medium. Other auxins, auxin conjugates and antiauxins tested were not effective or produced markedly fewer fruit. Additional IAA supplied to the fruit culture media before breaker stage resulted in an increase in the time period between breaker and red-ripe stages from 7 days without additional IAA to 12 days when 10-5m IAA was added. These results suggest that significant changes in the ripening period could be obtained by alteration of auxin relationships in tomato fruit.


1978 ◽  
Vol 79 (1) ◽  
pp. 10-19 ◽  
Author(s):  
B Baumgartner ◽  
K T Tokuyasu ◽  
M J Chrispeels

Vicilin peptidohydrolase, the protease that hydrolyzes the reserve proteins in the cotyledons of mung bean (Vigna radiata) seedlings, has been localized intracellularly by immunofluorescence microscopy using monospecific antibodies against the enzyme and rhodamine-coupled goat-anti-rabbit immunoglobulin G's. The enzyme can first be visualized after 3 days of seedling growth and is associated with small foci within the cytoplasm of the storage parenchyma cells farthest from the vascular bundles. On the 4th day of growth, the protease is also present in the numerous large protein bodies within these cells. Vicilin peptidohydrolase is known to be synthesized de novo starting on the 3rd day of growth. Our observations are therefore consistent with the interpretation that the enzyme is synthesized in the cytoplasm and subsequently transported to the protein bodies.


2021 ◽  
Vol 8 (1) ◽  
Author(s):  
Weihao Wang ◽  
Peiwen Wang ◽  
Xiaojing Li ◽  
Yuying Wang ◽  
Shiping Tian ◽  
...  

AbstractLight plays a critical role in plant growth and development, but the mechanisms through which light regulates fruit ripening and nutritional quality in horticultural crops remain largely unknown. Here, we found that ELONGATED HYPOCOTYL 5 (HY5), a master regulator in the light signaling pathway, is required for normal fruit ripening in tomato (Solanum lycopersicum). Loss of function of tomato HY5 (SlHY5) impairs pigment accumulation and ethylene biosynthesis. Transcriptome profiling identified 2948 differentially expressed genes, which included 1424 downregulated and 1524 upregulated genes, in the Slhy5 mutants. In addition, genes involved in carotenoid and anthocyanin biosynthesis and ethylene signaling were revealed as direct targets of SlHY5 by chromatin immunoprecipitation. Surprisingly, the expression of a large proportion of genes encoding ribosomal proteins was downregulated in the Slhy5 mutants, and this downregulation pattern was accompanied by a decrease in the abundance of ribosomal proteins. Further analysis demonstrated that SlHY5 affected the translation efficiency of numerous ripening-related genes. These data indicate that SlHY5 regulates fruit ripening both at the transcriptional level by targeting specific molecular pathways and at the translational level by affecting the protein translation machinery. Our findings unravel the regulatory mechanisms of SlHY5 in controlling fruit ripening and nutritional quality and uncover the multifaceted regulation of gene expression by transcription factors.


1985 ◽  
Vol 65 (4) ◽  
pp. 1011-1018 ◽  
Author(s):  
C. S. TAN ◽  
B. N. DHANVANTARI

Two tomato (Lycopersicon esculentum Mill.) cultivars, Heinz-2653 and Campbell-28, were grown on Fox loamy sand in the subhumid region of southern Ontario from 1979 to 1982. Irrigation increased the marketable yields of H-2653 in a dry year, 1982, but not in the other years. Irrigation substantially increased marketable yields of C-28 in 1979 and 1982. Irrigation, when the available soil moisture (ASM) level reached 50%, was no more effective than when the ASM level in the soil was allowed to drop to 25%. Without irrigation yield increased as plant population increased in normal and wet years, but not in a dry year. Blossom-end rot (BER) of C-28 cultivar was markedly reduced by irrigation. Effects of irrigation or plant population treatments on the incidence of fruit speck did not appear to be significant.Key words: Available soil moisture, Lycopersicon esculentum, Pseudomonas syringae pv. tomato, fruit speck


1987 ◽  
Vol 84 (3) ◽  
pp. 911-917 ◽  
Author(s):  
Birgit Piechulla ◽  
Richard E. Glick ◽  
Hubert Bahl ◽  
Anastasios Melis ◽  
Wilhelm Gruissem

1990 ◽  
Vol 2 (4) ◽  
pp. 243-254 ◽  
Author(s):  
Mandy J. Hetherington ◽  
Alan Martin ◽  
Douglas B. MacDougall ◽  
Keith R. Langley ◽  
Nick Bratchell

2009 ◽  
Vol 103 (1) ◽  
pp. 116-119 ◽  
Author(s):  
G.G. Romero ◽  
C.C. Martinez ◽  
E.E. Alanís ◽  
G.A. Salazar ◽  
V.G. Broglia ◽  
...  

1996 ◽  
Vol 271 (1) ◽  
pp. G211-G216 ◽  
Author(s):  
C. P. Corpe ◽  
C. F. Burant

In rodents, a number of intestinal digestive and absorptive processes demonstrate a diurnal pattern of activity. To investigate if the jejunal hexose transporters are regulated in such a diurnal fashion, the levels for the glucose and fructose transporter mRNA and proteins were determined at 6-h intervals over a 24-h control fed period. SGLT-1, GLUT-2, and GLUT-5 mRNA levels increased between two- and eightfold before the onset of peak feeding. GLUT-5 protein levels also varied in a diurnal fashion but were out of phase with the observed changes in GLUT-5 mRNA levels. In contrast, GLUT-2 protein levels remained relatively constant during the control fed 24-h period. The effect of dietary manipulations on the observed diurnal variation was also investigated. After only 3 h of feeding a 60% fructose-enriched diet, the levels of GLUT-5 mRNA and protein were significantly elevated. GLUT-5 mRNA and protein levels remained elevated relative to the level of control diet-fed animals over the ensuing 24 h and during the 7th day of fructose feeding. Exposure to elevated levels of fructose had no significant effect on the diurnal pattern of GLUT-2 and SGLT-1 mRNA. In contrast, GLUT-2 protein was rapidly downregulated during the length of the fructose feeding study. In conclusion, the data demonstrate a normal daily variation in the level of hexose transporter expression that can be rapidly modulated by diet.


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