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miRBase |
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![]() 5 publications mentioning csi-MIR159dOpen access articles that are associated with the species Citrus sinensis and mention the gene name MIR159d. Click the [+] symbols to view sentences that include the gene name, or the word cloud on the right for a summary. |
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Other miRNAs from this paper: csi-MIR160a, csi-MIR164a, csi-MIR166e, csi-MIR169a, csi-MIR172a, csi-MIR398a, csi-MIR166a, csi-MIR156a, csi-MIR3946, csi-MIR159a, csi-MIR166c, csi-MIR167c, csi-MIR167b, csi-MIR171b, csi-MIR171a, csi-MIR172c, csi-MIR393a, csi-MIR394a, csi-MIR395a, csi-MIR397, csi-MIR399c, csi-MIR399d, csi-MIR399a, csi-MIR399b, csi-MIR408, csi-MIR482f, csi-MIR477c, csi-MIR477a, csi-MIR477b, csi-MIR482a, csi-MIR482b, csi-MIR827, csi-MIR857, csi-MIR482c, csi-MIR3953, csi-MIR167a, csi-MIR156b, csi-MIR156c, csi-MIR156d, csi-MIR156e, csi-MIR156f, csi-MIR156g, csi-MIR159b, csi-MIR159c, csi-MIR160b, csi-MIR160c, csi-MIR164b, csi-MIR164c, csi-MIR166b, csi-MIR166d, csi-MIR166f, csi-MIR166g, csi-MIR166h, csi-MIR166i, csi-MIR166j, csi-MIR166k, csi-MIR167d, csi-MIR167e, csi-MIR169b, csi-MIR169c, csi-MIR169d, csi-MIR169e, csi-MIR169f, csi-MIR169g, csi-MIR169h, csi-MIR169i, csi-MIR169j, csi-MIR169k, csi-MIR169l, csi-MIR169m, csi-MIR169n, csi-MIR171c, csi-MIR171d, csi-MIR171e, csi-MIR171f, csi-MIR171g, csi-MIR171h, csi-MIR171i, csi-MIR172b, csi-MIR172d, csi-MIR393b, csi-MIR393c, csi-MIR394b, csi-MIR395b, csi-MIR395c, csi-MIR398b, csi-MIR399e, csi-MIR399f, csi-MIR477d, csi-MIR477e, csi-MIR482d, csi-MIR482e, csi-MIR482g, csi-MIR156h, csi-MIR156i, csi-MIR156j, csi-MIR164d, csi-MIR169o, csi-MIR169p, csi-MIR169q, csi-MIR169r
The adaptive responses of leaf miRNAs to B-deficiency might be associated with several aspects: (a) attenuation of plant growth and development by down -regulating TIR1, ARF and AFB due to up-regulated miR393 and miR160, and by lowering the expression of SAUR-like auxin-responsive protein family targeted by miR3946, thus enhancing plant stress tolerance; (b) improving the expression of NACs due to decreased expression miR159, miR782, miR3946 and miR7539, hence maintaining leaf phenotype and enhancing the stress tolerance; (c) activation of the stress responses and antioxidant system due to decreased expression of miR164, miR6260, miR5929, miR6214, miR3946 and miR3446; (d) decreased expression of MFS resulting from increased expression of miR5037, thus lowering B export from plants.
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The adaptive responses of miRNAs to B-deficiency might related to several aspects: (a) attenuation of plant growth and development by repressing auxin signaling due to decreased TIR1 level and ARF -mediated gene expression by altering the expression of miR393, miR160 and miR3946; (b) maintaining leaf phenotype and enhancing the stress tolerance by up -regulating NACs targeted by miR159, miR782, miR3946 and miR7539; (c) activation of the stress responses and antioxidant system through down -regulating the expression of miR164, miR6260, miR5929, miR6214, miR3946 and miR3446; (d) decreasing the expression of major facilitator superfamily protein genes targeted by miR5037, thus lowering B export from plants.
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Patade and Suprasanna showed that the up-regulation of MYB at 1 h of salt-stressed sugarcane leaves was accompanied by the down-regulation of miR159 [38].
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However, the expression of miR159 was up-regulated in P -deficient soybean (Glycine max) roots and leaves [39].
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Thus, B-deficiency -induced down-regulation of miR159 might increase the expression of MYBs (Table 2), thus improving the tolerance of plants to B-deficiency.
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94295432** miR158 −10.05808647** −3.35603222** miR2921 −10.13114959** −11.0611889** miR782 −10.76475548** −10.08402439** miR1446 −10.94721705** 5.01671689** miR5074 −10.94721705** 10.74971862** miR3443 −11.47199392** 9.96792062**Data from Additional file 3 and Lu et al. [8]; ** indicates a significant difference at P < 0.01 We found that miR159 was down-regulated in B -deficient leaves (Table 2), as previously obtained on salt stressed sugarcane leaves [38].
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In addition, many other P-deficiency-responsive miRNAs (i. e., miR1510, miR156, miR159, miR166, miR169, miR2109, miR395, miR397, miR398, miR408, miR447 and miR482) have been isolated from various plant species [15– 21].
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MiR159 plays important roles in maintaining leaf phenotype by negatively regulating MYB transcription factors [40].
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Other miRNAs from this paper: csi-MIR166e, csi-MIR172a, csi-MIR166a, csi-MIR156a, csi-MIR159a, csi-MIR166c, csi-MIR172c, csi-MIR482f, csi-MIR482a, csi-MIR482b, csi-MIR1515a, csi-MIR3950, csi-MIR482c, csi-MIR167a, csi-MIR156b, csi-MIR156c, csi-MIR156d, csi-MIR156e, csi-MIR156f, csi-MIR156g, csi-MIR159b, csi-MIR159c, csi-MIR166b, csi-MIR166d, csi-MIR166f, csi-MIR166g, csi-MIR166h, csi-MIR166i, csi-MIR166j, csi-MIR166k, csi-MIR172b, csi-MIR172d, csi-MIR482d, csi-MIR1515b, csi-MIR482e, csi-MIR482g, csi-MIR156h, csi-MIR156i, csi-MIR156j
In the present study, csi-miR159 was differentially expressed between MT and WT, and the targets of csi-miR159, including two GAMYBs, Polygalacturonase inhibitor 1 and NOZZLE, were also differentially expressed between MT and WT during fruit development and ripening (Table 2, Figures 4, 5).
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The GAMYB gene in barley is upregulated by the GA transduction pathway in both anthers and seeds (Murray et al., 2003) and over -expression of miR159 or disruption of the GA biosynthesis pathway delays flowering and reduces fertility (Achard et al., 2004; Cheng et al., 2004).
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Two strawberry miR159 family members display developmental-specific expression patterns in the fruit receptacle and cooperatively regulate Fa-GAMYB.
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Therefore, miR159, which regulates the spatiotemporal expression pattern of GAMYB genes, constitutes a major connection among at least three hormones—namely GA, ABA, and ETH (Curaba et al., 2014).
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The expression patterns of csi-miR159 differed in MT and WT before the 120 DAF stage.
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Several significant miRNAs and targets were identified in this study, such as csi-miR156k, csi-miR159, csi-miR166d, csi-miRN21, GAMYBs, SPLs, and ATHBs.
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These results indicated that csi-miR159 may be an important regulator of citrus fruit development and ripening and may play a significant role in the formation of later-ripening trait in MT (Figure 7).
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Csi-miR159 also targeted four genes, including two GAMYBs (Cs1g03470 and Cs3g06390) which play a central role during fruit ripening of strawberry (Vallarino et al., 2015).
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In tomato fruit, Zuo et al. (2012) reported that the expression of miR159 is efficiently repressed by ethylene (ETH) treatment.
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miR159 was shown to be involved in strawberry fruit ripening by regulating FaGAMYB which plays a central role in the transition of the strawberry receptacle from development to ripening (Csukasi et al., 2012; Vallarino et al., 2015).
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During Arabidopsis seed germination, ABA induces the accumulation of miR159, and over -expression of miR159 renders plants hyposensitive to ABA (Reyes and Chua, 2007).
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In previous studies, miR159 was characterized to regulate the expressions of GAMYB-like genes at the post-transcriptional level and play significant roles in leaf, flower and seed maturation (Millar and Gubler, 2005; Tsuji et al., 2006; Reyes and Chua, 2007).
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Among these, csi-miR159- GAMYBs module may play a central role in citrus fruit ripening, and this regulation may function in combination with plant hormones, including ABA, gibberellin (GA), and ethylene (ETH).
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ABA induction of miR159 controls transcript levels of two MYB factors during Arabidopsis seed germination.
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Other miRNAs from this paper: csi-MIR164a, csi-MIR166e, csi-MIR169a, csi-MIR172a, csi-MIR166a, csi-MIR390a, csi-MIR156a, csi-MIR159a, csi-MIR166c, csi-MIR171b, csi-MIR171a, csi-MIR172c, csi-MIR393a, csi-MIR396a, csi-MIR396b, csi-MIR477a, csi-MIR482a, csi-MIR827, csi-MIR3951a, csi-MIR396c, csi-MIR482c, csi-MIR3954, csi-MIR156b, csi-MIR156c, csi-MIR156d, csi-MIR156e, csi-MIR156f, csi-MIR156g, csi-MIR159b, csi-MIR159c, csi-MIR164b, csi-MIR164c, csi-MIR166b, csi-MIR166d, csi-MIR166f, csi-MIR166g, csi-MIR166h, csi-MIR166i, csi-MIR166j, csi-MIR166k, csi-MIR169b, csi-MIR169c, csi-MIR169d, csi-MIR169e, csi-MIR169f, csi-MIR169g, csi-MIR169h, csi-MIR169i, csi-MIR169j, csi-MIR169k, csi-MIR169l, csi-MIR169m, csi-MIR169n, csi-MIR171c, csi-MIR171d, csi-MIR171e, csi-MIR171f, csi-MIR171g, csi-MIR171h, csi-MIR171i, csi-MIR172b, csi-MIR172d, csi-MIR390b, csi-MIR393b, csi-MIR393c, csi-MIR396d, csi-MIR396e, csi-MIR396f, csi-MIR477d, csi-MIR168, csi-MIR156h, csi-MIR156i, csi-MIR156j, csi-MIR164d, csi-MIR169o, csi-MIR169p, csi-MIR169q, csi-MIR3951b, csi-MIR169r
Comparative analysis showed that some known miRNAs, such as csi-miR168a and csi-miR159 in this study, may fulfill specific function in specific tissues via target different genes.
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Another example is that csi-miR159 family was detected to target the transcription factor GAMYB in leaf and flower in consistency with previous reports [42, 43].
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However, in fruit, degraded fragments of GAMYB generated by csi-miR159 were absent and this miRNA was found to targete Cs8g05120 which was annotated as the LRR-containing protein DRT100 with potential roles in DNA damage repair (Additional file 5b).
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Additionally, miR156, miR159, miR319 and miR172 are involved in flowering regulation and phase changing from vegetative growth to reproductive growth [21, 25– 29].
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Furthermore, recent studies have shown that the MYB genes are post-transcriptionally regulated by microRNAs; for example, AtMYB33, AtMYB35, AtMYB65, and AtMYB101 genes involved in anther or pollen development are targeted by the miR159 family in Arabidopsis [23], [24].
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Other miRNAs from this paper: csi-MIR164a, csi-MIR166e, csi-MIR169a, csi-MIR398a, csi-MIR166a, csi-MIR156a, csi-MIR3946, csi-MIR159a, csi-MIR166c, csi-MIR167c, csi-MIR167b, csi-MIR395a, csi-MIR397, csi-MIR399c, csi-MIR399d, csi-MIR399a, csi-MIR399b, csi-MIR408, csi-MIR482f, csi-MIR482a, csi-MIR482b, csi-MIR535a, csi-MIR827, csi-MIR857, csi-MIR482c, csi-MIR167a, csi-MIR156b, csi-MIR156c, csi-MIR156d, csi-MIR156e, csi-MIR156f, csi-MIR156g, csi-MIR159b, csi-MIR159c, csi-MIR164b, csi-MIR164c, csi-MIR166b, csi-MIR166d, csi-MIR166f, csi-MIR166g, csi-MIR166h, csi-MIR166i, csi-MIR166j, csi-MIR166k, csi-MIR167d, csi-MIR167e, csi-MIR169b, csi-MIR169c, csi-MIR169d, csi-MIR169e, csi-MIR169f, csi-MIR169g, csi-MIR169h, csi-MIR169i, csi-MIR169j, csi-MIR169k, csi-MIR169l, csi-MIR169m, csi-MIR169n, csi-MIR395b, csi-MIR395c, csi-MIR398b, csi-MIR399e, csi-MIR399f, csi-MIR482d, csi-MIR535b, csi-MIR535c, csi-MIR482e, csi-MIR482g, csi-MIR156h, csi-MIR156i, csi-MIR156j, csi-MIR164d, csi-MIR169o, csi-MIR169p, csi-MIR169q, csi-MIR535d, csi-MIR535e, csi-MIR535f, csi-MIR169r
Also, many other miRNAs such as miR156, miR159, miR166, miR169, miR395, miR397, miR398, miR408, miR447, miR482, miR1510 and miR2109 are involved in plant response to P-limitation (Valdés-López et al., 2010; Hackenberg et al., 2013; Zhao et al., 2013; Paul et al., 2015).
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