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13 publications mentioning tae-MIR319

Open access articles that are associated with the species Triticum aestivum and mention the gene name MIR319. Click the [+] symbols to view sentences that include the gene name, or the word cloud on the right for a summary.

1
[+] score: 28
Compared with J19, tae-miR319 was up-regulated both in T349 and L21; tae-miR164 and tae-miR9678-3p were up-regulated both in T349 and J22 and tae-miR9659-3p was up-regulated in T349, L21 and J22 (Table 2). [score:9]
miR319 targets TCP transcription factors and miR164 targets NAC domain gene, which contributes to leaf development [33]. [score:6]
In another study, miRNA microarray analysis showed that miR156, miR167, miR164, miR319, miR396 and miR166 were up-regulated in leaf or root of bread wheat under drought stress [43]. [score:4]
It was reported that miR319 also target MYB transcription factors [41] that play significant roles in stress responses. [score:3]
miR319 regulates TCP transcription factors [33] and the NAC domain gene, which contributes to leaf development and drought stress response [38]. [score:3]
Several known miRNAs (miR319, miR164, miR167, and miR156) are involved in drought response. [score:1]
The log2 ratios varied from 1.01 to 1.20 and the maximum value was 1.20 for tae-miR319. [score:1]
tae-miR319 TCP and MYB transcription factor Glycosyl transferase, TC407332 CK212140 TC421314 TC368630 Histone H2B, BF485310 CA484819 TC455115 BE517710 Acyl-CoA synthetase, GH728978 TC438746 CA630893 TC398226 Trans-cinnamate 4-monooxygenase, TC432120 CK215833 CJ863381 Type 1 non specific lipid transfer protein precursor, Transcription factor PCF8, Ribosomal protein L3-A2-II. [score:1]
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2
[+] score: 23
Another miRNA from wheat, miR319 targeting a MYB transcription factor, also showed induced expression under cold stress although its expression is decreased under heat stress. [score:7]
Interestingly, AsNAC60, the NAC TF homolog of rice ONAC60, was downregulated by the overexpression of miR319 which enhanced drought and salinity tolerance in creeping bent-grass (Zhou et al. 2013). [score:6]
Several studies from dicots, such as tomato and Nicotiana, revealed jasmonic acid -associated differential expression of several miRNAs such as miR319 (Bozorov et al. 2012; Zhao et al. 2015). [score:3]
However, several studies revealed altered expression of numerous miRNAs such as miR159, miR164, miR167, miR172, miR319, and miR398 in response to both heat and cold stresses (Tang et al. 2012; Gupta et al. 2014; Wang et al. 2014) (Fig.   4). [score:3]
miR167, miR319, miR398, miR172, miR164, miR159, and miR169 are responsive to both heat and cold stresses Heat and cold stress result in distinct and independent modifications to cellular processes. [score:1]
dicocoides –Kantar et al. 2011a miR319 T. turgidum ssp. [score:1]
However, observations from genesis of miR159 and miR319 have suggested another cleavage pattern. [score:1]
miR167, miR319, miR398, miR172, miR164, miR159, and miR169 are responsive to both heat and cold stresses Heat and cold stress result in distinct and independent modifications to cellular processes. [score:1]
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3
[+] score: 15
In addition, miR319 -targeted TCP transcription factors can positively regulate the expression of miR164 and miR396, leading to reduced activities of NAC and GRF transcription factors and an inhibition of cell proliferation [11, 45]. [score:8]
For 13 highly conserved miRNA families differentially expressed in wheat grain development (Fig 3), five (miR165/166, miR171, miR393, miR396 and miR444), three (miR156, miR164 and miR168), two (miR319 and miR827), one (miR408) and two miRNAs (miR159 and miR167) belonged to Group I, II, III, IV and V, respectively. [score:4]
Most verified targets/miRNA modules were highly conserved among monocots and dicots, such as SPLs/miR156, NACs/miR164, HOXs/miR166, ARFs/miR167, SCL1/miR171, TCPs/miR319, GRFs/miR396, SPX/miR827 (Fig 4A). [score:3]
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4
[+] score: 10
Other cold responsive miRNAs, MiR319 and miR444, targeted TCP and MADS-box genes were involved flower development [51, 52]. [score:4]
Moreover, as shown in Table  2, a significant number of transcripts detected by degradome sequencing have been reported previously such as miR156- SBP, miR172- AP2, miR160- ARF (Auxin Response Factor), miR169-NFYA (Nuclear transcription Factor Y subunit A), miR319- TCP, and MiR9863- NBS, indicating conserved miRNA-target interaction in plants. [score:3]
In Arabidopsis, 16 miRNAs, including miR156, miR159, miR164, miR165, miR168, miR169, miR172, miR319, miR389, miR393, miR396, miR397, miR398, miR400, miR402, and miR408, were identified by RNA gel blot analysis [12], microarray analysis [13], and a computation -based approach to be related to cold response [14]. [score:1]
MiR169, miR172, miR156, miR319, miR159, and miR396 showed the cold-stress response in at least three species, and miR160, miR165, miR167, and miR171 overlapped with Populus, Arabidopsis, and Medicago (Additional file 1: Table S6). [score:1]
In addition, seven miRNAs, miR159, miR164, miR169, miR319, miR398, miR1029, and miR1126 were also identified to be cold-responsive in the seedling of wheat [9]. [score:1]
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5
[+] score: 10
c and d Screening of significant differentially expressed genes with Volcano chart by comparing SL1 and NN1, SL2 and NN2 There are several conserved miRNAs that have been reported to be essential for reproductive development in plants, including miR156/7, miR159, miR160, miR164, miR165/166, miR167, miR169, miR172, miR319 and miR396 [14]. [score:4]
Error bars indicated s. d. based on three biological replicates (** P < 0.01, Student’s t-test) There are several conserved miRNAs that have been reported to be essential for reproductive development in plants, including miR156/7, miR159, miR160, miR164, miR165/166, miR167, miR169, miR172, miR319 and miR396 [14]. [score:2]
According to previous studies, miR156, miR159, miR160, miR164, miR167, miR319, miR396 and miR5200 were mainly involved in floral development [14, 28]. [score:2]
In this study, miR156, miR159, miR160, miR164, miR167, miR319 and miR396 were identified from our data. [score:1]
tae-miR156 and tae-miR319 did not show two-fold change as RNA-seq data did. [score:1]
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6
[+] score: 8
In this study, the target of tae-miR159/tae-miR319 (Traes_1AL_041EBB4A6.2) was down-regulated significantly suggesting that tae-miR159 might be involved in regulation of anther development. [score:8]
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7
[+] score: 5
In addition, Arabidopsis miRNAs including miR160, miR166, and miR319 inhibit the expression of differentiation-promoting transcription factors such as ARF17, CNA, PHB, PHV, and TCP4 to enable proper embryonic patterning [66]. [score:5]
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8
[+] score: 4
Other miRNAs from this paper: tae-MIR159a, tae-MIR159b, tae-MIR156, tae-MIR398, tae-MIR397
“Role of microRNA miR319 in plant development,” in MicroRNAs in Plant Development and Stress Responses, Signaling and Communication in Plants Vol. [score:3]
In the present study, we developed amiR-PDS against endogenous PDS in wheat by using Arabidopsis miR319 precursor as backbone (Figures 1B, 7A). [score:1]
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9
[+] score: 3
Some miRNAs, such as miR166, tae-miR1130b-3p, tae-miR1120a, and ata-miR319-3p, were only differentially expressed in comparisons between stages of IME and/or ME. [score:3]
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10
[+] score: 3
A set of miRNA members, such as miR156, miR159, miR167, miR168, miR171, miR319, and miR396 of Arabidopsis, exhibit altered expression levels upon salt (Yu et al., 2005; Ding et al., 2009). [score:3]
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11
[+] score: 3
Other miRNAs from this paper: tae-MIR159a, tae-MIR159b, tae-MIR444b, tae-MIR9659
Sequence and expression differences underlie functional specialization of Arabidopsis, microRNAs miR159 and miR319. [score:3]
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12
[+] score: 3
Other miRNAs from this paper: osa-MIR156a, osa-MIR156b, osa-MIR156c, osa-MIR156d, osa-MIR156e, osa-MIR156f, osa-MIR156g, osa-MIR156h, osa-MIR156i, osa-MIR156j, osa-MIR160a, osa-MIR160b, osa-MIR160c, osa-MIR160d, osa-MIR164a, osa-MIR164b, osa-MIR167a, osa-MIR167b, osa-MIR167c, osa-MIR169a, osa-MIR171a, osa-MIR393a, osa-MIR396a, osa-MIR396b, osa-MIR396c, osa-MIR397a, osa-MIR397b, osa-MIR399a, osa-MIR399b, osa-MIR399c, osa-MIR399d, osa-MIR399e, osa-MIR399f, osa-MIR399g, osa-MIR399h, osa-MIR399i, osa-MIR399j, osa-MIR399k, osa-MIR156k, osa-MIR156l, osa-MIR159a, osa-MIR159b, osa-MIR159c, osa-MIR159d, osa-MIR159e, osa-MIR159f, osa-MIR319a, osa-MIR319b, osa-MIR160e, osa-MIR160f, osa-MIR164c, osa-MIR164d, osa-MIR164e, osa-MIR167d, osa-MIR167e, osa-MIR167f, osa-MIR167g, osa-MIR167h, osa-MIR167i, osa-MIR168a, osa-MIR168b, osa-MIR169b, osa-MIR169c, osa-MIR169d, osa-MIR169e, osa-MIR169f, osa-MIR169g, osa-MIR169h, osa-MIR169i, osa-MIR169j, osa-MIR169k, osa-MIR169l, osa-MIR169m, osa-MIR169n, osa-MIR169o, osa-MIR169p, osa-MIR169q, osa-MIR171b, osa-MIR171c, osa-MIR171d, osa-MIR171e, osa-MIR171f, osa-MIR171g, osa-MIR172a, osa-MIR172b, osa-MIR172c, osa-MIR171h, osa-MIR393b, osa-MIR408, osa-MIR172d, osa-MIR171i, osa-MIR167j, osa-MIR164f, osa-MIR390, osa-MIR439a, osa-MIR439b, osa-MIR439c, osa-MIR439d, osa-MIR439e, osa-MIR439f, osa-MIR439g, osa-MIR439h, osa-MIR439i, osa-MIR396e, osa-MIR444a, tae-MIR159a, tae-MIR159b, tae-MIR160, tae-MIR164, tae-MIR167a, tae-MIR171a, tae-MIR399, tae-MIR408, tae-MIR444a, osa-MIR169r, osa-MIR444b, osa-MIR444c, osa-MIR444d, osa-MIR444e, osa-MIR444f, osa-MIR396f, osa-MIR396g, osa-MIR396h, osa-MIR396d, tae-MIR156, tae-MIR167b, tae-MIR169, tae-MIR444b, tae-MIR171b, tae-MIR396, tae-MIR167c, tae-MIR397
Some of these miRNA families (for example, miR319, miR390, and miR165/166) are conserved deeply, including in lower plants such as Physcometrella [26- 28]. [score:1]
MiR169 was represented by five members, miR156, miR165/166, miR167, miR170/171 and miR172 were represented by three members each, and miR159, miR319 and miR168 were represented by two members each in the library. [score:1]
These include miRNA156/157, miR159, miR160, miR164, miR165/166, miR167, miR168, miR169, miR170/171, miR172, miR319, miR390, miR393, miR396, miR397, miR399 and miR408, which are conserved in diverse plant species (Table 2). [score:1]
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13
[+] score: 2
Some miRNAs including miR156, miR159 miR169 and miR319 are associated with coordination of the relationship between development and stress responses [61]. [score:2]
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