2018
DOI: 10.1016/j.scienta.2017.12.032
|View full text |Cite
|
Sign up to set email alerts
|

FaTT12-1 , a multidrug and toxin extrusion (MATE) member involved in proanthocyanidin transport in strawberry fruits

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

0
20
0

Year Published

2019
2019
2022
2022

Publication Types

Select...
7
1
1

Relationship

2
7

Authors

Journals

citations
Cited by 39 publications
(21 citation statements)
references
References 45 publications
0
20
0
Order By: Relevance
“…Recent research indicated that multi-drug and toxic extrusion MATE TT12 might be involved in transportation of anthocyanin across cell membranes in brown cotton, radish and strawberry (Gao et al, 2016, M’Mbone et al, 2018, Chen et al, 2018). In the present study, six MATE TT12 genes were identified in the strawberries and high ambient temperature up-regulate their genes expression, which was consistant with the increment of anthocyanidins levels (Table 1).…”
Section: Discussionmentioning
confidence: 99%
“…Recent research indicated that multi-drug and toxic extrusion MATE TT12 might be involved in transportation of anthocyanin across cell membranes in brown cotton, radish and strawberry (Gao et al, 2016, M’Mbone et al, 2018, Chen et al, 2018). In the present study, six MATE TT12 genes were identified in the strawberries and high ambient temperature up-regulate their genes expression, which was consistant with the increment of anthocyanidins levels (Table 1).…”
Section: Discussionmentioning
confidence: 99%
“…Subsequently, Equal volumes of TRV1 and TRV2/ TRV2-G6PDH-CY cultures were mixed together. Transient overexpression and VIGS by infiltration of corresponding construct into strawberry fruits followed the procedures described by Chen et al (2018) [ 45 ]. The treated strawberries were cultured in dark for 12 h, and then subjected to 4 °C treatment.…”
Section: Methodsmentioning
confidence: 99%
“…TRV2-CYC-B and TRV1 and TRV2 plasmids were transfected into Agrobacterium tumefaciens GV3101 competent cells by freeze-thaw. The method of Chen et al [32] and Zhai et al [31] were used for VIGS. Agrobacterium cells were spread in selective Luria Bertani (LB) solid medium containing Gentamicin (Gen, 40 mg/L), Kan (50 mg/L), and Rifampicin (Rif, 20 mg/L), then cultivated at 28 • C for 48 h-72 h. The growth of the colonies was observed.…”
Section: Agrobacterium Transformation and Injectionmentioning
confidence: 99%
“…The presence of the inserts was verified using 1 µL of bacterial solution as a template for PCR. TRV1 detection primers were created as described by Chen et al [32]. TRV2-CYC-B detection primers were the same as S1 primers.…”
Section: Agrobacterium Transformation and Injectionmentioning
confidence: 99%