Literature DB >> 24290763

Germ plasm anchoring is a dynamic state that requires persistent trafficking.

Kristina S Sinsimer1, Jack J Lee1, Stephan Y Thiberge2, Elizabeth R Gavis3.   

Abstract

Localized cytoplasmic determinants packaged as ribonucleoprotein (RNP) particles direct embryonic patterning and cell fate specification in a wide range of organisms. Once established, the asymmetric distributions of such RNP particles must be maintained, often over considerable developmental time. A striking example is the Drosophila germ plasm, which contains RNP particles whose localization to the posterior of the egg during oogenesis results in their asymmetric inheritance and segregation of germline from somatic fates in the embryo. Although actin-based anchoring mechanisms have been implicated, high-resolution live imaging revealed persistent trafficking of germ plasm RNP particles at the posterior cortex of the Drosophila oocyte. This motility relies on cortical microtubules, is mediated by kinesin and dynein motors, and requires coordination between the microtubule and actin cytoskeletons. Finally, we show that RNP particle motility is required for long-term germ plasm retention. We propose that anchoring is a dynamic state that renders asymmetries robust to developmental time and environmental perturbations.
Copyright © 2013 The Authors. Published by Elsevier Inc. All rights reserved.

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Year:  2013        PMID: 24290763      PMCID: PMC4149184          DOI: 10.1016/j.celrep.2013.10.045

Source DB:  PubMed          Journal:  Cell Rep            Impact factor:   9.423


  40 in total

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Review 4.  mRNA localization and the cytoskeleton.

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Review 4.  Dynamic droplets: the role of cytoplasmic inclusions in stress, function, and disease.

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6.  Drosophila pericentrin-like protein promotes the formation of primordial germ cells.

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Review 7.  Specifying and protecting germ cell fate.

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8.  Somatic insulin signaling regulates a germline starvation response in Drosophila egg chambers.

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9.  Sequence-Independent Self-Assembly of Germ Granule mRNAs into Homotypic Clusters.

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