pre-miRNA Information | |
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pre-miRNA | hsa-mir-3911 |
Genomic Coordinates | chr9: 127690687 - 127690795 |
Description | Homo sapiens miR-3911 stem-loop |
Comment | None |
RNA Secondary Structure |
Mature miRNA Information | ||||||||||||||||||||||||||||
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Mature miRNA | hsa-miR-3911 | |||||||||||||||||||||||||||
Sequence | 12| UGUGUGGAUCCUGGAGGAGGCA |33 | |||||||||||||||||||||||||||
Evidence | Experimental | |||||||||||||||||||||||||||
Experiments | Illumina | DRVs in miRNA |
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SNPs in miRNA |
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Putative Targets |
miRNA Expression profile | |
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Human miRNA Tissue Atlas | |
miRNAs in Extracellular Vesicles |
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Circulating MicroRNA Expression Profiling |
Gene Information | |||||||||||||||||||||
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Gene Symbol | MAT2A | ||||||||||||||||||||
Synonyms | MATA2, MATII, SAMS2 | ||||||||||||||||||||
Description | methionine adenosyltransferase 2A | ||||||||||||||||||||
Transcript | NM_005911 | ||||||||||||||||||||
Expression | |||||||||||||||||||||
Putative miRNA Targets on MAT2A | |||||||||||||||||||||
3'UTR of MAT2A (miRNA target sites are highlighted) |
>MAT2A|NM_005911|3'UTR 1 AAGTGTTAGCCTTTTTTCCCCAGACTTGTTGGCGTAGGCTACAGAGAAGCCTTCAAGCTCTGAGGGAAAGGGCCCTCCTT 81 CCTAAATTTTCCTGTCCTCTTTCAGCTCCTGACCAGTTGCAGTCACTCTAGTCAATGACATGAATTTTAGCTTTTGTGGG 161 GGACTGTAAGTTGGGCTTGCTATTCTGTCCCTAGGTGTTTTGTTCACCATTATAATGAATTTAGTGAGCATAGGTGATCC 241 ATGTAACTGCCTAGAAACAACACTGTAGTAAATAATGCTTTGAAATTGAACCTTTGTGCCCTATCACCCAACGCTCCAAA 321 GTCATAATTGCATTGACTTTCCCCACCAGATGCTGAAAATGTCCTTGTGATGTGCACGTAAAGTACTTGTAGTTCCACTT 401 ATAGCCTCTGTCTGGCAATGCCACAGCCCTGTCAGCATGAATTTGTAATGTCTTGAGCTCTATTATGAATGTGAAGCCTT 481 CCCCTTATCCTCCCTGTAACTTGATCCATTTCTAATTATGTAGCTCTTTGTCAGGGAGTGTTCCCTATCCAATCAATCTT 561 GCATGTAACGCAAGTTCCCAGTTGGAGCTCCAGCCTGACATCAAAAAAGGCAGTTACCATTAAACCATCTCCCTGGTGCT 641 TATGCTCTTAATTGCCACCTCTAACAGCACCAAATCAAAATCTCTCCACTTTCAGCTGTCTTTTGGAGGACGTACGTAAT 721 AAGGTTTTAATTTAGTAAACCAATCCTATGCATGGTTTCAGCACTAGCCAAACCTCACCAACTCCTAGTTCTAGAAAAAC 801 AGGCACTTGGCAGCCTTGTGATGTCATACAGAGAAGTCACAGGGCAGTACCTGAGGGTCTGTAGGTTGCACACTTTGGTA 881 CCAGATAACTTTTTTTTTTCTTTATAAGAAAGCCTGAGTACTCCACACTGCACAATAACTCCTCCCAGGGTTTTAACTTT 961 GTTTTATTTTCAAAACCAGGTCCAATGAGCTTTCTGAACAGCTGGTGTAGCTACAGAGAAACCAGCTTCCTTCAGAGAGC 1041 AGTGCTTTTGGCGGGGAGGAGGAAATCCCTTCATACTTGAACGTTTTCTAATTGCTTATTTATTGTATTCTGGGGTATGG 1121 CGTAAGTACAGAGAAGCCATCACCTCAGATGGCAGCTTTTAAAAGATTTTTTTTTTTTCTCTCAACACCATGATTCCTTT 1201 AACAACATGTTTCCAGCATTCCCAGGTAGGCCAAGGTGTCCTACAGAAAAACCTTGGGTTAGACCTACAGGGGGTCTGGC 1281 TGGTGTTAACAGAAGGGAGGGCAGAGCTGGTGCGGCTGGCCATGGAGAAAGCTGACTTGGCTGGTGTGGTACAGAGAAGC 1361 CAGCTTGTTTACATGCTTATTCCATGACTGCTTGCCCTAAGCAGAAAGTGCCTTTCAGGATCTATTTTTGGAGGTTTATT 1441 ACGTATGTCTGGTTCTCAATTCCAACAGTTTAATGAAGATCTAAATAAAATGCTAGGTTCTACCTTAAAAAAAAAAAAAA 1521 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 | HEK293 |
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 GSM545216. RNA binding protein: AGO2. Condition:miR-124 transfection
... - Hafner M; Landthaler M; Burger L; Khorshid et al., 2010, Cell. |
Article |
- Hafner M; Landthaler M; Burger L; Khorshid et al. - Cell, 2010
RNA transcripts are subject to posttranscriptional gene regulation involving hundreds of RNA-binding proteins (RBPs) and microRNA-containing ribonucleoprotein complexes (miRNPs) expressed in a cell-type dependent fashion. We developed a cell-based crosslinking approach to determine at high resolution and transcriptome-wide the binding sites of cellular RBPs and miRNPs. The crosslinked sites are revealed by thymidine to cytidine transitions in the cDNAs prepared from immunopurified RNPs of 4-thiouridine-treated cells. We determined the binding sites and regulatory consequences for several intensely studied RBPs and miRNPs, including PUM2, QKI, IGF2BP1-3, AGO/EIF2C1-4 and TNRC6A-C. Our study revealed that these factors bind thousands of sites containing defined sequence motifs and have distinct preferences for exonic versus intronic or coding versus untranslated transcript regions. The precise mapping of binding sites across the transcriptome will be critical to the interpretation of the rapidly emerging data on genetic variation between individuals and how these variations contribute to complex genetic diseases.
LinkOut: [PMID: 20371350]
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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 | HEK293 | ||||||
Disease | 4144.0 | ||||||
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 GSM1065669. RNA binding protein: AGO1. Condition:4-thiouridine
"PAR-CLIP data was present in GSM1065670. RNA binding protein: AGO2. 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 3 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) |
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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. |
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 GSM545216 | |
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Method / RBP | PAR-CLIP / AGO2 |
Cell line / Condition | HEK293 / miR-124 transfection |
Location of target site | ENST00000306434.3 | 3UTR | AUAACUUUUUUUUUUCUUUAUAAGAAAGCCUGAGUACUCCACACUGCACAAUAACUCCUCCCAGGGUUUUAACUUUGUUUUAUUUUCAAAACCAGGUCCAAUGAGCUUUC |
Tools used in this analysis | TargetScan, miRTarCLIP, and Piranha |
Article / Accession Series | PMID: 20371350 / GSE21578 |
CLIP-seq Viewer | Link |
CLIP-seq Support 2 for dataset GSM1065669 | |
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Method / RBP | PAR-CLIP / AGO1 |
Cell line / Condition | HEK293 / 4-thiouridine, ML_MM_8 |
Location of target site | ENST00000306434.3 | 3UTR | CCUGAGUACUCCACACUGCACAAUAACUCCUCCCAG |
Tools used in this analysis | TargetScan, miRTarCLIP, and Piranha |
Article / Accession Series | PMID: 23446348 / GSE43573 |
CLIP-seq Viewer | Link |
CLIP-seq Support 3 for dataset GSM1065670 | |
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Method / RBP | PAR-CLIP / AGO2 |
Cell line / Condition | HEK293 / 4-thiouridine, 3_ML_LG |
Location of target site | ENST00000306434.3 | 3UTR | UACUCCACACUGCACAAUAACUCCUCCCAGGGUUUU |
Tools used in this analysis | TargetScan, miRTarCLIP, and Piranha |
Article / Accession Series | PMID: 23446348 / GSE43573 |
CLIP-seq Viewer | Link |
CLIP-seq Support 4 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 | ENST00000306434.3 | 3UTR | UACUCCACACUGCACAAUAACUCCUCCCAG |
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-3911 Target Genes:
Functional analysis:
ID | Target | Description | Validation methods | |||||||||
Strong evidence | Less strong evidence | |||||||||||
MIRT207399 | MAT2A | methionine adenosyltransferase 2A | 2 | 6 | ||||||||
MIRT284537 | PDP2 | pyruvate dehyrogenase phosphatase catalytic subunit 2 | 2 | 2 | ||||||||
MIRT291946 | TPM4 | tropomyosin 4 | 2 | 2 | ||||||||
MIRT293609 | PVR | poliovirus receptor | 2 | 2 | ||||||||
MIRT357688 | PAIP2 | poly(A) binding protein interacting protein 2 | 2 | 2 | ||||||||
MIRT451607 | MEIS3P1 | Meis homeobox 3 pseudogene 1 | 2 | 2 | ||||||||
MIRT452110 | IFITM1 | interferon induced transmembrane protein 1 | 2 | 2 | ||||||||
MIRT457804 | KLHL25 | kelch like family member 25 | 2 | 2 | ||||||||
MIRT462730 | EFNB1 | ephrin B1 | 2 | 2 | ||||||||
MIRT463219 | ZNF131 | zinc finger protein 131 | 2 | 2 | ||||||||
MIRT464141 | VPS28 | VPS28, ESCRT-I subunit | 2 | 2 | ||||||||
MIRT467582 | SLC7A5 | solute carrier family 7 member 5 | 2 | 6 | ||||||||
MIRT470824 | PLXND1 | plexin D1 | 2 | 2 | ||||||||
MIRT474230 | LCLAT1 | lysocardiolipin acyltransferase 1 | 2 | 2 | ||||||||
MIRT478989 | COLGALT1 | collagen beta(1-O)galactosyltransferase 1 | 2 | 2 | ||||||||
MIRT479462 | CDK6 | cyclin dependent kinase 6 | 2 | 2 | ||||||||
MIRT483558 | SYT2 | synaptotagmin 2 | 2 | 2 | ||||||||
MIRT484483 | SLC9A1 | solute carrier family 9 member A1 | 2 | 2 | ||||||||
MIRT485224 | PRICKLE1 | prickle planar cell polarity protein 1 | 2 | 2 | ||||||||
MIRT490356 | DPYSL5 | dihydropyrimidinase like 5 | 2 | 4 | ||||||||
MIRT493177 | MKNK2 | MAP kinase interacting serine/threonine kinase 2 | 2 | 2 | ||||||||
MIRT509802 | CHAF1B | chromatin assembly factor 1 subunit B | 2 | 4 | ||||||||
MIRT511815 | HDGF | heparin binding growth factor | 2 | 2 | ||||||||
MIRT512254 | ARPP19 | cAMP regulated phosphoprotein 19 | 2 | 6 | ||||||||
MIRT513025 | GPT2 | glutamic--pyruvic transaminase 2 | 2 | 2 | ||||||||
MIRT519640 | ZNF772 | zinc finger protein 772 | 2 | 4 | ||||||||
MIRT531178 | SIGLEC12 | sialic acid binding Ig like lectin 12 (gene/pseudogene) | 2 | 2 | ||||||||
MIRT537870 | EDA2R | ectodysplasin A2 receptor | 2 | 2 | ||||||||
MIRT551914 | IGLON5 | IgLON family member 5 | 2 | 2 | ||||||||
MIRT558359 | DMTF1 | cyclin D binding myb like transcription factor 1 | 2 | 2 | ||||||||
MIRT559771 | URGCP-MRPS24 | URGCP-MRPS24 readthrough | 2 | 4 | ||||||||
MIRT559813 | ZNF83 | zinc finger protein 83 | 2 | 2 | ||||||||
MIRT561999 | LPP | LIM domain containing preferred translocation partner in lipoma | 2 | 2 | ||||||||
MIRT565754 | SERTAD2 | SERTA domain containing 2 | 2 | 2 | ||||||||
MIRT569423 | DCAF8 | DDB1 and CUL4 associated factor 8 | 2 | 2 | ||||||||
MIRT569845 | RGS5 | regulator of G protein signaling 5 | 2 | 2 | ||||||||
MIRT606928 | CDK15 | cyclin dependent kinase 15 | 2 | 2 | ||||||||
MIRT607616 | TMEM130 | transmembrane protein 130 | 2 | 4 | ||||||||
MIRT607629 | TRIOBP | TRIO and F-actin binding protein | 2 | 2 | ||||||||
MIRT607885 | SATB1 | SATB homeobox 1 | 2 | 2 | ||||||||
MIRT607942 | SSX2 | SSX family member 2 | 2 | 4 | ||||||||
MIRT608017 | CARNS1 | carnosine synthase 1 | 2 | 4 | ||||||||
MIRT608036 | UBLCP1 | ubiquitin like domain containing CTD phosphatase 1 | 2 | 2 | ||||||||
MIRT608063 | SSX2B | SSX family member 2B | 2 | 4 | ||||||||
MIRT608558 | SBK1 | SH3 domain binding kinase 1 | 2 | 6 | ||||||||
MIRT608915 | NCDN | neurochondrin | 2 | 6 | ||||||||
MIRT615876 | HIF1AN | hypoxia inducible factor 1 alpha subunit inhibitor | 2 | 4 | ||||||||
MIRT618023 | ELFN1 | extracellular leucine rich repeat and fibronectin type III domain containing 1 | 2 | 2 | ||||||||
MIRT620505 | SNRPD1 | small nuclear ribonucleoprotein D1 polypeptide | 2 | 2 | ||||||||
MIRT628101 | IL1RAPL1 | interleukin 1 receptor accessory protein like 1 | 2 | 2 | ||||||||
MIRT628700 | ZNF548 | zinc finger protein 548 | 2 | 2 | ||||||||
MIRT630658 | POU2F1 | POU class 2 homeobox 1 | 2 | 2 | ||||||||
MIRT643508 | ZNF28 | zinc finger protein 28 | 2 | 2 | ||||||||
MIRT646379 | SLC22A6 | solute carrier family 22 member 6 | 2 | 2 | ||||||||
MIRT660041 | C15orf61 | chromosome 15 open reading frame 61 | 2 | 2 | ||||||||
MIRT687700 | KRR1 | KRR1, small subunit processome component homolog | 2 | 2 | ||||||||
MIRT688858 | CAMKK2 | calcium/calmodulin dependent protein kinase kinase 2 | 2 | 2 | ||||||||
MIRT690443 | REPIN1 | replication initiator 1 | 2 | 2 | ||||||||
MIRT690456 | ZNF33A | zinc finger protein 33A | 2 | 2 | ||||||||
MIRT693796 | RHOG | ras homolog family member G | 2 | 2 | ||||||||
MIRT694274 | ZNF529 | zinc finger protein 529 | 2 | 4 | ||||||||
MIRT697697 | WAC | WW domain containing adaptor with coiled-coil | 2 | 2 | ||||||||
MIRT700242 | RCC2 | regulator of chromosome condensation 2 | 2 | 2 | ||||||||
MIRT701836 | MRPL37 | mitochondrial ribosomal protein L37 | 2 | 2 | ||||||||
MIRT704255 | DHCR24 | 24-dehydrocholesterol reductase | 2 | 2 | ||||||||
MIRT707203 | SDK2 | sidekick cell adhesion molecule 2 | 2 | 2 | ||||||||
MIRT710365 | CREB5 | cAMP responsive element binding protein 5 | 2 | 2 | ||||||||
MIRT711943 | WDFY1 | WD repeat and FYVE domain containing 1 | 2 | 2 | ||||||||
MIRT715496 | MAZ | MYC associated zinc finger protein | 2 | 2 | ||||||||
MIRT719250 | MS4A1 | membrane spanning 4-domains A1 | 2 | 2 |
miRNA-Drug Associations | ||||||||||||||||||
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miRNA-Drug Resistance Associations | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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