A Molecularly Defined Duplication Set for the X Chromosome of Drosophila melanogaster
Open Access
- 1 December 2010
- journal article
- Published by Oxford University Press (OUP) in Genetics
- Vol. 186 (4), 1111-1125
- https://doi.org/10.1534/genetics.110.121285
Abstract
We describe a molecularly defined duplication kit for the X chromosome of Drosophila melanogaster. A set of 408 overlapping P[acman] BAC clones was used to create small duplications (average length 88 kb) covering the 22-Mb sequenced portion of the chromosome. The BAC clones were inserted into an attP docking site on chromosome 3L using ΦC31 integrase, allowing direct comparison of different transgenes. The insertions complement 92% of the essential and viable mutations and deletions tested, demonstrating that almost all Drosophila genes are compact and that the current annotations of the genome are reasonably accurate. Moreover, almost all genes are tolerated at twice the normal dosage. Finally, we more precisely mapped two regions at which duplications cause diplo-lethality in males. This collection comprises the first molecularly defined duplication set to cover a whole chromosome in a multicellular organism. The work presented removes a long-standing barrier to genetic analysis of the Drosophila X chromosome, will greatly facilitate functional assays of X-linked genes in vivo, and provides a model for functional analyses of entire chromosomes in other species.Keywords
This publication has 71 references indexed in Scilit:
- Target-enrichment strategies for next-generation sequencingNature Methods, 2010
- The Vacuolar Proton Pump, V-ATPase, Is Required for Notch Signaling and Endosomal Trafficking in DrosophilaDevelopmental Cell, 2009
- Versatile P[acman] BAC libraries for transgenesis studies in Drosophila melanogasterNature Methods, 2009
- Recombineering: a homologous recombination-based method of genetic engineeringNature Protocols, 2009
- Recombineering-mediated tagging of Drosophila genomic constructs for in vivo localization and acute protein inactivationNucleic Acids Research, 2008
- A Sequence Motif within Chromatin Entry Sites Directs MSL Establishment on the Drosophila X ChromosomeCell, 2008
- BAC TransgeneOmics: a high-throughput method for exploration of protein function in mammalsNature Methods, 2008
- Exploiting position effects and the gypsy retrovirus insulator to engineer precisely expressed transgenesNature Genetics, 2008
- An optimized transgenesis system for Drosophila using germ-line-specific φC31 integrasesProceedings of the National Academy of Sciences, 2007
- Emerging technologies for gene manipulation in Drosophila melanogasterNature Reviews Genetics, 2005