Evolution of the A+T-rich region of mitochondrial DNA in the melanogaster species subgroup of Drosophila

• Published in: Journal of molecular evolution Vol. 55; no. 5; pp. 573 - 583
• Main Authors: Tsujino, Fumi, Kosemura, Akiko, Inohira, Kayo, Hara, Toshiko, Otsuka, Yoko F, Obara, Mari K, Matsuura, Etsuko T
• Format: Journal Article
• Language: English
• Published: Germany Springer Nature B.V 01-11-2002
• Subjects: Animals; Base Composition; Base Sequence; DNA, Mitochondrial - chemistry; DNA, Mitochondrial - genetics; Drosophila - classification; Drosophila - genetics; Drosophila melanogaster - classification; Drosophila melanogaster - genetics; Evolution, Molecular; Evolutionary biology; Genomics; Insects; Mitochondrial DNA; Molecular Sequence Data; Nucleic Acid Conformation; Phylogeny; Sequence Homology, Nucleic Acid; Species Specificity
• ISSN: 0022-2844; 1432-1432
• DOI: 10.1007/s00239-002-2353-x

We determined the nucleotide sequences of two regions in the A+T-rich region of mitochondrial DNA (mtDNA) in the siI and siII types of D. simulans, the maII type of D. mauritiana, and D. sechellia. The sequences were aligned with those of the corresponding regions of siIII of D. simulans and maI of D. mauritiana, D. melanogaster, and D. yakuba. The type I and type II elements and the T-stretches were detected in all eight of the mtDNA types compared, indicating that the three elements are essential in the A+T-rich region of this species subgroup. The alignment revealed several short repetitive sequences and relatively large deletions in the central portions of the region. In the highly conserved sequence elements in the type II elements, the substitution rates were not uniform among lineages and acceleration in the substitution rate might have been due to loss of functional constraint in the stem-loop-forming sequences predicted in the type II elements. Patterns of nucleotide substitutions observed in the A+T-rich region were further compared with those in the coding regions and in the intergenic regions of mtDNA. Substitutions between A and T were particularly repressed in the highly conserved sequence elements and in the intergenic regions compared with those in the A+T-rich region excluding the highly conserved sequence elements and in the fourfold degenerate sites in the coding regions. The functional and structural characteristics of the A+T-rich region that might be involved in this substitutional bias are discussed.