Abstract:Drought is the major abiotic stress that limits apple productivity and quality. To date, many important and divergent regulatory functions of miR156/SBP genes in plant growth and development have been well understood. However, little is known about the role of apple miR156 in response to abiotic stress. To better understand the functions of MdmiR156 in abiotic stress tolerance, we constructed the overexpression (OE) and short tandem target mimic (STTM) vector of MdmiR156n and performed its functional analysis … Show more
“…In the present study, we successfully knocked down csn-miR156f-2-5p and found that tea plants with csn-miR156f-2-5p knocked down might be more sensitive to drought ( Figure 6 ). This is consistent with previous findings showing that plants with miR156silence are more susceptible to drought stress than the corresponding WT with regard to Arabidopsis and apples [ 48 , 49 ].MicroRNAs function by cleaving the corresponding mRNA or inhibiting translation to regulate the expression of their target genes [ 12 ]. SPLs are genes with crucial roles in plants’ response to abiotic stress and their development, and they are the main target genes of miR156s [ 50 ].…”
The microRNA156 (miR156) family, one of the first miRNA families discovered in plants, plays various important roles in plant growth and resistance to various abiotic stresses. Previously, miR156s were shown to respond to drought stress, but miR156s in tea plants (Camellia sinensis (L.) O. Kuntze) have not been comprehensively identified and analyzed. Herein, we identify 47 mature sequences and 28 precursor sequences in tea plants. Our evolutionary analysis and multiple sequence alignment revealed that csn-miR156s were highly conserved during evolution and that the rates of the csn-miR156 members’ evolution were different. The precursor sequences formed typical and stable stem–loop structures. The prediction of cis-acting elements in the CsMIR156s promoter region showed that the CsMIR156s had diverse cis-acting elements; of these, 12 CsMIR156s were found to be drought-responsive elements. The results of reverse transcription quantitative PCR (RT-qPCR) testing showed that csn-miR156 family members respond to drought and demonstrate different expression patterns under the conditions of drought stress. This suggests that csn-miR156 family members may be significantly involved in the response of tea plants to drought stress. Csn-miR156f-2-5p knockdown significantly reduced the Fv/Fm value and chlorophyll content and led to the accumulation of more-reactive oxygen species and proline compared with the control. The results of target gene prediction showed that csn-miR156f-2-5p targeted SQUAMOSA promoter binding protein-like (SPL) genes. Further analyses showed that CsSPL14 was targeted by csn-miR156f-2-5p, as confirmed through RT-qPCR, 5′ RLM-RACE, and antisense oligonucleotide validation. Our results demonstrate that csn-miR156f-2-5p and CsSPL14 are involved in drought response and represent a new strategy for increasing drought tolerance via the breeding of tea plants.
“…In the present study, we successfully knocked down csn-miR156f-2-5p and found that tea plants with csn-miR156f-2-5p knocked down might be more sensitive to drought ( Figure 6 ). This is consistent with previous findings showing that plants with miR156silence are more susceptible to drought stress than the corresponding WT with regard to Arabidopsis and apples [ 48 , 49 ].MicroRNAs function by cleaving the corresponding mRNA or inhibiting translation to regulate the expression of their target genes [ 12 ]. SPLs are genes with crucial roles in plants’ response to abiotic stress and their development, and they are the main target genes of miR156s [ 50 ].…”
The microRNA156 (miR156) family, one of the first miRNA families discovered in plants, plays various important roles in plant growth and resistance to various abiotic stresses. Previously, miR156s were shown to respond to drought stress, but miR156s in tea plants (Camellia sinensis (L.) O. Kuntze) have not been comprehensively identified and analyzed. Herein, we identify 47 mature sequences and 28 precursor sequences in tea plants. Our evolutionary analysis and multiple sequence alignment revealed that csn-miR156s were highly conserved during evolution and that the rates of the csn-miR156 members’ evolution were different. The precursor sequences formed typical and stable stem–loop structures. The prediction of cis-acting elements in the CsMIR156s promoter region showed that the CsMIR156s had diverse cis-acting elements; of these, 12 CsMIR156s were found to be drought-responsive elements. The results of reverse transcription quantitative PCR (RT-qPCR) testing showed that csn-miR156 family members respond to drought and demonstrate different expression patterns under the conditions of drought stress. This suggests that csn-miR156 family members may be significantly involved in the response of tea plants to drought stress. Csn-miR156f-2-5p knockdown significantly reduced the Fv/Fm value and chlorophyll content and led to the accumulation of more-reactive oxygen species and proline compared with the control. The results of target gene prediction showed that csn-miR156f-2-5p targeted SQUAMOSA promoter binding protein-like (SPL) genes. Further analyses showed that CsSPL14 was targeted by csn-miR156f-2-5p, as confirmed through RT-qPCR, 5′ RLM-RACE, and antisense oligonucleotide validation. Our results demonstrate that csn-miR156f-2-5p and CsSPL14 are involved in drought response and represent a new strategy for increasing drought tolerance via the breeding of tea plants.
“…The higher level of flavonoids probably contribute to the cold tolerance in inbred line N28 waxy corn . Overexpression of MdmiR156n promoted the accumulation of flavonoids and reduced the accumulation of ROS under drought conditions in transgenic apple calli and Arabidopsis thaliana plants . The ectopic expression of flavonoids synthetase genes from Apocynum venetum including AvF3H , AvF3′H , and AvFLS notably increased the salt tolerance but reduced the ROS content in transgenic Arabidopsis, suggesting that the flavonoids improve the salt tolerance by increasing the ROS scavenging capacity in plants .…”
Section: Introductionmentioning
confidence: 98%
“…13 Overexpression of MdmiR156n promoted the accumulation of flavonoids and reduced the accumulation of ROS under drought conditions in transgenic apple calli and Arabidopsis thaliana plants. 14 The ectopic expression of flavonoids synthetase genes from Apocynum venetum including AvF3H, AvF3′H, and AvFLS notably increased the salt tolerance but reduced the ROS content in transgenic Arabidopsis, suggesting that the flavonoids improve the salt tolerance by increasing the ROS scavenging capacity in plants. 15 ABA induced the accumulation of flavonoids, including anthocyanin, naringin, quercetin, isorhamnetin, kaempferol, and catechin, to improve the antioxidant capacity of Nitraria tangutorum Bobr.…”
The color of the seed coat has great diversity and is regarded as a biomarker of metabolic variations. Here we isolated a soybean variant (BLK) from a population of recombinant inbred lines with a black seed coat, while its sibling plants have yellow seed coats (YL). The BLK and YL plants showed no obvious differences in vegetative growth and seed weight. However, the BLK seeds had higher anthocyanins and flavonoids level and showed tolerance to various abiotic stresses including herbicide, oxidation, salt, and alkalinity during germination. Integrated metabolomic and transcriptomic analyses revealed that the upregulation of biosynthetic genes probably contributed to the overaccumulation of flavonoids in BLK seeds. The transient expression of those biosynthetic genes in soybean root hairs increased the levels of total flavonoids or anthocyanins. Our study revealed the molecular basis of flavonoid accumulation in soybean seeds, leveraging genetic engineering for both nutritious and stress-tolerant soybean germplasm.
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