Literature DB >> 27730581

deGradFP: A System to Knockdown GFP-Tagged Proteins.

Emmanuel Caussinus1, Markus Affolter2.   

Abstract

Protein depletion by genetic means, in a very general sense including the use of RNA interference [1, 2] or CRISPR/Cas9-based methods, represents a central paradigm of modern biology to study protein functions in vivo. However, acting upstream the proteic level is a limiting factor if the turnover of the target protein is slow or the existing pool of the target protein is important (for instance, in insect embryos, as a consequence of a strong maternal contribution). In order to circumvent these problems, we developed deGradFP [3, 4]. deGradFP harnesses the ubiquitin-proteasome pathway to achieve direct depletion of GFP-tagged proteins. deGradFP is in essence a universal method because it relies on an evolutionarily conserved machinery for protein catabolism in eukaryotic cells; see refs. 5, 6 for review. deGradFP is particularly convenient in Drosophila melanogaster where it is implemented by a genetically encoded effector expressed under the control of the Gal4 system. deGradFP is a ready-to-use solution to perform knockdowns at the protein level if a fly line carrying a functional GFP-tagged version of the gene of interest is available. Many such lines have already been generated by the Drosophila community through different technologies allowing to make genomic rescue constructs or direct GFP knockins: protein-trap stock collections [7, 8] ( http://cooley.medicine.yale.edu/flytrap/ , http://www.flyprot.org/ ), P[acman] system [9], MiMIC lines [10, 11], and CRISPR/Cas9-driven homologous recombination.Two essential controls of a protein knockdown experiment are easily achieved using deGradFP. First, the removal of the target protein can be assessed by monitoring the disappearance of the GFP tag by fluorescence microscopy in parallel to the documentation of the phenotype of the protein knockdown (see Note 1 ). Second, the potential nonspecific effects of deGradFP can be assessed in control fly lacking a GFP-tagged target protein. So far, no nonspecific effects of the deGradFP effector have been reported [3].

Entities:  

Keywords:  F-Box; GFP; Gene expression; Nanobodies; Proteasome

Mesh:

Substances:

Year:  2016        PMID: 27730581     DOI: 10.1007/978-1-4939-6371-3_9

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  13 in total

1.  SILAC-based quantitative proteomic analysis of Drosophila gastrula stage embryos mutant for fibroblast growth factor signalling.

Authors:  Hamze Beati; Alistair Langlands; Sara Ten Have; H-Arno J Müller
Journal:  Fly (Austin)       Date:  2019-12-24       Impact factor: 2.160

Review 2.  Exploring cellular biochemistry with nanobodies.

Authors:  Ross W Cheloha; Thibault J Harmand; Charlotte Wijne; Thomas U Schwartz; Hidde L Ploegh
Journal:  J Biol Chem       Date:  2020-08-31       Impact factor: 5.157

3.  Context-Dependent Gene Regulation by Homeodomain Transcription Factor Complexes Revealed by Shape-Readout Deficient Proteins.

Authors:  Judith F Kribelbauer; Ryan E Loker; Siqian Feng; Chaitanya Rastogi; Namiko Abe; H Tomas Rube; Harmen J Bussemaker; Richard S Mann
Journal:  Mol Cell       Date:  2020-02-12       Impact factor: 17.970

4.  Protein visualization and manipulation in Drosophila through the use of epitope tags recognized by nanobodies.

Authors:  Jun Xu; Ah-Ram Kim; Ross W Cheloha; Fabian A Fischer; Joshua Shing Shun Li; Yuan Feng; Emily Stoneburner; Richard Binari; Stephanie E Mohr; Jonathan Zirin; Hidde L Ploegh; Norbert Perrimon
Journal:  Elife       Date:  2022-01-25       Impact factor: 8.140

5.  Targeted protein degradation using deGradFP in Trypanosoma brucei.

Authors:  Midori Ishii; Bungo Akiyoshi
Journal:  Wellcome Open Res       Date:  2022-06-23

6.  Rapid and Reversible Knockdown of Endogenously Tagged Endosomal Proteins via an Optimized HaloPROTAC Degrader.

Authors:  Hannah Tovell; Andrea Testa; Chiara Maniaci; Houjiang Zhou; Alan R Prescott; Thomas Macartney; Alessio Ciulli; Dario R Alessi
Journal:  ACS Chem Biol       Date:  2019-04-22       Impact factor: 5.100

7.  The Crk adapter protein is essential for Drosophila embryogenesis, where it regulates multiple actin-dependent morphogenic events.

Authors:  Andrew J Spracklen; Emma M Thornton-Kolbe; Alison N Bonner; Alexandru Florea; Peter J Compton; Rodrigo Fernandez-Gonzalez; Mark Peifer
Journal:  Mol Biol Cell       Date:  2019-07-18       Impact factor: 4.138

8.  Condensin I is required for faithful meiosis in Drosophila males.

Authors:  Kristina Kleinschnitz; Nina Vießmann; Mareike Jordan; Stefan K Heidmann
Journal:  Chromosoma       Date:  2020-04-08       Impact factor: 4.316

9.  Coupled oscillators coordinate collective germline growth.

Authors:  Caroline A Doherty; Rocky Diegmiller; Manisha Kapasiawala; Elizabeth R Gavis; Stanislav Y Shvartsman
Journal:  Dev Cell       Date:  2021-03-08       Impact factor: 12.270

10.  Combinations of DIPs and Dprs control organization of olfactory receptor neuron terminals in Drosophila.

Authors:  Scott Barish; Sarah Nuss; Ilya Strunilin; Suyang Bao; Sayan Mukherjee; Corbin D Jones; Pelin C Volkan
Journal:  PLoS Genet       Date:  2018-08-13       Impact factor: 5.917

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