Skip Navigation

This Article
Right arrow FREE Full Text (PDF) Freely available
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (81)
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Hugall, A.
Right arrow Articles by Moritz, C.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Hugall, A.
Right arrow Articles by Moritz, C.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Molecular Biology and Evolution, Vol 16, 157-164, Copyright © 1999 by Society for Molecular Biology and Evolution


ORIGINAL ARTICLE

Reticulate evolution and the origins of ribosomal internal transcribed spacer diversity in apomictic Meloidogyne

A Hugall, J Stanton and C Moritz
Co-operative Research Centre for Tropical Plant Pathology, Queensland, Australia. ahugall@zoology.uq.edu.au

Among root knot nematodes of the genus Meloidogyne, the polyploid obligate mitotic parthenogens M. arenaria, M. javanica, and M. incognita are widespread and common agricultural pests. Although these named forms are distinguishable by closely related mitochondrial DNA (mtDNA) haplotypes, detailed sequence analyses of internal transcribed spacers (ITSs) of nuclear ribosomal genes reveal extremely high diversity, even within individual nematodes. This ITS diversity is broadly structured into two very different groups that are 12%-18% divergent: one with low diversity (< 1.0%) and one with high diversity (6%-7%). In both of these groups, identical sequences can be found within individual nematodes of different mtDNA haplotypes (i.e., among species). Analysis of genetic variance indicates that more than 90% of ITS diversity can be found within an individual nematode, with small but statistically significant (5%-10%; P < 0.05) variance distributed among mtDNA lineages. The evolutionarily distinct parthenogen M. hapla shows a similar pattern of ITS diversity, with two divergent groups of ITSs within each individual. In contrast, two diploid amphimictic species have only one lineage of ITSs with low diversity (< 0.2%). The presence of divergent lineages of rDNA in the apomictic taxa is unlikely to be due to differences among pseudogenes. Instead, we suggest that the diversity of ITSs in M. arenaria, M. javanica, and M. incognita is due to hybrid origins from closely related females (as inferred from mtDNA) and combinations of more diverse paternal lineages.
Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Mol Biol EvolHome page
U. K. Simon and M. Weiss
Intragenomic Variation of Fungal Ribosomal Genes Is Higher than Previously Thought
Mol. Biol. Evol., November 1, 2008; 25(11): 2251 - 2254.
[Abstract] [Full Text] [PDF]


Home page
Mol Biol EvolHome page
N. Mestrovic, P. Castagnone-Sereno, and M. Plohl
Interplay of Selective Pressure and Stochastic Events Directs Evolution of the MEL172 Satellite DNA Library in Root-Knot Nematodes
Mol. Biol. Evol., December 1, 2006; 23(12): 2316 - 2325.
[Abstract] [Full Text] [PDF]


Home page
GeneticsHome page
I. Keller, I. C. Chintauan-Marquier, P. Veltsos, and R. A. Nichols
Ribosomal DNA in the Grasshopper Podisma pedestris: Escape From Concerted Evolution
Genetics, October 1, 2006; 174(2): 863 - 874.
[Abstract] [Full Text] [PDF]


Home page
Phil Trans R Soc BHome page
P. De Ley, I. T. De Ley, K. Morris, E. Abebe, M. Mundo-Ocampo, M. Yoder, J. Heras, D. Waumann, A. Rocha-Olivares, A.H Jay Burr, et al.
An integrated approach to fast and informative morphological vouchering of nematodes for applications in molecular barcoding
Phil Trans R Soc B, October 29, 2005; 360(1462): 1945 - 1958.
[Abstract] [Full Text] [PDF]


Home page
Integr. Comp. Biol.Home page
G. Worheide, A. M. Sole-Cava, and J. N. A. Hooper
Biodiversity, molecular ecology and phylogeography of marine sponges: patterns, implications and outlooks
Integr. Comp. Biol., April 1, 2005; 45(2): 377 - 385.
[Abstract] [Full Text] [PDF]


Home page
Mol Biol EvolHome page
A. Gandolfi, I. R. Sanders, V. Rossi, and P. Menozzi
Evidence of Recombination in Putative Ancient Asexuals
Mol. Biol. Evol., May 1, 2003; 20(5): 754 - 761.
[Abstract] [Full Text] [PDF]


Home page
Mol Biol EvolHome page
J. H. G. von der Schulenburg, J. M. Hancock, A. Pagnamenta, J. J. Sloggett, M. E. N. Majerus, and G. D. D. Hurst
Extreme Length and Length Variation in the First Ribosomal Internal Transcribed Spacer of Ladybird Beetles (Coleoptera: Coccinellidae)
Mol. Biol. Evol., April 1, 2001; 18(4): 648 - 660.
[Abstract] [Full Text] [PDF]


Home page
Mol Biol EvolHome page
G. Muir, C. C. Fleming, and C. Schlötterer
Three Divergent rDNA Clusters Predate the Species Divergence in Quercus petraea (Matt.) Liebl. and Quercus robur L
Mol. Biol. Evol., February 1, 2001; 18(2): 112 - 119.
[Abstract] [Full Text]


Home page
Mol Biol EvolHome page
K. W. Hughes and R. H. Petersen
Apparent Recombination or Gene Conversion in the Ribosomal ITS Region of a Flammulina (Fungi, Agaricales) Hybrid
Mol. Biol. Evol., January 1, 2001; 18(1): 94 - 96.
[Full Text] [PDF]


Home page
Mol Biol EvolHome page
D. J. Harris and K. A. Crandall
Intragenomic Variation Within ITS1 and ITS2 of Freshwater Crayfishes (Decapoda: Cambaridae): Implications for Phylogenetic and Microsatellite Studies
Mol. Biol. Evol., February 1, 2000; 17(2): 284 - 291.
[Abstract] [Full Text] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.