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  • 1
    ISSN: 1546-1718
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Medicine
    Notes: [Auszug] Sir — Closely related (confamilial) genera often retain large chromosomal tracts in which gene order is co linear, punctuated by structural mutations such as inversions and translocations1. To explore the possibility that conservation of gene order might extrapolate to more distantly related ...
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Journal of molecular evolution 36 (1993), S. 429-447 
    ISSN: 1432-1432
    Keywords: Retrotransposable elements ; Copia, retrotransposons ; Orthology ; Paralogy ; Gossypium ; Phylogenetic analysis ; Polyploidy ; Molecular evolution ; Horizontal transmission
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary Copia-like retrotransposable elements were identified in allotetraploid cotton,Gossypium hirsutum, and two species representing its diploid progenitors,G. herbaceum andG. raimondii. These elements are present in high copy number in all three species. Because the two diploid genomic groups have been isolated on opposite sides of the world for 6–11 million years, horizontal transfer of elements between these species is highly unlikely. Elements were intensively sampled to generate a model ofcopia-like retrotransposable element evolution in systems where vertical transmission is the sole probable means of descent.Copia-like retrotransposon diversity is equally great in all threeGossypium species. Despite this high heterogeneity, analysis of 89 partial reverse transcriptase sequences resulted in the recognition of nine sharply differentiated retrotransposon lineages, each containing elements that share high sequence similarity. No evidence of horizontal transfer from other taxa was obtained. Phylogenetic analyses demonstrate that element topologies are incongruent withGossypium phylogeny. Consideration of processes that obscure phylogenetic reconstruction of multigene families (including sampling error, variable degrees of orthology and paralogy, differential lineage age and lineage loss and/or proliferation) demonstrates that incongruence between organismal and retrotransposon trees is expected under conditions in which vertical processes are the sole means of transmission. Identification of closely related elements between species allowed rates ofcopia-like retrotransposon sequence evolution to be estimated as approximately 10−9 nucleotide substitutions/site/year. These rates are consistent with the interpretation that these retrotransposons have been evolving under functional constraints for most of the time frame bracketed by the species studied. Extrapolation of these results to previous studies that sampled from more highly divergent taxa indicates that horizontal transfer need not be invoked to explain observed phylogenetic patterns.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1573-4927
    Keywords: genetic linkage ; isozymes ; allozymes ; Zea mays L. ; adenylate kinase ; shikimate dehydrogenase ; aconitate hydratase ; NADH dehydrogenase
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract Electrophoretic variation and inheritance of four novel enzyme systems were studied in maize (Zea mays L.). A minimum of 10 genetic loci collectively encodes isozymes of aconitate hydratase (ACO; EC 4.2.1.3.), adenylate kinase (ADK; EC 2.7.4.3), NADH dehydrogenase (DIA; EC 1.6.99.—), and shikimate dehydrogenase (SAD; EC 1.1.1.25). At least four loci are responsible for the genetic control of ACO. Genetic data for two of the encoding loci,Aco1 andAco4, demonstrated that at least two maize ACOs are active as monomers. Analysis of organellar preparations suggests that ACO1 and ACO4 are localized in the cytosolic and mitochondrial subcellular fractions, respectively. Maize ADK is encoded by a single nuclear locus,Adk1, governing monomeric enzymes that are located in the chloroplasts. Two cytosolic and two mitochondrial forms of DIA were electrophoretically resolved. Segregation analyses demonstrated that the two cytosolic isozymes are controlled by separate loci,Dia1 andDia2, coding for products that are functional as monomers (DIA1) and dimers (DIA2). The major isozyme of SAD is apparently cytosolic, although an additional faintly staining plastid form may be present. Alleles atSad1 are each associated with two bands that cosegregate in controlled crosses. Linkage analyses and crosses with B-A translocation stocks were effective in determining the map locations of six loci, including the previously described but unmapped locusAcp4. Several of these loci were localized to sparsely mapped regions of the genome.Dia2 andAcp4 were placed on the distal portion of the long arm of chromosome 1, 12.6 map units apart.Dia1 was localized to chromosome 2, 22.2 centimorgans (cM) fromB1. Aco1 was mapped to chromosome 4, 6.2 cM fromsu1. Adk1 was placed on the poorly marked short arm of chromosome 6, 8.1 map units fromrgd1. Less than 1% recombination was observed betweenGlu1 (on chromosome 10) andSad1. In contrast to many other maize isozyme systems, there was little evidence of gene duplication or of parallel linkage relationships for these allozyme loci.
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  • 4
    ISSN: 1573-4927
    Keywords: genetic linkage ; isozymes ; allozymes ; Zea mays L. ; adenylate kinase ; shikimate dehydrogenase ; aconitate hydratase ; NADH dehydrogenase
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract Electrophoretic variation and inheritance of four novel enzyme systems were studied in maize (Zea mays L.). A minimum of 10 genetic loci collectively encodes isozymes of aconitate hydratase (ACO; EC 4.2.1.3.), adenylate kinase (ADK; EC 2.7.4.3), NADH dehydrogenase (DIA; EC 1.6.99.—), and shikimate dehydrogenase (SAD; EC 1.1.1.25). At least four loci are responsible for the genetic control of ACO. Genetic data for two of the encoding loci,Aco1 andAco4, demonstrated that at least two maize ACOs are active as monomers. Analysis of organellar preparations suggests that ACO1 and ACO4 are localized in the cytosolic and mitochondrial subcellular fractions, respectively. Maize ADK is encoded by a single nuclear locus,Adk1, governing monomeric enzymes that are located in the chloroplasts. Two cytosolic and two mitochondrial forms of DIA were electrophoretically resolved. Segregation analyses demonstrated that the two cytosolic isozymes are controlled by separate loci,Dia1 andDia2, coding for products that are functional as monomers (DIA1) and dimers (DIA2). The major isozyme of SAD is apparently cytosolic, although an additional faintly staining plastid form may be present. Alleles atSad1 are each associated with two bands that cosegregate in controlled crosses. Linkage analyses and crosses with B-A translocation stocks were effective in determining the map locations of six loci, including the previously described but unmapped locusAcp4. Several of these loci were localized to sparsely mapped regions of the genome.Dia2 andAcp4 were placed on the distal portion of the long arm of chromosome 1, 12.6 map units apart.Dia1 was localized to chromosome 2, 22.2 centimorgans (cM) fromB1. Aco1 was mapped to chromosome 4, 6.2 cM fromsu1. Adk1 was placed on the poorly marked short arm of chromosome 6, 8.1 map units fromrgd1. Less than 1% recombination was observed betweenGlu1 (on chromosome 10) andSad1. In contrast to many other maize isozyme systems, there was little evidence of gene duplication or of parallel linkage relationships for these allozyme loci.
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  • 5
    ISSN: 1573-6849
    Keywords: evolution ; genome ; Gossypium ; polyploidization ; repetitive element ; retrotransposon
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Retrotransposons constitute a ubiquitous and dynamic component of plant genomes. Intragenomic and intergenomic comparisons of related genomes offer potential insights into retrotransposon behavior and genomic effects. Here, we have used fluorescent in-situ hybridization to determine the chromosomal distributions of a Ty1-copia-like retrotransposon in the cotton AD-genome tetraploid Gossypium hirsutum and closely related putative A- and D-genome diploid ancestors. Retrotransposon clone A108 hybridized to all G. hirsutum chromosomes, approximately equal in intensity in the A- and D-subgenomes. Similar results were obtained by hybridization of A108 to the A-genome diploid G. arboreum, whereas no signal was detected on chromosomes of the D-genome diploid G. raimondii. The significance and potential causes of these observations are discussed.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Genetic resources and crop evolution 40 (1993), S. 165-170 
    ISSN: 1573-5109
    Keywords: crop evolution ; Gossypium hirsutum ; Gossypium lanceolatum ; allozymes ; polyploidy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Summary Gossypium lanceolatum comprises a group of laciniate-leaved commensal cottons from the Mexican states of Oaxaca and Guerrero. This geographically restricted, morphologically distinct group of perennial cottons has been considered conspecific with G. hirsutum, with which it is sympatric. In addition to its questionable specific status, G. lanceolatum has added importance because it represents the focal point of an hypothesis that New World tetraploid Gossypium have a polyphyletic origin—an hypothesis that conflicts with the more widely accepted view that New World tetraploid Gossypium have a monophyletic origin. To reassess the systematic and genetic relationships between G. lanceolatum and G. hirsutum, historical data were reconsidered in the context of recently published molecular marker based data. Chloroplast and nuclear DNA markers fail to discriminate G. lanceolatum from G. hirsutum, uniting both into a single phylogenetic lineage. A new analysis of allelic variability at 50 allozyme loci in 11 G. lanceolatum and 527 G. hirsutum accessions demonstrates that G. lanceolatum has no unique alleles relative to G. hirsutum. Genetic identity estimates were uniformly high (〉 0.96) among G. lanceolatum and geographically adjacent, mainland Mesoamerican groups of G. hirsutum accessions. Multivariate analyses demonstrated that G. lanceolatum is genetically embedded within geographically adjacent populations of G. hirsutum. These data, in conjunction with the complete interfertility between the two taxa and previous evidence for conspecificity, lead to the conclusion that G. lanceolatum does not warrant specific status. Rather, it is more properly recognized as a locally developed, domesticated form of G. hirsutum, i.e., G. hirsutum race ‘palmeri’.
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Biochemical genetics 22 (1984), S. 739-748 
    ISSN: 1573-4927
    Keywords: alcohol dehydrogenase ; isozymes ; Camellia japonica ; distorted segregation ; linkage
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract Alcohol dehydrogenase isozymes in Camellia japonica are encoded by two genes, Adh-1 and Adh-2. Both loci are expressed in seeds, and their products randomly associate into intragenic and intergenic dimers. Electrophoresis of leaf extracts reveals only the products of Adh-2. Formal genetic analysis indicated that the two Adh loci are tightly linked (combined estimate of r=0.004). Most segregations fit expected Mendelian ratios, but in some families distorted segregation was observed at Adh-1, Adh-2, or both loci. The deficient progeny class varied across families, and in two apparent backcrosses three rather than two phenotypic classes were recovered. The mechanism underlying these distortions is not known, but evidence is presented that suggests that the phenomenon is genic or segmental in nature. Plausible hypotheses include linkage of the Adh structural genes with a gametophytic self-incompatibility locus, translocation heterozygosity involving the segment bearing Adh-1 and Adh-2, or a combination of these two mechanisms.
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Plant molecular biology 42 (2000), S. 225-249 
    ISSN: 1573-5028
    Keywords: allopolyploidy ; duplication ; genome evolution ; genomic redundancy ; molecular evolution ; speciation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Polyploidy is a prominent process in plants and has been significant in the evolutionary history of vertebrates and other eukaryotes. In plants, interdisciplinary approaches combining phylogenetic and molecular genetic perspectives have enhanced our awareness of the myriad genetic interactions made possible by polyploidy. Here, processes and mechanisms of gene and genome evolution in polyploids are reviewed. Genes duplicated by polyploidy may retain their original or similar function, undergo diversification in protein function or regulation, or one copy may become silenced through mutational or epigenetic means. Duplicated genes also may interact through inter-locus recombination, gene conversion, or concerted evolution. Recent experiments have illuminated important processes in polyploids that operate above the organizational level of duplicated genes. These include inter-genomic chromosomal exchanges, saltational, non-Mendelian genomic evolution in nascent polyploids, inter-genomic invasion, and cytonuclear stabilization. Notwithstanding many recent insights, much remains to be learned about many aspects of polyploid evolution, including: the role of transposable elements in structural and regulatory gene evolution; processes and significance of epigenetic silencing; underlying controls of chromosome pairing; mechanisms and functional significance of rapid genome changes; cytonuclear accommodation; and coordination of regulatory factors contributed by two, sometimes divergent progenitor genomes. Continued application of molecular genetic approaches to questions of polyploid genome evolution holds promise for producing lasting insight into processes by which novel genotypes are generated and ultimately into how polyploidy facilitates evolution and adaptation.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Plant systematics and evolution 145 (1984), S. 223-226 
    ISSN: 1615-6110
    Keywords: Angiosperms ; Theaceae ; Camellia japonica ; Allozymes ; polyploidy ; origin of cultivars
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Electrophoretic examination of allozymes from 189Camellia japonica cultivars revealed some banding patterns not explainable by codominant diploid genetics. At several loci encoding dimeric enzymes, 5 and 6 banded patterns were observed in 7 cultivars. These patterns are interpreted as resulting from triploidy or aneuploidy, where three variant alleles code for products which are electrophoretically distinguishable and associate to form three homodimers and three heterodimers. The presence of allozyme multiplicity in these clones suggests a sexual rather than a somatic mode of triploid origin.
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  • 10
    ISSN: 1615-6110
    Keywords: Malvaceae ; Gossypium ; Allozymes ; genetic diversity ; cladistics ; phylogenetics ; endemism ; Flora of Brazil
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Gossypium mustelinum, one of five tetraploid species in the cotton genus, is geographically restricted to a few states in NE Brazil. Allozyme analysis was used to assess levels and patterns of genetic diversity inG. mustelinum and its relationship to the other tetraploid species. Genetic variation was low, with only 6 of 50 loci examined being polymorphic, a mean of 1.14 alleles per locus and a mean panmictic heterozygosity of 0.08. These estimates are low relative to other tetraploid cotton species, but are typical of island endemics. Interpopulational genetic identities were uniformly high, lending support to the concept of there being only one wild species of Brazilian cotton. The limited allelic diversity observed was correlated with geographical distribution, although variability is so limited in the species that geographically marginal populations are electrophoretically ordinary. Phylogenetic and phenetic analyses demonstrate thatG. mustelinum is isolated among polyploid cotton species, occupying one of the three basal clades resulting from an early radiation of polyploid taxa subsequent to polyploid formation. We suggest thatG. mustelinum represents a paleoendemic that presently exists as a series of widely scattered, relictual populations. Despite several centuries of sympatric cultivation ofG. barbadense andG. hirsutum, there was little evidence of interspecific introgression of alleles from cultivated cottons intoG. mustelinum.
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