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AGO1, AGO2 and AGO10 promoted anti-TuMV defense in a modular way in various organs, with AGO2 providing a prominent antiviral role in leaves. AGO5, AGO7 and AGO10 had minor effects in leaves.
Base pairing at the 15th nucleotide of a miRNA duplex is important for miRNA sorting in both Arabidopsis AGO1 (show EIF2C1 ELISA Kits) and AGO2. AGO2 favours miRNA duplexes with no middle mismatches.
Complementation analyses in ago mutant plants revealed that the catalytic residues of AGO1, AGO2, and AGO7 are required to restore the defects of Arabidopsis ago1-25, ago2-1, and zip-1 (AGO7-defective) mutants, respectively.
AGO2 and HEN1 (show HENMT1 ELISA Kits) participate in the DCL2-mediated antiviral defense to ensure the survival of Turnip crinkle virus-infected plants at high temperature.
This study reveals that miR408, which has a 5'A, regulates its target Plantacyanin through either AGO1 (show EIF2C1 ELISA Kits) or AGO2.
AGO1 (show EIF2C1 ELISA Kits) and AGO2 are involved in defense against mutant of Cucumber mosaic virus, which act downstream the biogenesis of viral secondary siRNAs in a nonredundant and cooperative manner.
Results show that AGO2-bound small RNA miR393b( *) targets a Golgi-localized SNARE (show NAPA ELISA Kits) gene, MEMB12.
second layer is activated when the first layer is suppressed because AGO2 is repressed by AGO1 (show EIF2C1 ELISA Kits) via miR403
This study employed molecular dynamics simulation to investigate the dynamic properties of human Ago2-RNA-duplex system and Ago2-free system to provide further understanding of the molecular mechanism of Ago2-RNA recognition.
WIG1 (show ZMAT3 ELISA Kits) governs the miRNA-dependent and the miRNA-independent recruitment of AGO2 to lower the stability of and suppress the translation of ACOT7 (show ACOT7 ELISA Kits) mRNA.
The adenovirus major late promoter produces a 31-nucleotide transcriptional start site small RNA (MLP (show MUC2 ELISA Kits)-TSS (show RPL38 ELISA Kits)-sRNA) that retains the 7-methylguanosine (m7G)-cap and is incorporated onto Ago2-containing RNA-induced silencing complexes (RISC (show SCPEP1 ELISA Kits)) in human adenovirus-37 infected cells.
Depletion of AUF1 (show HNRNPD ELISA Kits) abolishes the global interaction of miRNAs and AGO2. Single-molecule analysis revealed that AUF1 (show HNRNPD ELISA Kits) slowed down assembly of AGO2-let-7b-mRNA complex unexpectedly. AUF1 (show HNRNPD ELISA Kits) is a decay-promoting factor influencing multiple steps in AGO2-miRNA-mediated mRNA decay.
This lack of 21-3U HCV host factor activity correlated with reduced recruitment of Ago2 to the HCV S1 site. Additional experiments demonstrated strong preference for guanosine at nt 22 of miR (show MLXIP ELISA Kits)-122. Our findings reveal the importance of non-templated 3 miR (show MLXIP ELISA Kits)-122 modifications to its HCV host factor activity, and identify unexpected differences in miRNA requirements for host gene suppression versus RNA virus replication.
Low AGO2 expression is associated with melanoma.
Altogether, these data suggest that the phosphorylation state of the serine/threonine cluster is important for Argonaute-mRNA interactions.
data indicates that the aberrant expression of miR (show MLXIP ELISA Kits)-15b contributes to abnormal placentation by targeting argonaute 2 messenger RNA
findings support a model in which an AGO2 phosphorylation cycle stimulated by target engagement regulates miRNA:target interactions to maintain the global efficiency of miRNA-mediated silencing
deciphering Ago2:RNA interactions using crosslinking immunoprecipitation coupled with high-throughput sequencing (HITS-CLIP) to generate the first transcriptome-wide map of miR (show MLXIP ELISA Kits) targeting events in human myocardium, detecting 4000 cardiac Ago2 binding sites across 2200 target transcripts
This identified Ago2 as a key determinant of quiescence exit in Hematopoietic stem cells.
miR (show MLXIP ELISA Kits)-9, along with Argonaute proteins (Agos), is localized to the nucleus of quiescent neural stem cells, and manipulating their nuclear/cytoplasmic ratio impacts quiescence.
We propose that RISC (show SCPEP1 ELISA Kits)-mediated inhibition of specific sets of chromatin regulators is a primary mechanism for preserving embryonic stem cell pluripotency while inhibiting the onset of embryonic developmental programs
Increased AGO2 was detected in autophagy-deficient ATG5 (show ATG5 ELISA Kits)-/- and ATG16 (show ATG16L1 ELISA Kits)-/- mouse embryonic fibroblast cells. Chemical agents and VacA toxin, which disrupt autophagy, increased AGO2 expression in MEFs, epithelial cells lines, and human monocytes.
DIS3L2 (show DIS3L2 ELISA Kits) interacts with Ago2 and governs target RNA-directed miRNA degradation.
Results from the liver show that, siRNA targets 3'UTR (show UTS2R ELISA Kits) and the coding sequence (CDs (show ABHD5 ELISA Kits)) of endogenous genes in the presence Ago2 but in its absence, only 3'UTR (show UTS2R ELISA Kits)-targeted siRNA-mediated knockdown are active with the help of Ago1 (show EIF2C1 ELISA Kits) and Ago3 (show EIF2C3 ELISA Kits).
Roquin (show RC3H1 ELISA Kits) also directly binds Argonaute2, a central component of the RNA-induced silencing complex, and miR (show MLXIP ELISA Kits)-146a, a microRNA that targets Icos (show ICOS ELISA Kits) mRNA.
Target mRNAs induce tailing and trimming on Ago2-loaded miRNAs.
Mouse AGO2 binds tighter to miRNA targets than its RNAi cleavage product, even though the cleaved product contains more base pairs. By re-writing the rules for nucleic acid hybridization, Argonautes allow oligonucleotides to serve as specificity determinants with thermodynamic and kinetic properties more typical of RNA-binding proteins than of RNA or DNA.
Mouse Ago2 can be expressed as a fusion protein with the maltose binding protein in a soluble and enzymatically active form, without requiring coexpression with chaperones and cleave the complementary RNA in absence of other cellular factors.
Molecular evolution of AGO2 glutamine-rich repeat region
Mutation of T1149 or R1158 in the conserved PIWI (show PIWIL1 ELISA Kits) domain causes AGO2 protein instability, but only T1149 affects RNAi activity. Mass spec analysis shows that several proteasome components co-purify with both wildtype and mutant AGO2, and knockdown of two proteasome pathway components results in AGO2 protein accumulation.
We speculate that the repeated evolution of testis specificity in obscura group Ago2 genes, combined with their dynamic turnover and strong signatures of adaptive evolution, may be associated with highly derived roles in the suppression of transposable elements or meiotic drive
We find there are large differences in evolutionary rates and gene turnover between pathways, and that paralogs of Ago2, Ago3, and Piwi/Aub show contrasting rates of evolution after duplication.
Study shows that the Cricket Paralysis virus suppressor of RNA silencing, CrPV-1A but not B2 strongly interfere with the Ago-2-dependent miRNA silencing in Drosophila.
siRNA biogenesis does not stabilize AGO2 in Drosophila.
The results of this study found that mutations in Drosophila Argonaute 2 (Ago2) resulted in exacerbated transposon expression in the brain, progressive and age-dependent memory impairment, and shortened lifespan
analysis of regulation of Argonaute (show EIF2C1 ELISA Kits) slicer activity by guide RNA 3' end interactions with the N-terminal lobe
two new nuclear roles for Ago-2: one in pre-mRNA splicing and one in transcriptional repression.
Highlighting its role in antiviral defense, fly Ago2 dissociates so slowly from extensively complementary target RNAs that essentially every fully paired target is cleaved. Conversely, mouse AGO2, which mainly mediates miRNA-directed repression, dissociates rapidly and with similar rates for fully paired and seed-matched targets.
This gene encodes a member of the Argonaute family of proteins which play a role in RNA interference. The encoded protein is highly basic, and contains a PAZ domain and a PIWI domain. It may interact with dicer1 and play a role in short-interfering-RNA-mediated gene silencing. Multiple transcript variants encoding different isoforms have been found for this gene.
eukaryotic translation initiation factor 2C, 2
, protein argonaute-2-like
, PAZ Piwi domain protein
, argonaute 2
, eIF-2C 2
, eIF2C 2
, protein argonaute-2
, protein slicer
, golgi ER protein 95 kDa
, Protein slicer
, eukaryotic translation initiation factor 2C, 1
, Piwi/Argonaute family protein meIF2C2
, argonaute RISC catalytic component 2
, eukaryotic translation initiation factor 2C 2
, Eukaryotic translation initiation factor 2C 2
, translation initiation factor eIF2C