The KASH5 protein involved in meiotic chromosomal movements is a novel dynein activating adaptor
暂无分享,去创建一个
Morgan E. DeSantis | Jingjing Zhang | J. Nandakumar | Hiroki Shibuya | Sharon R. Garrott | Ritvija Agrawal | John P. Gillies | Juliana L. Zang
[1] A. Carter,et al. Structure of dynein-dynactin on microtubules shows tandem recruitment of cargo adaptors , 2022, bioRxiv.
[2] R. Dominguez,et al. A tunable LIC1-adaptor interaction modulates dynein activity in a cargo-specific manner , 2020, Nature Communications.
[3] R. McKenney,et al. New insights into the mechanism of dynein motor regulation by lissencephaly-1 , 2020, eLife.
[4] Meng-Han Tsai,et al. Impairment in dynein-mediated nuclear translocation by BICD2 C-terminal truncation leads to neuronal migration defect and human brain malformation , 2020, Acta Neuropathologica Communications.
[5] R. Vallee,et al. Nesprin-2 Recruitment of BicD2 to the Nuclear Envelope Controls Dynein/Kinesin-Mediated Neuronal Migration In Vivo , 2020, Current Biology.
[6] M. Gurusaran,et al. A molecular mechanism for LINC complex branching by structurally diverse SUN-KASH 6:6 assemblies , 2020, bioRxiv.
[7] S. Bullock,et al. Lis1 activates dynein motility by modulating its pairing with dynactin , 2020, Nature Cell Biology.
[8] Samara L. Reck-Peterson,et al. Lis1 promotes the formation of activated cytoplasmic dynein-1 complexes , 2020, Nature Cell Biology.
[9] Rongde Qiu,et al. LIS1 regulates cargo-adapter–mediated activation of dynein by overcoming its autoinhibition in vivo , 2019, The Journal of cell biology.
[10] S. Blanchard,et al. Cargo adaptors regulate stepping and force generation of mammalian dynein-dynactin , 2019, Nature Chemical Biology.
[11] E. Holzbaur,et al. Dynein activators and adaptors at a glance , 2019, Journal of Cell Science.
[12] R. Vale,et al. CRACR2a is a calcium-activated dynein adaptor protein that regulates endocytic traffic , 2019, The Journal of cell biology.
[13] Morkos A. Henen,et al. A transient helix in the disordered region of dynein light intermediate chain links the motor to structurally diverse adaptors for cargo transport , 2019, PLoS biology.
[14] Samara L. Reck-Peterson,et al. The cytoplasmic dynein transport machinery and its many cargoes , 2018, Nature Reviews Molecular Cell Biology.
[15] R. Dominguez,et al. A conserved interaction of the dynein light intermediate chain with dynein-dynactin effectors necessary for processivity , 2018, Nature Communications.
[16] A. Carter,et al. Cryo-EM shows how dynactin recruits two dyneins for faster movement , 2017, Nature.
[17] E. Smith,et al. Dissecting the telomere-inner nuclear membrane interface formed in meiosis , 2017, Nature Structural & Molecular Biology.
[18] Danielle A. Grotjahn,et al. Cryo-electron tomography reveals that dynactin recruits a team of dyneins for processive motility , 2017, Nature Structural & Molecular Biology.
[19] A. Bird,et al. Cryo-EM Reveals How Human Cytoplasmic Dynein Is Auto-inhibited and Activated , 2017, Cell.
[20] M. Vershinin,et al. Differential effects of the dynein-regulatory factor Lissencephaly-1 on processive dynein-dynactin motility , 2017, The Journal of Biological Chemistry.
[21] William B. Redwine,et al. Figures and figure supplements The human cytoplasmic dynein interactome reveals novel activators of motility , 2017 .
[22] Ha Thanh Thi Hoang,et al. Lissencephaly-1 is a context-dependent regulator of the human dynein complex , 2017, eLife.
[23] Helena R Pires,et al. Molecular mechanism of dynein recruitment to kinetochores by the Rod–Zw10–Zwilch complex and Spindly , 2017, The Journal of cell biology.
[24] R. Vale,et al. Disease-associated mutations in human BICD2 hyperactivate motility of dynein–dynactin , 2017, bioRxiv.
[25] M. Hieda. Implications for Diverse Functions of the LINC Complexes Based on the Structure , 2017, Cells.
[26] I. Meier. LINCing the eukaryotic tree of life – towards a broad evolutionary comparison of nucleocytoplasmic bridging complexes , 2016, Journal of Cell Science.
[27] R. Vale,et al. Assembly and activation of dynein–dynactin by the cargo adaptor protein Hook3 , 2016, bioRxiv.
[28] A. Carter,et al. How dynein and dynactin transport cargos: a structural perspective. , 2016, Current opinion in structural biology.
[29] Yoshinori Watanabe,et al. MAJIN Links Telomeric DNA to the Nuclear Membrane by Exchanging Telomere Cap , 2015, Cell.
[30] Samara L. Reck-Peterson,et al. Mechanism and regulation of cytoplasmic dynein. , 2015, Annual review of cell and developmental biology.
[31] N. Kleckner,et al. Recombination, Pairing, and Synapsis of Homologs during Meiosis. , 2015, Cold Spring Harbor perspectives in biology.
[32] C. Stewart,et al. Mechanism and regulation of rapid telomere prophase movements in mouse meiotic chromosomes. , 2015, Cell reports.
[33] Kai Zhang,et al. The structure of the dynactin complex and its interaction with dynein , 2015, Science.
[34] Yoshinori Watanabe,et al. The Dissection of Meiotic Chromosome Movement in Mice Using an In Vivo Electroporation Technique , 2014, PLoS genetics.
[35] R. Vale,et al. A Ras-like domain in the light intermediate chain bridges the dynein motor to a cargo-binding region , 2014, eLife.
[36] Gira Bhabha,et al. Activation of cytoplasmic dynein motility by dynactin-cargo adapter complexes , 2014, Science.
[37] Ha Thanh Thi Hoang,et al. In vitro reconstitution of a highly processive recombinant human dynein complex , 2014, The EMBO journal.
[38] Yoshinori Watanabe,et al. The meiosis-specific modification of mammalian telomeres , 2014, Cell cycle.
[39] Samara L. Reck-Peterson,et al. Reconstitution of dynein transport to the microtubule plus end by kinesin , 2014, eLife.
[40] Yoshinori Watanabe,et al. The TRF1-binding protein TERB1 promotes chromosome movement and telomere rigidity in meiosis , 2014, Nature Cell Biology.
[41] C. Stewart,et al. A mammalian KASH domain protein coupling meiotic chromosomes to the cytoskeleton , 2013, The Journal of cell biology.
[42] S. Burgess,et al. Functions and mechanics of dynein motor proteins , 2013, Nature Reviews Molecular Cell Biology.
[43] A. Carter. Crystal clear insights into how the dynein motor moves , 2013, Journal of Cell Science.
[44] A. Hyman,et al. BICD2, dynactin, and LIS1 cooperate in regulating dynein recruitment to cellular structures , 2012, Molecular biology of the cell.
[45] Samara L. Reck-Peterson,et al. Lis1 Acts as a “Clutch” between the ATPase and Microtubule-Binding Domains of the Dynein Motor , 2012, Cell.
[46] Min Han,et al. A conserved KASH domain protein associates with telomeres, SUN1, and dynactin during mammalian meiosis , 2012, The Journal of cell biology.
[47] Andrea Rothballer,et al. LINC Complexes Form by Binding of Three KASH Peptides to Domain Interfaces of Trimeric SUN Proteins , 2012, Cell.
[48] A. Dernburg,et al. Dynein-dependent processive chromosome motions promote homologous pairing in C. elegans meiosis , 2012, The Journal of cell biology.
[49] Xiulian Du,et al. Structure of Sad1-UNC84 Homology (SUN) Domain Defines Features of Molecular Bridge in Nuclear Envelope* , 2011, The Journal of Biological Chemistry.
[50] C. Horgan,et al. Rab GTPases and microtubule motors. , 2011, Biochemical Society transactions.
[51] Wilhelm Palm,et al. How shelterin protects mammalian telomeres. , 2008, Annual review of genetics.
[52] Karl Mechtler,et al. BAC TransgeneOmics: a high-throughput method for exploration of protein function in mammals , 2008, Nature Methods.
[53] Min Han,et al. SUN1 is required for telomere attachment to nuclear envelope and gametogenesis in mice. , 2007, Developmental cell.
[54] I. Jordens,et al. Rab Proteins, Connecting Transport and Vesicle Fusion , 2005, Traffic.
[55] H. Kawasaki,et al. Classification and evolution of EF-hand proteins , 1998, Biometals.
[56] Michael P. Sheetz,et al. Cytoplasmic dynein is a minus end-directed motor for membranous organelles , 1989, Cell.