Literature DB >> 10559989

Drosophila Lissencephaly-1 functions with Bic-D and dynein in oocyte determination and nuclear positioning.

A Swan1, T Nguyen, B Suter.   

Abstract

Here we show that the Drosophila homologue of Lissencephaly-1, DLis-1, acts together with Bicaudal-D (Bic-D), Egalitarian (Egl), dynein and microtubules to determine oocyte identity. DLis-1 is further required for nurse-cell-to-oocyte transport during oocyte growth, and for the positioning of the nucleus in the oocyte. Immunostaining of DLis-1 protein reveals a cortical localization that is independent of microtubules. DLis-1 may function in this position as a cortical anchor for the other nuclear-localization factors. DLis-1 and Bic-D are further required for nuclear localization in the developing nervous system, indicating that homologues of Bic-D, dynein and Egl-like proteins may also be involved in vertebrate neural migration and that their absence may cause a Miller-Dieker-like lissencephaly.

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Year:  1999        PMID: 10559989     DOI: 10.1038/15680

Source DB:  PubMed          Journal:  Nat Cell Biol        ISSN: 1465-7392            Impact factor:   28.824


  76 in total

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Review 5.  Making the LINC: SUN and KASH protein interactions.

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Journal:  Biol Chem       Date:  2015-04       Impact factor: 3.915

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7.  Drosophila klarsicht has distinct subcellular localization domains for nuclear envelope and microtubule localization in the eye.

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Journal:  Genetics       Date:  2004-11       Impact factor: 4.562

8.  Complete loss of Ndel1 results in neuronal migration defects and early embryonic lethality.

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9.  UNC-83 coordinates kinesin-1 and dynein activities at the nuclear envelope during nuclear migration.

Authors:  Heidi N Fridolfsson; Nina Ly; Marina Meyerzon; Daniel A Starr
Journal:  Dev Biol       Date:  2009-12-21       Impact factor: 3.582

Review 10.  Nuclear positioning.

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Journal:  Cell       Date:  2013-03-14       Impact factor: 41.582

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