The 3Ns chromosome of Psathyrostachys huashanica carries the gene(s) underlying wheat stripe rust resistance.

Abstract:

:Stripe rust (Puccinia striiformis tritici (Pst)) is one of the most destructive diseases of wheat in the world. Exploiting and utilizing stripe rust resistance genes of wild species has become an essential strategy for resistance breeding. Psathyrostachyshuashanica Keng ex Kuo is a wild species in Triticeae that has been used for wheat improvement because of its high resistance or immunity to stripe rust. In this study, 9 wheat-P. huashanica addition lines were characterized by Giemsa C-banding, genomic in situ hybridization (GISH), and disease resistance evaluation. Giemsa C-banding and GISH demonstrated that lines 163-5, 165-1, 183-5, 240-3, and 240-4 are P. huashanica 3Ns chromosome monosomic addition lines; lines 183-1 and 183-20 are P. huashanica 3Ns chromosome disomic addition lines; line 165-20 is a P. huashanica 3Ns and 4Ns chromosomes double disomic addition line, and line 219-1 is a P. huashanica 1Ns and 3Ns/5A chromosomes double disomic addition-substitution line. All these addition lines with P. huashanica 3Ns chromosome(s) expressed high resistance or immunity to stripe rust. By comparing the series of wheat-P. huashanica chromosome addition lines, we concluded that the P. huashanica 3Ns chromosome carries the gene(s) for resistance or immunity to stripe rust. These addition lines can be used as a donor source of novel stripe rust resistance to wheat breeding programs.

journal_name

Cytogenet Genome Res

authors

Wang Y,Yu K,Xie Q,Kang H,Lin L,Fan X,Sha L,Zhang H,Zhou Y

doi

10.1159/000324928

subject

Has Abstract

pub_date

2011-01-01 00:00:00

pages

136-43

issue

2

eissn

1424-8581

issn

1424-859X

pii

000324928

journal_volume

134

pub_type

杂志文章
  • Three cases with rare interstitial rearrangements of chromosome 1 characterized by multicolor banding.

    abstract::In this report, we describe three unrelated patients with similar symptoms such as mental retardation, growth delay and multiple phenotypic abnormalities. GTG-banding analysis revealed karyotypes with add(1p) in two cases and an add(1q) in the third. Fluorescence in situ hybridization (FISH) analysis using high resolu...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000086388

    authors: Polityko A,Starke H,Rumyantseva N,Claussen U,Liehr T,Raskin S

    更新日期:2005-01-01 00:00:00

  • Cytogenetic mapping of H1 histone and ribosomal RNA genes in hybrids between catfish species Pseudoplatystoma corruscans and Pseudoplatystoma reticulatum.

    abstract::A physical chromosome mapping of the H1 histone and 5S and 18S ribosomal RNA (rRNA) genes was performed in interspecific hybrids of Pseudoplatystoma corruscans and P. reticulatum. The results showed that 5S rRNA clusters were located in the terminal region of 2 chromosomes. H1 histone and 18S ribosomal genes were co-l...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000345299

    authors: Hashimoto DT,Ferguson-Smith MA,Rens W,Prado FD,Foresti F,Porto-Foresti F

    更新日期:2013-01-01 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

  • Different numbers of rye B chromosomes induce identical compaction changes in distinct A chromosome domains.

    abstract::In rye each B chromosome (B) represents 5.5% of the diploid A genome. Rye Bs have several nuclear to whole plant effects although they seem to bear no genes except for the ones that lead to their maintenance within a population. In this context, and considering that rye Bs are enriched in repetitive non-coding regions...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000079306

    authors: Delgado M,Caperta A,Ribeiro T,Viegas W,Jones RN,Morais-Cecílio L

    更新日期:2004-01-01 00:00:00

  • Genetic characterization of a sheep-dwarf goat hybrid.

    abstract::Twelve weeks after repeated spontaneous mating between a Bentheimer Landschaf ram and a West African dwarf doe was observed, the doe aborted a dead fetus. The aim of this study was to verify the parentage and the species of the supposed parents and the hybrid status of the fetus, using cytogenetic and molecular geneti...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000227841

    authors: Lühken G,Wagner HW,Seichter D,Hecht W,Erhardt G

    更新日期:2009-01-01 00:00:00

  • Comparative mapping in equids: the asine X chromosome is rearranged compared to horse and Hartmann's mountain zebra.

    abstract::The X chromosomes of the extant equids, in general, share morphology and banding pattern similarities. However, the donkey X is, in part, an exception because of significantly different centromeric index and variant banding patterns in the pericentromeric region. To verify the underlying molecular basis of this differ...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000063050

    authors: Raudsepp T,Lear TL,Chowdhary BP

    更新日期:2002-01-01 00:00:00

  • Coamplification of multiple regions of chromosome 2, including MYCN, in a single patchwork amplicon in cancer cell lines.

    abstract::Coamplification of multiple segments of chromosome 2, including an MYCN-bearing segment, was examined in 2 cancer cell lines, NCI-H69 (lung cancer) and IMR-32 (neuroblastoma). High-resolution array-CGH analysis revealed 13 and 6 highly amplified segments located at different sites in chromosome 2 in NCI-H69 and IMR-32...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000334349

    authors: Kitada K,Aida S,Aikawa S

    更新日期:2012-01-01 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

  • Happy together: the life and times of Ty retrotransposons and their hosts.

    abstract::The aim of this review is to describe the level of intimacy between Ty retrotransposons (Ty1-Ty5) and their host the yeast Saccharomyces cerevisiae. The effects of Ty location in the genome and of host proteins on the expression and mobility of Ty elements are highlighted. After a brief overview of Ty diversity and ev...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章,评审

    doi:10.1159/000084940

    authors: Lesage P,Todeschini AL

    更新日期:2005-01-01 00:00:00

  • Deletion 18p11.32p11.31 in a Child with Global Developmental Delay and Atypical, Drug-Resistant Absence Seizures.

    abstract::We report the first case of an 18p11.32 deletion, detected by array CGH, associated with a drug-resistant form of atypical absence epilepsy, global developmental delay and no signs of holoprosencephaly (HPE). In particular, this region encompasses 19 genes, and none of these genes have been strictly associated with ep...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000438502

    authors: Verrotti A,Palka C,Prezioso G,Alfonsi M,Calabrese G,Palka G,Chiarelli F

    更新日期:2015-01-01 00:00:00

  • A preliminary genetic map in Solea senegalensis (Pleuronectiformes, Soleidae) using BAC-FISH and next-generation sequencing.

    abstract::This article presents the first physical mapping carried out in the Senegalese sole (Solea senegalensis), an important marine fish species of Southern Europe. Eight probes were designated to pick up genes of interest in aquaculture (candidate genes) from a bacterial artificial chromosome (BAC) library using a method o...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000355001

    authors: García-Cegarra A,Merlo MA,Ponce M,Portela-Bens S,Cross I,Manchado M,Rebordinos L

    更新日期:2013-01-01 00:00:00

  • The temporal and spatial pattern of histone H3 phosphorylation at serine 28 and serine 10 is similar in plants but differs between mono- and polycentric chromosomes.

    abstract::Immunolabeling using site-specific antibodies against phosphorylated histone H3 at serine 10 or serine 28 revealed in plants an almost similar temporal and spatial pattern of both post-translational modification sites at mitosis and meiosis. During the first meiotic division the entire chromosomes are highly H3 phosph...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000074175

    authors: Gernand D,Demidov D,Houben A

    更新日期:2003-01-01 00:00:00

  • Mechanisms of the Evolutionary Chromosome Plasticity: Integrating the 'Centromere-from-Telomere' Hypothesis with Telomere Length Regulation.

    abstract::The 'centromere-from-telomere' hypothesis proposed by Villasante et al. [2007a] aims to explain the evolutionary origin of the eukaryotic chromosome. The hypothesis is based on the notion that the process of eukaryogenesis was initiated by adaptive responses of the symbiont eubacterium and its archaeal host to their n...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章,评审

    doi:10.1159/000447415

    authors: Slijepcevic P

    更新日期:2016-01-01 00:00:00

  • Karyotype Analysis of Four Blind Snake Species (Reptilia: Squamata: Scolecophidia) and Karyotypic Changes in Serpentes.

    abstract::The suborder Serpentes is divided into 2 infraorders, Scolecophidia and Alethinophidia, which diverged at an early stage of snake diversification. In this study, we examined karyotypes of 4 scolecophidian species (Letheobia simonii, Xerotyphlops vermicularis, Indotyphlops braminus, and Myriopholis macrorhyncha) and pe...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000496554

    authors: Matsubara K,Kumazawa Y,Ota H,Nishida C,Matsuda Y

    更新日期:2019-01-01 00:00:00

  • New insights into the karyotypic relationships of Chinese muntjac (Muntiacus reevesi), forest musk deer (Moschus berezovskii) and gayal (Bos frontalis).

    abstract::To investigate the karyotypic relationships between Chinese muntjac (Muntiacus reevesi), forest musk deer (Moschus berezovskii) and gayal (Bos frontalis), a complete set of Chinese muntjac chromosome-specific painting probes has been assigned to G-banded chromosomes of these three species. Sixteen autosomal probes (i....

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000081520

    authors: Chi J,Fu B,Nie W,Wang J,Graphodatsky AS,Yang F

    更新日期:2005-01-01 00:00:00

  • Assignment of linkage groups to turkey chromosome 1 (MGA1).

    abstract::Previous genetic mapping identified three linkage groups (M1, M18 and M26) in the turkey corresponding to chicken chromosome 1 (GGA1). This is inconsistent with previously described chromosomal differences between these species. FISH analysis of BAC clones corresponding to microsatellite markers from each of the three...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000095239

    authors: Reed KM,Sullivan LR,Foster LK,Chaves LD,Ponce de León FA

    更新日期:2006-01-01 00:00:00

  • Aneuploidy Detection and mtDNA Quantification in Bovine Embryos with Different Cleavage Onset Using a Next-Generation Sequencing-Based Protocol.

    abstract::Bovine embryos are now routinely used in agricultural systems as a means of disseminating superior genetics worldwide, ultimately with the aim of feeding an ever-growing population. Further investigations, common for human IVF embryos, thus have priority to improve cattle IVF, as has screening for aneuploidy (abnormal...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000452923

    authors: Hornak M,Kubicek D,Broz P,Hulinska P,Hanzalova K,Griffin D,Machatkova M,Rubes J

    更新日期:2016-01-01 00:00:00

  • Evidence of Rubus Yellow Net Virus Integration into the Red Raspberry Genome.

    abstract::Rubus yellow net virus (RYNV) infects Rubus spp., causing a severe decline when present in mixed infections with other viruses. RYNV belongs to the family Caulimoviridae, also known as plant pararetroviruses, which can exist as episomal or integrated elements (endogenous). Most of integrated pararetroviruses are nonin...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000509845

    authors: Diaz-Lara A,Mosier NJ,Stevens K,Keller KE,Martin RR

    更新日期:2020-01-01 00:00:00

  • Distribution of the tandem repeat sequences and karyotyping in cucumber (Cucumis sativus L.) by fluorescence in situ hybridization.

    abstract::We analyzed repeat sequences composition in the genome of cucumber inbred line 9930 using whole-genome shotgun reads. The analysis showed that satellite DNA sequences are the most dominant components in the cucumber genome. The distribution pattern of several tandem repeat sequences (Type I/II, Type III and Type IV) o...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000151320

    authors: Han YH,Zhang ZH,Liu JH,Lu JY,Huang SW,Jin WW

    更新日期:2008-01-01 00:00:00

  • Genomic organization and expression pattern of scapinin (PHACTR3) in mouse and human.

    abstract::Scapinin has been found to bind to cytoplasmic actin and is also a putative regulatory subunit of protein phosphatase-1 (PP1). It is found attached to the nuclear matrix-intermediate filament (NM-IF) and is down-regulated by differentiation of tumor cells. We have analyzed the genomic structure and tissue-specific exp...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000094797

    authors: Worch S,Fiedler E,Hansmann I,Schlote D

    更新日期:2006-01-01 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

  • Multicolor fluorescence in situ hybridization (FISH) applied to FISH-banding.

    abstract::During the last decade not only multicolor fluorescence in situ hybridization (FISH) using whole chromosome paints as probes, but also numerous chromosome banding techniques based on FISH have been developed for the human and for the murine genome. This review focuses on such FISH-banding techniques, which were recent...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章,评审

    doi:10.1159/000094207

    authors: Liehr T,Starke H,Heller A,Kosyakova N,Mrasek K,Gross M,Karst C,Steinhaeuser U,Hunstig F,Fickelscher I,Kuechler A,Trifonov V,Romanenko SA,Weise A

    更新日期:2006-01-01 00:00:00

  • Meiotic recombination in normal and clone bulls and their offspring.

    abstract::Homologous chromosome pairing and recombination are essential components of meiosis and sexual reproduction. The reshuffling of genetic material through breakage and reunion of chromatids ensure proper segregation of homologous chromosomes in reduction division and genetic diversity in the progeny. The advent of somat...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000118745

    authors: Hart EJ,Pinton A,Powell A,Wall R,King WA

    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

  • Chromosome Banding in Amphibia. XXXIII. Demonstration of 5-Methylcytosine-Rich Heterochromatin in Anura.

    abstract::An experimental approach using monoclonal anti-5-methylcytosine (5-MeC) antibodies and indirect immunofluorescence was elaborated for detecting 5-MeC-rich chromosome regions in anuran chromosomes. This technique was applied to mitotic metaphases of 6 neotropical frog species belonging to 6 genera and 4 families. The h...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000446141

    authors: Schmid M,Steinlein C

    更新日期:2016-01-01 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

  • Cytogenetic Characterization of a Small Evolutionary Rearrangement Involving Chromosomes BTA21 and OAR18.

    abstract::Both cattle (Bos taurus) and sheep (Ovis aries) belong to the Bovidae family but to different subfamilies, Bovinae and Caprinae, respectively. From a chromosomal point of view, apart from the already known centric fusions (that occurred during the evolutionary process in the Bovidae family) and the small differences i...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000507645

    authors: De Lorenzi L,Pauciullo A,Iannuzzi A,Parma P

    更新日期:2020-01-01 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

  • 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 ser...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000090812

    authors: Kono T

    更新日期:2006-01-01 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