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PMID: 6088060 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

The molecular basis of I-R hybrid dysgenesis in Drosophila melanogaster: identification, cloning, and properties of the I factor.

Cell ·Vol. 38 ·No. 1 ·1984-08-00 ·Pages 153-63

Bucheton A, Paro R, Sang HM, Pelisson A, Finnegan DJ

Abstract

We have analyzed two mutations of the white-eye gene, which arose in flies subject to I-R hybrid dysgenesis. These mutations are associated with insertions of apparently identical 5.4 kb sequences, which we have cloned. We believe that these insertions are copies of the I factor controlling I-R hybrid dysgenesis. The I factor is not a member of the copia-like or fold-back classes of transposable elements and has no sequence homology with the P factor that controls P-M dysgenesis. All strains of D. melanogaster contain I-factor sequences. Those present in reactive strains must represent inactive I elements. I elements have a remarkably similar sequence organization in all reactive strains and are located in peri-centromeric regions. Inducer strains appear to contain both I elements, located in peri-centromeric regions, and 10-15 copies of the complete I factor at sites on the chromosome arms.

MeSH Terms
Animals Base Sequence Chromosomes/ultrastructure Cloning, Molecular Crosses, Genetic DNA/isolation & purification DNA Restriction Enzymes DNA Transposable Elements Drosophila melanogaster/genetics Female Male Mutation Nucleic Acid Hybridization Plasmids
Chemicals
DNA Transposable Elements DNA DNA Restriction Enzymes
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Bucheton A
Paro R
Sang H M
Pelisson A
Finnegan D J
Article Info
Journal
Cell
Abbr.
Cell
ISSN
0092-8674
Published
1984-08-00
Pages
153-63
Language
English
Region
United States
NLM ID
0413066
Subset
IM
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