Chromosome pairing of individual genomes in tall fescue (Festuca arundinacea Schreb.), its progenitors, and hybrids with Italian ryegrass (Lolium multiflorum Lam.).

Abstract:

:A diploid-like pairing system prevents meiotic irregularities and improves the efficiency of gamete production in allopolyploid species. While the nature of the system is known in some polyploid crops including wheat, little is known about the control of chromosome pairing in polyploid fescues (Festuca spp.). In this work we studied chromosome pairing in allohexaploid F. arundinacea, its progenitors F. pratensis and F. glaucescens, and two intergeneric hybrids Lolium multiflorum (2x) x F. arundinacea (6x) and L. multiflorum (4x) x F. glaucescens (4x). The use of genomic in situ hybridization (GISH) permitted the analysis of homoeologous chromosome pairing and recombination of different genomes involved. We detected a diploid-like pairing system in polyploid fescues F. arundinacea and F. glaucescens, the latter being one of the progenitors of F. arundinacea. The pairing control system was absent in the second progenitor F. pratensis. Detailed analysis of intergeneric hybrids confirmed the presumed haploinsufficiency of the fescue system, which resulted in homoeologous pairing between all component genomes. This indicates that introgression of any specific chromosome segment from one genome to another is possible in all genome combinations. Our results not only contribute to the quest to discover the nature of the system controlling chromosome pairing in polyploid fescues, but may also have serious implications for design of hybrid breeding schemes in forage grasses.

journal_name

Cytogenet Genome Res

authors

Kopecký D,Bartos J,Zwierzykowski Z,Dolezel J

doi

10.1159/000207525

subject

Has Abstract

pub_date

2009-01-01 00:00:00

pages

170-8

issue

2

eissn

1424-8581

issn

1424-859X

pii

000207525

journal_volume

124

pub_type

杂志文章
  • 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

  • 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

  • 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

  • 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

  • Molecular cytogenetics and tandem repeat sequence evolution in the allopolyploid Nicotiana rustica compared with diploid progenitors N. paniculata and N. undulata.

    abstract::Nicotiana rustica (2n = 4x = 48) is a natural allotetraploid composed of P and U genomes which are closely related to genomes of diploid species N. paniculata and N. undulata. Genomic in situ hybridization (GISH) also confirms that the diploid parents, or close relatives, are the ancestors of N. rustica. In order to s...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000082413

    authors: Lim KY,Matyasek R,Kovarik A,Fulnecek J,Leitch AR

    更新日期:2005-01-01 00:00:00

  • Cryptic 13q34 and 4q35.2 Deletions in an Italian Family.

    abstract::Variations of DNA sequences in the human genome range from large, microscopically visible chromosome anomalies to single nucleotide changes. Submicroscopic genomic copy number variations, i.e. chromosomal imbalances which are undetectable by conventional cytogenetic analysis, play an intriguing clinical role. In this ...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000442068

    authors: Riccardi F,Rivolta GF,Uliana V,Grati FR,La Starza R,Marcato L,Di Perna C,Quintavalle G,Garavelli L,Rosato S,Sammarelli G,Neri TM,Tagliaferri A,Martorana D

    更新日期:2015-01-01 00:00:00

  • Molecular cytogenetics of forest trees.

    abstract::The economic and ecological importance of forest trees, as well as their unique biological features, has recently raised the level of interest in studies on their genomes, including sequencing of the entire poplar genome. However, cytogenetic studies have not moved in parallel with developments in genomics. This is es...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章,评审

    doi:10.1159/000121070

    authors: Ribeiro T,Barão A,Viegas W,Morais-Cecíli L

    更新日期:2008-01-01 00:00:00

  • A rare case of centric fission and fusion in a river buffalo (Bubalus bubalis, 2n = 50) cow with reduced fertility.

    abstract::A 5-year-old river buffalo cow underwent cytogenetic investigation since it had only one male offspring, apparently with normal body constitution, which died one month after birth. The female carrier had normal body conformation and internal sex adducts, as revealed by rectal palpation performed by a specialist veteri...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000318011

    authors: Di Meo GP,Perucatti A,Genualdo V,Iannuzzi A,Sarubbi F,Caputi-Jambrenghi A,Incarnato D,Peretti V,Vonghia G,Iannuzzi L

    更新日期:2011-01-01 00:00:00

  • Polymorphisms of the chicken antiviral MX gene.

    abstract::The Mx gene was originally found in laboratory mice in an infection experiment using influenza virus (Lindermann, 1962). Almost all of the mouse strains in that experiment died from the infection, and only the A2G strain had resistance to the virus. This resistant character was shown to be inherited as a single autoso...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000103200

    authors: Watanabe T

    更新日期:2007-01-01 00:00:00

  • Genomic signatures of chromosomal instability and osteosarcoma progression detected by high resolution array CGH and interphase FISH.

    abstract::Osteosarcoma (OS) is characterized by an unstable karyotype which typically has a heterogeneous pattern of complex chromosomal abnormalities. High-resolution array comparative genomic hybridization (CGH) in combination with interphase fluorescence in situ hybridization (FISH) analyses provides a complete description o...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000151310

    authors: Selvarajah S,Yoshimoto M,Ludkovski O,Park PC,Bayani J,Thorner P,Maire G,Squire JA,Zielenska M

    更新日期:2008-01-01 00:00:00

  • Distribution of Telomeric Sequences (TTAGGG)n in Rearranged Chromosomes of Phyllotine Rodents (Cricetidae, Sigmodontinae).

    abstract::Phyllotines are sigmodontine rodents endemic to South America with broad genetic variability, Robertsonian polymorphisms being the most frequent. Moreover, this taxon includes a species with multiple sex chromosomes, which is infrequent in mammals. However, molecular cytogenetic techniques have never been applied to p...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000444602

    authors: Lanzone C,Labaroni C,Suárez N,Rodríguez D,Herrera ML,Bolzán AD

    更新日期:2015-01-01 00:00:00

  • Assignment of 101 genes localized in HSA10 to a swine RH (IMpRH) map to generate a dense human-swine comparative map.

    abstract::Economically important traits such as growth and backfat in pigs have been shown to be influenced by genes in swine chromosome (SSC) 10q12-->qter corresponding to human chromosome (HSA) 10p. However, since gene information in the swine chromosomal region was limited, we attempted to generate a dense comparative map be...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000087523

    authors: Yasue H,Kiuchi S,Hiraiwa H,Ozawa A,Hayashi T

    更新日期:2006-01-01 00:00:00

  • Biallelic expression of Z-linked genes in male chickens.

    abstract::In birds, females are heterogametic (ZW), while males are homogametic (ZZ). It has been proposed that there is no dosage compensation for the expression of Z-linked genes in birds. In order to examine if the genes are inactivated on one of the two Z chromosomes, we analyzed the allelic expression of the B4GALT1 and CH...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000071609

    authors: Kuroiwa A,Yokomine T,Sasaki H,Tsudzuki M,Tanaka K,Namikawa T,Matsuda Y

    更新日期:2002-01-01 00:00:00

  • Satellite DNA spatial localization and transcriptional activity in mouse embryonic E-14 and IOUD2 stem cells.

    abstract::The formation of heterochromatin begins in the differentiating cells. The aim of this work was to study changes of satellite DNA distribution, transcriptional activity and interaction with certain proteins in mouse embryonic stem cells after induction with retinoic acid. We found that pericentromeric satellites entere...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000218132

    authors: Enukashvily NI,Malashicheva AB,Waisertreiger IS

    更新日期:2009-01-01 00:00:00

  • Genome stability in Arabidopsis cells exhibiting alternative lengthening of telomeres.

    abstract::Indefinite proliferation of eukaryotic cells depends on telomerase that counteracts the depletion of DNA from chromosome termini due to the end replication problem. The requirement for telomerase can, under certain conditions, be circumvented by employing homologous recombination-based mechanisms for telomere maintena...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000167827

    authors: Akimcheva S,Zellinger B,Riha K

    更新日期:2008-01-01 00:00:00

  • Histone H2AX phosphorylation is associated with most meiotic events in grasshopper.

    abstract::It is widely accepted that the H2AX histone in its phosphorylated form (gamma-H2AX) is related to the repair of DNA double-strand breaks (DSBs). In several organisms, gamma-H2AX presence has been demonstrated in meiotic processes such as recombination and sex chromosome inactivation during prophase I (from leptotene t...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000100416

    authors: Cabrero J,Teruel M,Carmona FD,Camacho JP

    更新日期:2007-01-01 00:00:00

  • Differential Dmrt1 transcripts in gonads of the protandrous black porgy, Acanthopagrus schlegeli.

    abstract::Black porgy, Acanthopagrus schlegeli Bleeker, is a marine protandrous hermaphrodite fish. A Dmrt1 cDNA was cloned and characterized and in order to study the process of sex change in this species, mRNA transcripts of Dmrt1 were monitored. Dmrt1 was specifically transcribed in testis and seminal vesicle in 2-year-old b...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000074354

    authors: He CL,Du JL,Wu GC,Lee YH,Sun LT,Chang CF

    更新日期:2003-01-01 00:00:00

  • Elimination of chromosomes in Hordeum vulgare x H. bulbosum crosses at mitosis and interphase involves micronucleus formation and progressive heterochromatinization.

    abstract::Uniparental chromosome elimination occurs in several interspecific hybrids of plants. We studied the mechanism underlying selective elimination of the paternal chromosomes during the development of Hordeum vulgare x H. bulbosum hybrid embryos that is restricted to an early stage of development. In almost all embryos m...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000093334

    authors: Gernand D,Rutten T,Pickering R,Houben A

    更新日期:2006-01-01 00:00:00

  • The mammalian mid-pachytene checkpoint: meiotic arrest in spermatocytes with a mutation in Atm alone or in combination with a Trp53 (p53) or Cdkn1a (p21/cip1) mutation.

    abstract::ATM, the protein product of the gene mutated in the human autosomal recessive disorder ataxia telangiectasia, is involved in detection of double strand breaks (DSBs) and is a key component of the damage surveillance network of cell cycle proteins. In somatic cells ATM phosphorylates many other proteins including p53, ...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000080603

    authors: Ashley T,Westphal C,Plug-de Maggio A,de Rooij DG

    更新日期:2004-01-01 00:00:00

  • Development of a linkage map and QTL scan for growth traits in North American bison.

    abstract::PCR protocols incorporating fluorescently labeled multiplexed primer combinations were developed to produce a linkage map for bison. Three hundred fifty eight microsatellite loci spanning all 29 autosomes were genotyped via 83 PCR multiplexes and nine individual amplifications. A total of 292 markers were integrated i...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000075726

    authors: Schnabel RD,Taylor JF,Derr JN

    更新日期:2003-01-01 00:00:00

  • Chromosomal Rearrangements during Turtle Evolution Altered the Synteny of Genes Involved in Vertebrate Sex Determination.

    abstract::Sex-determining mechanisms (SDMs) set an individual's sexual fate by its genotype (genotypic sex determination, GSD) or environmental factors like temperature (temperature- dependent sex determination, TSD), as in turtles where the GSD "trigger" remains unknown. SDMs co-evolve with turtle chromosome number, perhaps be...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000497302

    authors: Lee L,Montiel EE,Navarro-Domínguez BM,Valenzuela N

    更新日期:2019-01-01 00:00:00

  • Frequency and distribution of rob(1;29) in eight Portuguese cattle breeds.

    abstract::Cytogenetic investigations performed in eight Portuguese cattle breeds revealed the presence of rob(1;29) in both heterozygous and homozygous conditions in all, and five breeds, respectively, with variable percentages of carriers as follows: 41.0% in Arouquesa, 69.9% in Barrosa, 39.4% in Maronesa, 2.8% in Mirandesa, 8...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000118755

    authors: Iannuzzi A,Di Meo GP,Caputi Jambrenghi A,Vonghia G,Iannuzzi L,Rangel-Figueiredo T

    更新日期:2008-01-01 00:00:00

  • Mechanisms of formation of chromosomal aberrations: insights from studies with DNA repair-deficient cells.

    abstract::In order to understand the mechanisms of formation of chromosomal aberrations, studies performed on human syndromes with genomic instability can be fruitful. In this report, the results from studies in our laboratory on the importance of the transcription-coupled repair (TCR) pathway on the induction of chromosomal da...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章,评审

    doi:10.1159/000077471

    authors: Palitti F

    更新日期:2004-01-01 00:00:00

  • Chromosomal organization of repetitive DNA in Sorubim lima (Teleostei; Pimelodidae).

    abstract::Interspaced repetitive DNA elements and segmental duplications have been extensively analyzed in fishes through physical chromosome mapping methods, providing a better comprehension of the structure and organization of the genome of this group. In order to contribute to this scenario, a sequence integration study of d...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000353845

    authors: Sczepanski TS,Vicari MR,de Almeida MC,Nogaroto V,Artoni RF

    更新日期:2013-01-01 00:00:00

  • The role of DMDs in the maintenance of epigenetic states.

    abstract::An important aspect of genome reprogramming is the establishment and maintenance of gamete-specific DNA methylation patterns that distinguish the parental alleles of imprinted genes. Disrupting the accurate transmission of genomic imprints by interfering with these methylation patterns causes severe defects in fetal g...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章,评审

    doi:10.1159/000090822

    authors: Paoloni-Giacobino A,Chaillet JR

    更新日期:2006-01-01 00:00:00

  • Comparative Cytogenetics of the Congo African Grey Parrot (Psittacus erithacus).

    abstract::The Congo African grey parrot (Psittacus erithacus, PER) is an endemic species of Central Africa, valued for its intelligence and listed as vulnerable due to poaching and habitat destruction. Improved knowledge about the P. erithacus genome is needed to address key biological questions and conservation of this species...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000444136

    authors: Seibold-Torres C,Owens E,Chowdhary R,Ferguson-Smith MA,Tizard I,Raudsepp T

    更新日期:2015-01-01 00:00:00

  • Genome-wide experimental identification and functional analysis of human specific retroelements.

    abstract::Retroelements (REs) actively reshape genomes through genomic rearrangements, creation of new genes and modulation of the regulatory machinery of existing genes, thus introducing genomic novelties which potentially may be subject to natural selection. Thousands of RE integrations, presumably distinguishing the human an...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章,评审

    doi:10.1159/000084980

    authors: Buzdin A,Vinogradova T,Lebedev Y,Sverdlov E

    更新日期:2005-01-01 00:00:00

  • A model for genetic complementation controlling the chromosomal abnormalities and loss of heterozygosity formation in cancer.

    abstract::The relationship between the apparently random chromosomal changes found in aneuploidy and the genetic instability driving the progression of cancer is not clear. We report a test of the hypothesis that aneuploid chromosomal abnormalities might be selected to preserve cell-survival genes during loss of heterozygosity ...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000100406

    authors: Nestor AL,Hollopeter SL,Matsui SI,Allison D

    更新日期:2007-01-01 00:00:00

  • Heterologous Synapsis and Crossover Suppression in Heterozygotes for a Pericentric Inversion in the Zebra Finch.

    abstract::In the zebra finch, 2 alternative morphs regarding centromere position were described for chromosome 6. This polymorphism was interpreted to be the result of a pericentric inversion, but other causes of the centromere repositioning were not ruled out. We used immunofluorescence localization to examine the distribution...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000442656

    authors: del Priore L,Pigozzi MI

    更新日期:2015-01-01 00:00:00