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Reference
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| Citation |
Cook, H.A., Koppetsch, B.S., Wu, J., Theurkauf, W.E. (2004). The Drosophila SDE3 homolog armitage is required for oskar mRNA silencing and embryonic axis specification. Cell 116(6): 817--829. |
| FlyBase ID |
FBrf0174441 |
| Type of publication |
Research paper |
| Offprint Available |
No |
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External Crossreferences
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| PubMed ID |
15035984 |
| PubMed Abstract |
Polarization of the microtubule cytoskeleton during early oogenesis is required to specify the posterior of the Drosophila
oocyte, which is essential for asymmetric mRNA localization during mid-oogenesis and for embryonic axis specification. The
posterior determinant oskar mRNA is translationally silent until mid-oogenesis. We show that mutations in armitage and three
components of the RNAi pathway disrupt oskar mRNA translational silencing, polarization of the microtubule cytoskeleton, and
posterior localization of oskar mRNA. armitage encodes a homolog of SDE3, a presumptive RNA helicase involved in posttranscriptional
gene silencing (RNAi) in Arabidopsis, and is required for RNAi in Drosophila ovaries. Armitage forms an asymmetric network
associated with the polarized microtubule cytoskeleton and is concentrated with translationally silent oskar mRNA in the oocyte.
We conclude that RNA silencing is essential for establishment of the cytoskeletal polarity that initiates embryonic axis specification
and for translational control of oskar mRNA.
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| Biosis |
2004.261277 |
| Zoological record |
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Associated Information
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| Comments |
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| Text of personal communication |
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| Associated files |
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Related Publications
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Also Published As
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Other Reference Information
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| Secondary IDs |
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| Language of publication |
English |
| Additional language(s) of abstract |
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| ISBN |
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| Place of publication |
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Published In
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| Abbreviation |
Cell |
| Title |
Cell |
| Authors |
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| Volume range |
1- |
| Year range |
1974- |
| Page range |
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| Publisher |
Cell Press |
| Place of publication |
Cambridge, MA |
| Language of publication |
English |
| ISBN/ISSN |
0092-8674 |
| CODEN |
CELLB5 |
Data from Reference
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Aberrations (2)
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Alleles (11)
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Constructs (2)
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Genes (15)
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Insertions (1)
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