2017
DOI: 10.1016/j.bbrc.2017.01.185
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Base-pair opening dynamics of the microRNA precursor pri-miR156a affect temperature-responsive flowering in Arabidopsis

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Cited by 4 publications
(8 citation statements)
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“…It was predicted that the miRNA targets whose exogenous NO is down-regulated may play a positive regulatory role in drought stress response. mi156a are important miRNA for plant for abiotic stress responses, growth, and development [57]. miR156 can regulate plant stress tolerance by modulating SQUAMOSA promoter-binding-like protein (SPL) genes that function in anthocyanin biosynthesis [36].…”
Section: Discussionmentioning
confidence: 99%
“…It was predicted that the miRNA targets whose exogenous NO is down-regulated may play a positive regulatory role in drought stress response. mi156a are important miRNA for plant for abiotic stress responses, growth, and development [57]. miR156 can regulate plant stress tolerance by modulating SQUAMOSA promoter-binding-like protein (SPL) genes that function in anthocyanin biosynthesis [36].…”
Section: Discussionmentioning
confidence: 99%
“…There are at least two major processing mechanisms found in plant miRNAs (loop-to-base and base-to-loop processing), where the upper stem, lower stem, and bulges are the structural determinants that are important for the accuracy and efficiency of miRNA hairpin processing [ 121 , 123 , 124 , 125 , 126 , 127 ]. Indeed, mutations in the lower stem, upper stem, and bulges of pri-miR156a affect the production of miR156, thus altering the flowering time [ 121 , 128 , 129 ]. Interestingly, although the majority of the mutations in the upper stem and lower stem reduce the efficiency of miR156 formation at both lower and higher ambient temperatures, the effect of the disruption of base pairing in upper stem 2 (S2) was extraordinarily severe at lower temperature, suggesting the importance of S2 in the regulation of temperature-mediated flowering time [ 121 , 128 , 129 ].…”
Section: Non-coding Rnasmentioning
confidence: 99%
“…Indeed, mutations in the lower stem, upper stem, and bulges of pri-miR156a affect the production of miR156, thus altering the flowering time [ 121 , 128 , 129 ]. Interestingly, although the majority of the mutations in the upper stem and lower stem reduce the efficiency of miR156 formation at both lower and higher ambient temperatures, the effect of the disruption of base pairing in upper stem 2 (S2) was extraordinarily severe at lower temperature, suggesting the importance of S2 in the regulation of temperature-mediated flowering time [ 121 , 128 , 129 ]. Therefore, the S2 region likely acts as a structural determinant for temperature-responsive miR156 hairpin processing [ 121 ].…”
Section: Non-coding Rnasmentioning
confidence: 99%
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“…The opening ( k op ) and closing ( k cl ) rate constants and/or equilibrium constant for base-pair opening ( K op = k op / k cl ) can be determined by measuring the exchange using an external catalyst. These experiments have been used to probe base-pair opening in various DNA duplexes [[3], [4], [5], [6], [7], [8], [9], [10], [11], [12], [13], [14], [15], [16], [17], [18]], DNAs containing modified base such as 5-flurourasil, N6-methyl adenine, or modified guanine [[19], [20], [21]], UV-induced photoadduct-containing DNA [22], IHF-complexed DNA [23], interstrand cross-linked DNA [24], i-motif structure formed by the complementary C-rich DNA [25,26], various RNAs [15,[27], [28], [29], [30], [31], [32], [33], [34], [35], [36]], peptide nucleic acids (PNAs) [37,38], and threose nucleic acid (TNA) [39]. NMR exchange and single molecule FRET experiments could be used to study the protonation/deprotonation of adenine bases and formation of A + ·C wobble pair [[40], [41], [42], [43], [44]].…”
Section: Introductionmentioning
confidence: 99%