2023
DOI: 10.1016/j.indcrop.2022.116054
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Overexpression of the long non-coding RNA lncWOX5 negatively regulates the development of adventitious roots in Populus

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Cited by 3 publications
(3 citation statements)
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“…The lncWOX5 negatively regulated WOX5 , and lncWOX11 positively regulated WOX11 during the AR formation of poplar [ 46 ]. The overexpression of lncWOX5 negatively regulated the development of AR in Populus [ 83 ]. A total of 130 cis-acting lncRNAs were identified associated with the hub genes of modules significantly correlated with JA and DEGs in the phenylpropanoid biosynthesis, flavonoid biosynthesis, and isoflavonoid biosynthesis pathway, with 17 of them exhibiting significant differential expression during root cuttings in favorable conditions of other growth environment factors in E. ulmoides .…”
Section: Discussionmentioning
confidence: 99%
“…The lncWOX5 negatively regulated WOX5 , and lncWOX11 positively regulated WOX11 during the AR formation of poplar [ 46 ]. The overexpression of lncWOX5 negatively regulated the development of AR in Populus [ 83 ]. A total of 130 cis-acting lncRNAs were identified associated with the hub genes of modules significantly correlated with JA and DEGs in the phenylpropanoid biosynthesis, flavonoid biosynthesis, and isoflavonoid biosynthesis pathway, with 17 of them exhibiting significant differential expression during root cuttings in favorable conditions of other growth environment factors in E. ulmoides .…”
Section: Discussionmentioning
confidence: 99%
“…Plant-specific WUSCHEL-related homeobox (WOX) transcription factors (TFs), especially WOX11, LATERAL ORGAN BOUNDARIES DOMAIN 16, and SMALL AUXIN-UP RNA 36 (SAUR36), are essential regulators of AR formation via the auxin pathway [99]. Numerous lncRNAs that regulate the expression of WOX11 have been identified [97,100]. Among them, lncWOX11a is located 54,293 bp upstream of Pe-WOX11a on chromosome 13 and is mainly expressed in 1-week-old roots.…”
Section: Root Growth and Developmentmentioning
confidence: 99%
“…DNA from the frozen leaf tissue was extracted using a Plant Genomic DNA kit according to the manufacturer's instructions (Tiangen, Beijing, China). Elongation factor 1-alpha (EF1α) was used as an internal control fragment [18,19]. PCR amplification was performed using a Veriti ™ 96-Well Thermal Cycler (Thermo Fisher, Waltham, MA, USA) and the PCR mix (25 µL) contained 12.5 µL Premix Taq ™ (Takara, Beijing, China), 1 µL (10 µM) forward primer (5 -GGCAAGGAGAAGGTACACAT-3 ), 1 µL (10 µM) reverse primer (5 -CAATCACACGCTTGTCAATA-3 ), 3 µL (10 ng•µL −1 ) template DNA, and 7.5 µL ddH 2 O.…”
Section: Plant Materialsmentioning
confidence: 99%