Literature DB >> 9440270

Accumulation of transposable elements in laboratory lines of Drosophila melanogaster.

S V Nuzhdin1, E G Pasyukova, T F Mackay.   

Abstract

It is recognized that a stable number of transposable element (TE) copies per genome is maintained in natural populations of D. melanogaster as a result of the dynamic equilibrium between transposition to new sites and natural selection eliminating copies. The force of natural selection opposing TE multiplication is partly relaxed in inbred laboratory lines of flies. The average rate of TE transposition is from 2.6 x 10(-4) to 5.0 x 10(-4) per copy per generation, and the average rate of excision is at least two orders of magnitude lower; therefore inbred lines accumulate increasing numbers of copies with time. Correlations between the rate of transposition and TE copy number have been determined for copia, Doc, roo, and 412 and found to be either zero or positive. Because the rate of transposition is not a decreasing function of TE copy number, TE accumulation in inbred lines is self-accelerating. Transpositions cause a substantial fraction of mutations in D. melanogaster, therefore the mutation rate should increase with time in laboratory lines of this species. Inferences about the properties of spontaneous mutations from studies of mutation accumulation in laboratory lines should be reevaluated, because they are based on the assumption of a constant mutation rate.

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Year:  1997        PMID: 9440270

Source DB:  PubMed          Journal:  Genetica        ISSN: 0016-6707            Impact factor:   1.082


  19 in total

1.  Genetic variation of copia suppression in Drosophila melanogaster.

Authors:  W Vu; S Nuzhdin
Journal:  Heredity (Edinb)       Date:  2010-07-07       Impact factor: 3.821

2.  The dynamics of the roo transposable element in mutation-accumulation lines and segregating populations of Drosophila melanogaster.

Authors:  Montserrat Papaceit; Victoria Avila; Montserrat Aguadé; Aurora García-Dorado
Journal:  Genetics       Date:  2007-09       Impact factor: 4.562

3.  The impact of dissociation on transposon-mediated disease control strategies.

Authors:  John M Marshall
Journal:  Genetics       Date:  2008-02-03       Impact factor: 4.562

4.  Recent spread of a retrotransposon in the Silene latifolia genome, apart from the Y chromosome.

Authors:  Dmitry A Filatov; Elaine C Howell; Constantinos Groutides; Susan J Armstrong
Journal:  Genetics       Date:  2008-12-08       Impact factor: 4.562

5.  Quantitative genetic analysis of copia retrotransposon activity in inbred Drosophila melanogaster lines.

Authors:  S V Nuzhdin; E G Pasyukova; E A Morozova; A J Flavell
Journal:  Genetics       Date:  1998-10       Impact factor: 4.562

6.  Population genomics of transposable elements in Drosophila melanogaster.

Authors:  Dmitri A Petrov; Anna-Sophie Fiston-Lavier; Mikhail Lipatov; Kapa Lenkov; Josefa González
Journal:  Mol Biol Evol       Date:  2010-12-16       Impact factor: 16.240

7.  Population dynamics of PIWI-interacting RNAs (piRNAs) and their targets in Drosophila.

Authors:  Jian Lu; Andrew G Clark
Journal:  Genome Res       Date:  2009-11-30       Impact factor: 9.043

8.  Accelerating Mutational Load Is Not Due to Synergistic Epistasis or Mutator Alleles in Mutation Accumulation Lines of Yeast.

Authors:  Jean-Nicolas Jasmin; Thomas Lenormand
Journal:  Genetics       Date:  2015-11-23       Impact factor: 4.562

9.  R1 and R2 retrotransposition and deletion in the rDNA loci on the X and Y chromosomes of Drosophila melanogaster.

Authors:  César E Pérez-González; William D Burke; Thomas H Eickbush
Journal:  Genetics       Date:  2003-10       Impact factor: 4.562

10.  Recent LTR retrotransposon insertion contrasts with waves of non-LTR insertion since speciation in Drosophila melanogaster.

Authors:  Casey M Bergman; Douda Bensasson
Journal:  Proc Natl Acad Sci U S A       Date:  2007-06-25       Impact factor: 11.205

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