The KASH5 protein involved in meiotic chromosomal movements is a novel dynein activating adaptor

Dynein harnesses ATP hydrolysis to move cargo on microtubules in multiple biological contexts. Dynein meets a unique challenge in meiosis by moving chromosomes tethered to the nuclear envelope to facilitate homolog pairing essential for gametogenesis. Though processive dynein motility requires binding to an activating adaptor, the identity of the activating adaptor required for dynein to move meiotic chromosomes is unknown. We show that the meiosis-specific nuclear-envelope protein KASH5 is a dynein activating adaptor: KASH5 directly binds dynein using a mechanism conserved among activating adaptors and converts dynein into a processive motor. We map the dynein-binding surface of KASH5, identifying mutations that abrogate dynein binding in vitro and disrupt recruitment of the dynein machinery to the nuclear envelope in cultured cells and mouse spermatocytes in vivo. Our study identifies KASH5 as the first transmembrane dynein activating adaptor and provides molecular insights into how it activates dynein during meiosis.

[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.