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Plant miRNA regulation is environmentally and developmentally-sensitive

https://doi.org/10.1101/136762
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1007/978-3-642-37765-5_6openalex-snapshot
RNA Interference-Mediated Intrinsic Antiviral Immunity in Plants
inferredcites →https://doi.org/10.1016/j.cell.2007.07.039openalex-snapshot
Antiviral Immunity Directed by Small RNAs
inferredcites →https://doi.org/10.1016/j.cell.2009.01.046openalex-snapshot
Origin, Biogenesis, and Activity of Plant MicroRNAs
inferredcites →https://doi.org/10.1016/j.cell.2009.06.014openalex-snapshot
miR156-Regulated SPL Transcription Factors Define an Endogenous Flowering Pathway in Arabidopsis thaliana
inferredcites →https://doi.org/10.1016/j.cell.2009.06.031openalex-snapshot
The Sequential Action of miR156 and miR172 Regulates Developmental Timing in Arabidopsis
inferredcites →https://doi.org/10.1016/j.cell.2012.09.039openalex-snapshot
Fast-Forward Genetics Identifies Plant CPL Phosphatases as Regulators of miRNA Processing Factor HYL1
inferredcites →https://doi.org/10.1016/j.cub.2007.04.005openalex-snapshot
Identification of Nuclear Dicing Bodies Containing Proteins for MicroRNA Biogenesis in Living Arabidopsis Plants
inferredcites →https://doi.org/10.1016/j.cub.2013.05.055openalex-snapshot
Artificial microRNAs reveal cell-specific differences in small RNA activity in pollen
inferredcites →https://doi.org/10.1016/j.cub.2014.09.058openalex-snapshot
Temporal Control of Leaf Complexity by miRNA-Regulated Licensing of Protein Complexes
inferredcites →https://doi.org/10.1016/j.molcel.2014.08.028openalex-snapshot
mRNA Destabilization Is the Dominant Effect of Mammalian MicroRNAs by the Time Substantial Repression Ensues
inferredcites →https://doi.org/10.1016/j.tplants.2011.03.001openalex-snapshot
MicroRNA networks and developmental plasticity in plants
inferredcites →https://doi.org/10.1016/j.tplants.2012.01.010openalex-snapshot
Functions of microRNAs in plant stress responses
inferredcites →https://doi.org/10.1016/j.tplants.2015.08.003openalex-snapshot
Missing Pieces in the Puzzle of Plant MicroRNAs
inferredcites →https://doi.org/10.1016/j.tplants.2016.09.003openalex-snapshot
miRNA Biogenesis: A Dynamic Pathway
inferredcites →https://doi.org/10.1016/s0960-9822(02)01017-5openalex-snapshot
CARPEL FACTORY, a Dicer Homolog, and HEN1, a Novel Protein, Act in microRNA Metabolism in Arabidopsis thaliana
inferredcites →https://doi.org/10.1038/nature09267openalex-snapshot
Mammalian microRNAs predominantly act to decrease target mRNA levels
inferredcites →https://doi.org/10.1038/nature12633openalex-snapshot
Temperature-dependent regulation of flowering by antagonistic FLM variants
inferredcites →https://doi.org/10.1038/nbt1255openalex-snapshot
Expression of artificial microRNAs in transgenic Arabidopsis thaliana confers virus resistance
inferredcites →https://doi.org/10.1038/ncomms1303openalex-snapshot
Two splice variants of the IDD14 transcription factor competitively form nonfunctional heterodimers which may regulate starch metabolism
inferredcites →https://doi.org/10.1038/ncomms3145openalex-snapshot
The effects of carbon dioxide and temperature on microRNA expression in Arabidopsis development
inferredcites →https://doi.org/10.1038/nplants.2014.27openalex-snapshot
Gene regulation by translational inhibition is determined by Dicer partnering proteins
inferredcites →https://doi.org/10.1073/pnas.0307969100openalex-snapshot
The Arabidopsis double-stranded RNA-binding protein HYL1 plays a role in microRNA-mediated gene regulation
inferredcites →https://doi.org/10.1073/pnas.0405570102openalex-snapshot
Nuclear processing and export of microRNAs in Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.0802493105openalex-snapshot
Dual roles of the nuclear cap-binding complex and SERRATE in pre-mRNA splicing and microRNA processing in Arabidopsis thaliana
inferredcites →https://doi.org/10.1073/pnas.1512865112openalex-snapshot
KH domain protein RCF3 is a tissue-biased regulator of the plant miRNA biogenesis cofactor HYL1
inferredcites →https://doi.org/10.1073/pnas.200217597openalex-snapshot
AGO1, QDE-2, and RDE-1 are related proteins required for post-transcriptional gene silencing in plants, quelling in fungi, and RNA interference in animals
inferredcites →https://doi.org/10.1093/emboj/17.1.170openalex-snapshot
AGO1 defines a novel locus of Arabidopsis controlling leaf development
inferredcites →https://doi.org/10.1093/emboj/cdg74openalex-snapshot
Low temperature inhibits RNA silencing‐mediated defence by the control of siRNA generation
inferredcites →https://doi.org/10.1093/jxb/eru416openalex-snapshot
Control of flowering by ambient temperature
inferredcites →https://doi.org/10.1093/jxb/erw248openalex-snapshot
Structural determinants of miR156a precursor processing in temperature-responsive flowering in Arabidopsis
inferredcites →https://doi.org/10.1093/nar/gkp1240openalex-snapshot
Genetic framework for flowering-time regulation by ambient temperature-responsive miRNAs in Arabidopsis
inferredcites →https://doi.org/10.1093/nar/gkv578openalex-snapshot
microRNAs and the evolution of complex multicellularity: identification of a large, diverse complement of microRNAs in the brown algaEctocarpus
inferredcites →https://doi.org/10.1101/gad.307804openalex-snapshot
In vivo investigation of the transcription, processing, endonucleolytic activity, and functional relevance of the spatial distribution of a plant miRNA
inferredcites →https://doi.org/10.1104/pp.15.00073openalex-snapshot
Deciphering the Role of POLYCOMB REPRESSIVE COMPLEX1 Variants in Regulating the Acquisition of Flowering Competence in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.105.039834openalex-snapshot
Highly Specific Gene Silencing by Artificial MicroRNAs in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.2.8.755openalex-snapshot
Early Flower Development in Arabidopsis
inferredcites →https://doi.org/10.1111/j.1365-313x.2006.02835.xopenalex-snapshot
SERRATE is a novel nuclear regulator in primary microRNA processing in Arabidopsis
inferredcites →https://doi.org/10.1126/science.1159151openalex-snapshot
Widespread Translational Inhibition by Plant miRNAs and siRNAs
inferredcites →https://doi.org/10.1146/annurev-arplant-050312-120043openalex-snapshot
Classification and Comparison of Small RNAs from Plants
inferredcites →https://doi.org/10.1186/1746-4811-3-12openalex-snapshot
Protocol: a highly sensitive RT-PCR method for detection and quantification of microRNAs
inferredcites →https://doi.org/10.1186/1746-4811-7-7openalex-snapshot
Protocol: A simple phenol-based method for 96-well extraction of high quality RNA from Arabidopsis
inferredcites →https://doi.org/10.1242/dev.063511openalex-snapshot
The control of developmental phase transitions in plants
inferredcites →https://doi.org/10.1371/journal.pgen.1000646openalex-snapshot
Redundant and Specific Roles of the ARGONAUTE Proteins AGO1 and ZLL in Development and Small RNA-Directed Gene Silencing
inferredcites →https://doi.org/10.1371/journal.pgen.1001358openalex-snapshot
ARGONAUTE10 and ARGONAUTE1 Regulate the Termination of Floral Stem Cells through Two MicroRNAs in Arabidopsis
inferredcites →https://doi.org/10.1371/journal.pgen.1003875openalex-snapshot
A KH-Domain RNA-Binding Protein Interacts with FIERY2/CTD Phosphatase-Like 1 and Splicing Factors and Is Important for Pre-mRNA Splicing in Arabidopsis
inferredcites →https://doi.org/10.1371/journal.pgen.1006263openalex-snapshot
Developmental Functions of miR156-Regulated SQUAMOSA PROMOTER BINDING PROTEIN-LIKE (SPL) Genes in Arabidopsis thaliana
inferredcites →https://doi.org/10.1371/journal.pone.0035933openalex-snapshot
DRB2 Is Required for MicroRNA Biogenesis in Arabidopsis thaliana
inferredcites →https://doi.org/10.1371/journal.pone.0146534openalex-snapshot
Analysis of the Maize dicer-like1 Mutant, fuzzy tassel, Implicates MicroRNAs in Anther Maturation and Dehiscence
inferredcites →https://doi.org/10.14348/molcells.2016.0085openalex-snapshot
Post-Translational Regulation of miRNA Pathway Components, AGO1 and HYL1, in Plants

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.1007/s00299-020-02577-1openalex-snapshot
Plant rejuvenation: from phenotypes to mechanisms
inferred← citeshttps://doi.org/10.1016/j.scienta.2020.109435openalex-snapshot
MicroRNA regulation during the tomato fruit development and ripening: A review
inferred← citeshttps://doi.org/10.1093/jxb/ery172openalex-snapshot
Spatio-temporal expression of miRNA159 family members and their GAMYB target gene during the modulation of gibberellin-induced grapevine parthenocarpy
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