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Drosophila SWR1 and NuA4 complexes are defined by DOMINO isoforms.
Scacchetti, Alessandro; Schauer, Tamas; Reim, Alexander; Apostolou, Zivkos; Campos Sparr, Aline; Krause, Silke; Heun, Patrick; Wierer, Michael; Becker, Peter B.
Afiliación
  • Scacchetti A; Molecular Biology Division, Biomedical Center, Ludwig-Maximilians-University, Munich, Germany.
  • Schauer T; Bioinformatics Unit, Biomedical Center, Ludwig-Maximilians-University, Munich, Germany.
  • Reim A; Department of Proteomics and Signal Transduction, Max Planck Institute of Biochemistry, Munich, Germany.
  • Apostolou Z; Molecular Biology Division, Biomedical Center, Ludwig-Maximilians-University, Munich, Germany.
  • Campos Sparr A; Molecular Biology Division, Biomedical Center, Ludwig-Maximilians-University, Munich, Germany.
  • Krause S; Molecular Biology Division, Biomedical Center, Ludwig-Maximilians-University, Munich, Germany.
  • Heun P; Wellcome Trust Centre for Cell Biology and Institute of Cell Biology, School of Biological Sciences, The University of Edinburgh, Edinburgh, United Kingdom.
  • Wierer M; Department of Proteomics and Signal Transduction, Max Planck Institute of Biochemistry, Munich, Germany.
  • Becker PB; Molecular Biology Division, Biomedical Center, Ludwig-Maximilians-University, Munich, Germany.
Elife ; 92020 05 20.
Article en En | MEDLINE | ID: mdl-32432549
Cells contain a large number of proteins that control the activity of genes in response to various signals and changes in their environment. Often these proteins work together in groups called complexes. In the fruit fly Drosophila melanogaster, one of these complexes is called DOMINO. The DOMINO complex alters gene activity by interacting with other proteins called histones which influence how the genes are packaged and accessed within the cell. DOMINO works in two separate ways. First, it can replace certain histones with other variants that regulate genes differently. Second, it can modify histones by adding a chemical marker to them, which alters how they interact with genes. It was not clear how DOMINO can do both of these things and how that is controlled; but it was known that cells can make two different forms of the central component of the complex, called DOM-A and DOM-B, which are both encoded by the same gene. Scacchetti et al. have now studied fruit flies to understand the activities of these forms. This revealed that they do have different roles and that gene activity in cells changes if either one is lost. The two forms operate as part complexes with different compositions and only DOM-A includes the TIP60 enzyme that is needed to modify histones. As such, it seems that DOM-B primarily replaces histones with variant forms, while DOM-A modifies existing histones. This means that each form has a unique role associated with each of the two known behaviors of this complex. The presence of two different DOMINO complexes is common to flies and, probably, other insects. Yet, in other living things, such as mammals and yeast, their two roles are carried out by protein complexes originating from two distinct genes. This illustrates a concept called convergent evolution, where different organisms find different solutions for the same problem. As such, these findings provide an insight into the challenges encountered through evolution and the diverse solutions that have developed. They will also help us to understand the ways in which protein activities can adapt to different needs over evolutionary time.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Factores de Transcripción / Proteínas de Drosophila / Complejos Multiproteicos / Drosophila / Histona Acetiltransferasas Límite: Animals Idioma: En Revista: Elife Año: 2020 Tipo del documento: Article País de afiliación: Alemania Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Factores de Transcripción / Proteínas de Drosophila / Complejos Multiproteicos / Drosophila / Histona Acetiltransferasas Límite: Animals Idioma: En Revista: Elife Año: 2020 Tipo del documento: Article País de afiliación: Alemania Pais de publicación: Reino Unido