pre-miRNA Information | |
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pre-miRNA | hsa-mir-3618 |
Genomic Coordinates | chr22: 20085746 - 20085833 |
Description | Homo sapiens miR-3618 stem-loop |
Comment | None |
RNA Secondary Structure |
Mature miRNA Information | |||||||||||||||
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Mature miRNA | hsa-miR-3618 | ||||||||||||||
Sequence | 52| UGUCUACAUUAAUGAAAAGAGC |73 | ||||||||||||||
Evidence | Experimental | ||||||||||||||
Experiments | Illumina | ||||||||||||||
Editing Events in miRNAs |
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DRVs in miRNA |
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SNPs in miRNA |
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Putative Targets |
Gene Information | |||||||||||||||||||||
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Gene Symbol | PDE4DIP | ||||||||||||||||||||
Synonyms | CMYA2, MMGL | ||||||||||||||||||||
Description | phosphodiesterase 4D interacting protein | ||||||||||||||||||||
Transcript | NM_001002811 | ||||||||||||||||||||
Other Transcripts | NM_001002810 , NM_001002812 , NM_014644 , NM_022359 | ||||||||||||||||||||
Expression | |||||||||||||||||||||
Putative miRNA Targets on PDE4DIP | |||||||||||||||||||||
3'UTR of PDE4DIP (miRNA target sites are highlighted) |
>PDE4DIP|NM_001002811|3'UTR 1 CTTCAGAAGCATTTTTACTTGCAAGACGATGGACACATTCCCCTTGGGCTTTTTGTAACTGAAACGCACCACAGAAGACA 81 GGGAGTCATCGAAGGGCTGCTCGGGGAGGTGGCAGGGCGGAGGACCTGCTTGGGAAGAAACTCCAAGAAGATTGGAATGC 161 TTCCAAAGCAAGAATCTTTCTCAGTGAAATCTCATTATACAAAGAGAACCTTATGCAACCTGACAAACCACTGAGGTCAT 241 GGTGACTCAGTGATCAGCAGATGGTACTTCAACAGCAATCCCCTGTCAAACCTCAGAACTTGAGGCTGAAACATTGCTTC 321 CACCCACCATCAGTGAAGATGTAACTAGCATGTTACAAGAGTGAATAATCTGGACTTCAGAGATTAAGTCACCAATAGTG 401 ATCTCACAAGCACTCACCGGAACTCCTATAATGTCTCCACTTTGTCCATGCCATTTAGCAATCTCATCTCCTAAATGGAC 481 TGTGCCTATGATTCTTAAGGAGAAAGTGAATCATTGGTAGATATCCTGCACAAGCAGCTGGACTTTCCAGTAATAGCTTT 561 CTTGGGGCTATTAGGAAAATTAAACAAGAAATGAGGCTTTCTGGGTCTGCCTGTATGTCTTCTGCATAAGACAAAGAAGA 641 GACATCGAATCAACCAATAAGAAGAGCCCAAATAAGCATCCTCAAATCTTTTGGGATTTGGCACTTGGGGACATGAGTAG 721 TTGTCTGGGATACGTCATATTCTCAACAGTTTCTTTGTAGTAGTAGGATCACCTTCTTATAATAGGATCACCTTCTTGTT 801 GCTATAGCTGTACCCGACCTTCCCTTCTCCCTTGAGTGCTTGCATGAGCTCCACTTTTCCTTTTGCTTGAACAGCTTCTC 881 CTGAGTCCTCCTTACCGATGGTTGTGACTTTAATTATATACATCTCTGTCCCTCCAGACAGATCCCTCTGTCCTCACTCT 961 CTGATTTCATTGAGGATCTTGGGTGAGAGAGAGGGACCTGCAGGATGAACAAATGTCTACTCTAAGACAGCTAGATTGGG 1041 AGGTTGGCTGGTCACTGATGGTTATAATGACTGTGGGACAGGATTAACTTCAGAATAAATGAACAGGAGACACAGATATG 1121 AAGAAAGTTTCTGATTGATATGGTCTGAAGTACTCCTGGTATTGCAAGTCATTTGCTCTAATTCTCAATTGTAGGCAAAC 1201 TGATTTGTAAATTTGCTTCTTCAGCCTTCTTTCCTGTAGCCTAGCATGGAGAATCTGACCAGACCCCATTTTGAGAAGGT 1281 CAGCCTACACTGGAATGAACTTTTTACATTAGGGCATTTGTATTTCCCTCACAATACTTGCCACATTACTTGGCATAGGA 1361 GAGATGCTTAGTGTAATTATAAGTTAACAAGCCTTTGGATCAGGGCTTGACTCATGATAGACAAAGTATATGCCTGCTGG 1441 ATGGAAGAATCTCTTGGGCGAGCACCATTTTTCTTTCCATCACCTTTCCTTGAAAATATATCTTCAGCTTTGGGTAGGAG 1521 GAATCTTGGTGTATGAAATCATTGCAAATTTACTTCATCTTTTCTGGAGTTTGAAGTTGTGACTCTCCTGCTACCAATTA 1601 AATAAAGCTTACTTTGCCATAACAAAAAAAAA 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 | hESCs (WA-09) | ||||||
Disease | 9659.0 | ||||||
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 SRR359787. RNA binding protein: AGO2. Condition:4-thiouridine
... - Lipchina I; Elkabetz Y; Hafner M; Sheridan et al., 2011, Genes & development. |
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miRNA-target interactions (Provided by authors) |
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Article |
- Lipchina I; Elkabetz Y; Hafner M; Sheridan et al. - Genes & development, 2011
MicroRNAs are important regulators in many cellular processes, including stem cell self-renewal. Recent studies demonstrated their function as pluripotency factors with the capacity for somatic cell reprogramming. However, their role in human embryonic stem (ES) cells (hESCs) remains poorly understood, partially due to the lack of genome-wide strategies to identify their targets. Here, we performed comprehensive microRNA profiling in hESCs and in purified neural and mesenchymal derivatives. Using a combination of AGO cross-linking and microRNA perturbation experiments, together with computational prediction, we identified the targets of the miR-302/367 cluster, the most abundant microRNAs in hESCs. Functional studies identified novel roles of miR-302/367 in maintaining pluripotency and regulating hESC differentiation. We show that in addition to its role in TGF-beta signaling, miR-302/367 promotes bone morphogenetic protein (BMP) signaling by targeting BMP inhibitors TOB2, DAZAP2, and SLAIN1. This study broadens our understanding of microRNA function in hESCs and is a valuable resource for future studies in this area.
LinkOut: [PMID: 22012620]
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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/HeLa |
Location of target site | 3'UTR |
Tools used in this research | TargetScan , miRTarCLIP , Piranha |
Original Description (Extracted from the article) |
...
HITS-CLIP data was present in GSM1067869. RNA binding protein: AGO2. Condition:Ago2 IP-seq (asynchronous cells)
HITS-CLIP data was present in GSM1067870. RNA binding protein: AGO2. Condition:Ago2 IP-seq (mitotic cells)
... - Kishore S; Gruber AR; Jedlinski DJ; Syed et al., 2013, Genome biology. |
Article |
- Kishore S; Gruber AR; Jedlinski DJ; Syed et al. - Genome biology, 2013
BACKGROUND: In recent years, a variety of small RNAs derived from other RNAs with well-known functions such as tRNAs and snoRNAs, have been identified. The functional relevance of these RNAs is largely unknown. To gain insight into the complexity of snoRNA processing and the functional relevance of snoRNA-derived small RNAs, we sequence long and short RNAs, small RNAs that co-precipitate with the Argonaute 2 protein and RNA fragments obtained in photoreactive nucleotide-enhanced crosslinking and immunoprecipitation (PAR-CLIP) of core snoRNA-associated proteins. RESULTS: Analysis of these data sets reveals that many loci in the human genome reproducibly give rise to C/D box-like snoRNAs, whose expression and evolutionary conservation are typically less pronounced relative to the snoRNAs that are currently cataloged. We further find that virtually all C/D box snoRNAs are specifically processed inside the regions of terminal complementarity, retaining in the mature form only 4-5 nucleotides upstream of the C box and 2-5 nucleotides downstream of the D box. Sequencing of the total and Argonaute 2-associated populations of small RNAs reveals that despite their cellular abundance, C/D box-derived small RNAs are not efficiently incorporated into the Ago2 protein. CONCLUSIONS: We conclude that the human genome encodes a large number of snoRNAs that are processed along the canonical pathway and expressed at relatively low levels. Generation of snoRNA-derived processing products with alternative, particularly miRNA-like, functions appears to be uncommon.
LinkOut: [PMID: 23706177]
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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 | HEK293S |
Location of target site | 3'UTR |
Tools used in this research | TargetScan , miRTarCLIP , Piranha |
Original Description (Extracted from the article) |
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HITS-CLIP data was present in GSM1084046. RNA binding protein: AGO2. Condition:CLIP_noarsenite_rep4
HITS-CLIP data was present in GSM1084079. RNA binding protein: AGO2. Condition:CLIP_hippuristanol_rep2_AbnovaAb
... - Karginov FV; Hannon GJ, 2013, Genes & development. |
Article |
- Karginov FV; Hannon GJ - Genes & development, 2013
When adapting to environmental stress, cells attenuate and reprogram their translational output. In part, these altered translation profiles are established through changes in the interactions between RNA-binding proteins and mRNAs. The Argonaute 2 (Ago2)/microRNA (miRNA) machinery has been shown to participate in stress-induced translational up-regulation of a particular mRNA, CAT-1; however, a detailed, transcriptome-wide understanding of the involvement of Ago2 in the process has been lacking. Here, we profiled the overall changes in Ago2-mRNA interactions upon arsenite stress by cross-linking immunoprecipitation (CLIP) followed by high-throughput sequencing (CLIP-seq). Ago2 displayed a significant remodeling of its transcript occupancy, with the majority of 3' untranslated region (UTR) and coding sequence (CDS) sites exhibiting stronger interaction. Interestingly, target sites that were destined for release from Ago2 upon stress were depleted in miRNA complementarity signatures, suggesting an alternative mode of interaction. To compare the changes in Ago2-binding patterns across transcripts with changes in their translational states, we measured mRNA profiles on ribosome/polysome gradients by RNA sequencing (RNA-seq). Increased Ago2 occupancy correlated with stronger repression of translation for those mRNAs, as evidenced by a shift toward lighter gradient fractions upon stress, while release of Ago2 was associated with the limited number of transcripts that remained translated. Taken together, these data point to a role for Ago2 and the mammalian miRNAs in mediating the translational component of the stress response.
LinkOut: [PMID: 23824327]
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Experimental Support 4 for Functional miRNA-Target Interaction | |
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miRNA:Target | ---- |
Validation Method |
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Conditions | Cardiac Tissues |
Location of target site | 3'UTR |
Tools used in this research | TargetScan , miRTarCLIP , Piranha |
Original Description (Extracted from the article) |
...
HITS-CLIP data was present in GSM2202479. RNA binding protein: AGO2. Condition:S4_LV_29yo_Male_AGO2_bound_RNA
... - Spengler RM; Zhang X; Cheng C; McLendon JM; et al., 2016, Nucleic acids research. |
Article |
Elucidation of transcriptome-wide microRNA binding sites in human cardiac tissues by Ago2 HITS-CLIP.
- Spengler RM; Zhang X; Cheng C; McLendon JM; et al.- Nucleic acids research, 2016
MicroRNAs (miRs) have emerged as key biological effectors in human health and disease. These small noncoding RNAs are incorporated into Argonaute (Ago) proteins, where they direct post-transcriptional gene silencing via base-pairing with target transcripts. Although miRs have become intriguing biological entities and attractive therapeutic targets, the translational impacts of miR research remain limited by a paucity of empirical miR targeting data, particularly in human primary tissues. Here, to improve our understanding of the diverse roles miRs play in cardiovascular function and disease, we applied high-throughput methods to globally profile miR:target interactions in human heart tissues. We deciphered Ago2:RNA interactions using crosslinking immunoprecipitation coupled with high-throughput sequencing (HITS-CLIP) to generate the first transcriptome-wide map of miR targeting events in human myocardium, detecting 4000 cardiac Ago2 binding sites across >2200 target transcripts. Our initial exploration of this interactome revealed an abundance of miR target sites in gene coding regions, including several sites pointing to new miR-29 functions in regulating cardiomyocyte calcium, growth and metabolism. Also, we uncovered several clinically-relevant interactions involving common genetic variants that alter miR targeting events in cardiomyopathy-associated genes. Overall, these data provide a critical resource for bolstering translational miR research in heart, and likely beyond.
LinkOut: [PMID: 27418678]
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CLIP-seq Support 1 for dataset GSM1067869 | |
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Method / RBP | HITS-CLIP / AGO2 |
Cell line / Condition | HEK293/HeLa / Ago2 IP-seq (asynchronous cells) |
Location of target site | ENST00000369345.4 | 3UTR | GACCUCUCUCUCUCUCUCUCU |
Tools used in this analysis | TargetScan, miRTarCLIP, and Piranha |
Article / Accession Series | PMID: 23706177 / GSE43666 |
CLIP-seq Viewer | Link |
CLIP-seq Support 2 for dataset GSM1067870 | |
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Method / RBP | HITS-CLIP / AGO2 |
Cell line / Condition | HEK293/HeLa / Ago2 IP-seq (mitotic cells) |
Location of target site | ENST00000369345.4 | 3UTR | GACCUCUCUCUCUCUCUCUCUC |
Tools used in this analysis | TargetScan, miRTarCLIP, and Piranha |
Article / Accession Series | PMID: 23706177 / GSE43666 |
CLIP-seq Viewer | Link |
CLIP-seq Support 3 for dataset GSM1084046 | |
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Method / RBP | HITS-CLIP / AGO2 |
Cell line / Condition | HEK293S / CLIP_noarsenite_rep4 |
Location of target site | ENST00000369345.4 | 3UTR | UGUAGACCUCUCUCUCUCUCUCUCUCUCUCUC |
Tools used in this analysis | TargetScan, miRTarCLIP, and Piranha |
Article / Accession Series | PMID: 23824327 / GSE44404 |
CLIP-seq Viewer | Link |
CLIP-seq Support 4 for dataset GSM1084079 | |
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Method / RBP | HITS-CLIP / AGO2 |
Cell line / Condition | HEK293S / CLIP_hippuristanol_rep2_AbnovaAb |
Location of target site | ENST00000369345.4 | 3UTR | UAGACCUCUCUCUCUCUCUCUCUCU |
Tools used in this analysis | TargetScan, miRTarCLIP, and Piranha |
Article / Accession Series | PMID: 23824327 / GSE44404 |
CLIP-seq Viewer | Link |
CLIP-seq Support 5 for dataset SRR359787 | |
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Method / RBP | PAR-CLIP / AGO2 |
Cell line / Condition | hESCs (WA-09) / 4-thiouridine, RNase T1 |
Location of target site | ENST00000369345.4 | 3UTR | GAUGAACUGUAGACC |
Tools used in this analysis | TargetScan, miRTarCLIP, and Piranha |
Article / Accession Series | PMID: 22012620 / SRX103431 |
CLIP-seq Viewer | Link |
MiRNA-Target Expression Profile | |||||||
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MiRNA-Target Expression Profile (TCGA) | |||||||
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29 hsa-miR-3618 Target Genes:
Functional analysis:
ID | Target | Description | Validation methods | |||||||||
Strong evidence | Less strong evidence | |||||||||||
MIRT378435 | SOX4 | SRY-box 4 | 2 | 2 | ||||||||
MIRT459627 | GABARAP | GABA type A receptor-associated protein | 2 | 2 | ||||||||
MIRT471295 | PGAM4 | phosphoglycerate mutase family member 4 | 2 | 2 | ||||||||
MIRT471369 | PDZD8 | PDZ domain containing 8 | 2 | 2 | ||||||||
MIRT504886 | MRPL51 | mitochondrial ribosomal protein L51 | 2 | 2 | ||||||||
MIRT505938 | RBM33 | RNA binding motif protein 33 | 2 | 8 | ||||||||
MIRT525461 | TMPRSS12 | transmembrane protease, serine 12 | 2 | 2 | ||||||||
MIRT526767 | ZNF527 | zinc finger protein 527 | 2 | 2 | ||||||||
MIRT526990 | ARL8B | ADP ribosylation factor like GTPase 8B | 2 | 2 | ||||||||
MIRT528669 | PDE4DIP | phosphodiesterase 4D interacting protein | 2 | 6 | ||||||||
MIRT538462 | CNBP | CCHC-type zinc finger nucleic acid binding protein | 2 | 2 | ||||||||
MIRT542899 | HSBP1 | heat shock factor binding protein 1 | 2 | 2 | ||||||||
MIRT550274 | AHI1 | Abelson helper integration site 1 | 2 | 2 | ||||||||
MIRT551674 | BBS5 | Bardet-Biedl syndrome 5 | 2 | 2 | ||||||||
MIRT551689 | ASB16 | ankyrin repeat and SOCS box containing 16 | 2 | 2 | ||||||||
MIRT551755 | TRIM42 | tripartite motif containing 42 | 2 | 2 | ||||||||
MIRT555769 | PCMTD1 | protein-L-isoaspartate (D-aspartate) O-methyltransferase domain containing 1 | 2 | 2 | ||||||||
MIRT556241 | MARCH9 | membrane associated ring-CH-type finger 9 | 2 | 2 | ||||||||
MIRT556926 | IRF2BP2 | interferon regulatory factor 2 binding protein 2 | 2 | 4 | ||||||||
MIRT562638 | ARID1A | AT-rich interaction domain 1A | 2 | 2 | ||||||||
MIRT571348 | RPL37 | ribosomal protein L37 | 2 | 2 | ||||||||
MIRT612818 | KLHL3 | kelch like family member 3 | 2 | 2 | ||||||||
MIRT619329 | TIPRL | TOR signaling pathway regulator | 2 | 4 | ||||||||
MIRT653927 | SERPINC1 | serpin family C member 1 | 2 | 2 | ||||||||
MIRT659150 | DDHD1 | DDHD domain containing 1 | 2 | 2 | ||||||||
MIRT688334 | FAM126B | family with sequence similarity 126 member B | 2 | 2 | ||||||||
MIRT694760 | FZD2 | frizzled class receptor 2 | 2 | 2 | ||||||||
MIRT700477 | PUM1 | pumilio RNA binding family member 1 | 2 | 2 | ||||||||
MIRT702375 | KLF10 | Kruppel like factor 10 | 2 | 2 |
miRNA-Drug Resistance Associations | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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