2012
DOI: 10.4161/rna.19877
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The role of decapping proteins in the miRNA accumulation inArabidopsis thaliana

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Cited by 30 publications
(28 citation statements)
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References 55 publications
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“…DCP1 and VCS may be required for the degradation of some miRNA targets, suggesting a possible role in target destabilization; however, the decapping complex also has a broader role in the destabilization of many nontarget mRNAs (Xu et al, 2006;Goeres et al, 2007;Motomura et al, 2012). A relationship between decapping and slicing has not yet been established; therefore, a role for VCS in slicing-independent target destabilization may be an alternative explanation for target mRNA accumulation in vcs mutants.…”
Section: Decapping Complexmentioning
confidence: 99%
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“…DCP1 and VCS may be required for the degradation of some miRNA targets, suggesting a possible role in target destabilization; however, the decapping complex also has a broader role in the destabilization of many nontarget mRNAs (Xu et al, 2006;Goeres et al, 2007;Motomura et al, 2012). A relationship between decapping and slicing has not yet been established; therefore, a role for VCS in slicing-independent target destabilization may be an alternative explanation for target mRNA accumulation in vcs mutants.…”
Section: Decapping Complexmentioning
confidence: 99%
“…A relationship between decapping and slicing has not yet been established; therefore, a role for VCS in slicing-independent target destabilization may be an alternative explanation for target mRNA accumulation in vcs mutants. Alternatively, secondary effects of decapping mutants on miRNA levels may contribute to the observed target upregulation (Motomura et al, 2012). VCS also mediates translational repression as some targets are upregulated only at the protein level in vcs mutants (Brodersen et al, 2008).…”
Section: Decapping Complexmentioning
confidence: 99%
“…Total RNA was extracted from Arabidopsis inflorescences and the PrimeScript RT reagent Kit with gDNA Eraser (TaKaRa) was used to synthesize the cDNA according to the manufacturer's protocol. qPCR was performed with the StepOnePlus Real Time PCR System (Applied Biosystems; Life Technologies) using a KAPA SYBR Fast qPCR kit (KAPA BIOSYSTEMS) and reaction conditions as previously described (Motomura et al 2012). ACTIN2 was used as the internal control gene.…”
Section: Quantitative Rt-pcr (Qrt-pcr)mentioning
confidence: 99%
“…However, the causal relationship between translational repression and decay of target RNAs has not been established in plants. Mutations in VCS and decapping1 (DCP1; a P-body component required for mRNA decapping) reduce the levels of some target transcripts, indicating the presence of slicer-independent degradation of targets [158]. However, the upregulation of target transcripts in vcp and dcp1 may attribute to the decreased miRNA levels [158].…”
Section: Mirna-mediated Translational Inhibitionmentioning
confidence: 99%