Lunt, D. H., L. E. Whipple, and B. C. Hyman (1998) Mitochondrial DNA variable number tandem repeats (VNTRs): utility and problems in molecular ecology. MOLECULAR ECOLOGY 7:1441-1455. PDF
Analysis of mitochondrial (mt)DNA size polymorphism in the form of variable number tandem repeats (mtVNTRs) has become an increasingly popular methodology for addressing questions in molecular ecology. When detected by PCR, mtVNTR analysis can provide a sensitive, rapid, and cost-effective measure of genetic variability that may be exploited in studies of population differentiation and biogeography. Despite the emergence of this approach, there has been little critical evaluation of its success or utility as a practical tool. In this review, we identify problematic methodological, theoretical and interpretive factors that can influence the utility of mtVNTR analysis. The reliability of the procedure is considered in terms of both detection of alleles and scoring of intra-individual allele frequencies. While many of the potential technical problems of the technique do not raise serious practical concerns, this rapid and sensitive methodology is seriously compromised by the difficulty of reliably assessing allele frequencies, of assaying only germline tissue, and in our ignorance of the mechanisms generating mtVNTR diversity. Thus, although there is a considerable potential for mtVNTR pilot studies to assess genetic diversity, the utility of the technique to resolve broader questions in molecular ecology should be treated cautiously until such a time as the system is better understood.
Mitochondrial DNA variable number tandem repeats (VNTRs): utility and problems in molecular ecology
Mitochondrial DNA length variation in Meloidogyne incognita isolates of established genetic relationships: utility for nematode population studies
Whipple, L. E., D. H. Lunt, and B. C. Hyman (1998) Mitochondrial DNA length variation in Meloidogyne incognita isolates of established genetic relationships: utility for nematode population studies. FUNDAMENTAL AND APPLIED NEMATOLOGY 21:265-271. (PDF)
Six Meloidogyne incognita isolates with previously characterized genetic relationships were used to test the utility of a 63 base-pair mitochondrial Variable Number Tandem Repeat (VNTR) as a marker for population studies. The polymerase chain reaction (PCR) was used to amplify this locus and to measure copy number and allele frequencies of the 63 bp VNTR. Individual nematodes were typically heteroplasmic and maintained mitochondrial DNA (mtDNA) molecules containing up to thirteen distinguishable VNTR size classes. Each allele was composed of one to 21 repeat copies. Hierarchical statistics revealed that diversity was low (7%) among the isolates whereas 60% of the total genetic diversity measured for these six isolates resides within individuals. Likelihood ratio tests revealed that diversity indices were independent of genetic relatedness and race designation, limiting the utility of this locus for studies of population differentiation. As M. incognita is an obligate parthenogen, paternal contribution to heteroplasmy is excluded and diversity within individual nematodes at this mtDNA locus is primarily a consequence of mutation to different repeat copy numbers.
Animal mitochondrial DNA recombination
Lunt, D. H., and B. C. Hyman (1997) Nature 387:247-247. Animal mitochondrial DNA recombination
Genetic recombination is known to be a source of mitochondrial DNA (mtDNA) variability in plants, fungi and protists, but there continues to be a consensus (based on studies of somatic cell hybridization and DNA repair) that such processes do not operate on animal mtDNA. Contrary to this opinion we have now identified and characterized the end-products of recombination in the mitochondrial genome of the phytonematode Meloidogyne javanica. PDF PMID: 9153388