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Molecules and their functions in autophagy

Autophagy is a self-degradation system of cellular components through an autophagosomal-lysosomal pathway. Over the last 15 yr, yeast genetic screens led to the identification of a number of genes involved in the autophagic pathway. Most of these autophagy genes are present in higher eukaryotes and...

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Autores principales: Pyo, Jong-Ok, Nah, Jihoon, Jung, Yong-Keun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society for Biochemistry and Molecular Biology 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3296815/
https://www.ncbi.nlm.nih.gov/pubmed/22257882
http://dx.doi.org/10.3858/emm.2012.44.2.029
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author Pyo, Jong-Ok
Nah, Jihoon
Jung, Yong-Keun
author_facet Pyo, Jong-Ok
Nah, Jihoon
Jung, Yong-Keun
author_sort Pyo, Jong-Ok
collection PubMed
description Autophagy is a self-degradation system of cellular components through an autophagosomal-lysosomal pathway. Over the last 15 yr, yeast genetic screens led to the identification of a number of genes involved in the autophagic pathway. Most of these autophagy genes are present in higher eukaryotes and regulate autophagy process for cell survival and homeostasis. Significant progress has recently been made to better understand the molecular mechanisms of the autophagy machinery. Especially, autophagy process, including the regulation of autophagy induction through mTOR and the nucleation and elongation in autophagosome formation through class III phosphatidylinositol 3-kinase complex and ubiquitin-like conjugation systems, became evident. While many unanswered questions remain to be answered, here, we summarize the recent process of autophagy with emphasis on molecules and their protein complexes along with advanced molecular mechanisms that regulate the autophagy machinery.
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spelling pubmed-32968152012-03-12 Molecules and their functions in autophagy Pyo, Jong-Ok Nah, Jihoon Jung, Yong-Keun Exp Mol Med Review Autophagy is a self-degradation system of cellular components through an autophagosomal-lysosomal pathway. Over the last 15 yr, yeast genetic screens led to the identification of a number of genes involved in the autophagic pathway. Most of these autophagy genes are present in higher eukaryotes and regulate autophagy process for cell survival and homeostasis. Significant progress has recently been made to better understand the molecular mechanisms of the autophagy machinery. Especially, autophagy process, including the regulation of autophagy induction through mTOR and the nucleation and elongation in autophagosome formation through class III phosphatidylinositol 3-kinase complex and ubiquitin-like conjugation systems, became evident. While many unanswered questions remain to be answered, here, we summarize the recent process of autophagy with emphasis on molecules and their protein complexes along with advanced molecular mechanisms that regulate the autophagy machinery. Korean Society for Biochemistry and Molecular Biology 2012-02-29 2012-01-19 /pmc/articles/PMC3296815/ /pubmed/22257882 http://dx.doi.org/10.3858/emm.2012.44.2.029 Text en Copyright © 2012 by The Korean Society for Biochemistry and Molecular Biology http://creativecommons.org/licenses/by-nc/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Pyo, Jong-Ok
Nah, Jihoon
Jung, Yong-Keun
Molecules and their functions in autophagy
title Molecules and their functions in autophagy
title_full Molecules and their functions in autophagy
title_fullStr Molecules and their functions in autophagy
title_full_unstemmed Molecules and their functions in autophagy
title_short Molecules and their functions in autophagy
title_sort molecules and their functions in autophagy
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3296815/
https://www.ncbi.nlm.nih.gov/pubmed/22257882
http://dx.doi.org/10.3858/emm.2012.44.2.029
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