نتایج جستجو برای: dynein

تعداد نتایج: 4423  

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2017
Ha Thi Hoang Max A Schlager Andrew P Carter Simon L Bullock

Mutations in the human DYNC1H1 gene are associated with neurological diseases. DYNC1H1 encodes the heavy chain of cytoplasmic dynein-1, a 1.4-MDa motor complex that traffics organelles, vesicles, and macromolecules toward microtubule minus ends. The effects of the DYNC1H1 mutations on dynein motility, and consequently their links to neuropathology, are not understood. Here, we address this issu...

Journal: :Chemical reviews 2014
Benjamin H Blehm Paul R Selvin

1. INTRODUCTION Kinesin and dynein walking on microtubules are the two main drivers of long-distance intracellular transport in a huge variety of systems, from neurons to melanophores. These motors, however, are oppositely directed, with (most) kinesin driving cargos toward the plus ends of microtubules whereas dynein drives cargos toward the minus ends. 1 There are only two types of dynein, cy...

Journal: :Developmental cell 2006
Sandrine Grava Florian Schaerer Mahamadou Faty Peter Philippsen Yves Barral

The orientation of the mitotic spindle plays a key role in determining whether a polarized cell will divide symmetrically or asymmetrically. In most cell types, cytoplasmic dynein plays a critical role in spindle orientation. However, how dynein directs opposite spindle poles toward distinct and predetermined cell ends is poorly understood. Here, we show that dynein distributes preferentially t...

Journal: :Molecular biology of the cell 2003
Jun Zhang Shihe Li Reinhard Fischer Xin Xiang

The mechanism(s) by which microtubule plus-end tracking proteins are targeted is unknown. In the filamentous fungus Aspergillus nidulans, both cytoplasmic dynein and NUDF, the homolog of the LIS1 protein, localize to microtubule plus ends as comet-like structures. Herein, we show that NUDM, the p150 subunit of dynactin, also forms dynamic comet-like structures at microtubule plus ends. By exami...

Journal: :The Journal of Cell Biology 1998
Alistair Harrison Patricia Olds-Clarke Stephen M. King

The cytoplasmic dynein light chain Tctex1 is a candidate for one of the distorter products involved in the non-Mendelian transmission of mouse t haplotypes. It has been unclear, however, how the t-specific mutations in this protein, which is found associated with cytoplasmic dynein in many tissues, could result in a male germ cell-specific phenotype. Here, we demonstrate that Tctex1 is not only...

2009
Ying Wai Chan Luca L. Fava Andreas Uldschmid Michael H.A. Schmitz Daniel W. Gerlich Erich A. Nigg Anna Santamaria

Mitotic spindle formation and chromosome segregation depend critically on kinetochore-microtubule (KT-MT) interactions. A new protein, termed Spindly in Drosophila and SPDL-1 in C. elegans, was recently shown to regulate KT localization of dynein, but depletion phenotypes revealed striking differences, suggesting evolutionarily diverse roles of mitotic dynein. By characterizing the function of ...

2010
Jean-Baptiste Manneville Muguette Jehanno Sandrine Etienne-Manneville

Centrosome positioning is crucial during cell division, cell differentiation, and for a wide range of cell-polarized functions including migration. In multicellular organisms, centrosome movement across the cytoplasm is thought to result from a balance of forces exerted by the microtubule-associated motor dynein. However, the mechanisms regulating dynein-mediated forces are still unknown. We sh...

2012
Anja K. Dunsch Dean Hammond Jennifer Lloyd Lothar Schermelleh Ulrike Gruneberg Francis A. Barr

The cytoplasmic dynein motor generates pulling forces to center and orient the mitotic spindle within the cell. During this positioning process, dynein oscillates from one pole of the cell cortex to the other but only accumulates at the pole farthest from the spindle. Here, we show that dynein light chain 1 (DYNLL1) is required for this asymmetric cortical localization of dynein and has a speci...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2000
E Hirakawa H Higuchi Y Y Toyoshima

We have analyzed the movement of single 22S dynein molecules from Tetrahymena cilia by using a nanometer measuring system equipped with optical tweezers. Statistical analysis proved that a single molecule of 22S dynein can move processively and develop force at low concentrations of ATP (<20 microM). The maximum force was approximately 4.7 pN, and the force-velocity curve was convex down. Durin...

Journal: :The Journal of Cell Biology 2008
Noveera T. Ahmed Chunlei Gao Ben F. Lucker Douglas G. Cole David R. Mitchell

Formation of flagellar outer dynein arms in Chlamydomonas reinhardtii requires the ODA16 protein at a previously uncharacterized assembly step. Here, we show that dynein extracted from wild-type axonemes can rebind to oda16 axonemes in vitro, and dynein in oda16 cytoplasmic extracts can bind to docking sites on pf28 (oda) axonemes, which is consistent with a role for ODA16 in dynein transport, ...

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