AP-4 mediates export of ATG9A from thetrans-Golgi network to promote autophagosome formation
出版年份 2017 全文链接
标题
AP-4 mediates export of ATG9A from thetrans-Golgi network to promote autophagosome formation
作者
关键词
-
出版物
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
Volume 114, Issue 50, Pages E10697-E10706
出版商
Proceedings of the National Academy of Sciences
发表日期
2017-11-28
DOI
10.1073/pnas.1717327114
参考文献
相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。- Atg9a deficiency causes axon-specific lesions including neuronal circuit dysgenesis
- (2018) Junji Yamaguchi et al. Autophagy
- Segregation in the Golgi complex precedes export of endolysosomal proteins in distinct transport carriers
- (2017) Yu Chen et al. JOURNAL OF CELL BIOLOGY
- Amyloid precursor protein traffics from the Golgi directly to early endosomes in an Arl5b- and AP4-dependent pathway
- (2017) Wei Hong Toh et al. TRAFFIC
- Regulation of mATG9 trafficking by Src- and ULK1-mediated phosphorylation in basal and starvation-induced autophagy
- (2016) Changqian Zhou et al. CELL RESEARCH
- Atg9A trafficking through the recycling endosomes is required for autophagosome formation
- (2016) Kenta Imai et al. JOURNAL OF CELL SCIENCE
- Molecular Basis for the Interaction Between AP4 β4 and its Accessory Protein, Tepsin
- (2016) Meredith N. Frazier et al. TRAFFIC
- Loss of AP-5 results in accumulation of aberrant endolysosomes: defining a new type of lysosomal storage disease
- (2015) Jennifer Hirst et al. HUMAN MOLECULAR GENETICS
- Bivalent Motif-Ear Interactions Mediate the Association of the Accessory Protein Tepsin with the AP-4 Adaptor Complex
- (2015) Rafael Mattera et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- Role of the Atg9a gene in intrauterine growth and survival of fetal mice
- (2015) Takashi Kojima et al. Reproductive Biology
- In Vivo Evidence for Lysosome Depletion and Impaired Autophagic Clearance in Hereditary Spastic Paraplegia Type SPG11
- (2015) Rita-Eva Varga et al. PLoS Genetics
- Adaptor protein complexes and intracellular transport
- (2014) Sang Yoon Park et al. BIOSCIENCE REPORTS
- TBC1D5 and the AP2 complex regulate ATG9 trafficking and initiation of autophagy
- (2014) D. Popovic et al. EMBO REPORTS
- Ultrastructural analysis of autophagosome organization using mammalian autophagy-deficient cells
- (2014) C. Kishi-Itakura et al. JOURNAL OF CELL SCIENCE
- Spastic paraplegia proteins spastizin and spatacsin mediate autophagic lysosome reformation
- (2014) Jaerak Chang et al. JOURNAL OF CLINICAL INVESTIGATION
- Structural and Functional Characterization of Cargo-Binding Sites on the μ4-Subunit of Adaptor Protein Complex 4
- (2014) Breyan H. Ross et al. PLoS One
- Atg23 and Atg27 Act at the Early Stages of Atg9 Trafficking inS. cerevisiae
- (2014) Steven K. Backues et al. TRAFFIC
- Phosphatidylinositol 3-kinase and COPII generate LC3 lipidation vesicles from the ER-Golgi intermediate compartment
- (2014) Liang Ge et al. eLife
- ATG16L1 meets ATG9 in recycling endosomes
- (2013) Claudia Puri et al. Autophagy
- Defective autophagy in spastizin mutated patients with hereditary spastic paraparesis type 15
- (2013) Chiara Vantaggiato et al. BRAIN
- Diverse Autophagosome Membrane Sources Coalesce in Recycling Endosomes
- (2013) Claudia Puri et al. CELL
- The Adaptor Protein-1 μ1B Subunit Expands the Repertoire of Basolateral Sorting Signal Recognition in Epithelial Cells
- (2013) Xiaoli Guo et al. DEVELOPMENTAL CELL
- Interaction between AP-5 and the hereditary spastic paraplegia proteins SPG11 and SPG15
- (2013) Jennifer Hirst et al. MOLECULAR BIOLOGY OF THE CELL
- The role of autophagy in neurodegenerative disease
- (2013) Ralph A Nixon NATURE MEDICINE
- The CRAPome: a contaminant repository for affinity purification–mass spectrometry data
- (2013) Dattatreya Mellacheruvu et al. NATURE METHODS
- Multiplex Genome Engineering Using CRISPR/Cas Systems
- (2013) L. Cong et al. SCIENCE
- Cargo Recognition in Clathrin-Mediated Endocytosis
- (2013) L. M. Traub et al. Cold Spring Harbor Perspectives in Biology
- Physiological Functions of APP Family Proteins
- (2013) U. C. Muller et al. Cold Spring Harbor Perspectives in Medicine
- Mutation in TECPR2 Reveals a Role for Autophagy in Hereditary Spastic Paraparesis
- (2012) Danit Oz-Levi et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Cellular Pathways of Hereditary Spastic Paraplegia
- (2012) Craig Blackstone Annual Review of Neuroscience
- Mechanisms of Autophagosome Biogenesis
- (2012) David C. Rubinsztein et al. CURRENT BIOLOGY
- Multivariate proteomic profiling identifies novel accessory proteins of coated vesicles
- (2012) Georg H.H. Borner et al. JOURNAL OF CELL BIOLOGY
- Atg9 vesicles are an important membrane source during early steps of autophagosome formation
- (2012) Hayashi Yamamoto et al. JOURNAL OF CELL BIOLOGY
- AP1 is essential for generation of autophagosomes from the trans-Golgi network
- (2012) Y. Guo et al. JOURNAL OF CELL SCIENCE
- Dynamic and transient interactions of Atg9 with autophagosomes, but not membrane integration, are required for autophagy
- (2012) A. Orsi et al. MOLECULAR BIOLOGY OF THE CELL
- Amyloid precursor protein (APP) traffics from the cell surface via endosomes for amyloid β (Aβ) production in thetrans-Golgi network
- (2012) Regina Wai-Yan Choy et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Adaptor Protein Complex 4 Deficiency Causes Severe Autosomal-Recessive Intellectual Disability, Progressive Spastic Paraplegia, Shy Character, and Short Stature
- (2011) Rami Abou Jamra et al. AMERICAN JOURNAL OF HUMAN GENETICS
- The Fifth Adaptor Protein Complex
- (2011) Jennifer Hirst et al. PLOS BIOLOGY
- Mitochondria Supply Membranes for Autophagosome Biogenesis during Starvation
- (2010) Dale W. Hailey et al. CELL
- Sorting of the Alzheimer's Disease Amyloid Precursor Protein Mediated by the AP-4 Complex
- (2010) Patricia V. Burgos et al. DEVELOPMENTAL CELL
- Adaptor protein complex-4 (AP-4) deficiency causes a novel autosomal recessive cerebral palsy syndrome with microcephaly and intellectual disability
- (2010) A. Moreno-De-Luca et al. JOURNAL OF MEDICAL GENETICS
- A Genome-Scale DNA Repair RNAi Screen Identifies SPG48 as a Novel Gene Associated with Hereditary Spastic Paraplegia
- (2010) Mikołaj Słabicki et al. PLOS BIOLOGY
- Mutation in the AP4M1 Gene Provides a Model for Neuroaxonal Injury in Cerebral Palsy
- (2009) Annemieke J.M.H. Verkerk et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Atg9a controls dsDNA-driven dynamic translocation of STING and the innate immune response
- (2009) T. Saitoh et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Identification of the SPG15 Gene, Encoding Spastizin, as a Frequent Cause of Complicated Autosomal-Recessive Spastic Paraplegia, Including Kjellin Syndrome
- (2008) Sylvain Hanein et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Ubiquitin binding and conjugation regulate the recruitment of Rabex-5 to early endosomes
- (2008) Rafael Mattera et al. EMBO JOURNAL
- Accumulation of AMPA Receptors in Autophagosomes in Neuronal Axons Lacking Adaptor Protein AP-4
- (2008) Shinji Matsuda et al. NEURON
Discover Peeref hubs
Discuss science. Find collaborators. Network.
Join a conversationBecome a Peeref-certified reviewer
The Peeref Institute provides free reviewer training that teaches the core competencies of the academic peer review process.
Get Started