keyword
https://read.qxmd.com/read/38454149/structure-and-tethering-mechanism-of-dynein-2-intermediate-chains-in-intraflagellar-transport
#21
JOURNAL ARTICLE
Aakash G Mukhopadhyay, Katerina Toropova, Lydia Daly, Jennifer N Wells, Laura Vuolo, Miroslav Mladenov, Marian Seda, Dagan Jenkins, David J Stephens, Anthony J Roberts
Dynein-2 is a large multiprotein complex that powers retrograde intraflagellar transport (IFT) of cargoes within cilia/flagella, but the molecular mechanism underlying this function is still emerging. Distinctively, dynein-2 contains two identical force-generating heavy chains that interact with two different intermediate chains (WDR34 and WDR60). Here, we dissect regulation of dynein-2 function by WDR34 and WDR60 using an integrative approach including cryo-electron microscopy and CRISPR/Cas9-enabled cell biology...
March 7, 2024: EMBO Journal
https://read.qxmd.com/read/38448164/genome-scale-requirements-for-dynein-based-transport-revealed-by-a-high-content-arrayed-crispr-screen
#22
JOURNAL ARTICLE
Chun Hao Wong, Steven W Wingett, Chen Qian, Morag Rose Hunter, J Matthew Taliaferro, Douglas Ross-Thriepland, Simon L Bullock
The microtubule motor dynein plays a key role in cellular organization. However, little is known about how dynein's biosynthesis, assembly, and functional diversity are orchestrated. To address this issue, we have conducted an arrayed CRISPR loss-of-function screen in human cells using the distribution of dynein-tethered peroxisomes and early endosomes as readouts. From a genome-wide gRNA library, 195 validated hits were recovered and parsed into those impacting multiple dynein cargoes and those whose effects are restricted to a subset of cargoes...
May 6, 2024: Journal of Cell Biology
https://read.qxmd.com/read/38447793/swedish-alzheimer-s-disease-variant-perturbs-activity-of-retrograde-molecular-motors-and-causes-widespread-derangement-of-axonal-transport-pathways
#23
JOURNAL ARTICLE
Monica Feole, Victorio M Pozo Devoto, Neda Dragišić, Cayetana Arnaiz, Julieta Bianchelli, Kateřina Texlová, Kristina Kovačovicova, Jan S Novotny, Daniel Havas, Tomas L Falzone, Gorazd B Stokin
Experimental studies in flies, mice, and humans suggest a significant role of impaired axonal transport in the pathogenesis of Alzheimer's disease (AD). The mechanisms underlying these impairments in axonal transport, however, remain poorly understood. Here we report that the Swedish familial AD mutation causes a standstill of the Amyloid Precursor Protein (APP) in the axons at the expense of its reduced anterograde transport. The standstill reflects the perturbed directionality of the axonal transport of APP, which spends significantly more time traveling in the retrograde direction...
March 4, 2024: Journal of Biological Chemistry
https://read.qxmd.com/read/38445557/dynein-functions-in-galectin-3-mediated-processes-of-clathrin-independent-endocytosis
#24
JOURNAL ARTICLE
Chaithra Mayya, A Hema Naveena, Pankhuri Sinha, Dhiraj Bhatia
Multiple endocytic processes operate in cells in tandem to uptake multiple cargoes involved in diverse cellular functions, including cell adhesion and migration. The best-studied clathrin-mediated endocytosis (CME) involves the formation of a well-defined cytoplasmic clathrin coat to facilitate cargo uptake. According to the glycolipid-lectin (GL-Lect) hypothesis, galectin-3 (Gal3) binds to glycosylated membrane receptors and glycosphingolipids (GSLs) to drive membrane bending and tubular membrane invaginations that undergo scission to form a morphologically distinct class of uptake structures, termed clathrin-independent carriers (CLICs)...
2024: Journal of Biosciences
https://read.qxmd.com/read/38441532/nudc-is-critical-for-rod-photoreceptor-function-maintenance-and-survival
#25
JOURNAL ARTICLE
Mary Anne Garner, Meredith G Hubbard, Evan R Boitet, Seth T Hubbard, Anushree Gade, Guoxin Ying, Bryan W Jones, Wolfgang Baehr, Alecia K Gross
NUDC (nuclear distribution protein C) is a mitotic protein involved in nuclear migration and cytokinesis across species. Considered a cytoplasmic dynein (henceforth dynein) cofactor, NUDC was shown to associate with the dynein motor complex during neuronal migration. NUDC is also expressed in postmitotic vertebrate rod photoreceptors where its function is unknown. Here, we examined the role of NUDC in postmitotic rod photoreceptors by studying the consequences of a conditional NUDC knockout in mouse rods (rNudC-/- )...
March 15, 2024: FASEB Journal: Official Publication of the Federation of American Societies for Experimental Biology
https://read.qxmd.com/read/38432987/primary-ciliary-dyskinesia-caused-by-homozygous-dnaaf1-mutations-resulting-from-a-consanguineous-marriage-a-case-report-from-japan
#26
JOURNAL ARTICLE
Masashi Ito, Kozo Morimoto, Mikio Saotome, Akiko Miyabayashi, Keiko Wakabayashi, Hiroyuki Yamada, Minako Hijikata, Naoto Keicho, Ken Ohta
We present the case of a 58-year-old female patient with primary ciliary dyskinesia (PCD). She was born to parents with a consanguineous marriage. Chest computed tomography conducted at age 41 years indicated no situs inversus, and findings of bronchiectasis were limited to the middle and lingular lobes. Despite long-term macrolide therapy, bronchiectasis exacerbations frequently occurred. PCD was suspected because of the low nasal nitric oxide level (20.7 nL/min). Electron microscopy revealed outer and inner dynein arm defects, and a genetic analysis identified a homozygous single-nucleotide deletion in the DNAAF1 gene...
March 4, 2024: Internal Medicine
https://read.qxmd.com/read/38430911/the-mechanism-and-energetics-of-the-dynein-priming-stroke
#27
JOURNAL ARTICLE
Mert Golcuk, Sema Zeynep Yilmaz, Ahmet Yildiz, Mert Gur
Dyneins are an AAA+ motor responsible for motility and force generation toward the minus end of microtubules. Dynein motility is powered by nucleotide-dependent transitions of its linker domain, which transitions between straight (post-powerstroke) and bent (pre-powerstroke) conformations. To understand the dynamics and energetics of the linker, we performed all-atom molecular dynamics simulations of human dynein-2 primed for its power stroke. Simulations revealed that the linker can adopt either a bent conformation or a semi-bent conformation, separated by a 5...
February 28, 2024: Structure
https://read.qxmd.com/read/38426808/temperature-dependent-augmentation-of-ciliary-motility-by-the-trp2-channel-in-chlamydomonas-reinhardtii
#28
JOURNAL ARTICLE
Shunta Fueki, Taro Kaneko, Haruka Matsuki, Yuki Hashimoto, Megumi Yoshida, Atsuko Isu, Ken-Ichi Wakabayashi, Kenjiro Yoshimura
Temperature is a critical factor for living organisms. Many microorganisms migrate toward preferable temperatures, and this behavior is called thermotaxis. In this study, the molecular and physiological bases for thermotaxis are examined in Chlamydomonas reinhardtii. A mutant with knockout of a transient receptor potential (TRP) channel, trp2-3, showed defective thermotaxis. The swimming velocity and ciliary beat frequency of wild-type Chlamydomonas increase with temperature; however, this temperature-dependent enhancement of motility was almost absent in the trp2-3 mutant...
March 1, 2024: Cytoskeleton
https://read.qxmd.com/read/38408845/skewed-x-chromosome-inactivation-drives-the-proportion-of-dnaaf6-defective-airway-motile-cilia-and-variable-expressivity-in-primary-ciliary-dyskinesia
#29
JOURNAL ARTICLE
Lucie Thomas, Laurence Cuisset, Jean-Francois Papon, Aline Tamalet, Isabelle Pin, Rola Abou Taam, Catherine Faucon, Guy Montantin, Sylvie Tissier, Philippe Duquesnoy, Florence Dastot-Le Moal, Bruno Copin, Nathalie Carion, Bruno Louis, Sandra Chantot-Bastaraud, Jean-Pierre Siffroi, Rana Mitri, André Coste, Estelle Escudier, Guillaume Thouvenin, Serge Amselem, Marie Legendre
BACKGROUND: Primary ciliary dyskinesia (PCD) is a rare airway disorder caused by defective motile cilia. Only male patients have been reported with pathogenic mutations in X-linked DNAAF6 , which result in the absence of ciliary dynein arms, whereas their heterozygous mothers are supposedly healthy. Our objective was to assess the possible clinical and ciliary consequences of X-chromosome inactivation (XCI) in these mothers. METHODS: XCI patterns of six mothers of male patients with DNAAF6 -related PCD were determined by DNA-methylation studies and compared with their clinical phenotype (6/6 mothers), as well as their ciliary phenotype (4/6 mothers), as assessed by immunofluorescence and high-speed videomicroscopy analyses...
February 26, 2024: Journal of Medical Genetics
https://read.qxmd.com/read/38407313/dynein-and-dynactin-move-long-range-but-are-delivered-separately-to-the-axon-tip
#30
JOURNAL ARTICLE
Alexander D Fellows, Michaela Bruntraeger, Thomas Burgold, Andrew R Bassett, Andrew P Carter
Axonal transport is essential for neuronal survival. This is driven by microtubule motors including dynein, which transports cargo from the axon tip back to the cell body. This function requires its cofactor dynactin and regulators LIS1 and NDEL1. Due to difficulties imaging dynein at a single-molecule level, it is unclear how this motor and its regulators coordinate transport along the length of the axon. Here, we use a neuron-inducible human stem cell line (NGN2-OPTi-OX) to endogenously tag dynein components and visualize them at a near-single molecule regime...
May 6, 2024: Journal of Cell Biology
https://read.qxmd.com/read/38405875/unc-16-interacts-with-lrk-1-and-wdfy-3-to-regulate-the-termination-of-axon-growth
#31
Cody J Drozd, Tamjid A Chowdhury, Christopher C Quinn
MAPK8IP3 (unc-16/JIP3) is a neurodevelopmental-disorder associated gene that can regulate the termination of axon growth. However, its role in this process is not well understood. Here, we report that UNC-16 promotes axon termination through a process that includes the LRK-1(LRRK-1/LRRK-2) kinase and the WDFY-3 (WDFY3/Alfy) selective autophagy protein. Genetic analysis suggests that UNC-16 promotes axon termination through an interaction between its RH1 domain and the dynein complex. Loss of unc-16 function causes accumulation of late endosomes specifically in the distal axon...
February 16, 2024: bioRxiv
https://read.qxmd.com/read/38405786/torques-within-and-outside-the-human-spindle-balance-twist-at-anaphase
#32
Lila Neahring, Yifei He, Nathan H Cho, Gaoxiang Liu, Jonathan Fernandes, Caleb J Rux, Konstantinos Nakos, Radhika Subramanian, Srigokul Upadhyayula, Ahmet Yildiz, Sophie Dumont
At each cell division, nanometer-scale motors and microtubules give rise to the micron-scale spindle. Many mitotic motors step helically around microtubules in vitro, and most are predicted to twist the spindle in a left-handed direction. However, the human spindle exhibits only slight global twist, raising the question of how these molecular torques are balanced. Here, using lattice light sheet microscopy, we find that anaphase spindles in the epithelial cell line MCF10A have a high baseline twist, and we identify factors that both increase and decrease this twist...
December 10, 2023: bioRxiv
https://read.qxmd.com/read/38405740/immuno-scanning-electron-microscopy-of-islet-primary-cilia
#33
Sanja Sviben, Alexander J Polino, Isabella Melena, Jing W Hughes
The definitive demonstration of protein localization on primary cilia has been a challenge for cilia biologists. Primary cilia are solitary thread-like projections that contain specialized protein composition, but as the ciliary structure overlays the cell membrane and other cell parts, the identity of ciliary proteins are difficult to ascertain by conventional imaging approaches like immunofluorescence microscopy. Surface scanning electron microscopy combined with immuno-labeling (immuno-SEM) bypasses some of these indeterminacies by unambiguously showing protein expression in the context of the 3D ultrastructure of the cilium...
February 16, 2024: bioRxiv
https://read.qxmd.com/read/38391943/structure-and-function-of-dynein-s-non-catalytic-subunits
#34
REVIEW
Lu Rao, Arne Gennerich
Dynein, an ancient microtubule-based motor protein, performs diverse cellular functions in nearly all eukaryotic cells, with the exception of land plants. It has evolved into three subfamilies-cytoplasmic dynein-1, cytoplasmic dynein-2, and axonemal dyneins-each differentiated by their cellular functions. These megadalton complexes consist of multiple subunits, with the heavy chain being the largest subunit that generates motion and force along microtubules by converting the chemical energy of ATP hydrolysis into mechanical work...
February 11, 2024: Cells
https://read.qxmd.com/read/38382357/multidimensional-screening-of-pancreatic-cancer-spheroids-reveals-vulnerabilities-in-mitotic-and-cell-matrix-adhesion-signaling-that-associate-with-metastatic-progression-and-decreased-patient-survival
#35
JOURNAL ARTICLE
Albert-Fred Aquino, Farhana Runa, Jannatul F Shoma, Audrey Todd, Matthew Wallace, Natan Roberto de Barros, Jonathan A Kelber
Pancreatic ductal adenocarcinoma (PDAC) is a highly aggressive malignancy, with a median survival of less than 12 months and a 5-year survival of less than 10 %. Here, we have established an image-based screening pipeline for quantifying single PDAC spheroid dynamics in genetically and phenotypically diverse PDAC cell models. Wild-type KRas PDAC cells formed tight/compact spheroids - compaction of these structures was completely blocked by cytoplasmic dynein and focal adhesion kinase (FAK) inhibitors. In contrast, PDAC cells containing mutant KRas formed loosely aggregated spheroids that grew significantly slower following inhibition of polo-like kinase 1 (PLK1) or focal adhesion kinase (FAK)...
February 6, 2024: Biochemical and Biophysical Research Communications
https://read.qxmd.com/read/38378744/molecular-structure-and-function-of-mysterin-rnf213
#36
JOURNAL ARTICLE
Daisuke Morito
Mysterin is a large intracellular protein harboring a RING finger ubiquitin ligase domain and is also referred to as RING finger protein 213 (RNF213). The author performed the first molecular cloning of the mysterin gene as the final step in genetic exploration of cerebrovascular moyamoya disease (MMD) and initiated the next round of exploration to understand its molecular and cellular functions. Although much remains unknown, accumulating findings suggest that mysterin functions in cells by targeting massive intracellular structures such as lipid droplets (LDs) and various invasive pathogens...
February 20, 2024: Journal of Biochemistry
https://read.qxmd.com/read/38359560/application-of-sperm-motion-kinematics-and-motility-related-proteins-for-prediction-of-male-fertility
#37
JOURNAL ARTICLE
Jeong-Won Bae, Ju-Mi Hwang, Woo-Jin Lee, Dae-Hyun Kim, Jun Koo Yi, Jae Jung Ha, Dong Yep Oh, Woo-Sung Kwon
The selection of superior sires is paramount for enhancing the efficiency of animal production in the livestock industry. However, semen quality assessment still relies on conventional semen analysis techniques in both animals and humans. Despite extensive efforts to develop various biomarkers for more accurate and precise predictions of male fertility potential, more effective physiological indicators and advance potential biomarkers are needed. Herein, we aimed to develop new potential biomarkers related to sperm motion kinematics for male fertility prediction...
February 7, 2024: Theriogenology
https://read.qxmd.com/read/38354735/a-conserved-cenp-e-region-mediates-bubr1-independent-recruitment-to-the-outer-corona-at-mitotic-onset
#38
JOURNAL ARTICLE
Jeraldine Weber, Thibault Legal, Alicia Perez Lezcano, Agata Gluszek-Kustusz, Calum Paterson, Susana Eibes, Marin Barisic, Owen R Davies, Julie P I Welburn
The outer corona plays an essential role at the onset of mitosis by expanding to maximize microtubule attachment to kinetochores.1 , 2 The low-density structure of the corona forms through the expansion of unattached kinetochores. It comprises the RZZ complex, the dynein adaptor Spindly, the plus-end directed microtubule motor centromere protein E (CENP-E), and the Mad1/Mad2 spindle-assembly checkpoint proteins.3 , 4 , 5 , 6 , 7 , 8 , 9 , 10 CENP-E specifically associates with unattached kinetochores to facilitate chromosome congression,11 , 12 , 13 , 14 , 15 , 16 interacting with BubR1 at the kinetochore through its C-terminal region (2091-2358)...
February 8, 2024: Current Biology: CB
https://read.qxmd.com/read/38351062/docking-protein-6-dok6-selectively-docks-the-neurotrophic-signaling-transduction-to-restrain-peripheral-neuropathy
#39
JOURNAL ARTICLE
Yan Guo, Pan Xiang, Xiaojiao Sun, Wei Liu, Jiafeng Zhou, Bin Yin, Lin Hou, Boqin Qiang, Huiliang Li, Pengcheng Shu, Xiaozhong Peng
The appropriate and specific response of nerve cells to various external cues is essential for the establishment and maintenance of neural circuits, and this process requires the proper recruitment of adaptor molecules to selectively activate downstream pathways. Here, we identified that DOK6, a member of the Dok (downstream of tyrosine kinases) family, is required for the maintenance of peripheral axons, and that loss of Dok6 can cause typical peripheral neuropathy symptoms in mice, manifested as impaired sensory, abnormal posture, paw deformities, blocked nerve conduction, and dysmyelination...
February 14, 2024: Signal Transduction and Targeted Therapy
https://read.qxmd.com/read/38348540/dnali1-promotes-neurodegeneration-after-traumatic-brain-injury-via-inhibition-of-autophagosome-lysosome-fusion
#40
JOURNAL ARTICLE
Xulong Ding, Shuqiang Cao, Qing Wang, Bin Du, Kefeng Lu, Shiqian Qi, Ying Cheng, Qing-Zhang Tuo, Weibo Liang, Peng Lei
Traumatic brain injury (TBI) leads to progressive neurodegeneration that may be caused by chronic traumatic encephalopathy (CTE). However, the precise mechanism remains unclear. Herein, the study identifies a crucial protein, axonemal dynein light intermediate polypeptide 1 (DNALI1), and elucidated its potential pathogenic role in post-TBI neurodegeneration. The DNALI1 gene is systematically screened through analyses of Aging, Dementia, and TBI studies, confirming its elevated expression both in vitro and in vivo...
February 13, 2024: Advanced Science (Weinheim, Baden-Wurttemberg, Germany)
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