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Dynamic interplay of the SUMO and ERK pathways in regulating Elk-1 transcriptional activity.
Yang, Shen-Hsi; Jaffray, Ellis; Hay, Ron T; Sharrocks, Andrew D.
Afiliación
  • Yang SH; School of Biological Sciences, University of Manchester, 2.205 Stopford building, Oxford Road, Manchester M13 9PT, United Kingdom.
Mol Cell ; 12(1): 63-74, 2003 Jul.
Article en En | MEDLINE | ID: mdl-12887893
ABSTRACT
The ETS domain transcription factor Elk-1 is a direct target of the MAP kinase pathways. Phosphorylation of the Elk-1 transcriptional activation domain by MAP kinases triggers its activation. However, Elk-1 also contains two domains with repressive activities. One of these, the R motif, appears to function by suppressing the activity of the activation domain. Here, we demonstrate that SUMO modification of the R motif is required for this repressive activity. A dynamic interplay exists between the activating ERK MAP kinase pathway and the repressive SUMO pathway. ERK pathway activation leads to both phosphorylation of Elk-1 and loss of SUMO conjugation and, hence, to the loss of the repressive activity of the R motif. Thus, the reciprocal regulation of the activation and repressive activities are coupled by MAP kinase modification of Elk-1.
Asunto(s)
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Base de datos: MEDLINE Asunto principal: Proteínas Represoras / Factores de Transcripción / Transcripción Genética / Proteínas Proto-Oncogénicas / Proteínas Quinasas Activadas por Mitógenos / Proteína SUMO-1 / Proteínas de Unión al ADN / Células Eucariotas Límite: Animals / Humans Idioma: En Revista: Mol Cell Asunto de la revista: BIOLOGIA MOLECULAR Año: 2003 Tipo del documento: Article País de afiliación: Reino Unido
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Base de datos: MEDLINE Asunto principal: Proteínas Represoras / Factores de Transcripción / Transcripción Genética / Proteínas Proto-Oncogénicas / Proteínas Quinasas Activadas por Mitógenos / Proteína SUMO-1 / Proteínas de Unión al ADN / Células Eucariotas Límite: Animals / Humans Idioma: En Revista: Mol Cell Asunto de la revista: BIOLOGIA MOLECULAR Año: 2003 Tipo del documento: Article País de afiliación: Reino Unido