Development of Methods for the Target-Specific Protein Elimination in Plants


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Here we present the method for the target-specific elimination of certain intracellular proteins in plants using the ubiquitin-proteasome system. We modified the E3 ubiquitin ligase Chip of A. thaliana to obtain two variants carrying the deletions at the N-terminus and the GFP recognition domain. The interaction of the GFP protein and the chimeric ubiquitin ligase was confirmed via yeast two-hybrid assay. Fluorescence microscopy and fluorimetry showed that, when an infiltration of the gfp-expressing N. benthamiana plants was performed with agrobacteria carrying the hybrid E3 gene of the ubiquitin ligase Chip with the GFP recognition domain, a significant decrease in the fluorescence was observed for both variants: carrying the N-terminal deletion of 100 amino acids or the deletion of 140 amino acids.

作者简介

L. Maloshenok

Vavilov Institute of General Genetics, Russian Academy of Sciences

编辑信件的主要联系方式.
Email: maloshenoklg@mail.ru
俄罗斯联邦, Moscow, 119991

I. Abdeeva

Vavilov Institute of General Genetics, Russian Academy of Sciences

Email: maloshenoklg@mail.ru
俄罗斯联邦, Moscow, 119991

J. Panina

Vavilov Institute of General Genetics, Russian Academy of Sciences

Email: maloshenoklg@mail.ru
俄罗斯联邦, Moscow, 119991

E. Piruzian

Vavilov Institute of General Genetics, Russian Academy of Sciences

Email: maloshenoklg@mail.ru
俄罗斯联邦, Moscow, 119991

A. Zolotarenko

Vavilov Institute of General Genetics, Russian Academy of Sciences

Email: maloshenoklg@mail.ru
俄罗斯联邦, Moscow, 119991

S. Bruskin

Vavilov Institute of General Genetics, Russian Academy of Sciences

Email: maloshenoklg@mail.ru
俄罗斯联邦, Moscow, 119991


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