An Essential Role for Katanin p80 and Microtubule Severing in Male Gamete Production

Katanin is an evolutionarily conserved microtubule-severing complex implicated in multiple aspects of microtubule dynamics. Katanin consists of a p60 severing enzyme and a p80 regulatory subunit. The p80 subunit is thought to regulate complex targeting and severing activity, but its precise role remains elusive. In lower-order species, the katanin complex has been shown to modulate mitotic and female meiotic spindle dynamics and flagella development. The in vivo function of katanin p80 in mammals is unknown. Here we show that katanin p80 is essential for male fertility. Specifically, through an analysis of a mouse loss-of-function allele (the Taily line), we demonstrate that katanin p80, most likely in association with p60, has an essential role in male meiotic spindle assembly and dissolution and the removal of midbody microtubules and, thus, cytokinesis. Katanin p80 also controls the formation, function, and dissolution of a microtubule structure intimately involved in defining sperm head shaping and sperm tail formation, the manchette, and plays a role in the formation of axoneme microtubules. Perturbed katanin p80 function, as evidenced in the Taily mouse, results in male sterility characterized by decreased sperm production, sperm with abnormal head shape, and a virtual absence of progressive motility. Collectively these data demonstrate that katanin p80 serves an essential and evolutionarily conserved role in several aspects of male germ cell development.

[1]  F. McNally,et al.  Microtubule-severing enzymes. , 2010, Current opinion in cell biology.

[2]  F. Nédélec,et al.  Katanin Contributes to Interspecies Spindle Length Scaling in Xenopus , 2011, Cell.

[3]  J. Ross,et al.  Drosophila katanin-60 depolymerizes and severs at microtubule defects. , 2011, Biophysical journal.

[4]  P. Baas,et al.  Cell Migration: Katanin Gives Microtubules a Trim , 2011, Current Biology.

[5]  F. McNally,et al.  The spindle assembly function of Caenorhabditis elegans katanin does not require microtubule-severing activity , 2011, Molecular biology of the cell.

[6]  P. McIntyre,et al.  Cysteine-rich secretory protein 4 is an inhibitor of transient receptor potential M8 with a role in establishing sperm function , 2011, Proceedings of the National Academy of Sciences.

[7]  W. Marshall,et al.  Ciliogenesis: building the cell's antenna , 2011, Nature Reviews Molecular Cell Biology.

[8]  Shannon F. Stewman,et al.  Drosophila katanin is a microtubule depolymerase that regulates cortical-microtubule plus-end interactions and cell migration , 2011, Nature Cell Biology.

[9]  M. Bornens,et al.  GMAP210 and IFT88 are present in the spermatid golgi apparatus and participate in the development of the acrosome–acroplaxome complex, head–tail coupling apparatus and tail , 2011, Developmental dynamics : an official publication of the American Association of Anatomists.

[10]  M. O’Bryan,et al.  Spermiation: The process of sperm release. , 2011, Spermatogenesis.

[11]  M. O’Bryan,et al.  Genome-wide ENU Mutagenesis for the Discovery of Novel Male Fertility Regulators , 2010, Systems biology in reproductive medicine.

[12]  P. Baas,et al.  Acetylation of Microtubules Influences Their Sensitivity to Severing by Katanin in Neurons and Fibroblasts , 2010, The Journal of Neuroscience.

[13]  B. Nixon,et al.  Glioma pathogenesis-related 1-like 1 is testis enriched, dynamically modified, and redistributed during male germ cell maturation and has a potential role in sperm-oocyte binding. , 2010, Endocrinology.

[14]  R. Vallee,et al.  LIS1 and NudE Induce a Persistent Dynein Force-Producing State , 2010, Cell.

[15]  D. Cyr,et al.  Surfing the wave, cycle, life history, and genes/proteins expressed by testicular germ cells. Part 1: Background to spermatogenesis, spermatogonia, and spermatocytes , 2010, Microscopy research and technique.

[16]  D. Cyr,et al.  Surfing the wave, cycle, life history, and genes/proteins expressed by testicular germ cells. Part 2: Changes in spermatid organelles associated with development of spermatozoa , 2009, Microscopy research and technique.

[17]  M. O’Bryan,et al.  Phenotyping male infertility in the mouse: how to get the most out of a ‘non-performer’ , 2009, Human reproduction update.

[18]  Cecilia Conde,et al.  Microtubule assembly, organization and dynamics in axons and dendrites , 2009, Nature Reviews Neuroscience.

[19]  P. Bastien,et al.  Microtubule‐severing proteins are involved in flagellar length control and mitosis in Trypanosomatids , 2009, Molecular microbiology.

[20]  W. Marshall,et al.  Katanin knockdown supports a role for microtubule severing in release of basal bodies before mitosis in Chlamydomonas. , 2009, Molecular biology of the cell.

[21]  J. Gaertig,et al.  Katanin regulates dynamics of microtubules and biogenesis of motile cilia , 2007, The Journal of cell biology.

[22]  G. Schiavo,et al.  Spastin and microtubules: Functions in health and disease , 2007, Journal of neuroscience research.

[23]  H. Sudo,et al.  LAPSER1 is a putative cytokinetic tumor suppressor that shows the same centrosome and midbody subcellular localization pattern as p80 katanin , 2007, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[24]  Frédéric Chalmel,et al.  The conserved transcriptome in human and rodent male gametogenesis , 2007, Proceedings of the National Academy of Sciences.

[25]  G. C. Rogers,et al.  Three microtubule severing enzymes contribute to the “Pacman-flux” machinery that moves chromosomes , 2007, The Journal of cell biology.

[26]  R I McLachlan,et al.  Histological evaluation of the human testis--approaches to optimizing the clinical value of the assessment: mini review. , 2007, Human reproduction.

[27]  K. Oegema,et al.  Katanin controls mitotic and meiotic spindle length , 2006, The Journal of cell biology.

[28]  R. Vale,et al.  Making more microtubules by severing: a common theme of noncentrosomal microtubule arrays? , 2006, The Journal of cell biology.

[29]  Diego G. Silva,et al.  Fat aussie--a new Alström syndrome mouse showing a critical role for ALMS1 in obesity, diabetes, and spermatogenesis. , 2006, Molecular endocrinology.

[30]  J. Morrison,et al.  FGFR-1 signaling is involved in spermiogenesis and sperm capacitation , 2006, Journal of Cell Science.

[31]  Atsushi Yoshiki,et al.  Recruitment of katanin p60 by phosphorylated NDEL1, an LIS1 interacting protein, is essential for mitotic cell division and neuronal migration. , 2005, Human molecular genetics.

[32]  C. Hoogenraad,et al.  The microtubule plus-end-tracking protein CLIP-170 associates with the spermatid manchette and is essential for spermatogenesis. , 2005, Genes & development.

[33]  L. Qiang,et al.  Microtubules cut and run. , 2005, Trends in cell biology.

[34]  L. Qiang,et al.  Regulation of Microtubule Severing by Katanin Subunits during Neuronal Development , 2005, The Journal of Neuroscience.

[35]  L. Tres,et al.  The acrosome-acroplaxome-manchette complex and the shaping of the spermatid head. , 2004, Archives of histology and cytology.

[36]  P. Lefebvre,et al.  PF15p Is the Chlamydomonas Homologue of the Katanin p80 Subunit and Is Required for Assembly of Flagellar Central Microtubules , 2004, Eukaryotic Cell.

[37]  H. Arai,et al.  Expression of NUDEL in manchette and its implication in spermatogenesis , 2004, FEBS letters.

[38]  H. Arnold,et al.  Inactivation of a Testis-specific Lis1 Transcript in Mice Prevents Spermatid Differentiation and Causes Male Infertility* , 2003, Journal of Biological Chemistry.

[39]  A. Kierszenbaum Intramanchette transport (IMT): Managing the making of the spermatid head, centrosome, and tail , 2002, Molecular reproduction and development.

[40]  F. McNally,et al.  Katanin inhibition prevents the redistribution of γ-tubulin at mitosis , 2002 .

[41]  F. McNally,et al.  Katanin inhibition prevents the redistribution of gamma-tubulin at mitosis. , 2002, Journal of cell science.

[42]  C. Mahaffey,et al.  The mouse fidgetin gene defines a new role for AAA family proteins in mammalian development , 2000, Nature Genetics.

[43]  L. Quarmby,et al.  Cellular Samurai: katanin and the severing of microtubules. , 2000, Journal of cell science.

[44]  R. Mclachlan,et al.  Spermiation failure is a major contributor to early spermatogenic suppression caused by hormone withdrawal in adult rats. , 2000, Endocrinology.

[45]  F. McNally,et al.  Two domains of p80 katanin regulate microtubule severing and spindle pole targeting by p60 katanin. , 2000, Journal of cell science.

[46]  F. McNally,et al.  MEI-1/MEI-2 katanin-like microtubule severing activity is required for Caenorhabditis elegans meiosis. , 2000, Genes & development.

[47]  F. McNally Capturing a ring of samurai , 2000, Nature Cell Biology.

[48]  P. Baas,et al.  An Essential Role for Katanin in Severing Microtubules in the Neuron , 1999, The Journal of cell biology.

[49]  F. McNally,et al.  Katanin is responsible for the M-phase microtubule-severing activity in Xenopus eggs. , 1998, Molecular biology of the cell.

[50]  F. McNally,et al.  A role for katanin-mediated axonemal severing during Chlamydomonas deflagellation. , 1998, Molecular biology of the cell.

[51]  R. Vale,et al.  Katanin, a Microtubule-Severing Protein, Is a Novel AAA ATPase that Targets to the Centrosome Using a WD40-Containing Subunit , 1998, Cell.

[52]  R. Vale,et al.  Identification of katanin, an ATPase that severs and disassembles stable microtubules , 1993, Cell.

[53]  M. Meistrich,et al.  Linkage of manchette microtubules to the nuclear envelope and observations of the role of the manchette in nuclear shaping during spermiogenesis in rodents. , 1991, The American journal of anatomy.

[54]  K. Kemphues,et al.  Mutations affecting the meiotic and mitotic divisions of the early Caenorhabditis elegans embryo. , 1990, Genetics.

[55]  L. Romrell,et al.  Separation of mouse spermatogenic cells by sedimentation velocity. A morphological characterization. , 1976, Developmental biology.