dynamics of the roo transposable element in mutation-accumulation lines and segregating populations of Drosophila melanogaster
We estimated the number of copies for the long terminal repeat (LTR) retrotransposable element roo in a set of long-standing Drosophila melanogaster mutation-accumulation full-sib lines and in two large laboratory populations maintained with effective population size approximately 500, all of them d...
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Published in: | Genetics (Austin) Vol. 177; no. 1; pp. 511 - 522 |
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Main Authors: | , , , |
Format: | Journal Article |
Language: | English |
Published: |
United States
Genetics Soc America
01-09-2007
Genetics Society of America Copyright © 2007 by the Genetics Society of America |
Subjects: | |
Online Access: | Get full text |
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Summary: | We estimated the number of copies for the long terminal repeat (LTR) retrotransposable element roo in a set of long-standing Drosophila melanogaster mutation-accumulation full-sib lines and in two large laboratory populations maintained with effective population size approximately 500, all of them derived from the same isogenic origin. Estimates were based on real-time quantitative PCR and in situ hybridization. Considering previous estimates of roo copy numbers obtained at earlier stages of the experiment, the results imply a strong acceleration of the insertion rate in the accumulation lines. The detected acceleration is consistent with a model where only one (maybe a few) of the approximately 70 roo copies in the ancestral isogenic genome was active and each active copy caused new insertions with a relatively high rate ( approximately 10(-2)), with new inserts being active copies themselves. In the two laboratory populations, however, a stabilized copy number or no accelerated insertion was found. Our estimate of the average deleterious viability effects per accumulated insert [E(s) < 0.003] is too small to account for the latter finding, and we discuss the mechanisms that could contain copy number. |
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Bibliography: | http://www.genetics.org/ ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Communicating editor: M. J. Simmons Corresponding author: Departamento de Genética, Facultad de Biología, Universidad Complutense, 28040 Madrid, Spain. E-mail: augardo@bio.ucm.es |
ISSN: | 0016-6731 1943-2631 1943-2631 |
DOI: | 10.1534/genetics.107.076174 |