Multi-level and lineage-specific interactomes of the Hox transcription factor Ubx contribute to its functional specificity

• Verfasst von: Carnesecchi, Julie [VerfasserIn]
• Verfasst von: Sigismondo, Gianluca [VerfasserIn]
• Verfasst von: Domsch, Katrin [VerfasserIn]
• Verfasst von: Baader, Clara Eva Paula [VerfasserIn]
• Verfasst von: Rafiee, Mahmoud-Reza [VerfasserIn]
• Verfasst von: Krijgsveld, Jeroen [VerfasserIn]
• Verfasst von: Lohmann, Ingrid [VerfasserIn]
• Titel: Multi-level and lineage-specific interactomes of the Hox transcription factor Ubx contribute to its functional specificity
• Verf.angabe: Julie Carnesecchi, Gianluca Sigismondo, Katrin Domsch, Clara Eva Paula Baader, Mahmoud-Reza Rafiee, Jeroen Krijgsveld & Ingrid Lohmann
• E-Jahr: 2020
• Jahr: 13 March 2020
• Umfang: 17 S.
• Fussnoten: Gesehen am 08.10.2020
• Titel Quelle: Enthalten in: Nature Communications
• Ort Quelle: [London] : Nature Publishing Group UK, 2010
• Jahr Quelle: 2020
• Band/Heft Quelle: 11(2020) Artikel-Nummer 1388, 17 Seiten
• ISSN Quelle: 2041-1723
• DOI: doi:10.1038/s41467-020-15223-x
• Datenträger: Online-Ressource
• Sprache: eng
• K10plus-PPN: 1735209864

Abstract

Transcription factors (TFs) control cell fates by precisely orchestrating gene expression. However, how individual TFs promote transcriptional diversity remains unclear. Here, we use the Hox TF Ultrabithorax (Ubx) as a model to explore how a single TF specifies multiple cell types. Using proximity-dependent Biotin IDentification in Drosophila, we identify Ubx interactomes in three embryonic tissues. We find that Ubx interacts with largely non-overlapping sets of proteins with few having tissue-specific RNA expression. Instead most interactors are active in many cell types, controlling gene expression from chromatin regulation to the initiation of translation. Genetic interaction assays in vivo confirm that they act strictly lineage- and process-specific. Thus, functional specificity of Ubx seems to play out at several regulatory levels and to result from the controlled restriction of the interaction potential by the cellular environment. Thereby, it challenges long-standing assumptions such as differential RNA expression as determinant for protein complexes.