Evolutionary Diversification Indicated by Compensatory Base Changes in ITS2 Secondary Structures in a Complex Fungal Species, Rhizoctonia solani

被引:47
作者
Ahvenniemi, Paavo [1 ]
Wolf, Matthias [2 ]
Lehtonen, Mari J. [1 ]
Wilson, Paula [1 ]
German-Kinnari, Malgorzata [1 ]
Valkonen, Jari P. T. [1 ]
机构
[1] Univ Helsinki, Dept Appl Biol, FIN-00014 Helsinki, Finland
[2] Univ Wurzburg, Dept Bioinformat, Bioctr, D-97074 Wurzburg, Germany
关键词
ITS sequence heterogeneity; Compensatory base change; Secondary structure; Rhizoctonia solani; Concerted evolution; Anastomosis group; PRE-RIBOSOMAL-RNA; THANATEPHORUS-CUCUMERIS; PHYLOGENETIC UTILITY; GENETIC DIVERSITY; ANASTOMOSIS; POTATO; SEQUENCE; DNA; AG-3; POPULATIONS;
D O I
10.1007/s00239-009-9260-3
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The rRNA cistron (18S-ITS1-5.8S-ITS2-28S) is used widely for phylogenetic analyses. Recent studies show that compensatory base changes (CBC) in the secondary structure of ITS2 correlate with genetic incompatibility between organisms. Rhizoctonia solani consists of genetically incompatible strain groups (anastomosis groups, AG) distinguished by lack of anastomosis between hyphae of strains. Phylogenetic analysis of internal transcribed spacer (ITS) sequences shows a strong correlation with AG determination. In this study, ITS sequences were reannotated according to the flanking 5.8S and 28S regions which interact during ribogenesis. One or two CBCs were detected between the ITS2 secondary structure of AG-3 potato strains as compared to AG-3 tobacco strains, and between these two strains and all other AGs. When a binucleate Rhizoctonia species related to Ceratobasidiaceae was compared to the AGs of R. solani, which were multinucleate (3-21 nuclei per cell), 1-3 CBCs were detected. The CBCs in potato strains of AG-3 distinguish them from AG-3 tobacco strains and other AGs yielding further evidence that the potato strains of AG-3 originally described as R. solani are a species distinct from other AGs. The ITS1-5.8S-ITS2 sequences were analyzed by direct sequencing of PCR products from 497 strains of AG-3 isolated from potato. The same 10 and 4 positions in ITS1 and ITS2, respectively, contained variability in 425 strains (86%). Nine different unambiguous ITS sequences (haplotypes) could be detected in a single strain by sequencing cloned PCR products indicating that concerted evolution had not homogenized the rRNA cistrons in many AG-3 strains. Importantly, the sequence variability did not affect the secondary structure of ITS2 and CBCs in AG-3.
引用
收藏
页码:150 / 163
页数:14
相关论文
共 66 条
[1]   Parallels in rRNA processing:: Conserved features in the processing of the internal transcribed spacer 1 in the pre-rRNA from Schizosaccharomyces pombe [J].
Abeyrathne, PD ;
Nazar, RN .
BIOCHEMISTRY, 2005, 44 (51) :16977-16987
[2]  
[Anonymous], 1990, PCR Protocols. A Guide to Methods and Applications
[3]  
Bernard N., 1909, ANN SCI NAT BOT BIOL, V9, P1
[4]   Changing partners in the dark: isotopic and molecular evidence of ectomycorrhizal liaisons between forest orchids and trees [J].
Bidartondo, MI ;
Burghardt, B ;
Gebauer, G ;
Bruns, TD ;
Read, DJ .
PROCEEDINGS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES, 2004, 271 (1550) :1799-1806
[5]   Identification at strain level of Rhizoctonia solani AG4 isolates by direct sequence of asymmetric PCR products of the ITS regions [J].
Boysen, M ;
Borja, M ;
delMoral, C ;
Salazar, O ;
Rubio, V .
CURRENT GENETICS, 1996, 29 (02) :174-181
[6]  
Buckler ES, 1997, GENETICS, V145, P821
[7]  
BUTLER EE, 1970, RHIZOCTONIA SOLANI B, P32
[8]   Characterization of mycorrhizal isolates of Rhizoctonia solani from an orchid, including AG-12, a new anastomosis group [J].
Carling, DE ;
Pope, EJ ;
Brainard, KA ;
Carter, DA .
PHYTOPATHOLOGY, 1999, 89 (10) :942-946
[9]  
Carling DE, 1996, RHIZOCTONIA SPECIES: TAXONOMY, MOLECULAR BIOLOGY, ECOLOGY, PATHOLOGY AND DISEASE CONTROL, P37
[10]   Characterization of AG-13, a newly reported anastomosis group of Rhizoctonia solani [J].
Carling, DE ;
Baird, RE ;
Gitaitis, RD ;
Brainard, KA ;
Kuninaga, S .
PHYTOPATHOLOGY, 2002, 92 (08) :893-899