Literature DB >> 12477385

Polar transport in the Drosophila oocyte requires Dynein and Kinesin I cooperation.

Jens Januschke1, Louis Gervais, Sajith Dass, Julia A Kaltschmidt, Hernan Lopez-Schier, Daniel St Johnston, Andrea H Brand, Siegfried Roth, Antoine Guichet.   

Abstract

BACKGROUND: The cytoskeleton and associated motors play an important role in the establishment of intracellular polarity. Microtubule-based transport is required in many cell types for the asymmetric localization of mRNAs and organelles. A striking example is the Drosophila oocyte, where microtubule-dependent processes govern the asymmetric positioning of the nucleus and the localization to distinct cortical domains of mRNAs that function as cytoplasmic determinants. A conserved machinery for mRNA localization and nuclear positioning involving cytoplasmic Dynein has been postulated; however, the precise role of plus- and minus end-directed microtubule-based transport in axis formation is not yet understood.
RESULTS: Here, we show that mRNA localization and nuclear positioning at mid-oogenesis depend on two motor proteins, cytoplasmic Dynein and Kinesin I. Both of these microtubule motors cooperate in the polar transport of bicoid and gurken mRNAs to their respective cortical domains. In contrast, Kinesin I-mediated transport of oskar to the posterior pole appears to be independent of Dynein. Beside their roles in RNA transport, both motors are involved in nuclear positioning and in exocytosis of Gurken protein. Dynein-Dynactin complexes accumulate at two sites within the oocyte: around the nucleus in a microtubule-independent manner and at the posterior pole through Kinesin-mediated transport.
CONCLUSION: The microtubule motors cytoplasmic Dynein and Kinesin I, by driving transport to opposing microtubule ends, function in concert to establish intracellular polarity within the Drosophila oocyte. Furthermore, Kinesin-dependent localization of Dynein suggests that both motors are components of the same complex and therefore might cooperate in recycling each other to the opposite microtubule pole.

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Year:  2002        PMID: 12477385     DOI: 10.1016/s0960-9822(02)01302-7

Source DB:  PubMed          Journal:  Curr Biol        ISSN: 0960-9822            Impact factor:   10.834


  90 in total

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Authors:  Sarah E Cabral; Kimberly L Mowry
Journal:  Curr Top Dev Biol       Date:  2020-03-09       Impact factor: 4.897

2.  The origin of dorsoventral polarity in Drosophila.

Authors:  Siegfried Roth
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2003-08-29       Impact factor: 6.237

3.  Sm proteins specify germ cell fate by facilitating oskar mRNA localization.

Authors:  Graydon B Gonsalvez; T K Rajendra; Ying Wen; Kavita Praveen; A Gregory Matera
Journal:  Development       Date:  2010-07       Impact factor: 6.868

4.  Analyses of dynein heavy chain mutations reveal complex interactions between dynein motor domains and cellular dynein functions.

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Journal:  Genetics       Date:  2012-05-29       Impact factor: 4.562

5.  RNA localization.

Authors:  Yaron Shav-Tal; Robert H Singer
Journal:  J Cell Sci       Date:  2005-09-15       Impact factor: 5.285

6.  The positional, structural, and sequence requirements of the Drosophila TLS RNA localization element.

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7.  A dynein loading zone for retrograde endosome motility at microtubule plus-ends.

Authors:  J H Lenz; I Schuchardt; A Straube; G Steinberg
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Review 8.  mRNA trafficking in fungi.

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Review 9.  mRNA localization: gene expression in the spatial dimension.

Authors:  Kelsey C Martin; Anne Ephrussi
Journal:  Cell       Date:  2009-02-20       Impact factor: 41.582

10.  Dynein and the actin cytoskeleton control kinesin-driven cytoplasmic streaming in Drosophila oocytes.

Authors:  Laura R Serbus; Byeong-Jik Cha; William E Theurkauf; William M Saxton
Journal:  Development       Date:  2005-08       Impact factor: 6.868

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