1991
DOI: 10.1007/bf00226220
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Inheritance of chloroplast and mitochondrial DNA in Picea and composition of hybrids from introgression zones

Abstract: The cloning of white spruce (Picea glauca) mitochondrial DNA homologous to the cytochrome oxidase II and ATPaseα genes of maize is described. These probes were used to define restriction fragment length polymorphisms which distinguish the white, Engelmann (P. engelmannii) and Sitka spruce (P. sitchensis) populations that occur in British Columbia. Analysis of progeny from crosses between the species revealed that mitochondrial DNA was maternally inherited in all cases (32 progeny from five independent crosses)… Show more

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Cited by 94 publications
(63 citation statements)
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“…This result reflects the extremely slow mutation rate of the chloroplast genome in conifers (estimated to be 5.3 ϫ 10 Ϫ10 mutations per gene per generation for sequenced regions) (14). The slow mutation rate, along with the fact that spruce cpDNA is paternally inherited through widely dispersed pollen (15,16), could have resulted in minimal genetic differentiation and obliterated the cpDNA signature of refuge locations in modern samples. Nevertheless, we found significant patterns in the geographic distribution of the cpDNA haplotypes that unambiguously differentiate the two regions (i.e., within Alaska versus outside Alaska), unveiling several lines of evidence for a glacial refuge of white spruce in Alaska.…”
Section: Resultsmentioning
confidence: 99%
“…This result reflects the extremely slow mutation rate of the chloroplast genome in conifers (estimated to be 5.3 ϫ 10 Ϫ10 mutations per gene per generation for sequenced regions) (14). The slow mutation rate, along with the fact that spruce cpDNA is paternally inherited through widely dispersed pollen (15,16), could have resulted in minimal genetic differentiation and obliterated the cpDNA signature of refuge locations in modern samples. Nevertheless, we found significant patterns in the geographic distribution of the cpDNA haplotypes that unambiguously differentiate the two regions (i.e., within Alaska versus outside Alaska), unveiling several lines of evidence for a glacial refuge of white spruce in Alaska.…”
Section: Resultsmentioning
confidence: 99%
“…The hypothesis of nuclear inheritance is therefore an unlikely one, and maternal inheritance of the RFLP variation is a more parsimonious explanation for the results. Formal proof of maternal inheritance of cox1 variants detected by the same form of RFLP analysis has been given for interspecific crosses involving P. sylvestris and related conifers (Neale & Sederoff, 1989;Sutton et al, 1991;Wagner et al, 1991;DeVerno et al, 1993;Wang et al, 1996). It is therefore reasonable to assume that the variation analysed here is maternally inherited mtDNA variation.…”
Section: Discussionmentioning
confidence: 99%
“…For efficient RFLP analysis of the mtDNA in plants (which represents a small fraction of the total DNA) a homologous probe is required (Sutton et al, 1991). Sequences of the plant mitochondrial cox1 gene were extracted from the EMBL DNA database and aligned.…”
Section: Development Of Mtdna Markermentioning
confidence: 99%
“…Important issues are related to the reproducibility of the RAPD marker system [31], other limitations, such as the presence of null alleles in the case of SSR assays that may underestimate heterozygosity [32], or the dominance nature of the RAPD and AFLP marker systems, where heterozygous individuals cannot be distinguished from homozygous ones, and lastly, the inexpensive generation of a vast abundance of highly polymorphic DNA markers to tackle genome-wide genetic diversity studies. Dependent on the study focus, genetic markers were derived from nuclear or organelle sequences; for example, chloroplast-or mitochondrial-derived diagnostic markers [33][34][35], dependent on the evidence of their maternal inheritance in the species, were used to trace back the colonization history of angiosperm forest tree species and conifers, respectively [36,37]. Although it has been known that variability within protein-coding regions is far less than within non-coding genomic regions, due to lower mutation rates and purifying selection to maintain proper protein functions, the study of polymorphic sites within coding sequences has been deemed more relevant because of their putative functional associations and, in addition, the ease of their interspecific transferability for comparative genetic studies based on sequence conservation.…”
Section: Marker Types and Their Applicationsmentioning
confidence: 99%