Comparative analysis of MIR168 promoters in three plant species
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作者:
Qu, D.
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Northwest A&F Univ, Coll Hort, Yangling, Shaanxi, Peoples R China
Apple E&T Res Ctr Shaanxi Prov, Yangling, Shaanxi, Peoples R ChinaNorthwest A&F Univ, Coll Hort, Yangling, Shaanxi, Peoples R China
Qu, D.
[1
,2
]
Yan, F.
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Shaanxi Univ Technol, Shaanxi Prov Key Lab Bioresources, Hanzhong, Peoples R ChinaNorthwest A&F Univ, Coll Hort, Yangling, Shaanxi, Peoples R China
Yan, F.
[3
]
Li, M. A.
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机构:Northwest A&F Univ, Coll Hort, Yangling, Shaanxi, Peoples R China
Li, M. A.
Varotto, C.
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Fdn Edmund Mach, Dept Biodivers & Mol Ecol, Michele Alladige, TN, ItalyNorthwest A&F Univ, Coll Hort, Yangling, Shaanxi, Peoples R China
Varotto, C.
[4
]
Zhao, Z. Y.
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Northwest A&F Univ, Coll Hort, Yangling, Shaanxi, Peoples R China
Apple E&T Res Ctr Shaanxi Prov, Yangling, Shaanxi, Peoples R ChinaNorthwest A&F Univ, Coll Hort, Yangling, Shaanxi, Peoples R China
Zhao, Z. Y.
[1
,2
]
机构:
[1] Northwest A&F Univ, Coll Hort, Yangling, Shaanxi, Peoples R China
[2] Apple E&T Res Ctr Shaanxi Prov, Yangling, Shaanxi, Peoples R China
[3] Shaanxi Univ Technol, Shaanxi Prov Key Lab Bioresources, Hanzhong, Peoples R China
MicroRNAs (miRNAs) play important roles in the regulation of gene expression by post-transcriptionally targeting mRNAs for cleavage or translational repression. miR168 is a key miRNA because it regulates the expression of the slicer protein ARGONAUTE1 (AGO1), which catalyzes mRNA cleavage. Interestingly, plant miR168s are highly evolutionarily conserved; however, it is unclear whether MIR168 promoter elements and expression patterns are also conserved. Here, we isolated MIR168 promoters from monocot rice and dicot grape genomes. To determine the expression pattern, different promoters were fused to a beta-glucoronidase reporter gene and the resulting constructs were then transformed in Arabidopsis. The results revealed clear differences in the MIR168 promoter sequence of monocot and dicot plant species. Moreover, the pattern of MIR168 promoter expression differed between monocots and dicots. These results suggest that, unlike that of miR168, the MIR168 promoter is not conserved in monocots and dicots.
机构:
Max Planck Institute for Molecular Plant Physiology, 14476 Potsdam-Golm
LGC Genomics GmbH, 12459 BerlinMax Planck Institute for Molecular Plant Physiology, 14476 Potsdam-Golm
Lenz D.
May P.
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机构:
Luxembourg Centre for Systems Biomedicine, University of Luxembourg
Institute for Systems Biology, Seattle, WAMax Planck Institute for Molecular Plant Physiology, 14476 Potsdam-Golm
May P.
Walther D.
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Max Planck Institute for Molecular Plant Physiology, 14476 Potsdam-GolmMax Planck Institute for Molecular Plant Physiology, 14476 Potsdam-Golm