m6A Target Gene Information
General Information of the m6A Target Gene (ID: M6ATAR00565)
Full List of m6A Methylation Regulator of This Target Gene and Corresponding Disease/Drug Response(s)
MNK2
can be regulated by the following regulator(s), and cause disease/drug response(s). You can browse detail information of regulator(s) or disease/drug response(s).
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Methyltransferase-like 3 (METTL3) [WRITER]
Representative RNA-seq result indicating the expression of this target gene regulated by METTL3 | ||
Cell Line | LX2 cell line | Homo sapiens |
Treatment: shMETTL3 LX2 cells
Control: shLuc LX2 cells
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GSE207909 | |
Regulation |
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logFC: 1.09E+00 p-value: 4.06E-29 |
More Results | Click to View More RNA-seq Results | |
Representative RIP-seq result supporting the interaction between MNK2 and the regulator | ||
Cell Line | MDA-MB-231 | Homo sapiens |
Regulation | logFC: 1.25E+00 | GSE60213 |
In total 1 item(s) under this regulator | ||||
Experiment 1 Reporting the m6A Methylation Regulator of This Target Gene | [1] | |||
Response Summary | m6A writers METTL3/METTL14 and the m6A reader YTHDF1 orchestrate MAP kinase signal-integrating kinase 2 (MNK2) expression posttranscriptionally and thus control ERK signaling, which is required for the maintenance of muscle myogenesis and contributes to regeneration. | |||
Target Regulation | Up regulation | |||
Responsed Disease | Muscular dystrophies | ICD-11: 8C70 | ||
Pathway Response | MAPK signaling pathway | hsa04010 | ||
In-vitro Model | HEK293T | Normal | Homo sapiens | CVCL_0063 |
C2C12 | Normal | Mus musculus | CVCL_0188 | |
In-vivo Model | For mouse muscle injury and regeneration experiment, tibialis anterior (TA) muscles of 6-week-old male mice were injected with 25 uL of 10 uM cardiotoxin (CTX, Merck Millipore, 217503), 0.9% normal saline (Saline) were used as control. The regenerated muscles were collected at day 1, 3, 5, and 10 post-injection. TA muscles were isolated for Hematoxylin and eosin staining or frozen in liquid nitrogen for RNA and protein extraction. | |||
Methyltransferase-like 14 (METTL14) [WRITER]
In total 1 item(s) under this regulator | ||||
Experiment 1 Reporting the m6A Methylation Regulator of This Target Gene | [1] | |||
Response Summary | m6A writers METTL3/METTL14 and the m6A reader YTHDF1 orchestrate MAP kinase signal-integrating kinase 2 (MNK2) expression posttranscriptionally and thus control ERK signaling, which is required for the maintenance of muscle myogenesis and contributes to regeneration. | |||
Target Regulation | Up regulation | |||
Responsed Disease | Muscular dystrophies | ICD-11: 8C70 | ||
Pathway Response | MAPK signaling pathway | hsa04010 | ||
In-vitro Model | HEK293T | Normal | Homo sapiens | CVCL_0063 |
C2C12 | Normal | Mus musculus | CVCL_0188 | |
In-vivo Model | For mouse muscle injury and regeneration experiment, tibialis anterior (TA) muscles of 6-week-old male mice were injected with 25 uL of 10 uM cardiotoxin (CTX, Merck Millipore, 217503), 0.9% normal saline (Saline) were used as control. The regenerated muscles were collected at day 1, 3, 5, and 10 post-injection. TA muscles were isolated for Hematoxylin and eosin staining or frozen in liquid nitrogen for RNA and protein extraction. | |||
YTH domain-containing family protein 1 (YTHDF1) [READER]
In total 1 item(s) under this regulator | ||||
Experiment 1 Reporting the m6A Methylation Regulator of This Target Gene | [1] | |||
Response Summary | m6A writers METTL3/METTL14 and the m6A reader YTHDF1 orchestrate MAP kinase signal-integrating kinase 2 (MNK2) expression posttranscriptionally and thus control ERK signaling, which is required for the maintenance of muscle myogenesis contributes to regeneration. | |||
Target Regulation | Up regulation | |||
Responsed Disease | Muscular dystrophies | ICD-11: 8C70 | ||
Pathway Response | MAPK signaling pathway | hsa04010 | ||
In-vitro Model | HEK293T | Normal | Homo sapiens | CVCL_0063 |
C2C12 | Normal | Mus musculus | CVCL_0188 | |
In-vivo Model | For mouse muscle injury and regeneration experiment, tibialis anterior (TA) muscles of 6-week-old male mice were injected with 25 uL of 10 uM cardiotoxin (CTX, Merck Millipore, 217503), 0.9% normal saline (Saline) were used as control. The regenerated muscles were collected at day 1, 3, 5, and 10 post-injection. TA muscles were isolated for Hematoxylin and eosin staining or frozen in liquid nitrogen for RNA and protein extraction. | |||
Muscular dystrophies [ICD-11: 8C70]
In total 3 item(s) under this disease | ||||
Experiment 1 Reporting the m6A-centered Disease Response | [1] | |||
Response Summary | m6A writers METTL3/METTL14 and the m6A reader YTHDF1 orchestrate MAP kinase signal-integrating kinase 2 (MNK2) expression posttranscriptionally and thus control ERK signaling, which is required for the maintenance of muscle myogenesis and contributes to regeneration. | |||
Responsed Disease | Muscular dystrophies [ICD-11: 8C70] | |||
Target Regulator | Methyltransferase-like 14 (METTL14) | WRITER | ||
Target Regulation | Up regulation | |||
Pathway Response | MAPK signaling pathway | hsa04010 | ||
In-vitro Model | HEK293T | Normal | Homo sapiens | CVCL_0063 |
C2C12 | Normal | Mus musculus | CVCL_0188 | |
In-vivo Model | For mouse muscle injury and regeneration experiment, tibialis anterior (TA) muscles of 6-week-old male mice were injected with 25 uL of 10 uM cardiotoxin (CTX, Merck Millipore, 217503), 0.9% normal saline (Saline) were used as control. The regenerated muscles were collected at day 1, 3, 5, and 10 post-injection. TA muscles were isolated for Hematoxylin and eosin staining or frozen in liquid nitrogen for RNA and protein extraction. | |||
Experiment 2 Reporting the m6A-centered Disease Response | [1] | |||
Response Summary | m6A writers METTL3/METTL14 and the m6A reader YTHDF1 orchestrate MAP kinase signal-integrating kinase 2 (MNK2) expression posttranscriptionally and thus control ERK signaling, which is required for the maintenance of muscle myogenesis and contributes to regeneration. | |||
Responsed Disease | Muscular dystrophies [ICD-11: 8C70] | |||
Target Regulator | Methyltransferase-like 3 (METTL3) | WRITER | ||
Target Regulation | Up regulation | |||
Pathway Response | MAPK signaling pathway | hsa04010 | ||
In-vitro Model | HEK293T | Normal | Homo sapiens | CVCL_0063 |
C2C12 | Normal | Mus musculus | CVCL_0188 | |
In-vivo Model | For mouse muscle injury and regeneration experiment, tibialis anterior (TA) muscles of 6-week-old male mice were injected with 25 uL of 10 uM cardiotoxin (CTX, Merck Millipore, 217503), 0.9% normal saline (Saline) were used as control. The regenerated muscles were collected at day 1, 3, 5, and 10 post-injection. TA muscles were isolated for Hematoxylin and eosin staining or frozen in liquid nitrogen for RNA and protein extraction. | |||
Experiment 3 Reporting the m6A-centered Disease Response | [1] | |||
Response Summary | m6A writers METTL3/METTL14 and the m6A reader YTHDF1 orchestrate MAP kinase signal-integrating kinase 2 (MNK2) expression posttranscriptionally and thus control ERK signaling, which is required for the maintenance of muscle myogenesis contributes to regeneration. | |||
Responsed Disease | Muscular dystrophies [ICD-11: 8C70] | |||
Target Regulator | YTH domain-containing family protein 1 (YTHDF1) | READER | ||
Target Regulation | Up regulation | |||
Pathway Response | MAPK signaling pathway | hsa04010 | ||
In-vitro Model | HEK293T | Normal | Homo sapiens | CVCL_0063 |
C2C12 | Normal | Mus musculus | CVCL_0188 | |
In-vivo Model | For mouse muscle injury and regeneration experiment, tibialis anterior (TA) muscles of 6-week-old male mice were injected with 25 uL of 10 uM cardiotoxin (CTX, Merck Millipore, 217503), 0.9% normal saline (Saline) were used as control. The regenerated muscles were collected at day 1, 3, 5, and 10 post-injection. TA muscles were isolated for Hematoxylin and eosin staining or frozen in liquid nitrogen for RNA and protein extraction. | |||