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AID-ing Signaling in Toxoplasma gondii

The cyclic GMP-dependent protein kinase (PKG) of apicomplexan parasites is essential for secretion of micronemes and host cell invasion and egress. Both kinase specificity and localization can determine which substrates are phosphorylated. The functions of plasma membrane and cytosolic PKG isoforms...

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Autor principal: Kim, Kami
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5527314/
https://www.ncbi.nlm.nih.gov/pubmed/28743818
http://dx.doi.org/10.1128/mBio.01076-17
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author Kim, Kami
author_facet Kim, Kami
author_sort Kim, Kami
collection PubMed
description The cyclic GMP-dependent protein kinase (PKG) of apicomplexan parasites is essential for secretion of micronemes and host cell invasion and egress. Both kinase specificity and localization can determine which substrates are phosphorylated. The functions of plasma membrane and cytosolic PKG isoforms of Toxoplasma gondii were unknown because of difficulties precisely manipulating expression of essential genes. Brown et al. (K. M. Brown, S. Long, and L. D. Sibley, mBio 8:e00375-17, https://doi.org/10.1128/mBio.00375-17) adapted the auxin-inducible degron (AID) system for conditional expression of T. gondii proteins. AID, in combination with clustered regularly interspaced short palindromic repeat (CRISPR)-Cas9 gene editing, facilitated creation of a panel of PKG mutants to demonstrate that the membrane association via acylation of PKG is critical for its essential functions in tachyzoites. The cytosolic form of PKG is not sufficient for viability and is dispensable. These studies illuminate a critical role for targeting of kinase complexes for parasite viability. The AID system enables rapid, conditional regulation of protein expression that expands the molecular toolbox of T. gondii.
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spelling pubmed-55273142017-08-01 AID-ing Signaling in Toxoplasma gondii Kim, Kami mBio Commentary The cyclic GMP-dependent protein kinase (PKG) of apicomplexan parasites is essential for secretion of micronemes and host cell invasion and egress. Both kinase specificity and localization can determine which substrates are phosphorylated. The functions of plasma membrane and cytosolic PKG isoforms of Toxoplasma gondii were unknown because of difficulties precisely manipulating expression of essential genes. Brown et al. (K. M. Brown, S. Long, and L. D. Sibley, mBio 8:e00375-17, https://doi.org/10.1128/mBio.00375-17) adapted the auxin-inducible degron (AID) system for conditional expression of T. gondii proteins. AID, in combination with clustered regularly interspaced short palindromic repeat (CRISPR)-Cas9 gene editing, facilitated creation of a panel of PKG mutants to demonstrate that the membrane association via acylation of PKG is critical for its essential functions in tachyzoites. The cytosolic form of PKG is not sufficient for viability and is dispensable. These studies illuminate a critical role for targeting of kinase complexes for parasite viability. The AID system enables rapid, conditional regulation of protein expression that expands the molecular toolbox of T. gondii. American Society for Microbiology 2017-07-25 /pmc/articles/PMC5527314/ /pubmed/28743818 http://dx.doi.org/10.1128/mBio.01076-17 Text en Copyright © 2017 Kim. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Commentary
Kim, Kami
AID-ing Signaling in Toxoplasma gondii
title AID-ing Signaling in Toxoplasma gondii
title_full AID-ing Signaling in Toxoplasma gondii
title_fullStr AID-ing Signaling in Toxoplasma gondii
title_full_unstemmed AID-ing Signaling in Toxoplasma gondii
title_short AID-ing Signaling in Toxoplasma gondii
title_sort aid-ing signaling in toxoplasma gondii
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5527314/
https://www.ncbi.nlm.nih.gov/pubmed/28743818
http://dx.doi.org/10.1128/mBio.01076-17
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