Wing Membrane Biopsies for Bat Cytogenetics: Finding of 2n = 54 in Irish Rhinolophushipposideros (Rhinolophidae, Chiroptera, Mammalia) Supports Two Geographically Separated Chromosomal Variants in Europe.

Abstract:

:In Europe, 2 different diploid chromosome numbers, 2n = 54 and 2n = 56, have been described in the lesser horseshoe bat (Rhinolophushipposideros). The eastern form with 2n = 56 extends from the Czech Republic to Greece. To date, specimens with 54 chromosomes have been reported only from Spain and Germany. This study expands the distributional area of the western variant to Ireland. Strikingly, this distribution of European chromosomal variants is in contrast to the available molecular data that indicate little genetic differentiation of R. hipposideros populations spanning Northwestern to Central Europe. Further, we have developed an optimized protocol for establishing fibroblast cell cultures, suitable for karyotype analyses, from 3-mm wing membrane biopsies. This is a useful technique for cytogenetic studies of endangered bat species, as this non-lethal sampling method imposes only minimum stress to the animal without lasting adverse effects and is routinely used to sample tissue probes for molecular genetic studies in bats.

journal_name

Cytogenet Genome Res

authors

Kacprzyk J,Teeling EC,Kelleher C,Volleth M

doi

10.1159/000447111

subject

Has Abstract

pub_date

2016-01-01 00:00:00

pages

279-83

issue

4

eissn

1424-8581

issn

1424-859X

pii

000447111

journal_volume

148

pub_type

杂志文章
  • Why is SCA12 different from other SCAs?

    abstract::Spinocerebellar ataxia type 12 (SCA12), now described in European-American and Asian (Indian) pedigrees, is unique among the SCAs from clinical, pathological, and molecular perspectives. Clinically, the distinguishing feature is early and prominent action tremor with variability in other signs. Pathologically, brain M...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章,评审

    doi:10.1159/000072854

    authors: Holmes SE,O'Hearn E,Margolis RL

    更新日期:2003-01-01 00:00:00

  • Breakpoint analysis of the pericentric inversion between chimpanzee chromosome 10 and the homologous chromosome 12 in humans.

    abstract::During this study, we analysed the pericentric inversion that distinguishes human chromosome 12 (HSA12) from the homologous chimpanzee chromosome (PTR10). Two large chimpanzee-specific duplications of 86 and 23 kb were observed in the breakpoint regions, which most probably occurred associated with the inversion. The ...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000080806

    authors: Kehrer-Sawatzki H,Sandig CA,Goidts V,Hameister H

    更新日期:2005-01-01 00:00:00

  • Telomeric repeats far from the ends: mechanisms of origin and role in evolution.

    abstract::In addition to their location at terminal positions, telomeric-like repeats are also present at internal sites of the chromosomes (intrachromosomal or interstitial telomeric sequences, ITSs). According to their sequence organization and genomic location, two different kinds of ITSs can be identified: (1) heterochromat...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章,评审

    doi:10.1159/000167807

    authors: Ruiz-Herrera A,Nergadze SG,Santagostino M,Giulotto E

    更新日期:2008-01-01 00:00:00

  • Correlating the Genetic and Physical Map of Barley Chromosome 3H Revealed Limitations of the FISH-Based Mapping of Nearby Single-Copy Probes Caused by the Dynamic Structure of Metaphase Chromosomes.

    abstract::Genetic maps are based on the recombination frequency of molecular markers which often show different positions in comparison to the corresponding physical maps. To decipher the position and order of DNA sequences genetically mapped to terminal and interstitial regions of barley (Hordeum vulgare) chromosome 3H, fluore...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000478631

    authors: Bustamante FO,Aliyeva-Schnorr L,Fuchs J,Beier S,Houben A

    更新日期:2017-01-01 00:00:00

  • LIM-kinase as a regulator of actin dynamics in spermatogenesis.

    abstract::We have identified LIM-kinase (LIMK1 and LIMK2), the only known catalytic protein among LIM-family molecules. Both LIMK1 and LIMK2 phosphorylate (inactivate) cofilin, an actin depolymerizing factor, and induce actin cytoskeleton reorganization. We as well as others concurrently demonstrated that LIMK activation was re...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章,评审

    doi:10.1159/000076815

    authors: Takahashi H,Funakoshi H,Nakamura T

    更新日期:2003-01-01 00:00:00

  • Molecular characterization of the equine collagen, type IX, alpha 2 (COL9A2) gene on horse chromosome 2p16-->p15.

    abstract::The mammalian collagen, type IX, alpha 2 gene (COL9A2) encodes the alpha-2 chain of type IX collagen and is located on horse chromosome 2p16-->p14 harbouring a quantitative trait locus for osteochondrosis. We isolated a bacterial artificial chromosome (BAC) clone containing the equine COL9A2 gene and determined the co...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000095229

    authors: Boneker C,Kuiper H,Drögemüller C,Chowdhary BP,Distl O

    更新日期:2006-01-01 00:00:00

  • Application of molecular cytogenetics for chromosomal evolution of the Lemuriformes (Prosimians).

    abstract::R-banding chromosomal studies of 21 species of Lemuriformes allowed us to reconstruct the presumed ancestral karyotype of all the Lemuriformes except for Daubentoniidae and permitted the construction of their phylogenetic tree. Chromosome painting with fluorescently labeled heterologous DNA probes permitted comparativ...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000080816

    authors: Warter S,Hauwy M,Dutrillaux B,Rumpler Y

    更新日期:2005-01-01 00:00:00

  • A new translocation t(1p;18) in an Italian Mediterranean river buffalo (Bubalus bubalis, 2n = 50) bull: cytogenetic, fertility and inheritance studies.

    abstract::In recent years increasing attention has been paid to the cytogenetic control of Italian Mediterranean river buffalo (BBU) bulls authorized as sires which are registered in the stud book. Chromosome abnormalities described in this species are mainly numerical and affecting sex chromosomes. During routine cytogenetic a...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000342360

    authors: Albarella S,Ciotola F,Coletta A,Genualdo V,Iannuzzi L,Peretti V

    更新日期:2013-01-01 00:00:00

  • HIV-1/AIDS susceptibility and copy number variation in CCL3L1, a gene encoding a natural ligand for HIV-1 co-receptor CCR5.

    abstract::Variations of gene copy number in the human genome are increasingly recognized as a genetic factor in phenotypic variation. Human CC chemokine ligand 3-like 1 gene (CCL3L1), which is located on human chromosome 17q11.2, is highly variable in copy number owing to having a hot spot for segmental duplications. CCL3L1, a ...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章,评审

    doi:10.1159/000184703

    authors: Nakajima T,Kaur G,Mehra N,Kimura A

    更新日期:2008-01-01 00:00:00

  • Analysis using sperm-FISH of a putative interchromosomal effect in boars carrying reciprocal translocations.

    abstract::The occurrence of interchromosomal effects (ICE) in reciprocal translocation carriers still remains contradictory in the human literature. We used the pig as an animal model to investigate whether the structure of the reciprocal translocations as well as the size and/or type of the chromosomes not involved in the rear...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000245920

    authors: Bonnet-Garnier A,Guardia S,Pinton A,Ducos A,Yerle M

    更新日期:2009-01-01 00:00:00

  • Identification and Characterization of γ-Ray-Induced Mutations in Rice Cytoplasmic Genomes by Whole-Genome Sequencing.

    abstract::Chloroplasts and mitochondria are semi-autonomous organelles and have their own genomes (cytoplasmic genomes). Physical radiations (e.g., γ-rays) have been widely used in artificial mutation induction for plant germplasm enhancement and for breeding new cultivars. However, little is known at the genomic level about wh...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000506033

    authors: Zheng Y,Li S,Huang J,Fan L,Shu Q

    更新日期:2020-01-01 00:00:00

  • Chromosomal mechanisms underlying the karyotype evolution of the oriental voles (Muridae, Eothenomys).

    abstract::We have investigated the karyotype relationships of two oriental voles, i.e. the Yulong vole (Eothenomys proditor, 2n = 32) and the large oriental vole (Eothenomys miletus, 2n = 56) as well as the Clarke's vole (Microtus clarkei, 2n = 52), by a combined approach of cross-species chromosome painting and high-resolution...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000091928

    authors: Li T,Wang J,Su W,Yang F

    更新日期:2006-01-01 00:00:00

  • High-resolution organization of mouse centromeric and pericentromeric DNA.

    abstract::We studied the organization of mouse satellite 3 and 4 (MS3 and MS4) in comparison with major (MaSat) and minor (MiSat) DNA sequences, located in the centromeric and pericentromeric regions of mouse telocentric chromosomes by fiber-FISH. The centromeric region consists of a small block of MiSat and MS3 followed by a p...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000089878

    authors: Kuznetsova I,Podgornaya O,Ferguson-Smith MA

    更新日期:2006-01-01 00:00:00

  • Molecular Polymorphism and Divergence of Duplicated Genes in Tetraploid African Clawed Frogs (Xenopus).

    abstract::Genome duplication creates redundancy in proteins and their interaction networks, and subsequent smaller-scale gene duplication can further amplify genetic redundancy. Mutations then lead to the loss, maintenance or functional divergence of duplicated genes. Genome duplication occurred many times in African clawed fro...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章,评审

    doi:10.1159/000431108

    authors: Evans BJ,Kwon T

    更新日期:2015-01-01 00:00:00

  • Relating centromeric topography in fixed human chromosomes to α-satellite DNA and CENP-B distribution.

    abstract::Despite extensive analyses on the centromere and its associated proteins, detailed studies of centromeric DNA structure have provided limited information about its topography in condensed chromatin. We have developed a method with correlative fluorescence light microscopy and atomic force microscopy that investigates ...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000348744

    authors: Khan WA,Chisholm R,Tadayyon S,Subasinghe A,Norton P,Samarabandu J,Johnston LJ,Knoll JH,Rogan PK

    更新日期:2013-01-01 00:00:00

  • Meiotic mutations in rye Secale cereale L.

    abstract::Spontaneous meiotic mutations of winter rye Secale cereale L. (2n = 14) were revealed in inbred F2 progenies, which were obtained by self-pollination of F1 hybrids resulting from crosses of individual plants of cultivar Vyatka or weedy rye with plants of self-fertile inbred lines. The mutations cause partial or comple...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000082403

    authors: Sosnikhina SP,Mikhailova EI,Tikholiz OA,Priyatkina SN,Smirnov VG,Dadashev SY,Kolomiets OL,Bogdanov YF

    更新日期:2005-01-01 00:00:00

  • Identification of quantitative trait loci affecting shank length, body weight and carcass weight from the Japanese cockfighting chicken breed, Oh-Shamo (Japanese Large Game).

    abstract::We performed a quantitative trait locus (QTL) analysis to map QTLs controlling shank length, body weight, and carcass weight in a resource family of 245 F(2) birds developed from a cross of the large-sized, native, Japanese cockfighting breed, Oh-Shamo (Japanese Large Game), and the White Leghorn breed of chickens. In...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000103190

    authors: Tsudzuki M,Onitsuka S,Akiyama R,Iwamizu M,Goto N,Nishibori M,Takahashi H,Ishikawa A

    更新日期:2007-01-01 00:00:00

  • Equine FISH mapping of 36 genes known to locate on human chromosome ends.

    abstract::The INRA and the CHORI-241 horse BAC libraries were screened by hybridization with DNA probes and/or directly by PCR with primers designed in consensus sequences of genes localized at the end of each human chromosome. BAC clones were retrieved and 36 could be FISH mapped after the expected gene was confirmed in each B...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000085669

    authors: Perrocheau M,Boutreux V,Chadi-Taourit S,Di Meo GP,Perucatti A,Incarnato D,Cribiu EP,Guérin G,Iannuzzi L

    更新日期:2005-01-01 00:00:00

  • A prevalent Y;15 translocation in the Ethiopian Beta Israel community in Israel.

    abstract::We describe 7 cases of abnormal karyotypes involving chromosomes Y and 15 in Ethiopian Beta Israel patients: 46,XX, der(15)t(Y;15)(q12;p12) and 46,XY,der(15)t(Y;15)(q12;p12). Six cases were incidentally found in amniocentesis performed for various indications; the indication for karyotyping in 1 case was recurrent abo...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000336201

    authors: Chen-Shtoyerman R,Josefsberg Ben-Yehoshua S,Nissani R,Rosensaft J,Appelman Z

    更新日期:2012-01-01 00:00:00

  • The PMEL Gene and Merle in the Domestic Dog: A Continuum of Insertion Lengths Leads to a Spectrum of Coat Color Variations in Australian Shepherds and Related Breeds.

    abstract::Merle is a distinct coat color and pattern found in numerous species, including the domestic dog, characterized by patches of diluted eumelanin (black pigment) interspersed among areas of normal pigmentation. In dogs, this variegated pattern is caused by an insertion of a SINE element into the canine PMEL gene. Althou...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000491408

    authors: Ballif BC,Ramirez CJ,Carl CR,Sundin K,Krug M,Zahand A,Shaffer LG,Flores-Smith H

    更新日期:2018-08-03 00:00:00

  • Benchmarking Transcriptome Quantification Methods for Duplicated Genes in Xenopus laevis.

    abstract::Xenopus is an important model organism for the study of genome duplication in vertebrates. With the full genome sequence of diploid Xenopus tropicalis available, and that of allotetraploid X. laevis close to being finished, we will be able to expand our understanding of how duplicated genes have evolved. One of the ke...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000431386

    authors: Kwon T

    更新日期:2015-01-01 00:00:00

  • Visualization of fine-scale genomic structure by oligonucleotide-based high-resolution FISH.

    abstract::The discovery of complex structural variations that exist within individual genomes has prompted a need to visualize chromosomes at a higher resolution than previously possible. To address this concern, we established a robust, high-resolution fluorescence in situ hybridization (FISH) method that utilizes probes deriv...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000322717

    authors: Yamada NA,Rector LS,Tsang P,Carr E,Scheffer A,Sederberg MC,Aston ME,Ach RA,Tsalenko A,Sampas N,Peter B,Bruhn L,Brothman AR

    更新日期:2011-01-01 00:00:00

  • Heritable translocations induced by dermal exposure of male mice to acrylamide.

    abstract::Acrylamide (AA) is an important industrial chemical used mainly in the production of polymers. It can be absorbed through the skin. AA was shown to be a germ cell clastogen that entails a genetic risk for exposed workers. The genetic risk calculation was based on mouse heritable translocation test data obtained after ...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000077501

    authors: Adler ID,Gonda H,Hrabé de Angelis M,Jentsch I,Otten IS,Speicher MR

    更新日期:2004-01-01 00:00:00

  • Chromosomal mutagen sensitivity associated with mutations in BRCA genes.

    abstract::Chromosomal mutagen sensitivity is a common feature of cells from patients with different kinds of cancer. A portion of breast cancer patients also shows an elevated sensitivity to the induction of chromosome damage in cells exposed to ionizing radiation or chemical mutagens. Segregation analysis in families of patien...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章,评审

    doi:10.1159/000077511

    authors: Speit G,Trenz K

    更新日期:2004-01-01 00:00:00

  • Concurrent Loss of Heterozygosity and Mosaic Deletion of 12p13.32pter.

    abstract::Deletions in the short arm of chromosome 12 are the rarest subtelomeric imbalances. Less than 20 patients have been reported to date, and their microdeletions were identified either by FISH or array-CGH without SNP data. Here, we report a patient with a 12p13.32pter mosaic deletion detected by chromosome microarray an...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000445853

    authors: Faria RS,de Oliveira CP,da Costa MM,da S Rosa MT,Córdoba MS,Pic-Taylor A,Ferrari I,de Oliveira SF,Mazzeu JF

    更新日期:2016-01-01 00:00:00

  • An integrated and comparative genetic map of the turkey genome.

    abstract::An integrated genetic linkage map was developed for the turkey (Meleagris gallopavo) that combines the genetic markers from the three previous mapping efforts. The UMN integrated map includes 613 loci arranged into 41 linkage groups. An additional 105 markers are tentatively placed within linkage groups based on two-p...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000109627

    authors: Reed KM,Chaves LD,Mendoza KM

    更新日期:2007-01-01 00:00:00

  • Heteromorphic sex chromosome system with an exceptionally large Y chromosome in a catfish Steindachneridion sp. (Pimelodidae).

    abstract::The chromosomes and banding patterns of Steindachneridion sp., a large catfish (Pimelodidae), endemic to the Iguaçu River, Brazil, were analyzed using conventional (C-, G-banding) and restriction enzyme banding methods. The same diploid number (2n = 56) as in other members of the genus and the family was found but the...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000089888

    authors: Swarça AC,Fenocchio AS,Cestari MM,Bertollo LA,Dias AL

    更新日期:2006-01-01 00:00:00

  • Barley chromosome arms longer than half of the spindle axis interfere with nuclear divisions.

    abstract::We have tested the influence of recombinantly-elongated chromosome arms on nuclear divisions in barley and confirmed a rule according to which half the length of the average spindle axis defines the upper tolerance limit for chromosome arm length. A slightly longer chromosome arm caused incomplete separation of sister...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000068530

    authors: Hudakova S,Künzel G,Endo TR,Schubert I

    更新日期:2002-01-01 00:00:00

  • Characterisation of a GC-rich telomeric satellite DNA in Eumeces schneideri Daudin (Reptilia, Scincidae).

    abstract::A hitherto undescribed satellite DNA family (AvaII satDNA) has been isolated and characterised in Eumeces schneideri, a squamate reptile belonging to the family Scincidae. AvaII satDNA is characterised by a monomer length of 208 bp, a GC content of 59% and exhibits a certain degree of CpG methylation. FISH experiments...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000235933

    authors: Giovannotti M,Nisi Cerioni P,Caputo V,Olmo E

    更新日期:2009-01-01 00:00:00

  • Truncated RUNX1 Generated by the Fusion of RUNX1 to Antisense GRIK2 via a Cryptic Chromosome Translocation Enhances Sensitivity to Granulocyte Colony-Stimulating Factor.

    abstract::Fusions of the Runt-related transcription factor 1 (RUNX1) with different partner genes have been associated with various hematological disorders. Interestingly, the C-terminally truncated form of RUNX1 and RUNX1 fusion proteins are similarly considered important contributors to leukemogenesis. Here, we describe a 59-...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000508012

    authors: Abe A,Yamamoto Y,Katsumi A,Yamamoto H,Okamoto A,Inaguma Y,Iriyama C,Tokuda M,Okamoto M,Emi N,Tomita A

    更新日期:2020-01-01 00:00:00