Literature DB >> 18820457

Drosophila klaroid encodes a SUN domain protein required for Klarsicht localization to the nuclear envelope and nuclear migration in the eye.

Martin P Kracklauer1, Susan M L Banks, Xuanhua Xie, Yaning Wu, Janice A Fischer.   

Abstract

KASH (Klarsicht/Anc-1/Syne homology) domain proteins are cytoskeleton-associated proteins localized uniquely to the outer nuclear membrane. Klarsicht is a KASH protein required for nuclear migration in differentiating cells of the Drosophila eye. The C-terminal KASH domain of Klarsicht resides in the perinuclear space, and the cytoplasmic moiety connects to the microtubule organizing center. In C. elegans and vertebrate cells, SUN (Sad1/UNC-84) domain proteins reside in the inner nuclear membrane and tether KASH proteins to the outer nuclear membrane. Is there a Drosophila SUN protein that performs a similar function, and if so, is it like Klarsicht, obviously essential for nuclear positioning only in the eye? Here, we identify Drosophila Klaroid, a SUN protein that tethers Klarsicht. klaroid loss-of-function mutants are indistinguishable phenotypically from klarsicht mutants. Remarkably, neither gene is essential for Drosophila viability or fertility, and even in klaroid klorsicht double mutants, the only obvious external morphological defect is rough eyes. In addition, we find that klaroid and klarsicht are required for nuclear migration in differentiating neurons and in non-neural cells. Finally, while perinuclear Klaroid is ubiquitous in the eye, Klarsicht expression is limited to differentiating cells and may be part of the trigger for apical nuclear migration.

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Year:  2007        PMID: 18820457     DOI: 10.4161/fly.4254

Source DB:  PubMed          Journal:  Fly (Austin)        ISSN: 1933-6934            Impact factor:   2.160


  71 in total

1.  LINCing lamin B2 to neuronal migration: growing evidence for cell-specific roles of B-type lamins.

Authors:  Catherine Coffinier; Loren G Fong; Stephen G Young
Journal:  Nucleus       Date:  2010 Sep-Oct       Impact factor: 4.197

Review 2.  Lamin-binding Proteins.

Authors:  Katherine L Wilson; Roland Foisner
Journal:  Cold Spring Harb Perspect Biol       Date:  2010-02-17       Impact factor: 10.005

Review 3.  Interactions between nuclei and the cytoskeleton are mediated by SUN-KASH nuclear-envelope bridges.

Authors:  Daniel A Starr; Heidi N Fridolfsson
Journal:  Annu Rev Cell Dev Biol       Date:  2010       Impact factor: 13.827

4.  The Drosophila SUN protein Spag4 cooperates with the coiled-coil protein Yuri Gagarin to maintain association of the basal body and spermatid nucleus.

Authors:  Martin P Kracklauer; Heather M Wiora; William J Deery; Xin Chen; Benjamin Bolival; Dwight Romanowicz; Rebecca A Simonette; Margaret T Fuller; Janice A Fischer; Kathleen M Beckingham
Journal:  J Cell Sci       Date:  2010-07-20       Impact factor: 5.285

5.  Lamin Dysfunction Mediates Neurodegeneration in Tauopathies.

Authors:  Bess Frost; Farah H Bardai; Mel B Feany
Journal:  Curr Biol       Date:  2015-12-24       Impact factor: 10.834

6.  Affinity-based isolation of tagged nuclei from Drosophila tissues for gene expression analysis.

Authors:  Jingqun Ma; Vikki Marie Weake
Journal:  J Vis Exp       Date:  2014-03-25       Impact factor: 1.355

Review 7.  Making the LINC: SUN and KASH protein interactions.

Authors:  Dae In Kim; K C Birendra; Kyle J Roux
Journal:  Biol Chem       Date:  2015-04       Impact factor: 3.915

Review 8.  Communication between the cytoskeleton and the nuclear envelope to position the nucleus.

Authors:  Daniel A Starr
Journal:  Mol Biosyst       Date:  2007-07-16

9.  Temporal and tissue-specific disruption of LINC complexes in vivo.

Authors:  David Razafsky; Didier Hodzic
Journal:  Genesis       Date:  2014-03-10       Impact factor: 2.487

Review 10.  Nuclear positioning.

Authors:  Gregg G Gundersen; Howard J Worman
Journal:  Cell       Date:  2013-03-14       Impact factor: 41.582

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