Literature DB >> 2464689

Micropia: a retrotransposon of Drosophila combining structural features of DNA viruses, retroviruses and non-viral transposable elements.

D H Lankenau1, P Huijser, E Jansen, K Miedema, W Hennig.   

Abstract

The retrotransposon micropia was first described from Y-chromosomal fertility genes of Drosophila hydei. Screening a Drosophila melanogaster genomic library yielded several clones representing micropia elements in D. melanogaster. The DNA sequences of two elements from D. hydei (micropia-DhMiF2 and micropia-DhMiF8) and two elements from D. melanogaster (micropia-Dm2 and micropia-Dm11) permitted a detailed analysis of the spatial organization of micropia constituents. Micropia represents the typical gene organization represented by "core"-protein domains followed by a protease, reverse transcriptase, RNase and integrase domain. New features of the micropia family compared with other retrotransposons are: (1) a region of similarity to class I major histocompatibility complex antigens of mammals; (2) only one main open reading frame of about 4000 bases length; (3) a non-protein-coding region of about 500 base-pairs length between the 3' end of the open reading frame and the 5' start of the 3' long terminal repeat. This region includes 32 base-pair tandem repeats; (4) within the long terminal repeats, 82 base-pair tandem repeats with four potential ecdysteroid receptor binding sites. Because micropia combines many evolutionary features of different viruses, non-viral transposable elements, chromosomal genes and repetitive sequence organizations, this retrotransposon may be seen as a "minigenome" reflecting evolutionary principles of the construction of genomic components.

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Year:  1988        PMID: 2464689     DOI: 10.1016/0022-2836(88)90572-4

Source DB:  PubMed          Journal:  J Mol Biol        ISSN: 0022-2836            Impact factor:   5.469


  24 in total

1.  Towards a physical map of the fertility genes on the heterochromatic Y chromosome of Drosophila hydei: families of repetitive sequences transcribed on the lampbrush loops Nooses and Threads are organized in extended clusters of several hundred kilobases.

Authors:  P Trapitz; K H Glätzer; H Bünemann
Journal:  Mol Gen Genet       Date:  1992-11

2.  Retroviral-like element in a marine invertebrate.

Authors:  M S Springer; E H Davidson; R J Britten
Journal:  Proc Natl Acad Sci U S A       Date:  1991-10-01       Impact factor: 11.205

3.  Micropia-Dm2, the nucleotide sequence of a rearranged retrotransposon from Drosophila melanogaster.

Authors:  D H Lankenau; W Hennig
Journal:  Nucleic Acids Res       Date:  1990-07-25       Impact factor: 16.971

4.  Comparison of targeted-gene replacement frequencies in Drosophila melanogaster at the forked and white loci.

Authors:  D H Lankenau; V G Corces; W R Engels
Journal:  Mol Cell Biol       Date:  1996-07       Impact factor: 4.272

5.  Canalization by Selection of de Novo Induced Mutations.

Authors:  Laura Fanti; Lucia Piacentini; Ugo Cappucci; Assunta M Casale; Sergio Pimpinelli
Journal:  Genetics       Date:  2017-06-01       Impact factor: 4.562

6.  High transposition rates of Osvaldo, a new Drosophila buzzatii retrotransposon.

Authors:  M Labrador; A Fontdevila
Journal:  Mol Gen Genet       Date:  1994-12-15

7.  Evolution of the transposable element mariner in the Drosophila melanogaster species group.

Authors:  P Capy; J R David; D L Hartl
Journal:  Genetica       Date:  1992       Impact factor: 1.082

8.  Identification and genomic distribution of gypsy like retrotransposons in Citrus and Poncirus.

Authors:  G P Bernet; M J Asíns
Journal:  Theor Appl Genet       Date:  2003-08-22       Impact factor: 5.699

9.  The retrotransposon Tf1 assembles virus-like particles that contain excess Gag relative to integrase because of a regulated degradation process.

Authors:  A Atwood; J H Lin; H L Levin
Journal:  Mol Cell Biol       Date:  1996-01       Impact factor: 4.272

10.  Y enriched and Y specific DNA sequences from the genome of the Mediterranean fruit fly, Ceratitis capitata.

Authors:  J E Anleitner; D S Haymer
Journal:  Chromosoma       Date:  1992-03       Impact factor: 4.316

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