Systemic comparison of repression activity for miRNA and siRNA associated with different types of target sequences

► We did systemic comparison of repression activity for miRNA and siRNA associated with different types of target sequences. ► The level of repression could be ordered as follows: perfect-matched target≫dimeric targets≫monomeric targets. ► Fold repression of 8mer+7mer-1A lay between 2×8mer and 2×7me...

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Veröffentlicht in:Biochemical and biophysical research communications 2011-07, Vol.411 (2), p.393-396
Hauptverfasser: Lee, Han-Chia, Chen, Chih-Ying, Au, Lo-Chun
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Sprache:eng
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Zusammenfassung:► We did systemic comparison of repression activity for miRNA and siRNA associated with different types of target sequences. ► The level of repression could be ordered as follows: perfect-matched target≫dimeric targets≫monomeric targets. ► Fold repression of 8mer+7mer-1A lay between 2×8mer and 2×7mer-1A. ► A mismatch in one seed dramatically decreasing repressive activity of the dimer indicating cooperation of two monomers. ► Strong repression of miR-155 and siRNA-155 (siRNA carrying miR-155 sequence) with perfectly matched target was due primarily to translational attenuation. Most miRNA target sites are determined by Watson–Crick pairing via the seed region (positions ∼2–7nt of the mature miRNA). The binding sites of target mRNAs are categorized primarily as 7mer-m8, the 7mer-1A and the 8mer sites. This study analyzed post-transcriptional repression as a function of associations among various seed/target sequences. The target sequence of miR-155 from TP53INP1 was modified such that their various monomers and dimers could be inserted into the 3′UTR of a reporter gene for monitoring repression activity of miR-155. Results revealed that the level of repression could be ordered as follows: perfect-matched target≫dimeric targets≫monomeric targets. For dimeric targets, the order is 2×8mer>2×7mer-m8>2×7mer-1A. Fold repression of 8mer+7mer-1A lay between 2×8mer and 2×7mer-1A. A mismatch in one seed dramatically decreasing repressive activity of the dimer. This indicated that the degree of repression could be synergistically enhanced through the cooperation of the two miRISC-loaded monomers. The siRNA-155 (siRNA carrying miR-155 sequence) elicited higher repressive activity than miR-155, as they bound to the perfectly matched target. However, strong repression of miR-155 and siRNA-155 with a perfectly matched target was due primarily to translational attenuation. Cleavage/degradation of the target mRNA was not a major cause of the observed repression.
ISSN:0006-291X
1090-2104
DOI:10.1016/j.bbrc.2011.06.159