Inheritance of seed dormancy in Tibetan semi-wild wheat accession Q1028.

Abstract:

:Tibetan semi-wild wheat (Triticum aestivum ssp. tibetanum Shao) is one of the Chinese endemic hexaploid wheat genetic resources, distributed only in the Qinghai-Xizang Plateau of China. It has special characters, such as a hulled glume and spike disarticulation. However, seed dormancy, another important character for wheat resistance to pre-harvest sprouting, was rarely reported. Seed dormancy of more than 10 Tibetan semi-wild wheat accessions was evaluated, and their germinations were 0% or near 0% with both treatments of threshed seeds and intact spikes at hard dough stage. Tibetan semi-wild wheat accession Q1028 was investigated for its seed dormant characters by testing the seed germination percentages of intact spikes, seeds with bract powder, normal seeds, seeds with pierced coat, and sectioned embryos. It was observed that embryo dormancy of Q1028 accounted for its seed dormancy. Using threshed seeds and intact spikes at hard dough stage, the inheritance of seed dormancy was carried out using the F1, F2, F3 and F2BC1 populations of the cross between Q1028 and a wheat line 88-1643, susceptible to preharvest sprouting. The germinations of seeds and intact spikes in F1 plants were 1.0% and 0.9%, respectively. It indicated that seed dormancy of Q1028 was inherited as a dominant trait. From the genetic analysis of the F2, F3 and F2BC1 populations it was found that the strong seed dormancy of Q1028 was controlled by two dominant genes.

journal_name

J Appl Genet

authors

Lan XJ,Wei YM,Liu DC,Yan ZH,Zheng YL

subject

Has Abstract

pub_date

2005-01-01 00:00:00

pages

133-8

issue

2

eissn

1234-1983

issn

2190-3883

pii

260

journal_volume

46

pub_type

杂志文章
  • Founder event and its effect on genetic variation in translocated populations of noble crayfish (Astacus astacus).

    abstract::Establishing translocated populations is a common process to preserve and maintain genetic diversity of threatened species. In 2001, three translocated populations of noble crayfish (Astacus astacus) were established in the Czech Republic, founded by either adult or juvenile individuals from three particular source po...

    journal_title:Journal of applied genetics

    pub_type: 杂志文章

    doi:10.1007/s13353-015-0296-3

    authors: Bláha M,Žurovcová M,Kouba A,Policar T,Kozák P

    更新日期:2016-02-01 00:00:00

  • Localisation of rDNA in the Lupinus genome during the cell cycle.

    abstract::Observations of a specific rDNA locus behaviour during the cell cycle were made by fluorescent in situ hybridisation (FISH) in 12 Lupinus species. Due to the pattern of chromatin de-condensation in that locus, the number of relevant sites in interphase nuclei was twice as high as the number of signals on metaphase chr...

    journal_title:Journal of applied genetics

    pub_type: 杂志文章

    doi:

    authors: Naganowska B,Zielińska A

    更新日期:2004-01-01 00:00:00

  • A novel WDR62 missense mutation in microcephaly with abnormal cortical architecture and review of the literature.

    abstract::Autosomal recessive primary microcephaly (MCPH) is a group of rare neurodevelopmental diseases with severe microcephaly at birth. One type of the disorder, MCPH2, is caused by biallelic mutations in the WDR62 gene, which encodes the WD repeat-containing protein 62. Patients with WDR62 mutation may have a wide range of...

    journal_title:Journal of applied genetics

    pub_type: 杂志文章,评审

    doi:10.1007/s13353-019-00486-y

    authors: Zombor M,Kalmár T,Nagy N,Berényi M,Telcs B,Maróti Z,Brandau O,Sztriha L

    更新日期:2019-05-01 00:00:00

  • Aberrant methylation of ERBB pathway genes in sporadic colorectal cancer.

    abstract::The ErbB signalling network plays a crucial role in the growth and progression of several cancers, including colorectal cancer (CRC), and includes potentially drug-targetable genes. Oncogenic activation of the ErbB pathway by mutations and focal amplifications have emerged recently as an important predictive marker of...

    journal_title:Journal of applied genetics

    pub_type: 杂志文章

    doi:10.1007/s13353-014-0253-6

    authors: Szmida E,Karpiński P,Leszczynski P,Sedziak T,Kielan W,Ostasiewicz P,Sasiadek MM

    更新日期:2015-05-01 00:00:00

  • Novel insertion in exon 5 of the TCOF1 gene in twin sisters with Treacher Collins syndrome.

    abstract::Treacher Collins syndrome (TCS) is associated with an abnormal differentiation of the first and second pharyngeal arches during fetal development. This causes mostly craniofacial deformities, which require numerous corrective surgeries. TCS is an autosomal dominant disorder and it occurs in the general population at a...

    journal_title:Journal of applied genetics

    pub_type: 杂志文章

    doi:10.1007/s13353-012-0091-3

    authors: Marszałek-Kruk BA,Wójcicki P,Smigiel R,Trzeciak WH

    更新日期:2012-08-01 00:00:00

  • PRNP and SPRN genes polymorphism in atypical bovine spongiform encephalopathy cases diagnosed in Polish cattle.

    abstract::Polymorphisms in the coding region of the prion protein gene (PRNP) have been associated with the susceptibility and incubation period of prion diseases in humans and sheep. However, polymorphisms in this part of the bovine PRNP gene do not affect the classical bovine spongiform encephalopathy (BSE) susceptibility in ...

    journal_title:Journal of applied genetics

    pub_type: 杂志文章

    doi:10.1007/s13353-012-0102-4

    authors: Gurgul A,Polak MP,Larska M,Słota E

    更新日期:2012-08-01 00:00:00

  • Morphological diversity of androgenic carrot plants.

    abstract::The aim of this study was to evaluate phenotypic variation of R0 androgenic plants obtained from four seed sources and donor plants by anther culture. Several morphological traits (leaf size, petiole length, leaf division, cortex colour) and the range of diversity were evaluated. There was large variation in all trait...

    journal_title:Journal of applied genetics

    pub_type: 杂志文章

    doi:

    authors: Kozik EU,Nowak R,Kłosińska U,Górecka K,Krzyzanowska D,Górecki R

    更新日期:2002-01-01 00:00:00

  • Proteolytic enzymes from generative organs of flowering plants (Angiospermae).

    abstract::Pollen proteases were discovered over 100 years ago, whereas the enzymes from female tissues have been used since the Roman era in simple biotechnological processes. In the last decade a great progress has been made in studies on plant proteases, including those from the generative organs. This paper reviews reports p...

    journal_title:Journal of applied genetics

    pub_type: 杂志文章,评审

    doi:

    authors: Radłowski M

    更新日期:2005-01-01 00:00:00

  • Interactions between Glu-1 and Glu-3 loci and associations of selected molecular markers with quality traits in winter wheat (Triticum aestivum L.) DH lines.

    abstract::The quality of wheat depends on a large complex of genes and environmental factors. The objective of this study was to identify quantitative trait loci controlling technological quality traits and their stability across environments, and to assess the impact of interaction between alleles at loci Glu-1 and Glu-3 on gr...

    journal_title:Journal of applied genetics

    pub_type: 杂志文章

    doi:10.1007/s13353-016-0362-5

    authors: Krystkowiak K,Langner M,Adamski T,Salmanowicz BP,Kaczmarek Z,Krajewski P,Surma M

    更新日期:2017-02-01 00:00:00

  • Fingerprinting of common wheat cultivars with an Alw44I-based AFLP method.

    abstract::A simplified AFLP method, based on methylation-sensitive Alw44I restriction endonuclease, has been developed and evaluated for fingerprinting 15 wheat cultivars. The selected germplasms represented groups of spring and winter wheats with and without the 1BL.1RS translocation. Ten selective primers yielded 57 markers, ...

    journal_title:Journal of applied genetics

    pub_type: 杂志文章

    doi:

    authors: Tyrka M

    更新日期:2004-01-01 00:00:00

  • A comparative analysis of proteins that accumulate during the initial stage of root hair development in barley root hair mutants and their parent varieties.

    abstract::The mechanisms of root hair formation have been studied extensively in Arabidopsis but knowledge about these processes in monocot species is still limited, especially in relation to the proteome level. The aim of this study was to identify the proteins that are involved in the initiation and the early stage of root ha...

    journal_title:Journal of applied genetics

    pub_type: 杂志文章

    doi:10.1007/s13353-012-0105-1

    authors: Janiak A,Piórko S,Matros A,Mock HP,Kwaśniewski M,Chwiałkowska K,Chmielewska B,Szarejko I

    更新日期:2012-11-01 00:00:00

  • The F279Y polymorphism of the GHR gene and its relation to milk production and somatic cell score in German Holstein dairy cattle.

    abstract::The bovine growth hormone receptor (GHR) gene has been identified as a strong positional and functional candidate gene influencing milk production. A non-synonymous single nucleotide polymorphism (SNP) in exon 8 leads to a phenylalanine to tyrosine amino acid substitution (F279Y) in the receptor. The aim of the study ...

    journal_title:Journal of applied genetics

    pub_type: 杂志文章

    doi:10.1007/s13353-011-0051-3

    authors: Rahmatalla SA,Müller U,Strucken EM,Reissmann M,Brockmann GA

    更新日期:2011-11-01 00:00:00

  • Relaxed specificity of prokaryotic DNA methyltransferases results in DNA site-specific modification of RNA/DNA heteroduplexes.

    abstract::RNA/DNA hybrid duplexes regularly occur in nature, for example in transcriptional R loops. Their susceptibility to modification by DNA-specific or RNA-specific enzymes is, thus, a biologically relevant question, which, in addition, has possible biotechnological implications. In this study, we investigated the activity...

    journal_title:Journal of applied genetics

    pub_type: 杂志文章

    doi:10.1007/s13353-015-0279-4

    authors: Wons E,Mruk I,Kaczorowski T

    更新日期:2015-11-01 00:00:00

  • CRISPR/Cas9: targeted genome editing for the treatment of hereditary hearing loss.

    abstract::Hereditary hearing loss (HHL) is a neurosensory disorder that affects every 1/500 newborns worldwide and nearly 1/3 people over the age of 65. Congenital deafness is inherited as monogenetic or polygenic disorder. The delicacy, tissue heterogeneity, deep location of the inner ear down the brainstem, and minute quantit...

    journal_title:Journal of applied genetics

    pub_type: 杂志文章,评审

    doi:10.1007/s13353-019-00535-6

    authors: Farooq R,Hussain K,Tariq M,Farooq A,Mustafa M

    更新日期:2020-02-01 00:00:00

  • Homozygous 2p11.2 deletion supports the implication of ELMOD3 in hearing loss and reveals the potential association of CAPG with ASD/ID etiology.

    abstract::Autism spectrum disorder (ASD) is a set of neurodevelopmental conditions characterized by early-onset difficulties in social communication and unusually restricted, repetitive behavior and interests. Parental consanguinity may lead to higher risk of ASD and to more severe clinical presentations in the offspring. Studi...

    journal_title:Journal of applied genetics

    pub_type: 杂志文章

    doi:10.1007/s13353-018-0472-3

    authors: Lahbib S,Leblond CS,Hamza M,Regnault B,Lemée L,Mathieu A,Jaouadi H,Mkaouar R,Youssef-Turki IB,Belhadj A,Kraoua I,Bourgeron T,Abdelhak S

    更新日期:2019-02-01 00:00:00

  • A new PCR-RFLP within the domestic pigeon (Columba livia var. domestica) cytochrome b (MTCYB) gene.

    abstract::A total of 244 domestic pigeons (Columba livia var. domestica) were genotyped using the PCR-RFLP method. A 999 bp fragment of the MTCYB gene was amplified. The amplification products were digested with restriction enzymes. PCR-RFLP for MvaI restriction enzyme was observed. Frequencies of alleles were as follows: MTCYB...

    journal_title:Journal of applied genetics

    pub_type: 杂志文章

    doi:

    authors: Dybus A,Knapik K

    更新日期:2005-01-01 00:00:00

  • Current genetic methodologies in the identification of disaster victims and in forensic analysis.

    abstract::This review presents the basic problems and currently available molecular techniques used for genetic profiling in disaster victim identification (DVI). The environmental conditions of a mass disaster often result in severe fragmentation, decomposition and intermixing of the remains of victims. In such cases, traditio...

    journal_title:Journal of applied genetics

    pub_type: 杂志文章,评审

    doi:10.1007/s13353-011-0068-7

    authors: Ziętkiewicz E,Witt M,Daca P,Zebracka-Gala J,Goniewicz M,Jarząb B,Witt M

    更新日期:2012-02-01 00:00:00

  • Population biobanking in selected European countries and proposed model for a Polish national DNA bank.

    abstract::Population biobanks offer new opportunities for public health, are rudimentary for the development of its new branch called Public Health Genomics, and are important for translational research. This article presents organizational models of population biobanks in selected European countries. Review of bibliography and...

    journal_title:Journal of applied genetics

    pub_type: 杂志文章

    doi:10.1007/s13353-012-0082-4

    authors: Sak J,Pawlikowski J,Goniewicz M,Witt M

    更新日期:2012-05-01 00:00:00

  • A new assay based on terminal restriction fragment length polymorphism of homocitrate synthase gene fragments for Candida species identification.

    abstract::Candida sp. have been responsible for an increasing number of infections, especially in patients with immunodeficiency. Species-specific differentiation of Candida sp. is difficult in routine diagnosis. This identification can have a highly significant association in therapy and prophylaxis. This work has shown a new ...

    journal_title:Journal of applied genetics

    pub_type: 杂志文章

    doi:10.1007/s13353-017-0394-5

    authors: Szemiako K,Śledzińska A,Krawczyk B

    更新日期:2017-08-01 00:00:00

  • New PAH gene promoter KLF1 and 3'-region C/EBPalpha motifs influence transcription in vitro.

    abstract::Phenylketonuria (PKU) is a metabolic disease caused by mutations in the phenylalanine hydroxylase (PAH) gene. Although the PAH genotype remains the main determinant of PKU phenotype severity, genotype-phenotype inconsistencies have been reported. In this study, we focused on unanalysed sequences in non-coding PAH gene...

    journal_title:Journal of applied genetics

    pub_type: 杂志文章

    doi:10.1007/s13353-016-0359-0

    authors: Klaassen K,Stankovic B,Kotur N,Djordjevic M,Zukic B,Nikcevic G,Ugrin M,Spasovski V,Srzentic S,Pavlovic S,Stojiljkovic M

    更新日期:2017-02-01 00:00:00

  • Statistical measures of uncertainty for branches in phylogenetic trees inferred from molecular sequences by using model-based methods.

    abstract::In recent years, the emphasis of theoretical work on phylogenetic inference has shifted from the development of new tree inference methods to the development of methods to measure the statistical support for the topologies. This paper reviews 3 approaches to assign support values to branches in trees obtained in the a...

    journal_title:Journal of applied genetics

    pub_type: 杂志文章,评审

    doi:10.1007/BF03195249

    authors: Wróbel B

    更新日期:2008-01-01 00:00:00

  • Gene expression profiling in skeletal muscle of Holstein-Friesian bulls with single-nucleotide polymorphism in the myostatin gene 5'-flanking region.

    abstract::Myostatin (GDF-8) is a key protein responsible for skeletal muscle growth and development, thus mutations in the mstn gene can have major economic and breeding consequences. The aim of the present study was to investigate myostatin gene expression and transcriptional profile in skeletal muscle of Holstein-Friesian (Bl...

    journal_title:Journal of applied genetics

    pub_type: 杂志文章

    doi:10.1007/BF03195620

    authors: Sadkowski T,Jank M,Zwierzchowski L,Siadkowska E,Oprzadek J,Motyl T

    更新日期:2008-01-01 00:00:00

  • Association of 3 polymorphisms in porcine troponin I genes (TNNI1 and TNNI2) with meat quality traits.

    abstract::The contractile protein troponin I (TnI), a constituent protein of the troponin complex located on the thin filaments of striated muscle, is involved in inhibition of calcium-induced myosin ATPase activity (and thus contraction). TnI-slow (slow-twitch skeletal muscle isoform, named TNNI1) and TnI-fast (fast-twitch ske...

    journal_title:Journal of applied genetics

    pub_type: 杂志文章

    doi:10.1007/BF03195710

    authors: Yang H,Xu ZY,Lei MG,Li FE,Deng CY,Xiong YZ,Zuo B

    更新日期:2010-01-01 00:00:00

  • QTL mapping of 1000-kernel weight, kernel length, and kernel width in bread wheat (Triticum aestivum L.).

    abstract::Kernel size and morphology influence the market value and milling yield of bread wheat (Triticum aestivum L.). The objective of this study was to identify quantitative trait loci (QTLs) controlling kernel traits in hexaploid wheat. We recorded 1000-kernel weight, kernel length, and kernel width for 185 recombinant inb...

    journal_title:Journal of applied genetics

    pub_type: 杂志文章

    doi:10.1007/BF03208872

    authors: Ramya P,Chaubal A,Kulkarni K,Gupta L,Kadoo N,Dhaliwal HS,Chhuneja P,Lagu M,Gupta V

    更新日期:2010-01-01 00:00:00

  • Urological anomalies in children with renal agenesis or multicystic dysplastic kidney.

    abstract::This study aimed to determine the frequency of associated urological abnormalities in children with unilateral renal agenesis (RA) or multicystic dysplastic kidney (MCDK). In total, 38 children (10 girls, 28 boys) were studied: 21 with RA and 17 with MCDK. In 14 children (37%) anomalies of the urinary tract were suspe...

    journal_title:Journal of applied genetics

    pub_type: 杂志文章

    doi:10.1007/BF03194618

    authors: Krzemień G,Roszkowska-Blaim M,Kostro I,Wojnar J,Karpińska M,Sekowska R

    更新日期:2006-01-01 00:00:00

  • Expression of Npc1 in glial cells corrects sterility in Npc1(-/-) mice.

    abstract::Niemann-Pick type C1 (NPC) disease is an autosomal recessive neurodegenerative disorder. One feature of the mouse model of NPC1 is it's infertility. We have made transgenic mice which express the Npc1 protein exclusively in fibrillary astrocytes, using the glial fibrillary acidic protein (GFAP) promoter. This selectiv...

    journal_title:Journal of applied genetics

    pub_type: 杂志文章

    doi:10.1007/BF03195698

    authors: Donohue C,Marion S,Erickson RP

    更新日期:2009-01-01 00:00:00

  • Genetic background of cutaneous forms of lupus erythematosus: update on current evidence.

    abstract::This article reviews and updates current information on the possible genetic basis for cutaneous lupus erythematosus. The aetiology of this condition remains unknown and is believed to be multifactorial, involving genetic, environmental and retroviral factors. A genetic predisposition is probably the greatest risk fac...

    journal_title:Journal of applied genetics

    pub_type: 杂志文章,评审

    doi:

    authors: Osmola A,Namysł J,Jagodziński PP,Prokop J

    更新日期:2004-01-01 00:00:00

  • Chromosomal manipulation in Senegalese sole (Solea senegalensis Kaup, 1858): induction of triploidy and gynogenesis.

    abstract::In this study we have developed protocols for induced triploidy and gynogenesis of Senegalese sole (Solea senegalensis), a promising flatfish species for marine aquaculture, in order to: 1) identify the sex-determination mechanism; and 2) to improve its production by generating a) sterile fish, avoiding problems relat...

    journal_title:Journal of applied genetics

    pub_type: 杂志文章

    doi:10.1007/s13353-014-0233-x

    authors: Molina-Luzón MJ,López JR,Robles F,Navajas-Pérez R,Ruiz-Rejón C,De la Herrán R,Navas JI

    更新日期:2015-02-01 00:00:00

  • Interval mapping of QTLs controlling yield-related traits and seed protein content in Pisum sativum.

    abstract::A linkage map of garden pea was constructed on the basis of 114 plants (F2 generation) derived from a cross combination Wt10245 x Wt11238. The map, consisting of 204 morphological, isozyme, AFLP, ISSR, STS, CAPS and RAPD markers, was used for interval mapping of quantitative trait loci (QTLs) controlling seed number, ...

    journal_title:Journal of applied genetics

    pub_type: 杂志文章

    doi:

    authors: Irzykowska L,Wolko B

    更新日期:2004-01-01 00:00:00

  • Induction and characterization of streptomycin-resistant mutants in Capsicum praetermissum.

    abstract::Streptomycin-resistant mutants were isolated from mutagenised cotyledon explants of Capsicum praetermissum Heiser & Smith. The explants were mutagenised with N-ethyl-N-nitrosourea, which resulted in a high frequency of streptomycin-resistant mutants (18.0%) and a low frequency of chlorophyll-deficient (albino) mutants...

    journal_title:Journal of applied genetics

    pub_type: 杂志文章

    doi:

    authors: Venkataiah P,Christopher T,Subhash K

    更新日期:2005-01-01 00:00:00