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miRBase |
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![]() 5 publications mentioning csi-MIR169bOpen access articles that are associated with the species Citrus sinensis and mention the gene name MIR169b. 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-MIR159d, 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-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
In Arabidopsis, the expression of miR169 was inhibited by N-deficiency, while the expression levels of its target genes [i. e., NFYA2 (Nuclear Factor Y, subunit A2), NFYA3, NFYA5 and NFYA8] were increased [10, 13, 27, 29].
[score:9]
Transgenic Arabidopsis plants over -expressing miR169a had less accumulation of N and NFYA family members, and were more sensitive to N stress than the wild type, demonstrating a role for miR169 in the adaptation of plants to N-deficiency [29].
[score:3]
It is worth noting that some N-deficiency-responsive miRNAs (e. g., miR169, miR172, miR394, miR395, miR397, miR398, miR399, miR827, miR408 and miR857) are also responsive to other nutrient stresses (i. e., B, P, Fe, S and Cu deficiencies) in plants [8, 10], indicating the involvement of miRNA -mediated crosstalk among N, B, P, Fe, S and Cu under N-deficiency.
[score:1]
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].
[score:1]
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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-MIR159d, 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-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
In Arabidopsis, miR169 was greatly repressed and its target genes, NFYA (Nuclear Factor Y, subunit A) family members, were greatly up-regulated by N-deficiency.
[score:6]
Transgenic Arabidopsis plants over -expressing miR169a had lower N level, and displayed less tolerance to N-deficiency than the wild type, indicating the possible roles of miR169 in helping plants to deal with N-starvation (Zhao et al., 2011).
[score:3]
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).
[score:1]
Involvement of miR169 in the nitrogen-starvation responses in Arabidopsis.
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Other miRNAs from this paper: csi-MIR160a, csi-MIR169a, csi-MIR167c, csi-MIR167b, csi-MIR171b, csi-MIR171a, csi-MIR394a, csi-MIR399c, csi-MIR399d, csi-MIR399a, csi-MIR399b, csi-MIR827, csi-MIR167a, csi-MIR160b, csi-MIR160c, csi-MIR167d, csi-MIR167e, 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-MIR394b, csi-MIR399e, csi-MIR399f, csi-MIR169o, csi-MIR169p, csi-MIR169q, csi-MIR169r
N-deficiency -induced down-regulation of miR169 has been demonstrated to be an adaptive strategy of plants to N-starvation via N-uptake and remobilization [24, 30].
[score:4]
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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-MIR159d, 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-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
3, csi-miR4414.1, csi-miR391b, csi-miR1432a, the csi-miR169 family and the csi-miR171 family, were expressed in leaf and flower but were not detected in fruit.
[score:3]
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Other miRNAs from this paper: ath-MIR169a, ath-MIR169b, ath-MIR169c, ath-MIR169d, ath-MIR169e, ath-MIR169f, ath-MIR169g, ath-MIR169h, ath-MIR169i, ath-MIR169j, ath-MIR169k, ath-MIR169l, ath-MIR169m, ath-MIR169n, csi-MIR169a, 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-MIR169o, csi-MIR169p, csi-MIR169q, csi-MIR169r
NF-YA transcripts are also regulated at post-transcriptional level by the action of microRNA169 (miR169) that binds to the 3’-UTR and promotes their cleavage by the slicing protein Argonaute 1 [4, 8].
[score:2]
Involvement of miR169 in the nitrogen-starvation responses in Arabidopsis.
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