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Kemmer D Huang Y Shah SP Lim J Brumm J Yuen MM Ling J Xu T Wasserman WW Ouellette BF 《Genome biology》2005,6(12):R106
We developed Ulysses as a user-oriented system that uses a process called Interolog Analysis for the parallel analysis and
display of protein interactions detected in various species. Ulysses was designed to perform such Interolog Analysis by the
projection of model organism interaction data onto homologous human proteins, and thus serves as an accelerator for the analysis
of uncharacterized human proteins. The relevance of projections was assessed and validated against published reference collections.
All source code is freely available, and the Ulysses system can be accessed via a web interface . 相似文献
24.
Sohrab?P?Shah David?YM?He Jessica?N?Sawkins Jeffrey?C?Druce Gerald?Quon Drew?Lett Grace?XY?Zheng Tao?Xu BF?Francis?OuelletteEmail author 《BMC bioinformatics》2004,5(1):40
Background
We present Pegasys – a flexible, modular and customizable software system that facilitates the execution and data integration from heterogeneous biological sequence analysis tools. 相似文献25.
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N N Burtseva O A Gimadutdinov S N Bubenshchikova B F Vaniushin 《Nauchnye doklady vysshe? shkoly. Biologicheskie nauki》1985,(2):37-42
An express method for measuring the level of in vitro DNA methylation in homogenates and nuclei from animal tissues as well as during initial steps of DNA methylase isolation and purification when methylase activity is low and hardly testable by other methods has been suggested. The method is based on the measuring the radioactivity incorporated in filter adsorbed DNA (acid-insoluble material) 3H-label from S-adenosile-L-methionine as a result of in vitro DNA methylation. The advantage of the method consists in the replacement of a long-duration repeated deproteinization procedure traditionally used by a relatively simple procedure (15 min incubation of the mixture at 80 degrees C with 10 volumes of the 8M urea, 5 mM EDTA, 5% n-butanol, 2% sodium dodecilsulfate, 1 M sodium chloride solution) and the absence of any loss of DNA. The method is fit for the fast serial assay of DNA methylase activity taking into consideration that about one third of the total acid-insoluble radioactivity is due to the radioactivity in 5-methylcytosine residues in DNA. 相似文献
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Rat liver glucocorticoid-receptor complexes (GRC) acquire the ability to bind to DNA in a high affinity manner after activation by heating or precipitation with (NH)2SO4. DNA is practically non-saturable by GRC in low salt buffers as well as in 0.15 M NaCl-containing buffer, although in the latter case the binding decreases approximately 3--5 times. GRC bind to homo- and heterologous prokaryotic DNA in a similar way; in both cases an addition of KCl (up to 0.15 M) to the medium is followed by the same decrease of the binding. This data suggest that the association of GRC with DNA observed in vitro is not accompanied by "recognition" of any certain DNA site. Besides DNA, activated GRC can associate with other polymers, charged positively (DEAE-cellulose) or negatively (RNA, polyvinylsulfate). GRC interact very weakly with neutral compounds of the cellulose type but are strongly adsorbed on hydroxyapatite. Hence the activated GRC can be considered as an amphoteric protein. Salt solutions provoke dissociation of the GRC-DNA triple complexes: a complete dissociation is observed in the presence of 0,4 M NaCl or 0,4 M sodium phosphate buffer (pH 6,9). Sodium phosphate buffer also elutes GRC from other sorbents such as DEAE-cellulose or hydroxyapatite. No significant dissociation of the GRC-DNA complexes is observed at sucrose concentration up to 2 M. The data obtained are indicative of an essential role of electrostatic forces for the interaction of GRC with DNA. The non-ionic detergent Triton X-100 at a concentration as low as 0,05% completely destroys the GRC-DNA triple complexes. The models explicating the selectivity of the genome activation by GRC without their "recognition" of any specific DNA sequences are proposed. 相似文献
28.
Evolution of the WANCY region in amniote mitochondrial DNA 总被引:7,自引:1,他引:6
In most vertebrate mitochondrial genomes, the site for initiation of
light-strand replication, OL, is found within a cluster of five transfer
RNA (tRNA) genes (tRNA(Trp), tRNA(Ala), tRNA(Asn), tRNA(Cys), and
tRNA(Tyr)). This region and part of the adjacent cytochrome c oxydase
subunit I (COI) gene were sequenced for two crocodilian, two turtle, and
one snake species and for Sphenodon punctatus; part of the adjacent
nicotinamide adenine dinucleotide dehydrogenase subunit 2 (ND2) gene was
also sequenced for the crocodilian and turtle species. All had the typical
vertebrate gene order. The turtles and the snake have a lengthy noncoding
sequence between the tRNA(Asn) and tRNA(Cys) genes that we assumed to be
homologous to the mammalian OL. The crocodilians and Sphenodon lack such a
sequence, a condition they share with birds. Most proposed phylogenies for
the amniotes require that OL at this position was lost at least twice
during their diversification or was evolved independently more than once.
Within the five tRNA genes, frequencies of substitutions are much higher in
loops than in stems. Many loops vary dramatically in size among the
species; in the most extreme case, the D-arm of the Sphenodon tRNA(Cys) is
a "D-arm replacement" loop of seven nucleotides. Frequency of transitions
in stems is relatively uniform across tRNAs, but frequency of transversions
varies greatly. Mismatches in stems are infrequent, and their relative
frequency in a specific tRNA is unrelated to the frequency of substitution
in the corresponding gene. Several features of mammalian mitochondrial
tRNAs are conserved in WANCY tRNAs throughout amniotes. The inferred
initiation codon for COI is GTG in crocodilians, turtles, and the snake, a
condition they share with fishes, certain amphibians, and birds. TTG
appears to be the initiation codon for COI in Sphenodon; if correct, this
would be a novel initiation codon for vertebrate mitochondrial DNA.
Phylogenetic analyses of the inferred amino acid sequences of ND2 and COI
support the sister-group relationship of birds and crocodilians and suggest
that mammals are an early derived lineage within the amniotes.
相似文献
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A method of preparation of mitochondria free of nuclear DNA and its fragments by treatment of mitochondria with DEAE-cellulose has been developed. This method is based on binding nuclear nucleic acids and nucleoproteins to DEAE-cellulose particles in the media used for isolation of mitochondria. Treatment with DEAE-cellulose under the conditions described does not induce any visible degradation of mitochondria and mitochondrial DNA. The mitochondrial DNA preparations obtained from beef and rat liver are represented with closed circular molecules of contour length about 5.5 mu. The 5-methylcytosine content in beef and rat mitochondrial DNA (3.03 and 2.0 mole %, respectively) is twice as much as in corresponding nuclear DNA. Besides, mitochondrial DNA strongly differs from nuclear ones by a lower degree of pyrimidine clustering: the amount of mono- and dipyrimidine fragments (about 32 mole %) in mitochondrial DNA is 1.5 times as large and the content of long pyrimidine clusters (hexa- and others) is 2--4 times as low as those in nuclear DNA. The methylation level and the pyrimidine clustering degree may be used as criteria for the purity of mitochondrial DNA from nuclear DNA. 相似文献