The inhibition of SlIAA9 mimics an increase in endogenous auxin and mediates changes in auxin and gibberellin signalling during parthenocarpic fruit development in tomato

2020 ◽  
Vol 252 ◽  
pp. 153238
Author(s):  
Ji-Seong Kim ◽  
Kentaro Ezura ◽  
Jeongeun Lee ◽  
Mikkiko Kojima ◽  
Yumiko Takebayashi ◽  
...  
PLoS ONE ◽  
2015 ◽  
Vol 10 (10) ◽  
pp. e0139503 ◽  
Author(s):  
Orlando Alva ◽  
Rosa Nair Roa-Roco ◽  
Ricardo Pérez-Díaz ◽  
Mónica Yáñez ◽  
Jaime Tapia ◽  
...  

2002 ◽  
Vol 77 (1) ◽  
pp. 9-12
Author(s):  
O. Junttila ◽  
I. Martinussen ◽  
A. Ernstsen ◽  
G. Nilsen ◽  
T.V. Bhuvaneswari

2002 ◽  
pp. 101-104 ◽  
Author(s):  
B. Mezzetti ◽  
L. Landi ◽  
L. Scortichini ◽  
A. Spena ◽  
T. Pandolfini ◽  
...  

PLoS ONE ◽  
2013 ◽  
Vol 8 (7) ◽  
pp. e70080 ◽  
Author(s):  
Jiangang Ding ◽  
Biwei Chen ◽  
Xiaojian Xia ◽  
Weihua Mao ◽  
Kai Shi ◽  
...  

2015 ◽  
Vol 27 (1) ◽  
pp. 71-80
Author(s):  
S. Łukasik ◽  
W. Huszcza

It was found that parthenocarpy could be induced by morphactin IT 3456 (0.5 and 1 ppm) in prior emasculated flowers, those left to free-pollination and even flowers pollinated with the pollen of control plants (New Yorker). When morphactin IT 3456 in 0.5 and 1 ppm concentrations was used 88% and 100% of parthenocarpy was noted in the greenhouse, respectively (Earliest of All). The higest percentage of parthenocarpy in the total number of fruits in the field was recorded in the 'New Yorker' variety. The lowest percentage of parthenocarpy was observed in the variety 903. The symptoms of the destructive influence of morphactin IT 3456 (0.5 and 1 ppm) on plant development were noted, but they were stronger in the greenhouse than in the field.


PeerJ ◽  
2018 ◽  
Vol 6 ◽  
pp. e5975
Author(s):  
Suthasinee Somyong ◽  
Kitti Walayaporn ◽  
Nukoon Jomchai ◽  
Chaiwat Naktang ◽  
Tanapong Yodyingyong ◽  
...  

Oil palm parthenocarpic fruits, which are produced without fertilization, can be targeted to increase oil content because the majority of the fruit is occupied by mesocarp, the part in which palm oil is stored. Consequently, gaining an understanding of the parthenocarpic mechanism would be instrumental for producing parthenocarpic oil palm. This study aims to determine effects of auxin treatment and analyze differentially expressed genes in oil palm pistils at the pollination/anthesis stage, using an RNA sequencing (RNA seq) approach. The auxin treatment caused 100% parthenocarpy when auxin was sprayed before stigmas opened. The parthenocarpy decreased to 55%, 8% and 5% when the auxin was sprayed 1, 2 and 3 days after the opening of stigmas, respectively. Oil palm plants used for RNA seq were plants untreated with auxin as controls and auxin-treated plants on the day before pollination and 1 day after pollination. The number of raw reads ranged from 8,425,859 to 11,811,166 reads, with an average size ranging from 99 to 137 base pairs (bp). When compared with the oil palm transcriptome, the mapped reads ranged from 8,179,948 to 11,320,799 reads, representing 95.85–98.01% of the oil palm matching. Based on five comparisons between RNA seq of treatments and controls, and confirmation using reverse transcription polymerase chain reaction and quantitative real-time RT-PCR expression, five candidate genes, including probable indole-3-acetic acid (IAA)-amido synthetase GH3.8 (EgGH3.8), IAA-amido synthetase GH3.1 (EgGH3.1), IAA induced ARG7 like (EgARG7), tryptophan amino transferase-related protein 3-like (EgTAA3) and flavin-containing monooxygenase 1 (EgFMO1), were differentially expressed between auxin-treated and untreated samples. This evidence suggests a pathway of parthenocarpic fruit development at the beginning of fruit development. However, more research is needed to identify which genes are definitely involved in parthenocarpy.


1972 ◽  
Vol 52 (5) ◽  
pp. 781-785 ◽  
Author(s):  
D. J. CANTLIFFE

Nine growth-regulating chemicals were sprayed at concentrations of 50 and 100 ppm on pickling cucumbers (Cucumis sativus L., cult Pioneer) in an effort to induce parthenocarpic fruit development. A morphactin formulation, IT 3456 (methyl-2-chloro-9-hydroxyfluorene-(9)-carboxylate), and TIBA (2,3,5-triiodobenzoic acid) were the most effective in stimulating parthenocarpic fruit-set and development at both concentrations used. Between six and seven fruits per plant were induced parthenocarpically when 100 ppm IT 3456 morphactin was used. Two other morphactins tested, IT 3233 (n-butyl-9-hydroxyfluorene-(9)-carboxylate) and Bay 102614 (2,7-dichloro-9-hydroxyfluorene-carboxylate-(9)-methyl ester), produced no more fruits than the control. A new growth regulator, CCDP (3-carboxy-1-(p-chlorophenyl)-4,6-dimethyl-2-pridone), significantly increased the number of fruits per plant at the 100-ppm concentration, and also increased the number of female flowers per plant produced within 50 days of planting, at both concentrations. The other four compounds tested, designated EL 531 (α-cycloprophyl-α-(4-methoxyphenyl)-5-pyrimidine methanol), BAS 0660-W (N-dimethyl-morpholiniumchloride), TD 692 (mono-("coco" dimethylamine) succinate), and Chemagro 8728 (5-chloro-2-thenyl-tributylphosphonium), were not effective inducers of parthenocarpy in the cucumber.


Plant Biology ◽  
2005 ◽  
Vol 7 (2) ◽  
pp. 131-139 ◽  
Author(s):  
B. Gorguet ◽  
A. W. Heusden ◽  
P. Lindhout

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