2017
DOI: 10.1016/j.pbi.2016.11.006
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The evolution of microRNAs in plants

Abstract: MicroRNAs (miRNAs) are a central player in post-transcriptional regulation of gene expression and are involved in numerous biological processes in eukaryotes. Knowledge of the origins and divergence of miRNAs paves the way for a better understanding of the complexity of the regulatory networks that they participate in. The biogenesis, degradation, and regulatory activities of miRNAs are relatively better understood, but the evolutionary history of miRNAs still needs more exploration. Inverted duplication of ta… Show more

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Cited by 124 publications
(90 citation statements)
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References 49 publications
(57 reference statements)
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“…One strand of the duplex is associated with a member of the Argonaute (AGO) family. The resulting miRNA-AGO complex is the miRNA-induced silencing complex, which interacts with the complementary site of target mRNA transcript, thereby repressing the expression of the target transcripts at the post-transcriptional level [2]. …”
Section: Introductionmentioning
confidence: 99%
“…One strand of the duplex is associated with a member of the Argonaute (AGO) family. The resulting miRNA-AGO complex is the miRNA-induced silencing complex, which interacts with the complementary site of target mRNA transcript, thereby repressing the expression of the target transcripts at the post-transcriptional level [2]. …”
Section: Introductionmentioning
confidence: 99%
“…As proposed in a number of organisms 2, 20, 32, 47, 52 , low level transcription of inverted repeats or mutationally engendered hairpin structures could give rise to a diversity of RNAs recognized as substrates by the sRNA biogenesis machinery. However, most young miRNAs would likely be neutral 32, 47, 48, 52 , either by not being expressed at a high enough level or by not having enough sequence identity to regulate any meaningful target.…”
Section: Discussionmentioning
confidence: 99%
“…The 3' adapter was trimmed using perfect string matching on the first 7 nucleotides of the adapter (TGGAATT); the HD signatures, 4 assigned nucleotides at the 3' and 5' end of the insert (10, 16) were also trimmed. Next, the files were converted from redundant to non-redundant format (17,18) and the results were summarized into redundant and nonredundant size class distributions.…”
Section: Smallrnasmentioning
confidence: 99%
“…The abundances of the reads were normalized using the reads per total method (22)(23)(24). The replicate to replicate differential expression was called on offset fold change, offset = 20 (empirically determined) (18,25) calculated on the proximal ends of maximal confidence intervals built on the available replicates. The differential expression on loci (regions on the genome) was conducted using a simplified form of CoLIde (26) applicable on 2 samples, with 2 replicates each.…”
Section: Smallrnasmentioning
confidence: 99%