A Database of Drosophila Genes & Genomes

FB2008_07, released August 8, 2008
 

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Citation Ghabrial, A., Ray, R.P., Schupbach, T. (1998). okra and spindle-B encode components of the RAD52 DNA repair pathway and affect meiosis and patterning in Drosophila oogenesis.  Genes Dev. 12(17): 2711--2723.
FlyBase ID FBrf0104438
Type of publication Research paper
Offprint Available Yes
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PubMed ID 9732269
PubMed Abstract okra (okr), spindle-B (spnB), and spindle-D (spnD) are three members of a group of female sterile loci that produce defects in oocyte and egg morphology, including variable dorsal-ventral defects in the eggshell and embryo, anterior-posterior defects in the follicle cell epithelium and in the oocyte, and abnormalities in oocyte nuclear morphology. Many of these phenotypes reflect defects in grk-Egfr signaling processes, and can be accounted for by a failure to accumulate wild-type levels of Gurken and Fs(1)K10. We have cloned okr and spnB, and show that okr encodes the Drosophila homolog of the yeast DNA-repair protein Rad54, and spnB encodes a Rad51-like protein related to the meiosis-specific DMC1 gene. In functional tests of their role in DNA repair, we find that okr behaves like its yeast homolog in that it is required in both mitotic and meiotic cells. In contrast, spnB and spnD appear to be required only in meiosis. The fact that genes involved in meiotic DNA metabolism have specific effects on oocyte patterning implies that the progression of the meiotic cell cycle is coordinated with the regulation of certain developmental events during oogenesis.
Biosis 1447947
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Language of publication English
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Abbreviation Genes Dev.
Title Genes & Development
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Volume range 1-
Year range 1987-
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Place of publication Cold Spring Harbor, NY
Language of publication English
ISBN/ISSN 0890-9369
CODEN GEDEEP
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