Proteomic interactome of C. elegans mediator complex subunit 28 (MDT-28) reveals predominant association with a restricted aet of core mediator subunits and an affinity to additional structural and enzymatic proteins

Title:

Proteomic interactome of C. elegans mediator complex subunit 28 (MDT-28) reveals predominant association with a restricted aet of core mediator subunits and an affinity to additional structural and enzymatic proteins

Creator:

Yilma, P. , Kostrouchová, M. , Talacko, P., Kostrouchová, V., Kostrouch, D., Novák, P., and Kostrouchová, M.

Identifier:

https://cdk.lib.cas.cz/client/handle/uuid:0b2299c4-96ab-4a9a-88a5-b8c552aaf692
uuid:0b2299c4-96ab-4a9a-88a5-b8c552aaf692

Subject:

Caenorhabditis elegans, GPF-TRAP, interactome, head module, mass spectrometry, Mediator complex, MED28, MDT-28, and proteomic

Type:

model:article and TEXT

Format:

bez média and svazek

Description:

Transcription factors exert their regulatory potential on RNA polymerase II machinery through a multiprotein complex called Mediator complex or Mediator. The Mediator complex integrates regulatory signals from cell regulatory cascades with the regulation by transcription factors. The Mediator complex consists of 25 subunits in Saccharomyces cerevisiae and 30 or more subunits in multicellular eukaryotes. Mediator subunit 28 (MED28), along with MED30, MED23, MED25 and MED26, belong to presumably evolutionarily new subunits that seem to be absent in unicellular eukaryotes and are likely to have evolved together with multicellularity and cell differentiation. Previously, we have shown that an originally uncharacterized predicted gene, F28F8.5, is the true MED28 orthologue in Caenorhabditis elegans (mdt-28) and showed that it is involved in a spectrum of developmental processes. Here, we studied the proteomic interactome of MDT-28 edited as GFP::MDT-28 using Crispr/Cas9 technology or MDT-28::GFP expressed from extrachromosomal arrays in transgenic C. elegans exploiting the GFPTRAP system and mass spectrometry. The results show that MDT-28 associates with the Head module subunits MDT-6, MDT-8, MDT-11, MDT-17, MDT20, MDT-22, and MDT-30 and the Middle module subunit MDT-14. The analyses also identified additional proteins as preferential MDT-28 interactants, including chromatin-organizing proteins, structural proteins and enzymes. The results provide evidence for MDT-28 engagement in the Mediator Head module and support the possibility of physical (direct or indirect) interaction of MDT-28 with additional proteins, reflecting the transcription-regulating potential of primarily structural and enzymatic proteins at the level of the Mediator complex.

Language:

English

Rights:

http://creativecommons.org/publicdomain/mark/1.0/
policy:public

Coverage:

203-211

Source:

Folia biologica | 2019 Volume:65 | Number:5-6

Harvested from:

CDK

Metadata only:

false