pre-miRNA Information | |
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pre-miRNA | hsa-mir-4742 |
Genomic Coordinates | chr1: 224398227 - 224398311 |
Description | Homo sapiens miR-4742 stem-loop |
Comment | None |
RNA Secondary Structure |
Mature miRNA Information | |||||||||||||||||||||||||
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Mature miRNA | hsa-miR-4742-5p | ||||||||||||||||||||||||
Sequence | 1| UCAGGCAAAGGGAUAUUUACAGA |23 | ||||||||||||||||||||||||
Evidence | Experimental | ||||||||||||||||||||||||
Experiments | Illumina | ||||||||||||||||||||||||
SNPs in miRNA |
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Putative Targets |
Gene Information | |||||||||||||||||||||
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Gene Symbol | TMEM214 | ||||||||||||||||||||
Synonyms | - | ||||||||||||||||||||
Description | transmembrane protein 214 | ||||||||||||||||||||
Transcript | NM_001083590 | ||||||||||||||||||||
Other Transcripts | NM_017727 | ||||||||||||||||||||
Expression | |||||||||||||||||||||
Putative miRNA Targets on TMEM214 | |||||||||||||||||||||
3'UTR of TMEM214 (miRNA target sites are highlighted) |
>TMEM214|NM_001083590|3'UTR 1 GCCCTGCCTTCCTGGCCACTGATTTCTGCATGGGTAGACCATCCAAGACTGCAGCGGGTAGAAGGTGGCAGTTCTTCATG 81 GGAGTCTTTTTAACTTGGTGCCTGAGTTCTCTCCTAGGCAAGTGGCCAGTTGCCTCCACCTCAGTTCTTCCATCTTTGGT 161 GGGGACAGGGCCCAGCAGCATCTCAGCCTCCTACCCACAATTCCACTGAACACTTTTCTGGCCCTACTGCACATGGCCCC 241 CAGCCTCCATCCTTGTGCTGGTAGCCTCTCACAACTCCGCCCTTGCCCTCTGCCTTCCACTTCCTTCCATCTCATTTCTA 321 AACCCCAAACAGCTCATCTCTAAAAAGATAGAACTCCCAGCAGGTGGCTTCTGTGTTCTTCTGACAAATGATTCCTGCTT 401 CTCCAGACTTTAGCAGCCTCCTGTTCCCATTCTTGGTCACAGCTCTAGCCACAGCAGAAGGAAAGGGGCTTCCAGAAGAA 481 TATAGCACCGCATTGGGAAACAGCAGCCTCACCTCCACCTGAAGCCTGGGTGTGGCTGTCAGTGGACATGGGGAGCTGGA 561 TGGAAATGCCTCTCACTTCAAAATGCCCAGCCTGCCCCAAATGCCTCTAAGCCCCTCCCTGTCCCCTCCCTTGTAGTCCT 641 ACTTCTTCCAACTTTCCATTCCCCATCATGCTGGGGGTCTTGGTCACAAGGCTCAGCTTCTCTCCACTGTCCATCCCTCC 721 TATCATCTGTAGAGCAGAGCACAGGCAGTTGTGTGCCTTGGGCCCAGGGAACCCTCCATCAACCTGAGACAGGACTCAGT 801 ATATGGTTCTTGGGTATGCCCTACCAGGTGGAATAAAGGACACAGATTTGATTTCTAGCAAAAAAAAAAAAAAAAAAAAA 881 AAAA Target sites
Provided by authors
Predicted by miRanda
DRVs
SNPs
DRVs & SNPs
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miRNA-target interactions (Predicted by miRanda) |
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DRVs in gene 3'UTRs | |||||||||||||||||||||
SNPs in gene 3'UTRs |
Experimental Support 1 for Functional miRNA-Target Interaction | |||||||
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miRNA:Target | ---- | ||||||
Validation Method |
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Conditions | TZM-bl | ||||||
Location of target site | 3'UTR | ||||||
Tools used in this research | TargetScan , miRTarCLIP , Piranha | ||||||
Original Description (Extracted from the article) |
...
PAR-CLIP data was present in GSM1462574. RNA binding protein: AGO2. Condition:TZM-bl ami BaL
... - Whisnant AW; Bogerd HP; Flores O; Ho P; et al., 2013, mBio. |
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miRNA-target interactions (Provided by authors) |
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Article |
- Whisnant AW; Bogerd HP; Flores O; Ho P; et al. - mBio, 2013
UNLABELLED: The question of how HIV-1 interfaces with cellular microRNA (miRNA) biogenesis and effector mechanisms has been highly controversial. Here, we first used deep sequencing of small RNAs present in two different infected cell lines (TZM-bl and C8166) and two types of primary human cells (CD4(+) peripheral blood mononuclear cells [PBMCs] and macrophages) to unequivocally demonstrate that HIV-1 does not encode any viral miRNAs. Perhaps surprisingly, we also observed that infection of T cells by HIV-1 has only a modest effect on the expression of cellular miRNAs at early times after infection. Comprehensive analysis of miRNA binding to the HIV-1 genome using the photoactivatable ribonucleoside-induced cross-linking and immunoprecipitation (PAR-CLIP) technique revealed several binding sites for cellular miRNAs, a subset of which were shown to be capable of mediating miRNA-mediated repression of gene expression. However, the main finding from this analysis is that HIV-1 transcripts are largely refractory to miRNA binding, most probably due to extensive viral RNA secondary structure. Together, these data demonstrate that HIV-1 neither encodes viral miRNAs nor strongly influences cellular miRNA expression, at least early after infection, and imply that HIV-1 transcripts have evolved to avoid inhibition by preexisting cellular miRNAs by adopting extensive RNA secondary structures that occlude most potential miRNA binding sites. IMPORTANCE: MicroRNAs (miRNAs) are a ubiquitous class of small regulatory RNAs that serve as posttranscriptional regulators of gene expression. Previous work has suggested that HIV-1 might subvert the function of the cellular miRNA machinery by expressing viral miRNAs or by dramatically altering the level of cellular miRNA expression. Using very sensitive approaches, we now demonstrate that neither of these ideas is in fact correct. Moreover, HIV-1 transcripts appear to largely avoid regulation by cellular miRNAs by adopting an extensive RNA secondary structure that occludes the ability of cellular miRNAs to interact with viral mRNAs. Together, these data suggest that HIV-1, rather than seeking to control miRNA function in infected cells, has instead evolved a mechanism to become largely invisible to cellular miRNA effector mechanisms.
LinkOut: [PMID: 23592263]
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Experimental Support 2 for Functional miRNA-Target Interaction | |
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miRNA:Target | ---- |
Validation Method |
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Conditions | HCT116 |
Location of target site | 3'UTR |
Tools used in this research | TargetScan , miRTarCLIP , Piranha |
Original Description (Extracted from the article) |
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PAR-CLIP data was present in ERX177603. RNA binding protein: AGO2. Condition:p53_D_AGO_CLIP_2_5
PAR-CLIP data was present in ERX177615. RNA binding protein: AGO2. Condition:p53_D_AGO_CLIP_3_5
... - Krell J; Stebbing J; Carissimi C; Dabrowska et al., 2016, Genome research. |
Article |
- Krell J; Stebbing J; Carissimi C; Dabrowska et al. - Genome research, 2016
DNA damage activates TP53-regulated surveillance mechanisms that are crucial in suppressing tumorigenesis. TP53 orchestrates these responses directly by transcriptionally modulating genes, including microRNAs (miRNAs), and by regulating miRNA biogenesis through interacting with the DROSHA complex. However, whether the association between miRNAs and AGO2 is regulated following DNA damage is not yet known. Here, we show that, following DNA damage, TP53 interacts with AGO2 to induce or reduce AGO2's association of a subset of miRNAs, including multiple let-7 family members. Furthermore, we show that specific mutations in TP53 decrease rather than increase the association of let-7 family miRNAs, reducing their activity without preventing TP53 from interacting with AGO2. This is consistent with the oncogenic properties of these mutants. Using AGO2 RIP-seq and PAR-CLIP-seq, we show that the DNA damage-induced increase in binding of let-7 family members to the RISC complex is functional. We unambiguously determine the global miRNA-mRNA interaction networks involved in the DNA damage response, validating them through the identification of miRNA-target chimeras formed by endogenous ligation reactions. We find that the target complementary region of the let-7 seed tends to have highly fixed positions and more variable ones. Additionally, we observe that miRNAs, whose cellular abundance or differential association with AGO2 is regulated by TP53, are involved in an intricate network of regulatory feedback and feedforward circuits. TP53-mediated regulation of AGO2-miRNA interaction represents a new mechanism of miRNA regulation in carcinogenesis.
LinkOut: [PMID: 26701625]
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CLIP-seq Support 1 for dataset GSM1462574 | |
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Method / RBP | PAR-CLIP / AGO2 |
Cell line / Condition | TZM-bl / TZM-bl ami BaL |
Location of target site | ENST00000238788.9 | 3UTR | UCUUUUUAACUUGGUGCCUGAGUUCUCUCCU |
Tools used in this analysis | TargetScan, miRTarCLIP, and Piranha |
Article / Accession Series | PMID: 23592263 / GSE59944 |
CLIP-seq Viewer | Link |
MiRNA-Target Expression Profile | |||||||
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MiRNA-Target Expression Profile (TCGA) | |||||||
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70 hsa-miR-4742-5p Target Genes:
Functional analysis:
ID | Target | Description | Validation methods | |||||||||
Strong evidence | Less strong evidence | |||||||||||
MIRT065632 | CLIC4 | chloride intracellular channel 4 | 2 | 4 | ||||||||
MIRT068170 | TXLNA | taxilin alpha | 2 | 2 | ||||||||
MIRT119024 | TSN | translin | 2 | 2 | ||||||||
MIRT165212 | GRAMD3 | GRAM domain containing 2B | 2 | 2 | ||||||||
MIRT175254 | PSAT1 | phosphoserine aminotransferase 1 | 2 | 4 | ||||||||
MIRT213228 | REST | RE1 silencing transcription factor | 2 | 6 | ||||||||
MIRT296337 | PARD6B | par-6 family cell polarity regulator beta | 2 | 2 | ||||||||
MIRT316776 | FOXC1 | forkhead box C1 | 2 | 2 | ||||||||
MIRT453943 | XRCC6 | X-ray repair cross complementing 6 | 2 | 6 | ||||||||
MIRT454599 | RPL13A | ribosomal protein L13a | 2 | 2 | ||||||||
MIRT458485 | RMI1 | RecQ mediated genome instability 1 | 2 | 6 | ||||||||
MIRT458650 | SGPP2 | sphingosine-1-phosphate phosphatase 2 | 2 | 2 | ||||||||
MIRT459240 | ADRBK1 | G protein-coupled receptor kinase 2 | 2 | 2 | ||||||||
MIRT461008 | SYT7 | synaptotagmin 7 | 2 | 2 | ||||||||
MIRT462026 | RIF1 | replication timing regulatory factor 1 | 2 | 2 | ||||||||
MIRT462103 | TMEM214 | transmembrane protein 214 | 2 | 2 | ||||||||
MIRT463255 | ZIC5 | Zic family member 5 | 2 | 4 | ||||||||
MIRT465190 | TRPS1 | transcriptional repressor GATA binding 1 | 2 | 2 | ||||||||
MIRT470507 | PPP1R11 | protein phosphatase 1 regulatory inhibitor subunit 11 | 2 | 2 | ||||||||
MIRT472356 | TSPAN1 | tetraspanin 1 | 2 | 2 | ||||||||
MIRT473260 | MIDN | midnolin | 2 | 2 | ||||||||
MIRT477527 | EIF4G2 | eukaryotic translation initiation factor 4 gamma 2 | 2 | 4 | ||||||||
MIRT485182 | PTP4A1 | protein tyrosine phosphatase type IVA, member 1 | 2 | 4 | ||||||||
MIRT486461 | MDM2 | MDM2 proto-oncogene | 2 | 2 | ||||||||
MIRT492760 | PER1 | period circadian clock 1 | 2 | 8 | ||||||||
MIRT496703 | TRIM39 | tripartite motif containing 39 | 2 | 2 | ||||||||
MIRT497227 | MORC2 | MORC family CW-type zinc finger 2 | 2 | 2 | ||||||||
MIRT499582 | INTU | inturned planar cell polarity protein | 2 | 4 | ||||||||
MIRT504081 | C9orf40 | chromosome 9 open reading frame 40 | 2 | 6 | ||||||||
MIRT505484 | SRSF2 | serine and arginine rich splicing factor 2 | 2 | 2 | ||||||||
MIRT513255 | FBXO17 | F-box protein 17 | 2 | 2 | ||||||||
MIRT525061 | FRK | fyn related Src family tyrosine kinase | 2 | 2 | ||||||||
MIRT528798 | RAB32 | RAB32, member RAS oncogene family | 2 | 2 | ||||||||
MIRT534357 | SFT2D2 | SFT2 domain containing 2 | 2 | 2 | ||||||||
MIRT538731 | CAPN1 | calpain 1 | 2 | 2 | ||||||||
MIRT550792 | WARS2 | tryptophanyl tRNA synthetase 2, mitochondrial | 2 | 2 | ||||||||
MIRT553994 | SRPR | SRP receptor alpha subunit | 2 | 4 | ||||||||
MIRT568102 | CDKN1B | cyclin dependent kinase inhibitor 1B | 2 | 2 | ||||||||
MIRT570107 | SLC18B1 | solute carrier family 18 member B1 | 2 | 2 | ||||||||
MIRT570823 | RPL7L1 | ribosomal protein L7 like 1 | 2 | 2 | ||||||||
MIRT572004 | HMGB1 | high mobility group box 1 | 2 | 2 | ||||||||
MIRT572352 | PCYT2 | phosphate cytidylyltransferase 2, ethanolamine | 2 | 2 | ||||||||
MIRT609716 | TMEM132C | transmembrane protein 132C | 2 | 2 | ||||||||
MIRT613982 | LRRC40 | leucine rich repeat containing 40 | 2 | 2 | ||||||||
MIRT620740 | CCL16 | C-C motif chemokine ligand 16 | 2 | 2 | ||||||||
MIRT625074 | C15orf41 | chromosome 15 open reading frame 41 | 2 | 4 | ||||||||
MIRT627941 | NNT | nicotinamide nucleotide transhydrogenase | 2 | 2 | ||||||||
MIRT629941 | IGSF6 | immunoglobulin superfamily member 6 | 2 | 2 | ||||||||
MIRT633396 | FBXW8 | F-box and WD repeat domain containing 8 | 2 | 2 | ||||||||
MIRT635846 | ZNF264 | zinc finger protein 264 | 2 | 2 | ||||||||
MIRT638086 | ZNF652 | zinc finger protein 652 | 2 | 2 | ||||||||
MIRT643996 | TCHP | trichoplein keratin filament binding | 2 | 2 | ||||||||
MIRT660020 | C1GALT1 | core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase 1 | 2 | 2 | ||||||||
MIRT660161 | BRCC3 | BRCA1/BRCA2-containing complex subunit 3 | 2 | 2 | ||||||||
MIRT668887 | CSRP1 | cysteine and glycine rich protein 1 | 2 | 2 | ||||||||
MIRT676729 | METTL14 | methyltransferase like 14 | 2 | 2 | ||||||||
MIRT677210 | MURC | caveolae associated protein 4 | 2 | 2 | ||||||||
MIRT685949 | PTGIS | prostaglandin I2 synthase | 2 | 2 | ||||||||
MIRT687816 | ITPRIPL2 | inositol 1,4,5-trisphosphate receptor interacting protein like 2 | 2 | 2 | ||||||||
MIRT689900 | SOD2 | superoxide dismutase 2 | 2 | 2 | ||||||||
MIRT698214 | TMEM248 | transmembrane protein 248 | 2 | 2 | ||||||||
MIRT698279 | TMEM2 | transmembrane protein 2 | 2 | 2 | ||||||||
MIRT698758 | STK4 | serine/threonine kinase 4 | 2 | 2 | ||||||||
MIRT698789 | STK38 | serine/threonine kinase 38 | 2 | 2 | ||||||||
MIRT703152 | GPR137C | G protein-coupled receptor 137C | 2 | 2 | ||||||||
MIRT704408 | CTPS1 | CTP synthase 1 | 2 | 2 | ||||||||
MIRT705067 | C4orf32 | family with sequence similarity 241 member A | 2 | 2 | ||||||||
MIRT710201 | FLVCR1 | feline leukemia virus subgroup C cellular receptor 1 | 2 | 2 | ||||||||
MIRT714495 | HSPA4 | heat shock protein family A (Hsp70) member 4 | 2 | 2 | ||||||||
MIRT720082 | TNRC6B | trinucleotide repeat containing 6B | 2 | 2 |
miRNA-Drug Resistance Associations | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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