ArticleGenetics1999
Molecular evolution of two linked genes, Est-6 and Sod, in Drosophila melanogaster.
Article in Genetics, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.
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Who cites it
13 citing papers in PubMed, 27 citations in OpenAlex.
- Variation in the Local Grey Mullet Populations (Genes · 2024Article
- DNA polymorphism and selection at the bindin locus in three Strongylocentrotus sp. (Echinoidea).BMC genetics · 2016Article
- DNA variation in the phenotypically-diverse brown alga Saccharina japonica.BMC plant biology · 2012Article
- Complex interplay of evolutionary forces in the ladybird homeobox genes of Drosophila melanogaster.PloS one · 2011Article
- Positive and negative selection in the beta-esterase gene cluster of the Drosophila melanogaster subgroup.Journal of molecular evolution · 2006Article
- Nucleotide variation in the tinman and bagpipe homeobox genes of Drosophila melanogaster.Genetics · 2004Article
- Nucleotide variation of the Est-6 gene region in natural populations of Drosophila melanogaster.Genetics · 2003Article
- Molecular population genetics of the beta-esterase gene cluster of Drosophila melanogaster.Journal of genetics · 2003Article
- Article
- Patterns of DNA sequence polymorphism at Sod vicinities in Drosophila melanogaster: unraveling the footprint of a recent selective sweep.Proceedings of the National Academy of Sciences of the United States of America · 2003Article
- Article
- Article
- Contrasting patterns of nonneutral evolution in proteins encoded in nuclear and mitochondrial genomes.Genetics · 2000Article
Corrections and comments
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Authors and funding
4 authors at 3 institutions in 3 countries.
Funding
Abstract
We have obtained 15 sequences of Est-6 from a natural population of Drosophila melanogaster to test whether linkage disequilibrium exists between Est-6 and the closely linked Sod, and whether natural selection may be involved. An early experiment with allozymes had shown linkage disequilibrium between these two loci, while none was detected between other gene pairs. The Sod sequences for the same 15 haplotypes were obtained previously. The two genes exhibit similar levels of nucleotide polymorphism, but the patterns are different. In Est-6, there are nine amino acid replacement polymorphisms, one of which accounts for the S-F allozyme polymorphism. In Sod, there is only one replacement polymorphism, which corresponds to the S-F allozyme polymorphism. The transversion/transition ratio is more than five times larger in Sod than in Est-6. At the nucleotide level, the S and F alleles of Est-6 make up two allele families that are quite different from each other, while there is relatively little variation within each of them. There are also two families of alleles in Sod, one consisting of a subset of F alleles, and the other consisting of another subset of F alleles, designed F(A), plus all the S alleles. The Sod F(A) and S alleles are completely or nearly identical in nucleotide sequence, except for the replacement mutation that accounts for the allozyme difference. The two allele families have independent evolutionary histories in the two genes. There are traces of statistically significant linkage disequilibrium between the two genes that, we suggest, may have arisen as a consequence of selection favoring one particular sequence at each locus.
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