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FEBS Lett ; 596(16): 2056-2071, 2022 08.
Artigo em Inglês | MEDLINE | ID: mdl-35735777

RESUMO

p27Kip1 functions to coordinate cell cycle progression through the inhibition of cyclin-dependent kinase (CDK) complexes. p27Kip1 also exerts distinct activities beyond CDK-inhibition, including functioning as a transcriptional regulator. The aryl hydrocarbon receptor (AhR) is a ligand-activated transcription factor with diverse biological roles. The regulatory inputs that control AhR-mediated transcriptional responses are an active area of investigation. AhR was previously established as a direct regulator of p27Kip1 transcription. Here, we report the physical interaction of AhR and p27Kip1 and show that p27Kip1 expression negatively regulates AhR-mediated transcription. p27Kip1 knockout cells display increased AhR nuclear localisation and significantly higher expression of AhR target genes. This work thus identifies new regulatory cross-talk between p27Kip1 and AhR.


Assuntos
Quinases Ciclina-Dependentes , Receptores de Hidrocarboneto Arílico , Proteínas de Ciclo Celular , Inibidor de Quinase Dependente de Ciclina p27 , Regulação da Expressão Gênica
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