当前位置： SCI文献检索 > JOURNAL OF APPLIED GENETICS期刊下所有文献 > Genetic determination of variability of barley doubled haploids inoculated with Fusarium culmorum (W.G.Sm.) Sacc. with regard to mycotoxin accumulation and reduction in yield traits.

Genetic determination of variability of barley doubled haploids inoculated with Fusarium culmorum (W.G.Sm.) Sacc. with regard to mycotoxin accumulation and reduction in yield traits.

Abstract：

:The genetic determination of variability of barley doubled haploid (DH) lines in regard of their susceptibility to Fusarium head blight caused by Fusarium culmorum was studied. The susceptibility was evaluated in 3-year field experiment on the basis of reduction in yield traits and myotoxin accumulation in infected kernels. The following traits were analysed in inoculated and control plants: kernel number and weight per ear, 1000-kernel weight, percentage of plump kernels (>2.5 mm), deoxynivalenol (DON) content and nivalenol (NIV) content of kernels. On the basis of the obtained data, heritability coefficient (ratio of genotypic to phenotypic variance) was assessed, and genetic parameters as well as the number of effective factors were estimated. Heritability coefficients calculated from two-way analysis of variance, i.e.regarding the influence of years and year x genotype interaction, appeared to be exceptionally low and ranged from 5.2% for the reduction in plump kernels to 38.2% for the reduction in 1000-kernel weight. In the case of mycotoxin accumulation about 60% of the observed variability in NIV concentrations and 30% in DON concentration resulted form genetic differences among lines. Additive effects of genes were important for all the analysed traits. Significant effects of dominance and dominance x dominance were observed for 1000-kernel weight and percentage of plump kernels. Moreover, it was found that the observed variability in yield trait reduction resulted from segregation of 5-6 effective factors, DON contents from 4 factors, while NIV content from 5 factors.

journal_name

J Appl Genet

journal_title

Journal of applied genetics

authors

Surma M,Adamski T,Chełkowski J,Goliński P,Kaczmarek Z,Kostecki M,Perkowski J,Wiśniewska H

subject

Has Abstract

pub_date

2000-01-01 00:00:00

pages

237-46

issue

4

eissn

1234-1983

issn

2190-3883

pii

2

journal_volume

41

pub_type

杂志文章

相关文献

JOURNAL OF APPLIED GENETICS文献大全
  • 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 mutation profile of differentiated thyroid cancer coexisting with undifferentiated anaplastic cancer resembles that of anaplastic thyroid cancer but not that of archetypal differentiated thyroid cancer.

    abstract：:Differentiated thyroid cancer (DTC) has one of the lowest cancer mutational burdens, while anaplastic thyroid cancer (ATC) has a much higher mutation frequency. A fraction of ATC has an associated differentiated component, which suggests the coevolution of both cancers. Here, we aimed to compare mutation frequency in ...

    journal_title：Journal of applied genetics

    pub_type： 杂志文章

    doi：10.1007/s13353-020-00594-0

    authors： Mika J,Łabaj W,Chekan M,Abramowicz A,Pietrowska M,Polański A,Widłak P

    更新日期：2021-02-01 00:00:00

  • A doubled haploid rye linkage map with a QTL affecting α-amylase activity.

    abstract：:A rye doubled haploid (DH) mapping population (Amilo × Voima) segregating for pre-harvest sprouting (PHS) was generated through anther culture of F(1) plants. A linkage map was constructed using DHs, to our knowledge, for the first time in rye. The map was composed of 289 loci: amplified fragment length polymorphism (...

    journal_title：Journal of applied genetics

    pub_type： 杂志文章

    doi：10.1007/s13353-011-0029-1

    authors： Tenhola-Roininen T,Kalendar R,Schulman AH,Tanhuanpää P

    更新日期：2011-08-01 00:00:00

  • Inheritance of resistance to stripe rust in winter wheat cultivars Aquileja and Xian Nong 4.

    abstract：:Winter wheat cultivars Aquileja (AQ) and Xian Nong 4(XN) were previously reported to possess durable, quantitative resistance to stripe rust disease. In the present study, AQ, XN and a susceptible wheat cultivar were reciprocally crossed in all 6 combinations. Parents, F1, F2, F3, BCP1 and BCP2 were used to determine ...

    journal_title：Journal of applied genetics

    pub_type： 杂志文章

    doi：10.1007/BF03194656

    authors： Feng J,Zhang Z,Li G,Zhou Y,Wang H,Guo Q,Sun J

    更新日期：2007-01-01 00:00:00

  • Mouse models of atherosclerosis: explaining critical roles of lipid metabolism and inflammation.

    abstract：:Atherosclerosis is the most common cause of death globally. It is a complex disease involving morphological and cellular changes in vascular walls. Studying molecular mechanism of the disease is hindered by disease complexity and lack of robust noninvasive diagnostics in human. Mouse models are the most popular animal...

    journal_title：Journal of applied genetics

    pub_type： 杂志文章,评审

    doi：10.1007/s13353-013-0134-4

    authors： Mukhopadhyay R

    更新日期：2013-05-01 00:00:00

  • New allele of HvBRI1 gene encoding brassinosteroid receptor in barley.

    abstract：:The aim of these studies was to characterize nucleotide substitutions leading to the phenotype of brassinosteroid-insensitive, semi-dwarf barley mutant 093AR. Two substitutions in the sequence of barley HvBRI1 gene, encoding leucine-rich repeats receptor kinase (LRR-RK), which participates in brassinosteroid (BR) sign...

    journal_title：Journal of applied genetics

    pub_type： 杂志文章

    doi：10.1007/s13353-011-0031-7

    authors： Gruszka D,Szarejko I,Maluszynski M

    更新日期：2011-08-01 00:00:00

  • Molecular characterisation of tumour necrosis factor alpha and its potential connection with lipoprotein lipase and peroxisome proliferator-activated receptors in blunt snout bream (Megalobrama amblycephala).

    abstract：:Tumour necrosis factor alpha (TNF-α) is one kind of cytokines which is related to inflammation and lipid metabolism. TNF-α cDNA was cloned from the liver of blunt snout bream (Megalobrama amblycephala) through real-time polymerase chain reaction (PCR) and rapid amplification of cDNA ends (RACE) methods. The full-lengt...

    journal_title：Journal of applied genetics

    pub_type： 杂志文章

    doi：10.1007/s13353-017-0390-9

    authors： Zhou M,Mi HF,Liu WB,Wu YY,Wang KZ,Jiang GZ

    更新日期：2017-08-01 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

  • 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

  • A novel genotype c.1228C>G/c.1448C-1498C (L371V/Rec-NciI) in a 3-year-old child with type 1 Gaucher disease.

    abstract：:Gaucher disease (GD) is an autosomal recessive inborn error of metabolism, resulting from a deficiency of the enzyme glucocerebrosidase, causing an accumulation of the glycolipid glucocerebroside within lysosomes of macrophages in the reticuloendothelial system. Three major clinical forms have been assigned and more t...

    journal_title：Journal of applied genetics

    pub_type： 杂志文章

    doi：10.1007/BF03195642

    authors： Yassin NA,Muwakkit SA,Ibrahim AO,Kayim IM,Habbal MZ,Chamseddine NM,Musallam KM,Shamseddine AI

    更新日期：2008-01-01 00:00:00

  • Interstitial 11q24 deletion: a new case and review of the literature.

    abstract：:We describe a 19-month-old male presenting with right stenotic megaureter, anemia and thrombocytopenia, cardiac and ophthalmologic abnormalities. Analysis with array-based comparative genomic hybridization (aCGH) revealed an interstitial deletion of about 2.4 Mb of chromosome 11q24.2q24.3. We compared the phenotype of...

    journal_title：Journal of applied genetics

    pub_type： 杂志文章,评审

    doi：10.1007/s13353-015-0333-2

    authors： Tassano E,Janis S,Canepa A,Zanotto E,Torello C,Gimelli G,Cuoco C

    更新日期：2016-08-01 00:00:00

  • Length polymorphism of PCR-amplified genomic fragments of the Pregnancy-Associated Glycoprotein (PAG) gene family in the pig and some other domestic and wild mammals.

    abstract：:Porcine pregnancy-associated glycoprotein genes (pPAG) are known as a multigene family, in which five members have been cloned and sequences of their cDNAs identified. Porcine PAG1 and pPAG3 genes, belonging to the pPAG1-like subfamily, both encode enzymatically inactive precursors. In contrast, cDNAs of pPAG2, pPAG4 ...

    journal_title：Journal of applied genetics

    pub_type： 杂志文章

    doi：

    authors： Szafrańska B,Panasiewicz G,Wacławik A

    更新日期：2001-01-01 00:00:00

  • CCAAT/enhancer binding protein-beta negatively regulates the expression of glycerol-3-phosphate dehydrogenase 1 in pig PK-15 cells.

    abstract：:Soluble glycerol-3-phosphate dehydrogenase 1 (GPD1, EC 1.1.1.8) plays important roles in the synthesis of triacylglycerol and in the glycerol-3-phosphate shutter. Though GPD1 is expressed in most adult tissues, little is known about the regulation of its expression. In this study, we analyzed the characters, organizat...

    journal_title：Journal of applied genetics

    pub_type： 杂志文章

    doi：10.1007/s13353-011-0050-4

    authors： Gao Y,Pan Y

    更新日期：2011-11-01 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

  • Genetic analysis of a red tilapia (Oreochromis spp.) population undergoing three generations of selection for increased body weight at harvest.

    abstract：:Quantitative genetic analysis was performed on 10,919 data records collected over three generations from the selection programme for increased body weight at harvest in red tilapia (Oreochromis spp.). They were offspring of 224 sires and 226 dams (50 sires and 60 dams per generation, on average). Linear mixed models w...

    journal_title：Journal of applied genetics

    pub_type： 杂志文章

    doi：10.1007/s13353-017-0411-8

    authors： Hamzah A,Thoa NP,Nguyen NH

    更新日期：2017-11-01 00:00:00

  • QTL analysis of falling number and seed longevity in wheat (Triticum aestivum L.).

    abstract：:Pre-harvest sprouting (PHS) and seed longevity (SL) are complex biological processes of major importance for agricultural production. In the present study, a recombinant inbred line (RIL) population derived from a cross between the German winter wheat (Triticum aestivum L.) cultivars History and Rubens was used to ide...

    journal_title：Journal of applied genetics

    pub_type： 杂志文章

    doi：10.1007/s13353-017-0422-5

    authors： Börner A,Nagel M,Agacka-Mołdoch M,Gierke PU,Oberforster M,Albrecht T,Mohler V

    更新日期：2018-02-01 00:00:00

  • A novel TPM2 gene splice-site mutation causes severe congenital myopathy with arthrogryposis and dysmorphic features.

    abstract：:To date, only two splice-site mutations within the TPM2 gene have been shown to be causative for congenital myopathies. While the majority of TPM2 gene mutations are causative for nemaline myopathy, cap disease or distal arthrogryposis, some mutations in this gene have been found to be associated with non-specific con...

    journal_title：Journal of applied genetics

    pub_type： 杂志文章

    doi：10.1007/s13353-016-0368-z

    authors： Mroczek M,Kabzińska D,Chrzanowska KH,Pronicki M,Kochański A

    更新日期：2017-05-01 00:00:00

  • Decreased neural stem cell proliferation and olfaction in mouse models of Niemann-Pick C1 disease and the response to hydroxypropyl-β-cyclodextrin.

    abstract：:The Npc1nih/nih-null model and the Npc1nmf164/nmf164 hypomorph models of Niemann-Pick C1 (NPC1) disease show defects in olfaction. We have tested the effects of the life-prolonging treatment hydroxypropyl-beta-cyclodextrin (HPBCD) on olfaction and neural stem cell numbers when delivered either systemically or by nasal...

    journal_title：Journal of applied genetics

    pub_type： 杂志文章

    doi：10.1007/s13353-019-00517-8

    authors： Dragotto J,Palladino G,Canterini S,Caporali P,Patil R,Fiorenza MT,Erickson RP

    更新日期：2019-11-01 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

  • Molecular mapping of powdery mildew resistance gene Eg-3 in cultivated oat (Avena sativa L. cv. Rollo).

    abstract：:Powdery mildew is a prevalent fungal disease affecting oat (Avena sativa L.) production in Europe. Common oat cultivar Rollo was previously shown to carry the powdery mildew resistance gene Eg-3 in common with cultivar Mostyn. The resistance gene was mapped with restriction fragment length polymorphism (RFLP) markers ...

    journal_title：Journal of applied genetics

    pub_type： 杂志文章

    doi：10.1007/s13353-011-0077-6

    authors： Mohler V,Zeller FJ,Hsam SL

    更新日期：2012-05-01 00:00:00

  • Splicing mutations in human genetic disorders: examples, detection, and confirmation.

    abstract：:Precise pre-mRNA splicing, essential for appropriate protein translation, depends on the presence of consensus "cis" sequences that define exon-intron boundaries and regulatory sequences recognized by splicing machinery. Point mutations at these consensus sequences can cause improper exon and intron recognition and ma...

    journal_title：Journal of applied genetics

    pub_type： 杂志文章,评审

    doi：10.1007/s13353-018-0444-7

    authors： Anna A,Monika G

    更新日期：2018-08-01 00:00:00

  • Chromosome abnormalities without phenotypic consequences.

    abstract：:Some changes in chromosome morphology, detected during cytogenetic analysis, are not associated with clinical defects. Therefore a proper discrimination of harmless variants from true abnormalities, especially during prenatal diagnosis, is crucial to allow precise counseling. In this review we described chromosome var...

    journal_title：Journal of applied genetics

    pub_type： 杂志文章,评审

    doi：10.1007/BF03194674

    authors： Kowalczyk M,Srebniak M,Tomaszewska A

    更新日期：2007-01-01 00:00:00

  • Mapping QTLs for pre-harvest sprouting tolerance on chromosome 2D in a synthetic hexaploid wheat x common wheat cross.

    abstract：:Based on segregation distortion of simple sequence repeat (SSR) molecular markers, we detected a significant quantitative trait loci (QTL) for pre-harvest sprouting (PHS) tolerance on the short arm of chromosome 2D (2DS) in the extremely susceptible population of F2 progeny generated from the cross of PHS tolerant syn...

    journal_title：Journal of applied genetics

    pub_type： 杂志文章

    doi：10.1007/BF03195631

    authors： Ren XB,Lan XJ,Liu DC,Wang JL,Zheng YL

    更新日期：2008-01-01 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

  • A simplified AFLP method for fingerprinting of common wheat (Triticum aestivum L.) cultivars.

    abstract：:The simplified AFLP method was developed and evaluated for identification and genetic diversity studies of wheat cultivars. Selective primers exploited in AFLP assay based on a single cutting enzyme PstI ((PstI)AFLP) generated total of 111 robust fragments, including 67 (60%) monomorphic and 12 (11%) cultivar-specific...

    journal_title：Journal of applied genetics

    pub_type： 杂志文章

    doi：

    authors： Tyrka M

    更新日期：2002-01-01 00:00:00

  • Biallelic mutations in CYP24A1 or SLC34A1 as a cause of infantile idiopathic hypercalcemia (IIH) with vitamin D hypersensitivity: molecular study of 11 historical IIH cases.

    abstract：:Idiopathic infantile hypercalcemia (IIH) is a mineral metabolism disorder characterized by severe hypercalcemia, failure to thrive, vomiting, dehydration, and nephrocalcinosis. The periodical increase in incidence of IIH, which occurred in the twentieth century in the United Kingdom, Poland, and West Germany, turned o...

    journal_title：Journal of applied genetics

    pub_type： 杂志文章

    doi：10.1007/s13353-017-0397-2

    authors： Pronicka E,Ciara E,Halat P,Janiec A,Wójcik M,Rowińska E,Rokicki D,Płudowski P,Wojciechowska E,Wierzbicka A,Książyk JB,Jacoszek A,Konrad M,Schlingmann KP,Litwin M

    更新日期：2017-08-01 00:00:00

  • Genetic relationships among wheat genotypes, as revealed by microsatellite markers and pedigree analysis.

    abstract：:Genetic relationships among 20 elite wheat genotypes were studied using microsatellite markers and pedigree analysis. A total of 93 polymorphic bands were obtained with 25 microsatellite primer pairs. Coefficient of parentage (COP) values were calculated using parentage information at the expansion level of 5. The ped...

    journal_title：Journal of applied genetics

    pub_type： 杂志文章

    doi：

    authors： Sud S,Bains NS,Nanda GS

    更新日期：2005-01-01 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

  • Identification of novel candidate genes for the inverted teat defect in sows using a genome-wide marker panel.

    abstract：:The number of functional teats is an important selection criterion in pig breeding. Inherited defects of the udder, such as the inverted teat, do have a considerable negative impact on the nursing ability of the sow. To investigate the genetic background of this defect and the number of functional teats in Swedish mat...

    journal_title：Journal of applied genetics

    pub_type： 杂志文章

    doi：10.1007/s13353-016-0382-1

    authors： Chalkias H,Jonas E,Andersson LS,Jacobson M,de Koning DJ,Lundeheim N,Lindgren G

    更新日期：2017-05-01 00:00:00

  • Subtelomeric rearrangements in Polish subjects with intellectual disability and dysmorphic features.

    abstract：:Fluorescent in situ hybridization (FISH) was performed in 76 patients referred to our department because of intellectual disability and dysmorphic features that can be related to subtelomeric microaberrations. In all the patients, conventional cytogenetic methods revealed normal karyotype. Four (5.3%) subtelomeric rea...

    journal_title：Journal of applied genetics

    pub_type： 杂志文章

    doi：10.1007/BF03195731

    authors： Bogdanowicz J,Pawłowska B,Ilnicka A,Gawlik-Zawiślak S,Jóźwiak A,Sobiczewska B,Zdzienicka E,Korniszewski L,Zaremba J

    更新日期：2010-01-01 00:00:00