Dynamics of concerted evolution of ribosomal DNA and histone gene families in the melanogaster species subgroup of Drosophila

1982 ◽  
Vol 158 (1) ◽  
pp. 17-35 ◽  
Author(s):  
Enrico Coen ◽  
Tom Strachan ◽  
Gabriel Dover
1997 ◽  
Vol 17 (3) ◽  
pp. 1666-1673 ◽  
Author(s):  
R Bishop ◽  
A Musoke ◽  
S Morzaria ◽  
B Sohanpal ◽  
E Gobright

Concerted evolution of multicopy gene families in vertebrates is recognized as an important force in the generation of biological novelty but has not been documented for the multicopy genes of protozoa. A multicopy locus, Tpr, which consists of tandemly arrayed open reading frames (ORFs) containing several repeated elements has been described for Theileria parva. Herein we show that probes derived from the 5'/N-terminal ends of ORFs in the genomic DNAs of T. parva Uganda (1,108 codons) and Boleni (699 codons) hybridized with multicopy sequences in homologous DNA but did not detect similar sequences in the DNA of 14 heterologous T. parva stocks and clones. The probe sequences were, however, protein coding according to predictive algorithms and codon usage. The 3'/C-terminal ends of the Uganda and Boleni ORFs exhibited 75% similarity and identity, respectively, to the previously identified Tpr1 and Tpr2 repetitive elements of T. parva Muguga. Tpr1-homologous sequences were detected in two additional species of Theileria. Eight different Tpr1-homologous transcripts were present in piroplasm mRNA from a single T. parva Muguga-infected animal. The Tpr1 and Tpr2 amino acid sequences contained six predicted membrane-associated segments. The ratio of synonymous to nonsynonymous substitutions indicates that Tpr1 evolves like protein-encoding DNA. The previously determined nucleotide sequence of the gene encoding the p67 antigen is completely identical in T. parva Muguga, Boleni, and Uganda, including the third base in codons. The data suggest that concerted evolution can lead to the radical divergence of coding sequences and that this can be a mechanism for the generation of novel genes.


Genetics ◽  
2006 ◽  
Vol 174 (2) ◽  
pp. 863-874 ◽  
Author(s):  
Irene Keller ◽  
Ioana C. Chintauan-Marquier ◽  
Paris Veltsos ◽  
Richard A. Nichols

Genetics ◽  
2005 ◽  
Vol 169 (2) ◽  
pp. 931-944 ◽  
Author(s):  
A. Kovarik ◽  
J. C. Pires ◽  
A. R. Leitch ◽  
K. Y. Lim ◽  
A. M. Sherwood ◽  
...  

1996 ◽  
Vol 42 (6) ◽  
pp. 685-705 ◽  
Author(s):  
Richard C. Cronn ◽  
Xinping Zhao ◽  
Andrew H. Paterson ◽  
Jonathan F. Wendell

Genetics ◽  
1997 ◽  
Vol 145 (3) ◽  
pp. 821-832 ◽  
Author(s):  
Edward S Buckler ◽  
Anthony Ippolito ◽  
Timothy P Holtsford

Although nuclear ribosomal DNA (rDNA) repeats evolve together through concerted evolution, some genomes contain a considerable diversity of paralogous rDNA. This diversity includes not only multiple functional loci but also putative pseudogenes and recombinants. We examined the occurrence of divergent paralogues and recombinants in Gossypium, Nicotiana, Tripsacum, Winteraceae, and Zea ribosomal internal transcribed spacer (ITS) sequences. Some of the divergent paralogues are probably rDNA pseudogenes, since they have low predicted secondary structure stability, high substitution rates, and many deamination-driven substitutions at methylation sites. Under standard PCR conditions, the low stability paralogues amplified well, while many high-stability paralogues amplified poorly. Under highly denaturing PCR conditions (i.e., with dimethylsulfoxide), both low- and high-stability paralogues amplified well. We also found recombination between divergent paralogues. For phylogenetics, divergent ribosomal paralogues can aid in reconstructing ancestral states and thus serveas good outgroups. Divergent paralogues can also provide companion rDNA phylogenies. However, phylogeneticists must discriminate among families of divergent paralogues and recombinants or suffer from muddled and inaccurate organismal phylogenies.


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