Isolation and characterization of the genomic region from Drosophila kuntzei containing the Adh and Adhr genes

Autor: Wilke Van Delden, Louis van de Zande, Jantien E. Oppentocht
Přispěvatelé: Population Genetics, Van de Zande lab
Rok vydání: 2002
Předmět:
Polymerase Chain Reaction
NUCLEOTIDE-SEQUENCE
Gene Duplication
codon bias
FAT-BODY
Genomic library
Drosophila kuntzei
Cloning
Molecular

Promoter Regions
Genetic

Phylogeny
Genetics
MELANOGASTER
Structural gene
Nucleic acid sequence
myr
SPECIES GROUP
Blotting
Southern

Codon usage bias
ALCOHOL-DEHYDROGENASE EXPRESSION
Drosophila
Nuclear gene
Molecular Sequence Data
NUCLEAR GENES
Biology
nucleotide diversity
Evolution
Molecular

Species Specificity
CODON USAGE
Sequence Homology
Nucleic Acid

Animals
Amino Acid Sequence
RNA
Messenger

Enhancer
Codon
Molecular Biology
Gene
Ecology
Evolution
Behavior and Systematics

DNA Primers
Gene Library
Repetitive Sequences
Nucleic Acid

BASE COMPOSITION
Base Sequence
Sequence Homology
Amino Acid

quinaria group
Alcohol Dehydrogenase
Genetic Variation
DNA
Blotting
Northern

Molecular biology
MOLECULAR EVOLUTION
Amino Acid Substitution
Zdroj: Molecular Biology and Evolution, 19(7), 1026-1040. Oxford University Press
ISSN: 0737-4038
Popis: The nucleotide sequences of the Adh and Adhr genes of Drosophila kuntzei were derived from combined overlapping sequences of clones isolated from a genomic library and from cloned PCR and inverse-PCR fragments. Only a proximal promoter was detected upstream of the Adh gene, indicating that D. kuntzei Adh is regulated by a one-promoter system. Further upstream of the Adh structural gene, an adult enhancer region (AAE) was found that contains most of the regulatory sequences described for AAEs of other Drosophila species. Analysis of the ADH protein showed an amino acid change from valine to threonine in the active site at position 189 which is also found in D. funebris but is otherwise unique among Drosophila. This difference alone may be responsible for the very low ADH activity found in this species and may cause a difference in substrate usage pattern. Codon bias in Adh and Adhr was comparable and found to be very low compared with other species. Phylogenetic analysis showed that D. kuntzei is closest related to D. funebris and D. immigrans. The time of divergence between D. kuntzei and D. funebris was estimated to be 14.2-20.2 Myr and that between D. kuntzei-D. funebris and D. immigrans to be 30.8-44.0 Myr. An analysis of the genetic variation in the Adh gene and upstream sequences Of four European strains showed that this gene was highly variable. Overall nucleotide diversity (pi) was 0.0139, which is two times higher than that in D. melanogaster.
Databáze: OpenAIRE