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      Variation in genome size and karyotype among closely related aphid parasitoids (Hymenoptera, Aphelinidae).

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          Abstract

          Genome sizes were measured and determined for the karyotypes of nine species of aphid parasitoids in the genus Aphelinus Dalman,1820. Large differences in genome size and karyotype were found between Aphelinus species, which is surprising given the similarity in their morphology and life history. Genome sizes estimated from flow cytometry were larger for species in the Aphelinus mali (Haldeman, 1851) complex than those for the species in the Aphelinus daucicola Kurdjumov, 1913 and Aphelinus varipes (Förster,1841) complexes. Haploid karyotypes of the Aphelinus daucicola and Aphelinus mali complexes comprised five metacentric chromosomes of similar size, whereas those of the Aphelinus varipes complex had four chromosomes, including a larger and a smaller metacentric chromosome and two small acrocentric chromosomes or a large metacentric and three smaller acrocentric chromosomes. Total lengths of female haploid chromosome sets correlated with genome sizes estimated from flow cytometry. Phylogenetic analysis of karyotypic variation revealed a chromosomal fusion together with pericentric inversions in the common ancestor of the Aphelinus varipes complex and further pericentric inversions in the clade comprising Aphelinus kurdjumovi Mercet, 1930 and Aphelinus hordei Kurdjumov, 1913. Fluorescence in situ hybridization with a 28S ribosomal DNA probe revealed a single site on chromosomes of the haploid karyotype of Aphelinus coreae Hopper & Woolley, 2012. The differences in genome size and total chromosome length between species complexes matched the phylogenetic divergence between them.

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          Rapid flow cytometric analysis of the cell cycle in intact plant tissues.

          Mechanical chopping of plant tissues in the presence of mithramycin released intact nuclei representative of the cells within the tissues. The amount of nuclear DNA in the homogenates of monocotyledonous and dicotyledonous plants was accurately and rapidly determined by flow microfluorometry, and the distribution of nuclei involved in the cell cycle was charted for tissues selected from different physical locations or developmental stages.
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            Cytogenetic analysis using quantitative, high-sensitivity, fluorescence hybridization.

            This report describes the use of fluorescence in situ hybridization for chromosome classification and detection of chromosome aberrations. Biotin-labeled DNA was hybridized to target chromosomes and subsequently rendered fluorescent by successive treatments with fluorescein-labeled avidin and biotinylated anti-avidin antibody. Human chromosomes in human-hamster hybrid cell lines were intensely and uniformly stained in metaphase spreads and interphase nuclei when human genomic DNA was used as a probe. Interspecies translocations were detected easily at metaphase. The human-specific fluorescence intensity from cell nuclei and chromosomes was proportional to the amount of target human DNA. Human Y chromosomes were fluorescently stained in metaphase and interphase nuclei by using a 0.8-kilobase DNA probe specific for the Y chromosome. Cells from males were 40 times brighter than those from females. Both Y chromosomal domains were visible in most interphase nuclei of XYY amniocytes. Human 28S ribosomal RNA genes on metaphase chromosomes were distinctly stained by using a 1.5-kilobase DNA probe.
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              A phylogenetic analysis of the megadiverse Chalcidoidea (Hymenoptera)

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                Author and article information

                Journal
                Comp Cytogenet
                Comparative cytogenetics
                Pensoft Publishers
                1993-0771
                1993-0771
                2017
                : 11
                : 1
                Affiliations
                [1 ] Botanical Garden, Moscow State University, Moscow, Russia.
                [2 ] Beneficial Insects Introduction Research Unit, ARS-USDA, 501 South Chapel Street, Newark, Delaware, United States of America.
                [3 ] Department of Entomology, Texas A&M University, College Station, Texas, United States of America.
                Article
                10.3897/CompCytogen.v11i1.10872
                5599701
                28919952
                384f0cc3-2a6c-4ecc-a9a4-efcf9d6322d6
                History

                Aphelinidae,Aphelinus,flow cytometry,genome size,karyotype,parasitoid

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