Genome Research

Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
 QUICK SEARCH:   [advanced]


     


Genome Res. 13:2213-2219, 2003
©2003 by Cold Spring Harbor Laboratory Press; ISSN 1088-9051/03 $5.00
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Domazet-Loso, T.
Right arrow Articles by Tautz, D.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Domazet-Loso, T.
Right arrow Articles by Tautz, D.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati  
What's this?

An Evolutionary Analysis of Orphan Genes in Drosophila

Tomislav Domazet-Loso and Diethard Tautz1

Institut für Genetik der Universität zu Köln, 50931 Köln, Germany

Orphan genes are protein-coding regions that have no recognizable homolog in distantly related species. A substantial fraction of coding regions in any genome sequenced consists of orphan genes, but the evolutionary and functional significance of orphan genes is not understood. We present a reanalysis of the Drosophila melanogaster proteome that shows that there are still between 26% and 29% of all proteins without a significant match with noninsect sequences, and that these orphans are underrepresented in genetic screens. To analyze the characteristics of orphan genes in Drosophila, we used sequence comparisons between cDNAs retrieved from two Drosophila yakuba libraries and their corresponding D. melanogaster orthologs. We find that a cDNA library from adults yields twice as many orphan genes as such a library from embryos. The orphan genes evolve on average more than three times faster than nonorphan genes, although the width of the evolutionary rate distribution is similar for the two classes. In particular, some orphan genes show very low substitution rates that are comparable to otherwise highly conserved genes. We propose a model suggesting that orphans may be involved in the evolution of adaptive traits, and that slow-evolving orphan genes may be particularly interesting candidate genes for identifying lineage-specific adaptations.


1 Corresponding author.
E-MAIL tautz{at}uni-koeln.de; FAX +49221 470 5975.

[The sequence data from this study have been submitted to GenBank under accession nos. AF531914-AF532036 and AY231640-AY232253.]

Article and publication are at http://www.genome.org/cgi/doi/10.1101/gr.1311003.


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati    What's this?


This article has been cited by other articles:


Home page
Plant Physiol.Home page
M. A. Campbell, W. Zhu, N. Jiang, H. Lin, S. Ouyang, K. L. Childs, B. J. Haas, J. P. Hamilton, and C. R. Buell
Identification and Characterization of Lineage-Specific Genes within the Poaceae
Plant Physiology, December 1, 2007; 145(4): 1311 - 1322.
[Abstract] [Full Text] [PDF]


Home page
Mol Biol EvolHome page
H.-R. Chung, U. Lohr, and H. Jackle
Lineage-specific expansion of the Zinc Finger Associated Domain ZAD
Mol. Biol. Evol., September 1, 2007; 24(9): 1934 - 1943.
[Abstract] [Full Text] [PDF]


Home page
Physiol. GenomicsHome page
N. Lopez-Sanchez, Z. Gonzalez-Fernandez, M. Niinobe, K. Yoshikawa, and J. M. Frade
Single mage gene in the chicken genome encodes CMage, a protein with functional similarities to mammalian type II Mage proteins
Physiol Genomics, July 18, 2007; 30(2): 156 - 171.
[Abstract] [Full Text] [PDF]


Home page
Appl. Environ. Microbiol.Home page
M. Marzorati, F. de Ferra, H. Van Raemdonck, S. Borin, E. Allifranchini, G. Carpani, L. Serbolisca, W. Verstraete, N. Boon, and D. Daffonchio
A Novel Reductive Dehalogenase, Identified in a Contaminated Groundwater Enrichment Culture and in Desulfitobacterium dichloroeliminans Strain DCA1, Is Linked to Dehalogenation of 1,2-Dichloroethane
Appl. Envir. Microbiol., May 1, 2007; 73(9): 2990 - 2999.
[Abstract] [Full Text] [PDF]


Home page
Mol Biol EvolHome page
A. Aouacheria, C. Geourjon, N. Aghajari, V. Navratil, G. Deleage, C. Lethias, and J.-Y. Exposito
Insights into Early Extracellular Matrix Evolution: Spongin Short Chain Collagen-Related Proteins Are Homologous to Basement Membrane Type IV Collagens and Form a Novel Family Widely Distributed in Invertebrates
Mol. Biol. Evol., December 1, 2006; 23(12): 2288 - 2302.
[Abstract] [Full Text] [PDF]


Home page
GeneticsHome page
M. Proschel, Z. Zhang, and J. Parsch
Widespread Adaptive Evolution of Drosophila Genes With Sex-Biased Expression
Genetics, October 1, 2006; 174(2): 893 - 900.
[Abstract] [Full Text] [PDF]


Home page
GeneticsHome page
S. R. Schulze, B. F. McAllister, D. A. R. Sinclair, K. A. Fitzpatrick, M. Marchetti, S. Pimpinelli, and B. M. Honda
Heterochromatic Genes in Drosophila: A Comparative Analysis of Two Genes
Genetics, July 1, 2006; 173(3): 1433 - 1445.
[Abstract] [Full Text] [PDF]


Home page
Mol Biol EvolHome page
P. Siwach, S. D. Pophaly, and S. Ganesh
Genomic and Evolutionary Insights into Genes Encoding Proteins with Single Amino Acid Repeats
Mol. Biol. Evol., July 1, 2006; 23(7): 1357 - 1369.
[Abstract] [Full Text] [PDF]


Home page
Nucleic Acids ResHome page
S. Steigele and K. Nieselt
Open reading frames provide a rich pool of potential natural antisense transcripts in fungal genomes
Nucleic Acids Res., September 7, 2005; 33(16): 5034 - 5044.
[Abstract] [Full Text] [PDF]


Home page
Genome Res.Home page
L. Ma, C. Chen, X. Liu, Y. Jiao, N. Su, L. Li, X. Wang, M. Cao, N. Sun, X. Zhang, et al.
A microarray analysis of the rice transcriptome and its comparison to Arabidopsis
Genome Res., September 1, 2005; 15(9): 1274 - 1283.
[Abstract] [Full Text] [PDF]


Home page
Genome Res.Home page
W. Wang, H. Zheng, S. Yang, H. Yu, J. Li, H. Jiang, J. Su, L. Yang, J. Zhang, J. McDermott, et al.
Origin and evolution of new exons in rodents
Genome Res., September 1, 2005; 15(9): 1258 - 1264.
[Abstract] [Full Text] [PDF]


Home page
GeneticsHome page
J. L. Mueller, K. R. Ram, L. A. McGraw, M. C. Bloch Qazi, E. D. Siggia, A. G. Clark, C. F. Aquadro, and M. F. Wolfner
Cross-Species Comparison of Drosophila Male Accessory Gland Protein Genes
Genetics, September 1, 2005; 171(1): 131 - 143.
[Abstract] [Full Text] [PDF]


Home page
GeneticsHome page
T. M. Hambuch and J. Parsch
Patterns of Synonymous Codon Usage in Drosophila melanogaster Genes With Sex-Biased Expression
Genetics, August 1, 2005; 170(4): 1691 - 1700.
[Abstract] [Full Text] [PDF]


Home page
GeneticsHome page
G. Marais, P. Nouvellet, P. D. Keightley, and B. Charlesworth
Intron Size and Exon Evolution in Drosophila
Genetics, May 1, 2005; 170(1): 481 - 485.
[Abstract] [Full Text] [PDF]


Home page
Mol Biol EvolHome page
M. M. Alba and J. Castresana
Inverse Relationship Between Evolutionary Rate and Age of Mammalian Genes
Mol. Biol. Evol., March 1, 2005; 22(3): 598 - 606.
[Abstract] [Full Text] [PDF]


Home page
Mol Biol EvolHome page
Z. Zhang, T. M. Hambuch, and J. Parsch
Molecular Evolution of Sex-Biased Genes in Drosophila
Mol. Biol. Evol., November 1, 2004; 21(11): 2130 - 2139.
[Abstract] [Full Text] [PDF]


Home page
Genome Res.Home page
V. Daubin and H. Ochman
Bacterial Genomes as New Gene Homes: The Genealogy of ORFans in E. coli
Genome Res., June 1, 2004; 14(6): 1036 - 1042.
[Abstract] [Full Text] [PDF]




Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
Genes Dev. Learn. Mem.
Protein Science RNA Genome Res.
Copyright © 2003 by Cold Spring Harbor Laboratory Press.