Skip to content
DraconiticResearch
Search Sources API
197,768 studies31 sourcesUpdated 56 min ago
PreprintCC BYbioRxiv

Fluorescent Ubiquitination-based Trbl Turnover Indicator (FUTTI): A tool to detect activity of the Tribbles pseudokinase in vivo

Abstract

Targeted protein turnover of the transcription factor C/EBP is enhanced by the Tribbles (Trib) pseudokinase family of adaptor proteins, which bind to a conserved degron motif in C/EBP substrate and recruit a cognate COP1 E3 ligase to ubiquitinate C/EBP for degradation. We identified a conserved degron in the Drosophila C/EBP ortholog Slbo and fused this motif to a fluorescent protein (GFP or RFP) under the control of a constitutive promoter. Transgenic flies expressing this fluorescent protein (FP)::degron transgene, which we call the Fluorescent Ubiquitination-based Trbl Turnover Indicator (or FUTTI) sensor, showed reduced levels of fluorescence in response to increased levels of Drosophila Tribbles (Trbl) and conversely, increased levels when Trbl activity was reduced. Mutations in the Trbl conserved pseudokinase substrate binding pocket and in a divergent PEST-like motif in the C-terminal tail region disrupted Trbl activity in the FUTTI assay. These data indicate that FUTTI will be a valuable tool to identify sites of Trbl activity in vivo and the critical features of the protein required for function.

Related

  1. A Tandem Fluorescent Rh1::eGFP mCherry Reporter Reveals Rhodopsin 1 Trafficking and Turnover In Vivo in Drosophila Photoreceptors
    H. Gheflati, C. Steiner, N. Feizy
    bioRxivPreprintCC BYFull textCell biologybioRxiv
  2. A nucleocapsid-tagged fluorescent pangolin coronavirus enables authentic-virus neutralization assays and localizes the antiviral activity of cepharanthine to viral entry
    Y. Ma, S. Lu, S. Luo +8
    bioRxivPreprintAll rights reservedFull textMicrobiologybioRxiv
  3. Cell cycle-coupled CK1δ turnover, autoinhibition, and activity
    Fidel Emmanuel Serrano, Bianca Ruppert, Axel CR Diernfellner +1
    eLifePeer-reviewedCC BY 4.0Full textCell biologyeLifeEurope PMCPMC
  4. Map-based cloning of the susceptibility locus conditioning bs6 resistance in pepper (Capsicum annuum L.) encoding mutant alleles of pseudokinase proteins.
    Zoltan Toth, Zoltan Gabor Toth, Peter Kalo +2
    TAG. Theoretical and applied genetics. Theoretische und angewandte GenetikPeer-reviewedCC BYFull textPlant biologyEurope PMC
  5. Integrative Multi-Omics and Single-Cell Analysis Prioritizes YWHAB Within Ubiquitination-Related Transcriptional Programs in Endometrial Carcinoma
    Jiaxi Wang, Hongwen Zhu, Yue Li +6
    GenesPeer-reviewedCC BYFull textGenetics & genomicsEurope PMC
BibTeX
@misc{nauman2026fluorescent,
  title = {{Fluorescent Ubiquitination-based Trbl Turnover Indicator (FUTTI): A tool to detect activity of the Tribbles pseudokinase in vivo}},
  author = {C. Nauman and S. Shayestehpour and S. O'Connor and Z. Fischer and L. Dobens},
  howpublished = {bioRxiv},
  year = {2026},
  month = sep,
  doi = {10.64898/2026.09.25.753906},
  url = {https://www.biorxiv.org/content/10.64898/2026.09.25.753906v1},
  note = {CC BY},
}
RIS
TY  - UNPB
TI  - Fluorescent Ubiquitination-based Trbl Turnover Indicator (FUTTI): A tool to detect activity of the Tribbles pseudokinase in vivo
AU  - C. Nauman
AU  - S. Shayestehpour
AU  - S. O'Connor
AU  - Z. Fischer
AU  - L. Dobens
PY  - 2026
DA  - 2026/09/25
PB  - bioRxiv
DO  - 10.64898/2026.09.25.753906
UR  - https://www.biorxiv.org/content/10.64898/2026.09.25.753906v1
AB  - Targeted protein turnover of the transcription factor C/EBP is enhanced by the Tribbles (Trib) pseudokinase family of adaptor proteins, which bind to a conserved degron motif in C/EBP substrate and recruit a cognate COP1 E3 ligase to ubiquitinate C/EBP for degradation. We identified a conserved degron in the Drosophila C/EBP ortholog Slbo and fused this motif to a fluorescent protein (GFP or RFP) under the control of a constitutive promoter. Transgenic flies expressing this fluorescent protein (FP)::degron transgene, which we call the Fluorescent Ubiquitination-based Trbl Turnover Indicator (or FUTTI) sensor, showed reduced levels of fluorescence in response to increased levels of Drosophila Tribbles (Trbl) and conversely, increased levels when Trbl activity was reduced. Mutations in the Trbl conserved pseudokinase substrate binding pocket and in a divergent PEST-like motif in the C-terminal tail region disrupted Trbl activity in the FUTTI assay. These data indicate that FUTTI will be a valuable tool to identify sites of Trbl activity in vivo and the critical features of the protein required for function.
ER  -