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2022
DOI: 10.1016/j.indcrop.2021.114460
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Gene expression analysis revealed Hbr-miR396b as a key piece participating in reaction wood formation of Hevea brasiliensis (rubber tree)

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Cited by 5 publications
(6 citation statements)
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“…MiRNAs are an important class of non-coding factors that regulate genes expression at the post-transcriptional level in nearly every aspect of plant development such as germination, growth, tissue differentiation, and flowering ( Das et al, 2019 ; Glazińska et al, 2019 ; Qiu et al, 2019 ). The results of small RNA-seq demonstrate that the xylem of D. odorifera contains a large and diverse small RNA population, a finding similar to previous studies in rubber tree ( Meng et al, 2022 ) and Chinese fir ( Wan et al, 2012 ).…”
Section: Discussionsupporting
confidence: 87%
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“…MiRNAs are an important class of non-coding factors that regulate genes expression at the post-transcriptional level in nearly every aspect of plant development such as germination, growth, tissue differentiation, and flowering ( Das et al, 2019 ; Glazińska et al, 2019 ; Qiu et al, 2019 ). The results of small RNA-seq demonstrate that the xylem of D. odorifera contains a large and diverse small RNA population, a finding similar to previous studies in rubber tree ( Meng et al, 2022 ) and Chinese fir ( Wan et al, 2012 ).…”
Section: Discussionsupporting
confidence: 87%
“…A total of 40 known miRNAs belonging to 22 miRNA families and 123 novel miRNAs were identified in these small RNA libraries, among which 14 miRNAs were differentially expressed ( Figure 4 ). Similarly, the miR156, miR159, miR166, miR319, miR396, miR398, and miR408 families have also been identified in the xylem of rubber tree ( Meng et al, 2022 ). The miR396a and miR156g are also differentially expressed in the primary stem, transition stem, and secondary stem of Populus trichocarpa ( Wang R et al, 2021 ).…”
Section: Discussionmentioning
confidence: 99%
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“…qPCR was performed with TB Green Premix Ex Taq II (Tli RNase H Plus; Takara, Beijing, China) for the target genes according to the manufacturer’s instructions. PCR conditions were as follows: denaturation at 94°C for 2 min, then 40 cycles of 95°C for 5 s and 60°C for 30 s. Ubiquitin was used as internal reference for normalization of expression data of rubber tree samples ( Meng et al., 2022 ), and β-actin was used for N. benthamiana ( Nawaz et al., 2019 ). For miRNA, a miRNA RT-qPCR Detection Kit (Aidlab, Beijing, China) was used following the manufacturer’s instructions.…”
Section: Methodsmentioning
confidence: 99%
“…qPCR was performed with TB Green Premix Ex Taq II (Tli RNase H Plus; Takara, Beijing, China) for the target genes according to the manufacturer's instructions. PCR conditions were as follows: denaturation at 94°C for 2 min, then 40 cycles of 95°C for 5 s and 60°C for 30 s. Ubiquitin was used as internal reference for normalization of expression data of rubber tree samples (Meng et al, 2022), and b-actin was used for N. benthamiana (Nawaz et al, 2019). For miRNA, a miRNA RT-qPCR Detection Kit (Aidlab, Beijing, China) was used following the manufacturer's instructions.…”
Section: Validation Of Mirna Expression and That Of Their Target Gene...mentioning
confidence: 99%