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      New data on karyotypes of lace bugs (Tingidae, Cimicomorpha, Hemiptera) with analysis of the 18S rDNA clusters distribution

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          Abstract

          Abstract

          The karyotypes of 10 species from 9 genera of the family Tingidae ( Hemiptera , Heteroptera , Cimicomorpha ) are described and illustrated for the first time. These species are: Agramma atricapillum (Spinola, 1837), Catoplatus carthusianus (Goeze, 1778), Dictyla platyoma (Fieber, 1861), Lasiacantha hermani Vásárhelyi, 1977, Oncochila simplex (Herrich-Schaeffer, 1830), Tingis ( Neolasiotropis) pilosa Hummel, 1825, and T. ( Tropidocheila) reticulata Herrich-Schaeffer, 1835, all with 2n = 12A + XY, as well as Acalypta marginata (Wolff, 1804), Derephysia ( Paraderephysia) longispina Golub, 1974, and Dictyonota strichnocera Fieber, 1844, all with 2n = 12A + X(0). Moreover, genera Catoplatus Spinola, 1837, Derephysia Spinola, 1837, and Oncochila (Herrich-Schaeffer, 1830) were explored cytogenetically for the first time. Much as all other hitherto studied lace bugs, the species studied here have 12 autosomes but differ in their sex chromosome systems. The ribosomal clusters were localized on male meiotic cells of all ten species already mentioned and, additionally, in Acalypta carinata Panzer, 1806 known to have 2n = 12A + X ( Grozeva and Nokkala 2001) by fluorescence in situ hybridization (FISH) using a PCR amplified 18S rDNA fragment as a probe. In all cases, rDNA loci were located interstitially on a pair of autosomes. Furthermore, two species possessed some additional rDNA clusters. Thus, Acalypta marginata showed clearly defined interstitial clusters on one more pair of autosomes, whereas Derephysia longispina had a terminal cluster on the X-chromosome. FISH performed with the telomeric (TTAGG) n probe did not reveal labelling in chromosomes of any species studied. Hence, the results obtained provide additional evidence for the karyotype conservatism, at least regarding the number of autosomes, for variation in chromosomal distribution of rDNA loci between species and for the lack of the ancestral insect telomeric sequence TTAGG in lace bugs. Preliminary taxonomic comments are made basing on some cytogenetic evidence.

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          Phylogenetic distribution of TTAGG telomeric repeats in insects.

          We examined the presence of TTAGG telomeric repeats in 22 species from 20 insect orders with no or inconclusive information on the telomere composition by single-primer polymerase chain reaction with (TTAGG)6 primers, Southern hybridization of genomic DNAs, and fluorescence in situ hybridization of chromosomes with (TTAGG)n probes. The (TTAGG)n sequence was present in 15 species and absent in 7 species. In a compilation of new and published data, we combined the distribution of (TTAGG)n telomere motif with the insect phylogenetic tree. The pattern of phylogenetic distribution of the TTAGG repeats clearly supported a hypothesis that the sequence was an ancestral motif of insect telomeres but was lost repeatedly during insect evolution. The motif was conserved in the "primitive" apterous insect orders, the Archaeognatha and Zygentoma, in the "lower" Neoptera (Plecoptera, Phasmida, Orthoptera, Blattaria, Mantodea, and Isoptera) with the exception of Dermaptera, and in Paraneoptera (Psocoptera, Thysanoptera, Auchenorrhyncha, and Sternorrhyncha) with the exception of Heteroptera. Surprisingly, the (TTAGG)n motif was not found in the "primitive" pterygotes, the Palaeoptera (Ephemeroptera and Odonata). The Endopterygota were heterogeneous for the occurrence of TTAGG repeats. The motif was conserved in Hymenoptera, Lepidoptera, and Trichoptera but was lost in one clade formed by Diptera, Siphonaptera, and Mecoptera. It was also lost in Raphidioptera, whereas it was present in Megaloptera. In contrast with previous authors, we did not find the motif in Neuroptera. Finally, both TTAGG-positive and TTAGG-negative species were reported in Coleoptera. The repeated losses of TTAGG in different branches of the insect phylogenetic tree and, in particular, in the most successful lineage of insect evolution, the Endopterygota, suggest a backup mechanism in the genome of insects that enabled them frequent evolutionary changes in telomere composition.
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            High dynamics of rDNA cluster location in kissing bug holocentric chromosomes (Triatominae, Heteroptera).

            In this paper, we determine by fluorescent in situ hybridization the variability in the chromosomal location of 45S rDNA clusters in 38 species belonging to 7 genera of the Triatominae subfamily, using a triatomine-specific 18S rDNA probe. Our results show a striking variability at the inter- and intraspecific level, never reported so far in holocentric chromosomes, revealing the extraordinary genomic dynamics that occurred during the evolution in this group of insects. Our results also demonstrate that the chromosomal position of rDNA clusters is an important marker to disclose chromosomal differentiation in species karyotypically homogenous in their chromosome number. Copyright © 2012 S. Karger AG, Basel.
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              Chromosomes and their Meiotic Behavior in Two Families of the Primitive Infraorder Dipsocoromorpha (Heteroptera)

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                Author and article information

                Contributors
                Journal
                Comp Cytogenet
                Comp Cytogenet
                CompCytogen
                Comparative Cytogenetics
                Pensoft Publishers
                1993-0771
                1993-078X
                2018
                13 December 2018
                : 12
                : 4
                : 515-528
                Affiliations
                [1 ] Zoological Institute, Russian Academy of Sciences, Universitetskaya nab. 1, St. Petersburg 199034, Russia Zoological Institute, Russian Academy of Sciences St. Petersburg Russia
                [2 ] Voronezh State University, Universitetskaya pl. 1, Voronezh, 394006, Russia Voronezh State University Voronezh Russia
                Author notes
                Corresponding author: Natalia Golub ( nvgolub@ 123456mail.ru )

                Academic editor: I. Gavrilov-Zimin

                Article
                10.3897/CompCytogen.v12i4.30431
                6302064
                beb035b9-b6e6-49d6-96b6-36f71f1af402
                Natalia V. Golub, Viktor B. Golub, Valentina G. Kuznetsova

                This is an open access article distributed under the terms of the Creative Commons Attribution License (CC BY 4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

                History
                : 9 October 2018
                : 8 November 2018
                Categories
                Data Paper
                Animalia
                Arthropoda
                Cimicomorpha
                Hemiptera
                Heteroptera
                Hexapoda
                Insecta
                Invertebrata
                Tingidae
                Tingoidea
                Karyosystematics
                Molecular Cytogenetics
                Neogene
                Russia

                karyotype,chromosome number,sex chromosomes,fish,rdna,(ttagg)n,lace bugs, tingidae , heteroptera

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