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Phylogenetic relationships of bolitoglossine salamanders: a demonstration of the effects of combining morphological and molecular data sets 总被引:2,自引:0,他引:2
We analyzed sequence data for 555 bp of the mitochondrial gene cytochrome b
in plethodontid salamanders, taken from 18 ingroup (tribe Bolitoglossini)
and 4 outgroup (tribe Plethodontini) taxa. There were 257 variable sites,
of which 219 were phylogenetically informative. Sequence differences among
taxa exceeded 20%, and there were up to 15% amino acid differences among
the sequences. We also analyzed 37 morphological (including karyological)
characters, taken from the literature. Data were analyzed separately and
then combined using parsimony and likelihood approaches. There is little
conflict between the morphological and DNA data, and that which occurs is
at nodes that are weakly supported by one or both of the data sets. Treated
separately, the morphological and DNA data provide strong support for some
nodes but not for others. The combined data act synergistically so that
good support is obtained for nearly all of the nodes in the tree. Recent
divergences are supported by silent transitions, and older divergences are
supported by a combination of morphological, karyological, DNA
transversion, and amino acid changes. Eliminating silent changes from the
DNA data improves the consistency index and improves some bootstrap and
decay index values for several deeper branches in the tree. However, the
combined data set with all characters included provides a better supported
tree overall. Maximum likelihood and parsimony with all of the data give
not only the same topology but also remarkably similar branch lengths.
Results of this analysis support the monopoly of the supergenera
Hydromantes and Batrachoseps, and of a sister group relationship of
Batrachoseps and the supergenus Bolitoglossa (represented in this study one
species of the genus Bolitoglossa).
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Elena Ian Dmitry B. Malko Olga N. Sekurova Harald Bredholt Christian Rückert Marina E. Borisova Andreas Albersmeier J?rn Kalinowski Mikhail S. Gelfand Sergey B. Zotchev 《PloS one》2014,9(5)
A total of 74 actinomycete isolates were cultivated from two marine sponges, Geodia barretti and Phakellia ventilabrum collected at the same spot at the bottom of the Trondheim fjord (Norway). Phylogenetic analyses of sponge-associated actinomycetes based on the 16S rRNA gene sequences demonstrated the presence of species belonging to the genera Streptomyces, Nocardiopsis, Rhodococcus, Pseudonocardia and Micromonospora. Most isolates required sea water for growth, suggesting them being adapted to the marine environment. Phylogenetic analysis of Streptomyces spp. revealed two isolates that originated from different sponges and had 99.7% identity in their 16S rRNA gene sequences, indicating that they represent very closely related strains. Sequencing, annotation, and analyses of the genomes of these Streptomyces isolates demonstrated that they are sister organisms closely related to terrestrial Streptomyces albus J1074. Unlike S. albus J1074, the two sponge streptomycetes grew and differentiated faster on the medium containing sea water. Comparative genomics revealed several genes presumably responsible for partial marine adaptation of these isolates. Genome mining targeted to secondary metabolite biosynthesis gene clusters identified several of those, which were not present in S. albus J1074, and likely to have been retained from a common ancestor, or acquired from other actinomycetes. Certain genes and gene clusters were shown to be differentially acquired or lost, supporting the hypothesis of divergent evolution of the two Streptomyces species in different sponge hosts. 相似文献
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We have used a clinical magnetic resonance imager to search for the possible effects of a 1.5 T magnetic fields on the growth of the yeast Saccharomyces cerevisiae. Yeast samples were grown in nutrient broth contained in constant-temperature boxes, both in and out of the magnetic field of the imager. Growth was measured by using a hemocytometer and light microscope to calculate cell densities. Over the time span corresponding to approximately seven cell divisions, we find no convincing statistical evidence for an effect of magnetic field on cell density. © 1994 Wiley-Liss, Inc. 相似文献
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DC White JO Stair DB Ringelberg 《Journal of industrial microbiology & biotechnology》1996,17(3-4):185-196
Microscopic examinations have convinced microbial ecologists that the culturable microbes recovered from environmental samples represent a tiny proportion of the extant microbiota. Methods for recovery and enzymatic amplification of nucleic acids from environmental samples have shown that a huge diversity existsin situ, far exceeding any expectations which were based on direct microscopy. It is now theoretically possible to extract, amplify and sequence all the nucleic acids from a community and thereby gain a comprehensive measure of the diversity as well as some insights into the phylogeny of the various elements within this community. Unfortunately, this analysis becomes economically prohibitive if applied to the multitude of niches in a single biome let alone to a diverse set of environments. It is also difficult to utilize PCR amplification on nucleic acids from some biomes because of coextracting enzymatic inhibitors. Signature biomarker analysis which potentially combines gene probe and lipid analysis on the same sample, can serve as a complement to massive environmental genome analysis in providing quantitative comparisons between microniches in the biome under study. This analysis can also give indications of the magnitude of differences in biodiversity in the blome as well as provide insight into the phenotypic activities of each community in a rapid and cost-effective manner. Applications of signature lipid biomarker analysis to define quantitatively the microbial viable biomass of portions of an Eastern USA deciduous forest, are presented. 相似文献
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