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 related with sexual maturation, and b) all-female stocks, of higher growth rate. Triploidy was induced by means of a cold shock. Gynogenesis was induced by activating eggs with UV-irradiated sperm, and to prompt diploid gynogenesis, a cold-shock step was also used. Ploidy of putative triploid larvae and gynogenetic embryos were determined by means of karyotyping and microsatellite analysis. Haploid gynogenetic embryos showed the typical "haploid syndrome". As expected, triploid and gynogenetic groups showed lower fertilization, hatching, and survival rates than in the diploid control group. Survival rate, calculated 49 days after hatching, for haploid and diploid gynogenetic groups was similar to those observed in other fish species (0% and 62.5%, respectively), whereas triploids showed worse values (45%). Sex was determined macroscopically and by histological procedures, revealing that all the diploid gynogenetic individuals were females. In conclusion, we have successfully applied chromosomal-manipulation techniques in the flatfish species Senegalese sole in order to produce triploid, haploid, and diploid gynogenetic progenies.
journal_name
J Appl Genetjournal_title
Journal of applied geneticsauthors
Molina-Luzón MJ,López JR,Robles F,Navajas-Pérez R,Ruiz-Rejón C,De la Herrán R,Navas JIdoi
10.1007/s13353-014-0233-xsubject
Has Abstractpub_date
2015-02-01 00:00:00pages
77-84issue
1eissn
1234-1983issn
2190-3883journal_volume
56pub_type
杂志文章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
更新日期:2008-01-01 00:00:00
abstract::Selective DNA pooling is an advanced methodology for linkage mapping of quantitative trait loci (QTL) in farm animals. The principle is based on densitometric estimates of marker allele frequency in pooled DNA samples of phenotypically extreme individuals from half-sib, backcross and F(2) experimental designs in farm ...
journal_title:Journal of applied genetics
pub_type: 杂志文章,评审
doi:
更新日期:2002-01-01 00:00:00
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
更新日期:2012-08-01 00:00:00
abstract::The glyceraldehyde-3-phosphate dehydrogenase promoter of the food yeast Candida utilis strain NRRL Y-660 was cloned to create a novel integrative vector for Agrobacterium tumefaciens-mediated transformation. The new binary vector harbors β-glucuronidase activity as reporter and kanamicin/geneticin resistance as select...
journal_title:Journal of applied genetics
pub_type: 杂志文章
doi:10.1007/s13353-013-0162-0
更新日期:2013-11-01 00:00:00
abstract::Proper epigenetic regulation processes are crucial in the normal development of the human brain. An ever-increasing group of neurodevelopmental disorders due to derangements of epigenetic regulation involve both microdeletion and monogenic syndromes. Some of these syndromes have overlapping clinical phenotypes due to ...
journal_title:Journal of applied genetics
pub_type: 杂志文章
doi:10.1007/s13353-017-0408-3
更新日期:2017-11-01 00:00:00
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:
更新日期:2005-01-01 00:00:00
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
更新日期:2015-05-01 00:00:00
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 ke...
journal_title:Journal of applied genetics
pub_type: 杂志文章
doi:
更新日期:2000-01-01 00:00:00
abstract::The type-B authentic response regulators (ARR-Bs) function as positive regulators of cytokinin signal transduction and play important roles in abiotic stress resistance and plant development. However, little of ARR-B family is known in tomato. In this study, we performed a comprehensive analysis of ARR-B family factor...
journal_title:Journal of applied genetics
pub_type: 杂志文章
doi:10.1007/s13353-020-00565-5
更新日期:2020-09-01 00:00:00
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
更新日期:2017-02-01 00:00:00
abstract::Laminopathies, a group of heterogeneous disorders associated with lamin A/C gene (LMNA) mutations, encompass a wide spectrum of clinical phenotypes, which may present as separate disease or as overlapping syndromes. We describe a 35-year-old female in whom a novel sporadic heterozygous mutation c.1001_1003delGCC (p.Se...
journal_title:Journal of applied genetics
pub_type: 杂志文章
doi:10.1007/s13353-016-0365-2
更新日期:2017-02-01 00:00:00
abstract::The milk fatty acid (FA) profile is far from the optimal fat composition in regards to human health. The natural sources of variation, such as feeding or genetics, could be used to increase the concentrations of unsaturated fatty acids. The impact of feeding is well described. However, genetic effects on the milk FA c...
journal_title:Journal of applied genetics
pub_type: 杂志文章
doi:10.1007/BF03195649
更新日期:2009-01-01 00:00:00
abstract::Deoxyguanosine kinase deficiency (dGK) is a frequent cause of the hepatocerebral form of mitochondrial depletion syndrome (MDS). A group of 28 infants with severe progressive liver failure of unknown cause was recruited for post mortem search for deoxyguanosine kinase (DGUOK) gene mutations. Four affected patients (14...
journal_title:Journal of applied genetics
pub_type: 杂志文章
doi:10.1007/s13353-010-0008-y
更新日期:2011-02-01 00:00:00
abstract::Investigations on the impact of chemicals on the environment and human health have led to the development of an exposome concept. The exposome refers to the totality of exposures received by a person during life, including exposures to life-style factors, from the prenatal period to death. The exposure to genotoxic ch...
journal_title:Journal of applied genetics
pub_type: 杂志文章,评审
doi:10.1007/s13353-016-0380-3
更新日期:2017-08-01 00:00:00
abstract::Hemp (Cannabis sativa L.) is a species considered as having one of the most complicated mechanisms of sex determination. Peroxidase and esterase isoenzymes in leaves of the two sexual phenotypes of hemp were studied. Significant differences in isoperoxidase and isoesterase patterns were found between male and female p...
journal_title:Journal of applied genetics
pub_type: 杂志文章
doi:
更新日期:2002-01-01 00:00:00
abstract::Functional lox-like sequences have been identified within the yeast and mammalian genome. These hetero-specific lox sites also allow Cre recombinase to specifically target efficient integration of exogenous DNA into the endogenous pseudo-lox (ψlox) sequences that occur naturally in the host genome using a Cre/loxP int...
journal_title:Journal of applied genetics
pub_type: 杂志文章
doi:10.1007/s13353-010-0011-3
更新日期:2011-02-01 00:00:00
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:
更新日期:2004-01-01 00:00:00
abstract::The long QT syndrome (LQTS) is an inherited cardiac arrhythmia that may lead to sudden death in the absence of structural heart disease. Mutations in the cardiac potassium and sodium channel genes can be found in approximately 70 percent of patients with a highly probable clinical diagnosis. In this study, we aimed to...
journal_title:Journal of applied genetics
pub_type: 杂志文章
doi:10.1007/BF03208882
更新日期:2010-01-01 00:00:00
abstract::The distinctness, uniformity and stability (DUS) requirements involve expensive, space- and time-consuming measurements of morphological traits. Moreover, for a majority of traits, interactions between genotype and environment complicate the evaluation. Molecular markers have a potential to facilitate this procedure, ...
journal_title:Journal of applied genetics
pub_type: 杂志文章
doi:10.1007/BF03195609
更新日期:2008-01-01 00:00:00
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
更新日期:2017-05-01 00:00:00
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
更新日期:2011-11-01 00:00:00
abstract::The role of genetic background in childhood-onset combined pituitary hormone deficiency (CPHD) has been extensively studied. The major contributors are the PROP1, POU1F1, LHX3, LHX4 and HESX1 genes coding transcription factors implicated in pituitary organogenesis. The clinical consequences of mutations encompass impa...
journal_title:Journal of applied genetics
pub_type: 杂志文章
doi:10.1007/s13353-015-0328-z
更新日期:2016-08-01 00:00:00
abstract::Mutagenicity refers to the induction of permanent changes in the DNA sequence of an organism, which may result in a heritable change in the characteristics of living systems. Antimutagenic agents are able to counteract the effects of mutagens. This group of agents includes both natural and synthetic compounds. Based o...
journal_title:Journal of applied genetics
pub_type: 杂志文章,评审
doi:10.1007/s13353-014-0198-9
更新日期:2014-05-01 00:00:00
abstract::The aim of this study was to assess the frequencies of three hemochromatosis gene (HFE) mutations in ethnic Roma/Gypsies in Slovakia. A cohort of 367 individuals representing general population and not preselected for health status was genotyped by TaqMan real-time PCR assay for C282Y, H63D and S65C mutations in HFE g...
journal_title:Journal of applied genetics
pub_type: 杂志文章
doi:10.1007/s13353-012-0088-y
更新日期:2012-05-01 00:00:00
abstract::Myogenic factor 5 (myf-5) is the product of the MYF5 gene, belonging to the MyoD family. This transcription factor participates in the control of myogenesis. We identified 3 new mutations in the promoter region of the gene: A65C, C580T and C613T. The aim of this study was to evaluate the influence of the A65C transver...
journal_title:Journal of applied genetics
pub_type: 杂志文章
doi:10.1007/BF03194600
更新日期:2006-01-01 00:00:00
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:
更新日期:2005-01-01 00:00:00
abstract::In addition to their normal developmental processes, plants have evolved complex genetic and epigenetic regulatory mechanisms to cope with various environmental stresses. It has been shown that both DNA methylation and histone modifications are involved in DNA damage response to various types of stresses. In this stud...
journal_title:Journal of applied genetics
pub_type: 杂志文章
doi:10.1007/s13353-014-0226-9
更新日期:2014-11-01 00:00:00
abstract::Starting from two datasets of codon usage in coding sequences from mesophilic and thermophilic bacteria, we used internal correspondence analysis to study the variability of codon usage within and between species, and within and between amino acids. The first dataset included 18,958,458 codons from 58,482 coding seque...
journal_title:Journal of applied genetics
pub_type: 杂志文章
doi:
更新日期:2003-01-01 00:00:00
abstract::The matrix metalloproteinase-2 gene (MMP2) was found to be associated with hip structure in pigs. Recently three quantitative trait loci (QTLs) for loin muscle area were found on chromosome 6, to which MMP2 was mapped. In the present study, association analyses were conducted in two pig populations for a single-nucleo...
journal_title:Journal of applied genetics
pub_type: 杂志文章
doi:10.1007/BF03195679
更新日期:2009-01-01 00:00:00
abstract::Arylamine N-acetyltransferase (NAT) genes were targeted for inhibition using short hairpin RNA (shRNA) using two different RNA polymerase III promoters. Constructs were developed for NAT1 and NAT2, the endogenous mouse genes, and for human NAT1. There were fetal and neonatal deaths with these constructs, perhaps due i...
journal_title:Journal of applied genetics
pub_type: 杂志文章
doi:
更新日期:2005-01-01 00:00:00