pre-miRNA Information | |
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pre-miRNA | hsa-mir-4666a |
Genomic Coordinates | chr1: 228462074 - 228462152 |
Description | Homo sapiens miR-4666a stem-loop |
Comment | None |
RNA Secondary Structure |
Mature miRNA Information | ||||||||||||||||||||||||||||
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Mature miRNA | hsa-miR-4666a-5p | |||||||||||||||||||||||||||
Sequence | 10| AUACAUGUCAGAUUGUAUGCC |30 | |||||||||||||||||||||||||||
Evidence | Experimental | |||||||||||||||||||||||||||
Experiments | Illumina | |||||||||||||||||||||||||||
SNPs in miRNA |
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Putative Targets |
Gene Information | |||||||||||||||||||||
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Gene Symbol | TSPAN6 | ||||||||||||||||||||
Synonyms | T245, TM4SF6, TSPAN-6 | ||||||||||||||||||||
Description | tetraspanin 6 | ||||||||||||||||||||
Transcript | NM_003270 | ||||||||||||||||||||
Expression | |||||||||||||||||||||
Putative miRNA Targets on TSPAN6 | |||||||||||||||||||||
3'UTR of TSPAN6 (miRNA target sites are highlighted) |
>TSPAN6|NM_003270|3'UTR 1 CCCAATGTATCTGTGGGCCTATTCCTCTCTACCTTTAAGGACATTTAGGGTCCCCCCTGTGAATTAGAAAGTTGCTTGGC 81 TGGAGAACTGACAACACTACTTACTGATAGACCAAAAAACTACACCAGTAGGTTGATTCAATCAAGATGTATGTAGACCT 161 AAAACTACACCAATAGGCTGATTCAATCAAGATCCGTGCTCGCAGTGGGCTGATTCAATCAAGATGTATGTTTGCTATGT 241 TCTAAGTCCACCTTCTATCCCATTCATGTTAGATCGTTGAAACCCTGTATCCCTCTGAAACACTGGAAGAGCTAGTAAAT 321 TGTAAATGAAGTAATACTGTGTTCCTCTTGACTGTTATTTTTCTTAGTAGGGGGCCTTTGGAAGGCACTGTGAATTTGCT 401 ATTTTGATGTAGTGTTACAAGATGGAAAATTGATTCCTCTGACTTTGCTATTGATGTAGTGTGATAGAAAATTCACCCCT 481 CTGAACTGGCTCCTTCCCAGTCAAGGTTATCTGGTTTGATTGTATAATTTGCACCAAGAAGTTAAAATGTTTTATGACTC 561 TCTGTTCTGCTGACAGGCAGAGAGTCACATTGTGTAATTTAATTTCAGTCAGTCAATAGATGGCATCCCTCATCAGGGTT 641 GCCAGATGGTGATAACAGTGTAAGGCCTTGGGTCTAAGGCATCCACGACTGGAAGGGACTACTGATGTTCTGTGATACAT 721 CAGGTTTCAGCACACAACTTACATTTCTTTGCCTCCAAATTGAGGCATTTATTATGATGTTCATACTTTCCCTCTTGTTT 801 GAAAGTTTCTAATTATTAAATGGTGTCGGAATTGTTGTATTTTCCTTAGGAATTCAGTGGAACTTATCTTCATTAAATTT 881 AGCTGGTACCAGGTTGATATGACTTGTCAATATTATGGTCAACTTTAAGTCTTAGTTTTCGTTTGTGCCTTTGATTAATA 961 AGTATAACTCTTATACAATAAATACTGCTTTCCTCTAAAAAGATCGTGTTTAAATTAACTTGTAGAAAATCTGCTGGAAT 1041 GGTTGTTGTTTTCCACTGAGAAAGCTAAGCCCTACATTTCTATTCAGAGTACTGTTTTTAGATGTGAAATATAAGCCTGC 1121 GGCCTTAACTCTGTATTAAAAAAAATGTTTTTGTTTAAAAAAAACTGTTCCCATAGGTGCAGCAAACCACCATGGCACAT 1201 GTATACCTATGTAACAAACCTGCACATTCTGCACATGTATCCCAGAACTTAATGTAAACAAAAAAATCTTAAAGTGCAAA 1281 TATTAAAAAAAACTGTTCTCTGTGAAAAAAATTATATTCCATGTTATAAAGTAGCATATGACTAGTGTTCTCCTAGAGAT 1361 CAGACTTTTTTGATTGTATAGTTTGCATTAAAAAGTTGTACAGGGAGGGATGTAACCTGTATCTTCAGGATAATAGGGAA 1441 ATTAATAAGGAAAATAATAATTACTAAAATTTGAGTTGAAGTCAGGGAATTATTTCTTTGGTTTTGAGTCTCTTTATACA 1521 TCCATTAGTAGAACCTGTCTAGTCTGATTGCCACAGTCCTTGAATTGATGGTAAGGGGGAGTCAGTTACAGTTAGAAAAA 1601 AACCTGGGCAAAAACTACTAGTTAAATGATCATGAATTTTGAGTATGTGTTTTAAAATGCTTGGAGTTATTGCAGAAAAA 1681 TGATATTCTCCATTAGAACATTTGATGTGTGACTTTTGACATAGGATAAGGTGATAAGAAAATTAAGTTGAAAAATAGTG 1761 ACTCAAGTACAGCAAATCAGATTTTTGGCTACTGAGATTAAAGAAGCAAATATTTAAAGGATTATCAGCAATTTTCAAAT 1841 ACATATTTTTCACTGCAGTGGTTTTGAAGAATGTTTTAAGGTTATATTTAGAGTTTTTAAAAAAGTTTTCCCTCAGCCAG 1921 CCATGGTGGCTCACATCTGTAATCCCAGCACTTTGAGAGGCTGAGGCGGGCGGATCACCTGAGGTCAGGAGTTCTAGACC 2001 AGCCTGGCCAACATGGTAAAACACCGTCTCTAATAAAAATGCAAAAATTAGCTGGGTGTGGTGGCAAGCACCTGTAATCC 2081 CAGCTACTTGGGAGACTGAGGCAGGAGAATCACTTGAATCCAGGAGTCAGAGGTTGCAGTGAGCCGAGATCACACCACTG 2161 CACTCCAGCCTGGGCGATAAGAGTGAACCTGCATCTCAGAAAAAAAAAAAAAGTTTTCCCTCATTATTAAAAAGGAAAAA 2241 TTATAGAAAATTAAAATATAGAATGTAGAAAGAGGAAAAACACCACACATCACTCGTCAGGTGGATTGGTTTGTTTATTT 2321 TTAAGATGGGTTTATTTTGGATAGCCAGTTAGAAAACGCCCTTATAGCTGATGTGTGCTTGTGCATACTGAATTGTATAC 2401 TTAATTCTGAAAGTAATGAGGAAACATTTCACCTAATGATAACTGGTACAAAGGAAAGTTCACGTGTCTTTAATAGTTTG 2481 CTAATTAGACTAGCTGGTTAGAAAGAGGGATCACTAGATTGGAGAGAGAGATCCAGTTTCCACTGGAGGCAGTAGGTCTG 2561 CTCATTTCCATGGTGACAATCCTAATGGCAGAGGGAGTGAGTTTCCCTTAGTGGCACAGGCTGGGGGTTTTGAGCTTTTA 2641 AGTTTTGTTTTATAGAAATCTGGAGAATTTTACATTTTACTTCACTATATATCTATGTTTAAAATAATTCATTTTTGATG 2721 TCCCAAAATTGATGTGGGTTGCCTTATTTCCAGGCACCAGGTTGCTCACTGCAAGGTGACATTTTGAGAAGCAGAAATCT 2801 CTAGGTATATCTTAAGTGTGAAAAGCTTGTTAGATTTCCATGGCCTATTCCAGGTGGGTTGTTGGGTTTATGTTGTAAGC 2881 ATCAAACTTTTGTGGAAATAAATACCTAATACAAGGTAAAAAAAAAAAAAAA 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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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 | HEK293 | ||||||
Disease | 7105.0 | ||||||
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 GSM1065667. RNA binding protein: AGO1. Condition:4-thiouridine
... - Memczak S; Jens M; Elefsinioti A; Torti F; et al., 2013, Nature. |
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miRNA-target interactions (Provided by authors) |
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Article |
- Memczak S; Jens M; Elefsinioti A; Torti F; et al. - Nature, 2013
Circular RNAs (circRNAs) in animals are an enigmatic class of RNA with unknown function. To explore circRNAs systematically, we sequenced and computationally analysed human, mouse and nematode RNA. We detected thousands of well-expressed, stable circRNAs, often showing tissue/developmental-stage-specific expression. Sequence analysis indicated important regulatory functions for circRNAs. We found that a human circRNA, antisense to the cerebellar degeneration-related protein 1 transcript (CDR1as), is densely bound by microRNA (miRNA) effector complexes and harbours 63 conserved binding sites for the ancient miRNA miR-7. Further analyses indicated that CDR1as functions to bind miR-7 in neuronal tissues. Human CDR1as expression in zebrafish impaired midbrain development, similar to knocking down miR-7, suggesting that CDR1as is a miRNA antagonist with a miRNA-binding capacity ten times higher than any other known transcript. Together, our data provide evidence that circRNAs form a large class of post-transcriptional regulators. Numerous circRNAs form by head-to-tail splicing of exons, suggesting previously unrecognized regulatory potential of coding sequences.
LinkOut: [PMID: 23446348]
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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 | 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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CLIP-seq Support 1 for dataset GSM1065667 | |
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Method / RBP | PAR-CLIP / AGO1 |
Cell line / Condition | HEK293 / 4-thiouridine, ML_MM_6 |
Location of target site | ENST00000373020.4 | 3UTR | UAUACCUAUGUAACAAACCUGCACAUUCUGCACAUG |
Tools used in this analysis | TargetScan, miRTarCLIP, and Piranha |
Article / Accession Series | PMID: 23446348 / GSE43573 |
CLIP-seq Viewer | Link |
CLIP-seq Support 2 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 | ENST00000373020.4 | 3UTR | AUACCUAUGUAACAAACCUGCACAUUCUGCACAUG |
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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83 hsa-miR-4666a-5p Target Genes:
Functional analysis:
ID | Target | Description | Validation methods | |||||||||
Strong evidence | Less strong evidence | |||||||||||
MIRT057266 | FAM35A | family with sequence similarity 35 member A | 2 | 2 | ||||||||
MIRT059969 | PATL1 | PAT1 homolog 1, processing body mRNA decay factor | 2 | 6 | ||||||||
MIRT079031 | TNRC6C | trinucleotide repeat containing 6C | 2 | 2 | ||||||||
MIRT079631 | DNAJB4 | DnaJ heat shock protein family (Hsp40) member B4 | 2 | 2 | ||||||||
MIRT086974 | LANCL1 | LanC like 1 | 2 | 2 | ||||||||
MIRT091804 | GOLGA4 | golgin A4 | 2 | 2 | ||||||||
MIRT229501 | EIF1AX | eukaryotic translation initiation factor 1A, X-linked | 2 | 4 | ||||||||
MIRT255972 | WDR17 | WD repeat domain 17 | 2 | 2 | ||||||||
MIRT262975 | ADO | 2-aminoethanethiol dioxygenase | 2 | 2 | ||||||||
MIRT264774 | PAFAH1B2 | platelet activating factor acetylhydrolase 1b catalytic subunit 2 | 2 | 2 | ||||||||
MIRT334169 | CCND1 | cyclin D1 | 2 | 6 | ||||||||
MIRT345868 | SRSF2 | serine and arginine rich splicing factor 2 | 2 | 2 | ||||||||
MIRT452477 | DDX4 | DEAD-box helicase 4 | 2 | 2 | ||||||||
MIRT455764 | TSPAN6 | tetraspanin 6 | 2 | 4 | ||||||||
MIRT461627 | DCAF15 | DDB1 and CUL4 associated factor 15 | 2 | 4 | ||||||||
MIRT465169 | TRPV2 | transient receptor potential cation channel subfamily V member 2 | 2 | 4 | ||||||||
MIRT468950 | RPS14 | ribosomal protein S14 | 2 | 6 | ||||||||
MIRT483236 | C2orf72 | chromosome 2 open reading frame 72 | 2 | 8 | ||||||||
MIRT498544 | TMEM30B | transmembrane protein 30B | 2 | 2 | ||||||||
MIRT500633 | TXNIP | thioredoxin interacting protein | 2 | 4 | ||||||||
MIRT504113 | GPR158 | G protein-coupled receptor 158 | 2 | 2 | ||||||||
MIRT504428 | ZNF85 | zinc finger protein 85 | 2 | 6 | ||||||||
MIRT505036 | ZNF451 | zinc finger protein 451 | 2 | 2 | ||||||||
MIRT506526 | MRPL17 | mitochondrial ribosomal protein L17 | 2 | 6 | ||||||||
MIRT508773 | GSG1 | germ cell associated 1 | 2 | 2 | ||||||||
MIRT517297 | ELF4 | E74 like ETS transcription factor 4 | 2 | 6 | ||||||||
MIRT519353 | OBFC1 | STN1, CST complex subunit | 2 | 4 | ||||||||
MIRT523891 | ENPP6 | ectonucleotide pyrophosphatase/phosphodiesterase 6 | 2 | 6 | ||||||||
MIRT527509 | ZNF134 | zinc finger protein 134 | 2 | 2 | ||||||||
MIRT531218 | IFNGR2 | interferon gamma receptor 2 | 2 | 2 | ||||||||
MIRT535957 | MOGAT1 | monoacylglycerol O-acyltransferase 1 | 2 | 2 | ||||||||
MIRT537229 | GALNT7 | polypeptide N-acetylgalactosaminyltransferase 7 | 2 | 4 | ||||||||
MIRT537337 | FKBP5 | FK506 binding protein 5 | 2 | 2 | ||||||||
MIRT539125 | ARHGEF17 | Rho guanine nucleotide exchange factor 17 | 2 | 2 | ||||||||
MIRT539910 | ISPD | isoprenoid synthase domain containing | 2 | 2 | ||||||||
MIRT541527 | MGAT4C | MGAT4 family member C | 2 | 2 | ||||||||
MIRT546119 | USP25 | ubiquitin specific peptidase 25 | 2 | 2 | ||||||||
MIRT548846 | CERCAM | cerebral endothelial cell adhesion molecule | 2 | 2 | ||||||||
MIRT549892 | LINC00955 | long intergenic non-protein coding RNA 955 | 2 | 2 | ||||||||
MIRT549898 | ADH4 | alcohol dehydrogenase 4 (class II), pi polypeptide | 2 | 2 | ||||||||
MIRT550763 | ENOX2 | ecto-NOX disulfide-thiol exchanger 2 | 2 | 4 | ||||||||
MIRT553200 | UBE2A | ubiquitin conjugating enzyme E2 A | 2 | 2 | ||||||||
MIRT553970 | SRSF10 | serine and arginine rich splicing factor 10 | 2 | 2 | ||||||||
MIRT554092 | SMU1 | DNA replication regulator and spliceosomal factor | 2 | 2 | ||||||||
MIRT555208 | PROX1 | prospero homeobox 1 | 2 | 4 | ||||||||
MIRT555834 | PAX5 | paired box 5 | 2 | 4 | ||||||||
MIRT556865 | JAZF1 | JAZF zinc finger 1 | 2 | 2 | ||||||||
MIRT558594 | CREBL2 | cAMP responsive element binding protein like 2 | 2 | 2 | ||||||||
MIRT559690 | AGO2 | argonaute 2, RISC catalytic component | 2 | 4 | ||||||||
MIRT563312 | ORC4 | origin recognition complex subunit 4 | 2 | 2 | ||||||||
MIRT563585 | FAM229B | family with sequence similarity 229 member B | 2 | 2 | ||||||||
MIRT563853 | ALYREF | Aly/REF export factor | 2 | 4 | ||||||||
MIRT565146 | TUBB2A | tubulin beta 2A class IIa | 2 | 2 | ||||||||
MIRT565769 | SEPHS1 | selenophosphate synthetase 1 | 2 | 2 | ||||||||
MIRT568317 | BACH1 | BTB domain and CNC homolog 1 | 2 | 2 | ||||||||
MIRT575387 | Unc5b | unc-5 netrin receptor B | 2 | 4 | ||||||||
MIRT607728 | BDH1 | 3-hydroxybutyrate dehydrogenase 1 | 2 | 8 | ||||||||
MIRT612691 | PLXNA4 | plexin A4 | 2 | 4 | ||||||||
MIRT615916 | GDPD1 | glycerophosphodiester phosphodiesterase domain containing 1 | 2 | 2 | ||||||||
MIRT629792 | P2RY1 | purinergic receptor P2Y1 | 2 | 2 | ||||||||
MIRT632119 | FKBP9 | FK506 binding protein 9 | 2 | 2 | ||||||||
MIRT645554 | ZDHHC15 | zinc finger DHHC-type containing 15 | 2 | 4 | ||||||||
MIRT651479 | WWC3 | WWC family member 3 | 2 | 2 | ||||||||
MIRT654138 | RPH3A | rabphilin 3A | 2 | 6 | ||||||||
MIRT655191 | PHAX | phosphorylated adaptor for RNA export | 2 | 2 | ||||||||
MIRT665543 | UNC5B | unc-5 netrin receptor B | 2 | 5 | ||||||||
MIRT668057 | GRIK3 | glutamate ionotropic receptor kainate type subunit 3 | 2 | 2 | ||||||||
MIRT678978 | CERS4 | ceramide synthase 4 | 2 | 4 | ||||||||
MIRT679124 | RBM3 | RNA binding motif (RNP1, RRM) protein 3 | 2 | 2 | ||||||||
MIRT686776 | AZF1 | azoospermia factor 1 | 2 | 2 | ||||||||
MIRT687144 | PTPN12 | protein tyrosine phosphatase, non-receptor type 12 | 2 | 2 | ||||||||
MIRT691453 | C21orf58 | chromosome 21 open reading frame 58 | 2 | 2 | ||||||||
MIRT691469 | FAM98B | family with sequence similarity 98 member B | 2 | 2 | ||||||||
MIRT697031 | UHRF1BP1 | UHRF1 binding protein 1 | 2 | 2 | ||||||||
MIRT698401 | TM9SF3 | transmembrane 9 superfamily member 3 | 2 | 2 | ||||||||
MIRT702056 | RNMT | RNA guanine-7 methyltransferase | 2 | 2 | ||||||||
MIRT705903 | ADAM9 | ADAM metallopeptidase domain 9 | 2 | 2 | ||||||||
MIRT707491 | MMADHC | methylmalonic aciduria and homocystinuria, cblD type | 2 | 2 | ||||||||
MIRT708080 | KLHL23 | kelch like family member 23 | 2 | 2 | ||||||||
MIRT709738 | TRIM27 | tripartite motif containing 27 | 2 | 2 | ||||||||
MIRT710056 | RWDD2A | RWD domain containing 2A | 2 | 2 | ||||||||
MIRT710226 | KCNK1 | potassium two pore domain channel subfamily K member 1 | 2 | 2 | ||||||||
MIRT712043 | STYK1 | serine/threonine/tyrosine kinase 1 | 2 | 2 |