MEG3 (original) (raw)
MEG3 (maternally expressed 3) is a maternally expressed, imprinted long non-coding RNA gene. At least 12 different isoforms of MEG3 are generated by alternative splicing. Expression of MEG3 is lost in cancer cells. It acts as a growth suppressor in tumour cells, and activates p53. A pituitary transcript variant has been associated with inhibited cell proliferation. Studies in mouse and sheep suggest that an upstream intergenic differentially methylated region regulates imprinting of the region. The expression profile in mouse of the co-regulated Meg3 and Dlk1 genes suggests a causative role in the pathologies found in uniparental disomy animals, characterized by defects in skeletal muscle maturation, bone formation, placenta size and organization and prenatal lethality. The sheep homolo
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dbo:abstract | MEG3 (maternally expressed 3) is a maternally expressed, imprinted long non-coding RNA gene. At least 12 different isoforms of MEG3 are generated by alternative splicing. Expression of MEG3 is lost in cancer cells. It acts as a growth suppressor in tumour cells, and activates p53. A pituitary transcript variant has been associated with inhibited cell proliferation. Studies in mouse and sheep suggest that an upstream intergenic differentially methylated region regulates imprinting of the region. The expression profile in mouse of the co-regulated Meg3 and Dlk1 genes suggests a causative role in the pathologies found in uniparental disomy animals, characterized by defects in skeletal muscle maturation, bone formation, placenta size and organization and prenatal lethality. The sheep homolog is associated with the callipyge mutation which in heterozygous individuals affects a muscle-specific long-range control element located in the DLK1-GTL2 intergenic region and results in the callipyge muscular hypertrophy. The non-Mendelian inheritance pattern, known as polar overdominance, likely results from the combination of the cis-effect on the expression levels of genes in the DLK1-GTL2 imprinted domain, and trans interaction between the products of reciprocally imprinted genes. (en) |
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dbo:wikiPageWikiLink | dbr:Mouse dbr:Bone dbr:P53 dbr:Genomic_imprinting dbr:Gene dbr:Long_noncoding_RNA dbr:Polar_overdominance dbc:Non-coding_RNA dbr:Cis-acting dbr:DLK1 dbr:Alternative_splicing dbr:Cell_proliferation dbr:Glossary_of_sheep_husbandry dbr:Heterozygous dbr:Hypertrophy dbr:Homology_(biology) dbr:Trans-acting dbr:Methylated dbr:Sheep dbr:Long_non-coding_RNA dbr:Placenta dbr:Uniparental_disomy dbr:Skeletal_muscle dbr:Mendelian dbr:Tumour dbr:Pituitary dbr:Intergenic dbr:Prenatal dbr:IG-DMR |
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dcterms:subject | dbc:Non-coding_RNA |
rdf:type | owl:Thing dbo:Biomolecule dbo:Gene wikidata:Q206229 wikidata:Q7187 dbo:HumanGene |
rdfs:comment | MEG3 (maternally expressed 3) is a maternally expressed, imprinted long non-coding RNA gene. At least 12 different isoforms of MEG3 are generated by alternative splicing. Expression of MEG3 is lost in cancer cells. It acts as a growth suppressor in tumour cells, and activates p53. A pituitary transcript variant has been associated with inhibited cell proliferation. Studies in mouse and sheep suggest that an upstream intergenic differentially methylated region regulates imprinting of the region. The expression profile in mouse of the co-regulated Meg3 and Dlk1 genes suggests a causative role in the pathologies found in uniparental disomy animals, characterized by defects in skeletal muscle maturation, bone formation, placenta size and organization and prenatal lethality. The sheep homolo (en) |
rdfs:label | MEG3 (en) |
owl:sameAs | freebase:MEG3 http://purl.org/net/tcm/tcm.lifescience.ntu.edu.tw/id/gene/MEG3 wikidata:MEG3 https://global.dbpedia.org/id/kBXd |
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is foaf:primaryTopic of | wikipedia-en:MEG3 |