m6A-centered Crosstalk Information
Mechanism of Crosstalk between m6A Modification and Epigenetic Regulation
| Crosstalk ID |
M6ACROT05657
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[1] | |||
m6A modification
Circ_SETD2
Circ_SETD2
METTL3
Methylation
: m6A sites
Direct
Enhancement
Non-coding RNA
circSETD2
miR-181a-5p
lncRNA miRNA circRNA
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| m6A Modification: | |||||
|---|---|---|---|---|---|
| m6A Regulator | Methyltransferase-like 3 (METTL3) | WRITER | |||
| m6A Target | Circ_SETD2 | ||||
| Epigenetic Regulation that have Cross-talk with This m6A Modification: | |||||
| Epigenetic Regulation Type | Non-coding RNA (ncRNA) | ||||
| Epigenetic Regulator | Circ_SETD2 | circRNA | View Details | ||
| Regulated Target | hsa-miR-181a-5p | View Details | |||
| Crosstalk Relationship | m6A → ncRNA | Enhancement | |||
| Crosstalk Mechanism | m6A regulators directly modulate the functionality of ncRNAs through specific targeting ncRNA | ||||
| Crosstalk Summary | METTL3 overexpression increased total m6A, Circ_SETD2 m6A, and circSETD2 levels. m6A modification mediated circSETD2 upregulation. circSETD2 was a sponge of hsa-miR-181a-5p to elevate MCL1 transcription. miR-181a-5p overexpression or MCL1 silencing annulled the role of m6A-modified circSETD2. circSETD2 inhibition negated suppression of METTL3 overexpression on chorionic trophoblast apoptosis in vivo. Collectively, m6A modification of circSETD2 suppressed miR-181a-5p and increased MCL1 transcription, thus regulating trophoblasts. | ||||
| Responsed Disease | Pre-eclampsia | ICD-11: JA24 | |||
| Cell Process | Cell proliferation | ||||
| Cell invasion | |||||
| Cell apoptosis | |||||
In-vitro Model |
HTR-8/SVneo | Normal | Homo sapiens | CVCL_7162 | |
| In-vivo Model | Pregnant rats were randomly assigned to 5 groups: normal pregnancy (normal) group, PE group, circSETD2 overexpression (PE + oe-circSETD2) group, METTL3 overexpression (PE + oe-METTL3) group, overexpression control (PE + oe-NC) group, joint treatment (PE + oe-METTL3 + si-circSETD2) group, and joint treatment control (PE + oe-METTL3 + si-NC) group, with 6 rats in each group. After continuous injection of L-NAME for 4 days, the rats in the overexpression and overexpression control groups were further injected with 30 μl lentivirus vector oe-circSETD2, oe-METTL3 or oe-NC solution (GenePharma, Shanghai, China) through the tail vein; after continuous injection of L-NAME for 4 days, the rats in the PE + oe-METTL3 + si-circSETD2 group were further injected with 30 μl lentiviral vector oe-circSETD2 and si-circSETD2 (GenePharma) at the virus titer of 5 × 107 PFU/mL. The rats were euthanized on the 16th day of pregnancy. Then, the chorionic trophoblast tissues were isolated from the placenta of pregnant rats and divided into 2 parts, with 1 part for extraction and detection of tissue RNA, and the other part fixed in the buffer containing 10% formalin, embedded in paraffin, and made into 5 μm sections. | ||||
Full List of Potential Compound(s) Related to This m6A-centered Crosstalk
| JA24: Pre-eclampsia | 1 Compound(s) Regulating the Disease | Click to Show/Hide the Full List | ||
| Digibind | Phase 2 | [2] | ||
| Synonyms |
Digoxin Immune Fab (ovine); Ovine antidigoxin polyclonal antibody fragments (pre-eclampsia), BTG; Ovine antidigoxin polyclonal antibody fragments (pre-eclampsia), GlaxoSmithKline/Glenveigh
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| External Link | ||||
References
: m6A sites