To investigate its role in proton translocation, we characterized the electron transfer and proton translocation activity of complex I variants lacking either NuoL or parts of the C-terminal domain. Our data suggest that the H(+)/2e(-) stoichiometry of the Delta NuoL variant is 2, indicating a different stoichiometry for proton translocation as proposed from structural data. In addition, the same H(+)/e(-) stoichiometry is obtained with the variant lacking the C-terminal transmembraneous KU-57788 solubility dmso helix of NuoL, indicating its role in energy transmission.”
“Today, the reconstruction

of the organismal evolutionary tree is basedmainly on molecular sequence data. However, sequence data are sometimes insufficient to reliably resolve in particular deep branches. Thus, it is highly desirable to find novel, more reliable types of phylogenetic markers that can be derived from the wealth of genomic data. Here, we consider the gain of introns close to older preexisting ones. Because correct splicing is impeded by very small exons, nearby pairs of introns very rarely coexist, that is, the gain of the new intron

is nearly always associated with the loss of the old intron. Both events may even be directly connected as in cases of intron migration. Therefore, it should be possible to identify one of the introns as ancient ( plesiomorphic) and the other as novel ( derived or apomorphic). To test the suitability of such near intron pairs ( NIPs) as a marker class for phylogenetic MEK inhibitor drugs analysis, we undertook an analysis of the evolutionary positions of bees and wasps ( Hymenoptera) and beetles

( Coleoptera) in relation to moths ( Lepidoptera) and dipterans ( Diptera) using recently completed genome project data. By scanning 758 putatively orthologous gene structures of Apis mellifera ( Hymenoptera) and Tribolium castaneum ( Coleoptera), we identified 189 pairs of introns, one from each species, which are located less than 50 nt from each other. A comparison with genes from 5 other holometabolan and 9 metazoan outgroup genomes resulted in 22 shared derived OICR-9429 mouse intron positions found in beetle as well as in butterflies and/ or dipterans. This strongly supports a basal position of hymenopterans in the holometabolous insect tree. In addition, we found 31 and 12 intron positions apomorphic for A. mellifera and T. castaneum, respectively, which seem to represent changes inside these branches. Another 12 intron pairs indicate parallel intron gains or extraordinarily small exons. In conclusion, we show here that the analysis of phylogenetically nested, nearby intron pairs is suitable to identify evolutionarily younger intron positions and to determine their relative age, which should be of equal importance for the understanding of intron evolution and the reconstruction of the eukaryotic tree.