Literature DB >> 10871377

The global intrinsic curvature of archaeal and eubacterial genomes is mostly contained in their dinucleotide composition and is probably not an adaptation.

E Merino1, A Garciarrubio.   

Abstract

Until now, the genomic DNA of all eubacteria analyzed has been hyper-curved, its global intrinsic curvature being higher than that of a random sequence. In contrast, that rule failed for archaea or eukaryotes, which could be either hypo- or hyper-curved. The existence of the rule suggested that, at least for eubacteria, global intrinsic curvature is adaptive. However, the present results from analyzing 21 eubacterial and six archaeal genomes argue against adaptation. First, there are two eubacterial exceptions to the former rule. More significantly, we found that the dinucleotide composition of the genome alone (which lacks all sequence information) is enough to determine the genome curvature. Additional evidence against adaptation came from showing that the global curvature of bacterial genomes could not have evolved under either of two complementary models of curvature selection: (i) that curvature is selected locally from unbiased variability; (ii) that curvature is established globally through the selection of a curvature-altering mutational bias. We found that the observed relationship between curvature and dinucleotide composition is incompatible with model (i). We also found that, contrary to the predictions of model (ii), the dinucleo-tide compositions of bacterial genomes were not statistically special in their curvature-related properties (when compared to stochastically generated dinucleotide compositions).

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Year:  2000        PMID: 10871377      PMCID: PMC102725          DOI: 10.1093/nar/28.12.2431

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN: 0305-1048            Impact factor:   16.971


  39 in total

1.  Curvature of mouse satellite DNA and condensation of heterochromatin.

Authors:  M Z Radic; K Lundgren; B A Hamkalo
Journal:  Cell       Date:  1987-09-25       Impact factor: 41.582

2.  Direct evidence for DNA bending at the lambda replication origin.

Authors:  K Zahn; F R Blattner
Journal:  Science       Date:  1987-04-24       Impact factor: 47.728

3.  Sequence periodicities in chicken nucleosome core DNA.

Authors:  S C Satchwell; H R Drew; A A Travers
Journal:  J Mol Biol       Date:  1986-10-20       Impact factor: 5.469

4.  Detection, sequence patterns and function of unusual DNA structures.

Authors:  J N Anderson
Journal:  Nucleic Acids Res       Date:  1986-11-11       Impact factor: 16.971

5.  Static and initiator protein-enhanced bending of DNA at a replication origin.

Authors:  R R Koepsel; S A Khan
Journal:  Science       Date:  1986-09-19       Impact factor: 47.728

6.  The isolation of restriction fragments containing the primary and secondary (galT) bacterial att sites of phage lambda.

Authors:  J C Marini; R Weisberg; A Landy
Journal:  Virology       Date:  1977-12       Impact factor: 3.616

7.  Physical characterization of a kinetoplast DNA fragment with unusual properties.

Authors:  J C Marini; P N Effron; T C Goodman; C K Singleton; R D Wells; R M Wartell; P T Englund
Journal:  J Biol Chem       Date:  1984-07-25       Impact factor: 5.157

8.  Structure and function of an AT-rich, interspersed repetitive sequence from Chironomus thummi: solenoidal DNA, 142 bp palindrome-frame and homologies with the sequence for site-specific recombination of bacterial transposons.

Authors:  N Israelewski
Journal:  Nucleic Acids Res       Date:  1983-10-25       Impact factor: 16.971

9.  The pitch of chromatin DNA is reflected in its nucleotide sequence.

Authors:  E N Trifonov; J L Sussman
Journal:  Proc Natl Acad Sci U S A       Date:  1980-07       Impact factor: 11.205

Review 10.  Probing the three-dimensional structures of DNA and RNA oligonucleotides in solution by nuclear Overhauser enhancement measurements.

Authors:  G M Clore; A M Gronenborn
Journal:  FEBS Lett       Date:  1985-01-07       Impact factor: 4.124

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