2012
DOI: 10.1016/j.jplph.2012.06.011
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Identification and characterization of miRNAs and their potential targets in flax

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Cited by 43 publications
(38 citation statements)
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“…The lengths of these identified mature miRNA sequences ranged from 19 to 24 nucleotides; however, most of the potential miRNAs (17 of 27 or 62.96%) were 21 nt in length (Table 1). This length was quite similar to other mature miRNAs already identified in other plants (Zhang et al, 2006a;Xie et al, 2010;Barozai et al, 2012;Neutelings et al, 2012). The A+U contents of these predicted P. vulgaris pre-miRNA sequences ranged from 30.34 to 68.37%, with an average of 57.95 ± 8.53% (Table 1), which closely matched the results of previous studies (Ambros et al, 2003;Neutelings et al, 2012).…”
Section: Identification Of Potential Mirnassupporting
confidence: 88%
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“…The lengths of these identified mature miRNA sequences ranged from 19 to 24 nucleotides; however, most of the potential miRNAs (17 of 27 or 62.96%) were 21 nt in length (Table 1). This length was quite similar to other mature miRNAs already identified in other plants (Zhang et al, 2006a;Xie et al, 2010;Barozai et al, 2012;Neutelings et al, 2012). The A+U contents of these predicted P. vulgaris pre-miRNA sequences ranged from 30.34 to 68.37%, with an average of 57.95 ± 8.53% (Table 1), which closely matched the results of previous studies (Ambros et al, 2003;Neutelings et al, 2012).…”
Section: Identification Of Potential Mirnassupporting
confidence: 88%
“…The identified P. vulgaris pre-miRNAs were between 68 and 202 nt in length, with an average of 111.37 ± 34.17 nt; however, the majority of the pre-miRNAs (24 of 27 or 88.89%) were 60-150 nt in length (Table 1). These results matched the lengths of most previously predicted premiRNAs in plant species (Zhang et al, 2007;Unver and Budak, 2009;Barozai et al, 2012;Neutelings et al, 2012). Although the identified P. vulgaris miRNA precursors were of a wide range of lengths, they could be folded into the typical miRNA secondary structures (Figure 2).…”
Section: Identification Of Potential Mirnassupporting
confidence: 85%
“…It was shown that miR408 was also responsive to phosphate limitation and became more abundant during phosphate limitation (Pant et al, 2009). Functions of lus-miR408 predicted targets in flax were metabolism, transport and transcription factor (Neutelings et al, 2012). In our study we observed miR408 up-regulation induced by Pi deficiency, and this could indicate that this miRNA takes part in expression regulation during mineral nutrient stress in flax.…”
Section: Mir408 Up-regulation In Flax Under Pi Deficiencysupporting
confidence: 56%
“…In Arabidopsis miR398 is up-regulated during copper deficiency (Zhu et al, 2011) and down-regulated under N starvation conditions (Liang, He, & Yu, 2012). Lus-miR398 targets were predicted in flax; their functions were: metabolism, signaling, transport and transcription factor (Neutelings, Fenart, Lucau-Danila, & Hawkins, 2012;Barvkar et al, 2013). In our investigation of flax miRNAs, the up-regulation of miR398 under nutrient deficiency was observed.…”
Section: Role Of Mir398 In Flax Pi Homeostasis Regulationmentioning
confidence: 67%
“…The NormFinder analysis, which considers the intra-and intergroup variation of gene expression, identified the gm-miR171a as the top ranking house-keeping gene. The miR168 belongs to the group of potential biomarkers of plant stress response (Bej and Basak, 2014;Neutelings et al, 2012). Under different types of abiotic stress (drought, salinity, cold, UV, mechanical, and heat stress), up-regulation of miR168 expression (Bej and Basak, 2014;Sunkar, 2010) has been observed.…”
Section: Characterisation Of Selected Mirnamentioning
confidence: 99%