Abstract
The cyanobacterial radiation consists of several lineages of phyletically (morphologically and genetically) related organisms. Several of these organisms show a striking resemblance to fossil counterparts. To investigate the molecular mechanisms responsible for stabilizing or homogenizing cyanobacterial characters, we compared the evolutionary rates and phylogenetic origins of the small-subunit rRNA-encoding DNA (16S rDNA), the conserved gene rbcL (encoding D-ribulose 1,5-bisphosphate carboxylase-oxygenase large subunit), and the less conserved gene rbcX. This survey includes four categories of phyletically related organisms: 16 strains of Microcystis, 6 strains of Tychonema, 10 strains of Planktothrix, and 12 strains of Nostoc. Both rbcL and rbcX can be regarded as neutrally evolving genes, with 95 to 100% and 50 to 80% synonymous nucleotide substitutions, respectively. There is generally low sequence divergence within the Microcystis, Tychonema, and Planktothrix categories both for rbcLX and 16S rDNA. The Nostoc category, on the other hand, consists of three genetically clustered lineages for these loci. The 16S rDNA and rbcLX phylogenies are not congruent for strains within the clustered groups. Furthermore, analysis of the phyletic structure for rbcLX indicates recombinational events between the informative sites within this locus. Thus, our results are best explained by a model involving both intergenic and intragenic recombinations. This evolutionary model explains the DNA sequence clustering for the modern species as a result of sequence homogenization (concerted evolution) caused by exchange of genetic material for neutrally evolving genes. The morphological clustering, on the other hand, is explained by structural and functional stability of these characters. We also suggest that exchange of genetic material for neutrally evolving genes may explain the apparent stability of cyanobacterial morphological characters, perhaps over billions of years.
MeSH Terms
Base Sequence
Biological Evolution
Chromosome Mapping
Chromosomes, Bacterial
Cyanobacteria/classification,genetics
DNA, Ribosomal/genetics
Genetic Variation
Phylogeny
Polymerase Chain Reaction
RNA, Ribosomal, 16S/genetics
Sequence Alignment
Sequence Homology, Nucleic Acid
Species Specificity
Chemicals
DNA, Ribosomal
RNA, Ribosomal, 16S
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Rudi K
Department of Biology, University of Oslo, Norway. knut.rudi@bio.uio.no
Skulberg O M
Jakobsen K S
References (25)
25 references, click to expand
-
Signal, noise, and reliability in molecular phylogenetic analyses.
J Hered. 1992 May-Jun;83(3):189-95
PMID: 1624764
-
Bacterial evolution.
Microbiol Rev. 1987 Jun;51(2):221-71
PMID: 2439888
-
Fast and sensitive multiple sequence alignments on a microcomputer.
Comput Appl Biosci. 1989 Apr;5(2):151-3
PMID: 2720464
-
CONFIDENCE LIMITS ON PHYLOGENIES: AN APPROACH USING THE BOOTSTRAP.
Evolution. 1985 Jul;39(4):783-791
PMID: 28561359
-
PHYLOGENETIC INFERENCE FROM RESTRICTION ENDONUCLEASE CLEAVAGE SITE MAPS WITH PARTICULAR REFERENCE TO THE EVOLUTION OF HUMANS AND THE APES.
Evolution. 1983 Mar;37(2):221-244
PMID: 28568373
-
DOES RECOMBINATION CONSTRAIN NEUTRAL DIVERGENCE AMONG BACTERIAL TAXA?
Evolution. 1995 Feb;49(1):164-175
PMID: 28593680
-
Methods for identifying proteins by using partial sequences.
Proc Natl Acad Sci U S A. 1979 May;76(5):2170-4
PMID: 287054
-
Homologous recombination in Escherichia coli: dependence on substrate length and homology.
Genetics. 1986 Mar;112(3):441-57
PMID: 3007275
-
Genetic exchange among natural isolates of bacteria: recombination within the phoA gene of Escherichia coli.
Proc Natl Acad Sci U S A. 1988 Sep;85(18):7036-40
PMID: 3045828
-
The neighbor-joining method: a new method for reconstructing phylogenetic trees.
Mol Biol Evol. 1987 Jul;4(4):406-25
PMID: 3447015
-
Parallel gradualistic evolution of Ordovician trilobites.
Nature. 1987 Dec 10-16;330(6148):561-3
PMID: 3683573
-
Statistical methods of DNA sequence analysis: detection of intragenic recombination or gene conversion.
Mol Biol Evol. 1985 Nov;2(6):539-56
PMID: 3870876
-
A simple method for estimating evolutionary rates of base substitutions through comparative studies of nucleotide sequences.
J Mol Evol. 1980 Dec;16(2):111-20
PMID: 7463489
-
Interspecies gene exchange in bacteria: the role of SOS and mismatch repair systems in evolution of species.
Cell. 1995 Feb 10;80(3):507-15
PMID: 7859291
-
Bacterial gene transfer by natural genetic transformation in the environment.
Microbiol Rev. 1994 Sep;58(3):563-602
PMID: 7968924
-
Punctuated equilibrium comes of age.
Nature. 1993 Nov 18;366(6452):223-7
PMID: 8232582
-
Determining divergence times of the major kingdoms of living organisms with a protein clock.
Science. 1996 Jan 26;271(5248):470-7
PMID: 8560259
-
Bridging the protein sequence-structure gap by structure predictions.
Annu Rev Biophys Biomol Struct. 1996;25:113-36
PMID: 8800466
-
Dating the cenancester of organisms.
Science. 1996 Dec 6;274(5293):1750; author reply 1751-3
PMID: 8984636
-
Dating the cenancester of organisms.
Science. 1996 Dec 6;274(5293):1750-1; author reply 1751-3
PMID: 8984637
-
Episodic adaptive evolution of primate lysozymes.
Nature. 1997 Jan 9;385(6612):151-4
PMID: 8990116
-
Rapid, universal method to isolate PCR-ready DNA using magnetic beads.
Biotechniques. 1997 Mar;22(3):506-11
PMID: 9067030
-
Maximum activity of recombinant ribulose 1,5-bisphosphate carboxylase/oxygenase of Anabaena sp. strain CA requires the product of the rbcX gene.
J Bacteriol. 1997 Jun;179(11):3793-6
PMID: 9171433
-
Strain characterization and classification of oxyphotobacteria in clone cultures on the basis of 16S rRNA sequences from the variable regions V6, V7, and V8.
Appl Environ Microbiol. 1997 Jul;63(7):2593-9
PMID: 9212409
-
A graphical method for detecting recombination in phylogenetic data sets.
Mol Biol Evol. 1997 Nov;14(11):1125-31
PMID: 9364770