PRMT5- mediated symmetric arginine dimethylation is attenuated by mutant huntingtin and is impaired in Huntington's disease (HD).
Cell Cycle
; 14(11): 1716-29, 2015.
Article
en En
| MEDLINE
| ID: mdl-25927346
Palabras clave
BDNF, brain-derived neurotrophic factor; CB, Cajal body; ChIP, the chromatin immunoprecipitation; DMEM, Dulbecco's modified Eagle's medium; FBS, fetal bovine serum; HD, Huntington's disease; HEK, human embryonic kidney; Htt, huntingtin; Huntington's disease mechanism; IP, immunoprecipitation; IgG, immunoglobulin; PIC, protease inhibitors cocktail; PRMT5, protein arginine methyltransferase; RNA processing; SMN, survival of motor neurons; Sm proteins, spleceosomal small nuclear ribonucleoproteins; gene transcription; huntingtin; neurodegeneration; polyQ, polyglutamine; protein interactions; protein methylation; sDMA, symmetrical arginine dimethylation; snRNPs, small nuclear ribonucleoprotein particles
Texto completo:
1
Banco de datos:
MEDLINE
Asunto principal:
Arginina
/
Proteína-Arginina N-Metiltransferasas
/
Regulación de la Expresión Génica
/
Enfermedad de Huntington
/
Epigénesis Genética
/
Proteínas del Tejido Nervioso
Tipo de estudio:
Prognostic_studies
Límite:
Animals
/
Humans
Idioma:
En
Revista:
Cell Cycle
Año:
2015
Tipo del documento:
Article
País de afiliación:
Estados Unidos