rdf:type |
|
lifeskim:mentions |
umls-concept:C0010834,
umls-concept:C0013139,
umls-concept:C0017262,
umls-concept:C0029045,
umls-concept:C0033684,
umls-concept:C0185117,
umls-concept:C0449774,
umls-concept:C1423524,
umls-concept:C1427622,
umls-concept:C1514925,
umls-concept:C1521761,
umls-concept:C1706089,
umls-concept:C2911684
|
pubmed:issue |
2
|
pubmed:dateCreated |
1999-3-9
|
pubmed:abstractText |
To study the expression of the I factor, a non-long-terminal-repeat retrotransposon responsible for I-R hybrid dysgenesis in Drosophila melanogaster, we have tagged the ORF1 protein (ORF1p) by inserting the HA epitope in its N-terminal region. In transgenic flies, this modification is compatible with a high rate of autonomous transposition and allows direct estimation of the transposition frequency. I factor transposes in the germline of females (SF) that are daughters from crosses between I strain males (which contain active copies of the I factor) and R strain females (which do not). We analyzed the expression pattern of ORF1p by indirect immunofluorescence. Its expression correlates with retrotransposition. During oogenesis ORF1p appears unexpectedly as a cytoplasmic product, which accumulates with a specific pattern into the oocyte. A comparison of the expression patterns under conditions that modify the transposing activity of the element clarifies some aspects of I-factor functioning in the transposition process.
|
pubmed:commentsCorrections |
http://linkedlifedata.com/resource/pubmed/commentcorrection/9927467-106029,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9927467-109354,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9927467-1330483,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9927467-1647020,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9927467-1698618,
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http://linkedlifedata.com/resource/pubmed/commentcorrection/9927467-9475738
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pubmed:language |
eng
|
pubmed:journal |
|
pubmed:citationSubset |
IM
|
pubmed:chemical |
|
pubmed:status |
MEDLINE
|
pubmed:month |
Feb
|
pubmed:issn |
0016-6731
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pubmed:author |
|
pubmed:issnType |
Print
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pubmed:volume |
151
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
761-71
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pubmed:dateRevised |
2009-11-18
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pubmed:meshHeading |
pubmed-meshheading:9927467-Amino Acid Sequence,
pubmed-meshheading:9927467-Animals,
pubmed-meshheading:9927467-Animals, Genetically Modified,
pubmed-meshheading:9927467-Base Sequence,
pubmed-meshheading:9927467-Drosophila Proteins,
pubmed-meshheading:9927467-Drosophila melanogaster,
pubmed-meshheading:9927467-Female,
pubmed-meshheading:9927467-Gene Expression Regulation,
pubmed-meshheading:9927467-Genes, Insect,
pubmed-meshheading:9927467-Insect Proteins,
pubmed-meshheading:9927467-Molecular Sequence Data,
pubmed-meshheading:9927467-Oocytes,
pubmed-meshheading:9927467-Retroelements
|
pubmed:year |
1999
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pubmed:articleTitle |
High-frequency retrotransposition of a marked I factor in Drosophila melanogaster correlates with a dynamic expression pattern of the ORF1 protein in the cytoplasm of oocytes.
|
pubmed:affiliation |
Centre de Génétique Moléculaire, CNRS, 91198 Gif sur Yvette Cedex, France.
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|