Cargando…

REEP3 and REEP4 determine the tubular morphology of the endoplasmic reticulum during mitosis

The endoplasmic reticulum (ER) is extensively remodeled during metazoan open mitosis. However, whether the ER becomes more tubular or more cisternal during mitosis is controversial, and dedicated factors governing the morphology of the mitotic ER have remained elusive. Here, we describe the ER membr...

Descripción completa

Detalles Bibliográficos
Autores principales:	Kumar, Darshan, Golchoubian, Banafsheh, Belevich, Ilya, Jokitalo, Eija, Schlaitz, Anne-Lore
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	The American Society for Cell Biology 2019
Materias:	Articles
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6724692/ https://www.ncbi.nlm.nih.gov/pubmed/30995177 http://dx.doi.org/10.1091/mbc.E18-11-0698

Ejemplares similares

Reticulon-like REEP4 at the inner nuclear membrane promotes nuclear pore complex formation
por: Golchoubian, Banafsheh, et al.
Publicado: (2021)

REEP5 depletion causes sarco-endoplasmic reticulum vacuolization and cardiac functional defects
por: Lee, Shin-Haw, et al.
Publicado: (2020)

The accessory proteins REEP5 and REEP6 refine CXCR1-mediated cellular responses and lung cancer progression
por: Park, Cho Rong, et al.
Publicado: (2016)

Mutations in REEP6 Cause Autosomal-Recessive Retinitis Pigmentosa
por: Arno, Gavin, et al.
Publicado: (2016)

Further supporting evidence for REEP1 phenotypic and allelic heterogeneity
por: Maroofian, Reza, et al.
Publicado: (2019)

Converging Role for REEP1/SPG31 in Oxidative Stress
por: Naef, Valentina, et al.
Publicado: (2023)

Progressive sheet-to-tubule transformation is a general mechanism for endoplasmic reticulum partitioning in dividing mammalian cells
por: Puhka, Maija, et al.
Publicado: (2012)

Recessive REEP1 mutation is associated with congenital axonal neuropathy and diaphragmatic palsy
por: Schottmann, Gudrun, et al.
Publicado: (2015)

De novo REEP2 missense mutation in pure hereditary spastic paraplegia
por: Roda, Ricardo H., et al.
Publicado: (2017)

Screening for REEP1 Mutations in 31 Chinese Hereditary Spastic Paraplegia Families
por: Ma, Xinran, et al.
Publicado: (2020)

Naringenin Ameliorates Drosophila ReepA Hereditary Spastic Paraplegia-Linked Phenotypes
por: Napoli, Barbara, et al.
Publicado: (2019)

REEP5 (Receptor Accessory Protein 5) Acts as a Sarcoplasmic Reticulum Membrane Sculptor to Modulate Cardiac Function
por: Yao, Lei, et al.
Publicado: (2018)

Enhanced reticulospinal output in patients with (REEP1) hereditary spastic paraplegia type 31
por: Fisher, K. M., et al.
Publicado: (2013)

Autosomal dominant hereditary spastic paraplegia: Novel mutations in the REEP1 gene (SPG31)
por: Schlang, Katharina J, et al.
Publicado: (2008)

Mutation analysis of SPAST, ATL1, and REEP1 in Korean Patients with Hereditary Spastic Paraplegia
por: Kim, Tae-Hyoung, et al.
Publicado: (2014)

Pathogenic Variant of REEP1 in a Korean Family with Autosomal-Dominant Hereditary Spastic Paraplegia
por: Park, Hyung Jun, et al.
Publicado: (2018)

REEP6 deficiency leads to retinal degeneration through disruption of ER homeostasis and protein trafficking
por: Agrawal, Smriti A., et al.
Publicado: (2017)

Autosomal Recessive Retinitis Pigmentosa Associated with Three Novel REEP6 Variants in Chinese Population
por: Zhang, Lujia, et al.
Publicado: (2021)

Erratum: Mutation Analysis of SPAST, ATL1, and REEP1 in Korean Patients with Hereditary Spastic Paraplegia
por: Kim, Tae-Hyoung, et al.
Publicado: (2014)

Towards understanding the role of Receptor Expression Enhancing Protein 5 (REEP5) in cardiac muscle and beyond
por: Lee, Shin-Haw, et al.
Publicado: (2020)

Microscopy Image Browser: A Platform for Segmentation and Analysis of Multidimensional Datasets
por: Belevich, Ilya, et al.
Publicado: (2016)

Morphological Heterogeneity of the Endoplasmic Reticulum within Neurons and Its Implications in Neurodegeneration
por: Sree, Sreesha, et al.
Publicado: (2021)

Hereditary spastic paraplegia due to a novel mutation of the REEP1 gene: Case report and literature review
por: Richard, Sébastien, et al.
Publicado: (2017)

REEP6 mediates trafficking of a subset of Clathrin-coated vesicles and is critical for rod photoreceptor function and survival
por: Veleri, Shobi, et al.
Publicado: (2017)

The ortholog of human REEP1-4 is required for autophagosomal enclosure of ER-phagy/nucleophagy cargos in fission yeast
por: Zou, Chen-Xi, et al.
Publicado: (2023)

circREEP3 Drives Colorectal Cancer Progression via Activation of FKBP10 Transcription and Restriction of Antitumor Immunity
por: Chen, Zhenzhen, et al.
Publicado: (2022)

Chidamide suppresses adipogenic differentiation of bone marrow derived mesenchymal stem cells via increasing REEP2 expression
por: Zhang, Xianning, et al.
Publicado: (2023)

The REEP5/TRAM1 complex binds SARS-CoV-2 NSP3 and promotes virus replication
por: Li, Jie, et al.
Publicado: (2023)

DeepMIB: User-friendly and open-source software for training of deep learning network for biological image segmentation
por: Belevich, Ilya, et al.
Publicado: (2021)

REEPs Are Membrane Shaping Adapter Proteins That Modulate Specific G Protein-Coupled Receptor Trafficking by Affecting ER Cargo Capacity
por: Björk, Susann, et al.
Publicado: (2013)

Inhibition of ER stress improves progressive motor deficits in a REEP1-null mouse model of hereditary spastic paraplegia
por: Wang, Bingjie, et al.
Publicado: (2020)

Exploring the eukaryotic Yip and REEP/Yop superfamily of membrane-shaping adapter proteins (MSAPs): A cacophony or harmony of structure and function?
por: Angelotti, Timothy
Publicado: (2022)

Correction: REEPs Are Membrane Shaping Adapter Proteins That Modulate Specific G Protein-Coupled Receptor Trafficking by Affecting ER Cargo Capacity
por: Björk, Susann, et al.
Publicado: (2013)

CircFAT1 promotes hepatocellular carcinoma progression via miR‐30a‐5p/REEP3 pathway
por: Wei, Hailiang, et al.
Publicado: (2020)

A 3.9-Mb Deletion on 2p11.2 Comprising the REEP1 Gene Causes Early-Onset Atypical Parkinsonism
por: Baviera-Muñoz, Raquel, et al.
Publicado: (2021)

Golgi clusters and vesicles mediate mitotic inheritance independently of the endoplasmic reticulum
por: Jokitalo, Eija, et al.
Publicado: (2001)

NOGO-A/RTN4A and NOGO-B/RTN4B are simultaneously expressed in epithelial, fibroblast and neuronal cells and maintain ER morphology
por: Rämö, Olli, et al.
Publicado: (2016)

Endoplasmic reticulum remains continuous and undergoes sheet-to-tubule transformation during cell division in mammalian cells
por: Puhka, Maija, et al.
Publicado: (2007)

Automated 3D Axonal Morphometry of White Matter
por: Abdollahzadeh, Ali, et al.
Publicado: (2019)

DeepACSON automated segmentation of white matter in 3D electron microscopy
por: Abdollahzadeh, Ali, et al.
Publicado: (2021)

Cannot write session to /tmp/vufind_sessions/sess_h0eu9jhci2802k12snlst3n2v3