Genomic imprinting is a barrier to parthenogenesis in mammals.

Abstract:

:Only mammals have relinquished parthenogenesis as a means of producing descendants. Bi-parental reproduction is necessary due to parent-specific epigenetic modification of the genome during gametogenesis, which leads to non-equivalent expression of imprinted genes from the maternal and paternal alleles. However, a series of our work showed that alteration of maternal imprinting by oocyte reconstruction using non-growing oocytes, together with deletion of the H19 gene provide appropriate expression of imprinted genes from the maternal genome. The resulting ng (non-growing)/fg (fully-grown) parthenogenic embryos were developed to term. Here, we discuss how the parthenogenetic embryos survived as normal individuals.

journal_name

Cytogenet Genome Res

authors

Kono T

doi

10.1159/000090812

keywords:

subject

Has Abstract

pub_date

2006-01-01 00:00:00

pages

31-5

issue

1-4

eissn

1424-8581

issn

1424-859X

pii

90812

journal_volume

113

pub_type

杂志文章
  • The Mobilome of Reptiles: Evolution, Structure, and Function.

    abstract::Transposable elements (TE) constitute one of the most variable genomic features among vertebrates, impacting genome size, structure, and composition. Despite their important role in shaping genomic diversity, they have mostly been studied in mammals, which display one of the least diverse genomes in terms of TE divers...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章,评审

    doi:10.1159/000496416

    authors: Boissinot S,Bourgeois Y,Manthey JD,Ruggiero RP

    更新日期:2019-01-01 00:00:00

  • The Persevering Cytotaxonomy: Discovery of a Unique XX/XY Sex Chromosome System in Catfishes Suggests the Existence of a New, Endemic and Rare Species.

    abstract::The genus Hypostomus has a broad geographic distribution in Brazilian rivers and comprises armored catfishes with a very complicated taxonomy due to the absence of morphological autapomorphies. The existence of nearly 10 allopatric populations with different karyotypes suggests that Hypostomusancistroides represents a...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000492959

    authors: Rocha-Reis DA,de Oliveira Brandão K,de Almeida-Toledo LF,Pazza R,Kavalco KF

    更新日期:2018-09-28 00:00:00

  • Cytogenetic Assessment of the Rat Cell Line CLS-ACI-1: An in vitro Cell Model for Mycn Overexpression.

    abstract::Breast cancer is a complex and heterogeneous disease, and the establishment of cell models in order to properly study the disease at the molecular and cellular level is of utmost importance. Here, we present the cytogenetic characterization and gene expression analysis of the tumoral mammary rat cell line CLS-ACI-1. T...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000441374

    authors: Meles S,Adega F,Castro J,Chaves R

    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

  • Polyploidy and hybridization as main factors of speciation: complex reticulate evolution within the grass genus Helictochloa.

    abstract::To study the origin and evolution of naturally occurring polyploids, we performed phylogenetic analyses of nuclear ribosomal DNA spacers combined with molecular cytogenetics in 55 accessions of 27 taxa of the oat genus Helictochloa. A complex pattern of reticulate evolution was revealed with many diploid species and e...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000361002

    authors: Winterfeld G,Schneider J,Perner K,Röser M

    更新日期:2014-01-01 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

  • Transposable DNA Elements in Amazonian Fish: From Genome Enlargement to Genetic Adaptation to Stressful Environments.

    abstract::Transposable elements have driven genome evolution and plasticity in many ways across a range of organisms. Different types of biotic and abiotic stresses can stimulate the expression or transposition of these mobile elements. Here, we cytogenetically analyzed natural fish populations of the same species living under ...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000507104

    authors: da Silva FA,Corrêa Guimarães EM,Carvalho NDM,Ferreira AMV,Schneider CH,Carvalho-Zilse GA,Feldberg E,Gross MC

    更新日期:2020-01-01 00:00:00

  • Karyotypic evolution in the Galliformes: an examination of the process of karyotypic evolution by comparison of the molecular cytogenetic findings with the molecular phylogeny.

    abstract::To define the process of karyotypic evolution in the Galliformes on a molecular basis, we conducted genome-wide comparative chromosome painting for eight species, i.e. silver pheasant (Lophura nycthemera), Lady Amherst's pheasant (Chrysolophus amherstiae), ring-necked pheasant (Phasianus colchicus), turkey (Meleagris ...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000078570

    authors: Shibusawa M,Nishibori M,Nishida-Umehara C,Tsudzuki M,Masabanda J,Griffin DK,Matsuda Y

    更新日期:2004-01-01 00:00:00

  • Recurrent inversion events at 17q21.31 microdeletion locus are linked to the MAPT H2 haplotype.

    abstract::The chromosomal band 17q21.31, containing the microtubule-associated protein tau (MAPT) gene, is a hotspot for chromosomal rearrangements. It is known to contain a common inversion polymorphism of approximately 900 kb in populations with European ancestry. The inverted configuration is linked to a distinct MAPT haplot...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000315901

    authors: Rao PN,Li W,Vissers LE,Veltman JA,Ophoff RA

    更新日期:2010-01-01 00:00:00

  • 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 ...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000207525

    authors: Kopecký D,Bartos J,Zwierzykowski Z,Dolezel J

    更新日期:2009-01-01 00:00:00

  • The genomic structure, chromosomal localization, and analysis of SIL as a candidate gene for holoprosencephaly.

    abstract::Holoprosencephaly (HPE) is the most common congenital malformation of the brain and face in humans. In this study we report the analysis of SIL (Sumacr;CL iumacr;nterrupting lumacr;ocus) as a candidate gene for HPE. Fluorescent in situ hybridization (FISH) analysis using a BAC 246e16 confirmed the assignment of SIL to...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000064057

    authors: Karkera JD,Izraeli S,Roessler E,Dutra A,Kirsch I,Muenke M

    更新日期:2002-01-01 00:00:00

  • Telomere dysfunction and telomerase activation in cancer--a pathological paradox?

    abstract::Telomerase is expressed in more than 90% of human cancers. Telomere maintenance by this enzyme is believed to safeguard genomic integrity in neoplastic cells. Nevertheless, many telomerase-expressing tumours exhibit chromosomal instability triggered by short, dysfunctional telomeres, implying that active telomerase is...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章,评审

    doi:10.1159/000108310

    authors: Calcagnile O,Gisselsson D

    更新日期:2007-01-01 00:00:00

  • DNA methylation profiles of CpG islands for cellular differentiation and development in mammals.

    abstract::DNA methylation has been implicated in mammalian development. Transcription units contain CpG islands, but expression of CpG island associated genes in normal tissues was not believed to be controlled by DNA methylation. There are, however, numerous CpG islands containing tissue-dependent and differentially methylated...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000078205

    authors: Shiota K

    更新日期:2004-01-01 00:00:00

  • Involvement of the mitochondrial pathway in p53-independent apoptosis induced by p28GANK knockdown in Hep3B cells.

    abstract::It is well known that TP53 may mediate apoptosis triggered by anticancer drugs. However, accumulating evidence indicates that TP53 may be inactivated by mutations and/or deletions in about 50% of human cancers and, as such, may lead to pronounced resistance to therapeutic agents. Thus, the development of new approache...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000227831

    authors: Wang J,Wang XF,Zhang LG,Xie SY,Li ZL,Li YJ,Li HH,Jiao F

    更新日期:2009-01-01 00:00:00

  • Elevated chromosome translocation frequencies in New Zealand nuclear test veterans.

    abstract::In 1957/58 the British Government conducted a series of nuclear tests in the mid-Pacific codenamed Operation Grapple, which involved several naval vessels from Britain and New Zealand. Two New Zealand frigates with 551 personnel onboard were stationed at various distances between 20 and 150 nautical miles from ground ...

    journal_title:Cytogenetic and genome research

    pub_type: 历史文章,杂志文章

    doi:10.1159/000125832

    authors: Wahab MA,Nickless EM,Najar-M'kacher R,Parmentier C,Podd JV,Rowland RE

    更新日期:2008-01-01 00:00:00

  • Chromosome banding in Amphibia. XXIX. The primitive XY/XX sex chromosomes of Hyla femoralis (Anura, Hylidae).

    abstract::The karyotype of the pine woods treefrog, Hyla femoralis, is characterized by primitive XY female/XX male sex chromosomes. The sole difference between the X and the Y is the presence of a nucleolus organizer region (NOR) in the X. Due to a deletion of the NOR in the Y, this chromosome is distinctly smaller than the X....

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000073421

    authors: Schmid M,Steinlein C

    更新日期:2003-01-01 00:00:00

  • Integration of chicken genomic resources to enable whole-genome sequencing.

    abstract::Different genomic resources in chicken were integrated through the Wageningen chicken BAC library. First, a BAC anchor map was created by screening this library with two sets of markers: microsatellite markers from the consensus linkage map and markers created from BAC end sequencing in chromosome walking experiments....

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000075766

    authors: Aerts J,Crooijmans R,Cornelissen S,Hemmatian K,Veenendaal T,Jaadar A,van der Poel J,Fillon V,Vignal A,Groenen M

    更新日期:2003-01-01 00:00:00

  • Mechanisms of nondisjunction in human spermatogenesis.

    abstract::A reduction in recombination in the pseudoautosomal region is associated with an increased frequency of aneuploid 24,XY human sperm. Similarly, individuals with paternally derived Klinefelter syndrome (47,XXY) also have a paucity of recombination in the chromosomes that have undergone nondisjunction. Meiotic studies u...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000086895

    authors: Martin RH

    更新日期:2005-01-01 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

  • Z and W chromosomes of chickens: studies on their gene functions in sex determination and sex differentiation.

    abstract::Since the discovery of SRY/SRY as a testis-determining gene on the mammalian Y chromosome in 1990, extensive studies have been carried out on the immediate target of SRY/SRY and genes functioning in the course of testis development. Comparative studies in non-mammalian vertebrates including birds have failed to find a...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章,评审

    doi:10.1159/000071599

    authors: Mizuno S,Kunita R,Nakabayashi O,Kuroda Y,Arai N,Harata M,Ogawa A,Itoh Y,Teranishi M,Hori T

    更新日期:2002-01-01 00:00:00

  • Comparative mapping of CDY and DAZ in higher primates.

    abstract::The human male specific expressed gene families CDY and DAZ are known to be repetitively clustered in the Y-specific region of the human Y chromosome. Comparative FISH-mapping of DNA clones specific for CDY and DAZ resulted in a Y-specific but diverse signal pattern within the non-recombining region of the Y-chromosom...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000063021

    authors: Wimmer R,Kühl H,Röttger S,Schempp W

    更新日期:2002-01-01 00:00:00

  • Assessing the Clinical Utility of SNP Microarray for Prader-Willi Syndrome due to Uniparental Disomy.

    abstract::Maternal uniparental disomy (UPD) 15 is one of the molecular causes of Prader-Willi syndrome (PWS), a multisystem disorder which presents with neonatal hypotonia and feeding difficulty. Current diagnostic algorithms differ regarding the use of SNP microarray to detect PWS. We retrospectively examined the frequency wit...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000478921

    authors: Santoro SL,Hashimoto S,McKinney A,Mihalic Mosher T,Pyatt R,Reshmi SC,Astbury C,Hickey SE

    更新日期:2017-01-01 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

  • 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

  • The controversial telomeres of lily plants.

    abstract::The molecular structure of the exceptional telomeres of six plant species belonging to the order Asparagales and two species of the order Liliales was analyzed using Southern blot and fluorescence in situ hybridization. Three different situations were found, namely: i) In the two Liliales species, Tulipa australis (Li...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000082393

    authors: de la Herrán R,Cuñado N,Navajas-Pérez R,Santos JL,Ruiz Rejón C,Garrido-Ramos MA,Ruiz Rejón M

    更新日期:2005-01-01 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

  • Pesticides and the induction of aneuploidy in human sperm.

    abstract::Pesticides are some of the most frequently released toxic chemicals into the environment. Exposure to them has been associated with reproductive dysfunction, but the knowledge of the genotoxic risks of these substances is still limited. In vitro and in vivo, many pesticides are shown to induce aneuploidy. Analysis of ...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章,评审

    doi:10.1159/000086915

    authors: Härkönen K

    更新日期:2005-01-01 00:00:00

  • Overexpression of KLF13 and FGFR3 in oral cancer cells.

    abstract::KLF13 and FGFR3 have important cellular functions and each is believed to play a role in cancer. KLF13 is a transcription factor required for the expression of several oncogenes. FGFR3 is a fibroblast growth factor receptor that initiates a signaling cascade leading to the activation of numerous cellular pathways. Her...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000308303

    authors: Henson BJ,Gollin SM

    更新日期:2010-06-01 00:00:00

  • Methods to detect CNVs in the human genome.

    abstract::The detection of quantitative changes in genomic DNA, i.e. deletions and duplications or Copy Number Variants (CNVs), has recently gained considerable interest. First, detailed analysis of the human genome showed a surprising amount of CNVs, involving thousands of genes. Second, it was realised that the detection of C...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000184723

    authors: Aten E,White SJ,Kalf ME,Vossen RH,Thygesen HH,Ruivenkamp CA,Kriek M,Breuning MH,den Dunnen JT

    更新日期:2008-01-01 00:00:00

  • Strand-specific fluorescence in situ hybridization: the CO-FISH family.

    abstract::The ability to prepare single-stranded chromosomal target DNA allows innovative uses of FISH technology for studies of chromosome organization. Standard FISH methodologies require functionally single-stranded DNAs in order to facilitate hybridization between the probe and the complementary chromosomal target sequence....

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章,评审

    doi:10.1159/000079565

    authors: Bailey SM,Goodwin EH,Cornforth MN

    更新日期:2004-01-01 00:00:00