Screening and identification of a microsatellite marker associated with sex in Wami tilapia, Oreochromis urolepis hornorum.

Abstract:

:In this study, primer pairs of 15 microsatellite markers associated with sex determination of tilapia were selected and amplified in Wami tilapia, Oreochromis urolepis hornorum. While one marker, UNH168, on linkage group 3 (LG3) was associated (P <0.001) with the phenotypic sex in the experimental population, nine genotypes were detected in both sexes. Only 99-bp allele was detected in the female samples, while 141, 149 and 157-bp alleles were present in both male and female samples. UNH168 was localized by fluorescence in situ hybridization (FISH) on the long arm of the largest tilapia chromosome pair (chromosome 1, equivalent to LG3). This sex-linked microsatellite marker could potentially be used for marker-assisted selection in tilapia breeding programmes to produce monosex male tilapia.

journal_name

J Genet

journal_title

Journal of genetics

authors

Zhu H,Liu Z,Lu M,Gao F,Ke X,Ma D,Huang Z,Cao J,Wang M

doi

10.1007/s12041-016-0653-y

subject

Has Abstract

pub_date

2016-06-01 00:00:00

pages

283-9

issue

2

eissn

0022-1333

issn

0973-7731

journal_volume

95

pub_type

杂志文章
  • Signatures of positive selection on the hepatic lipase gene in human populations.

    abstract::The hepatic lipase plays a central role in the lipid metabolism, catalyzing the hydrolysis of phospholipids, monoglycerides, diglycerides, and triglycerides, and acyl-CoA. It is also implied in the conversion of very low-density lipoprotein and intermediate density lipoprotein to low density lipoproteins. As a consequ...

    journal_title:Journal of genetics

    pub_type: 杂志文章

    doi:

    authors: Flores SV,Olivari CF,Prado LF

    更新日期:2020-03-01 00:00:00

  • Molecular population genetics of the beta-esterase gene cluster of Drosophila melanogaster.

    abstract::We have investigated nucleotide polymorphism at the beta-esterase gene cluster including the Est-6 gene and psiEst-6 putative pseudogene in four samples of Drosophila melanogaster derived from natural populations of southern Africa (Zimbabwe), Europe (Spain), North America (USA: California), and South America (Venezue...

    journal_title:Journal of genetics

    pub_type: 杂志文章

    doi:10.1007/BF02715813

    authors: Balakirev ES,Ayala FJ

    更新日期:2003-12-01 00:00:00

  • Eight paths of ERK1/2 signalling pathway regulating hepatocyte proliferation in rat liver regeneration.

    abstract::Although it is known that hormones, growth factors and integrin promote hepatocyte proliferation in liver regeneration (LR) through ERK1/2 signalling pathway, reports about regulating processes of its intracellular paths in hepatocytes of LR are limited. This study aims at exploring which paths of ERK1/2 signalling pa...

    journal_title:Journal of genetics

    pub_type: 杂志文章

    doi:

    authors: Li JW,Wang GP,Fan JY,Chang CF,Xu CS

    更新日期:2011-12-01 00:00:00

  • Accelerated molecular evolution of insect orthologues of ERG28/C14orf1: a link with ecdysteroid metabolism?

    abstract::We have analysed the evolution of ERG28/C14orf1, a gene coding for a protein involved in sterol biosynthesis. While primary sequence of the protein is well conserved in all organisms able to synthesize sterols de novo, strong divergence is noticed in insects, which are cholesterol auxotrophs. In spite of this virtual ...

    journal_title:Journal of genetics

    pub_type: 杂志文章

    doi:10.1007/BF02811414

    authors: Veitia RA,Hurst LD

    更新日期:2001-04-01 00:00:00

  • Genetic diversity, population structure and marker trait associations for seed quality traits in cotton (Gossypium hirsutum).

    abstract::Cottonseed contains 16% seed oil and 23% seed protein by weight. High levels of palmitic acid provides a degree of stability to the oil, while the presence of bound gossypol in proteins considerably changes their properties, including their biological value. This study uses genetic principles to identify genomic regio...

    journal_title:Journal of genetics

    pub_type: 杂志文章

    doi:10.1007/s12041-015-0489-x

    authors: Badigannavar A,Myers GO

    更新日期:2015-03-01 00:00:00

  • Pleiotropic phenotypes of the salt-tolerant and cytosine hypomethylated leafless inflorescence, evergreen dwarf and irregular leaf lamina mutants of Catharanthus roseus possessing Mendelian inheritance.

    abstract::In Catharanthus roseus, three morphological cum salt-tolerant chemically induced mutants of Mendelian inheritance and their wild-type parent cv Nirmal were characterized for overall cytosine methylation at DNA repeats, expression of 119 protein coding and seven miRNA-coding genes and 50 quantitative traits. The mutant...

    journal_title:Journal of genetics

    pub_type: 杂志文章

    doi:10.1007/s12041-013-0271-x

    authors: Kumari R,Sharma V,Sharma V,Kumar S

    更新日期:2013-12-01 00:00:00

  • Genetics of fruit yield and its component traits under different fruiting habit backgrounds in chilli (Capsicum annuum L.).

    abstract::The six basic generations (two parents, F1, F2 and backcrosses) of 14 crosses developed from nine parents differing in fruits node-1 and fruit orientation were evaluated to decipher the genetics of three quantitative traits (average fruit weight, fruits plant-1 and green fruit yield plant-1) during the rainly season o...

    journal_title:Journal of genetics

    pub_type: 杂志文章

    doi:

    authors: Anilkumar C,Mohan Rao A,Ramesh S,Bhavani B,Pranesh

    更新日期:2019-09-01 00:00:00

  • Analysis of novel domain-specific mutations in the zebrafish ndr2/cyclops gene generated using CRISPR-Cas9 RNPs.

    abstract::Nodal-related protein (ndr2) is amember of the transforming growth factor type β superfamily of factors and is required for ventral midline patterning of the embryonic central nervous system in zebrafish. In humans, mutations in the gene encoding nodal cause holoprosencephaly and heterotaxy. Mutations in the ndr2 gene...

    journal_title:Journal of genetics

    pub_type: 杂志文章

    doi:

    authors: Turner AN,Andersen RS,Bookout IE,Brashear LN,Davis JC,Gahan DM,Davis JC,Gotham JP,Hijaz BA,Kaushik AS,Mcgill JB,Miller VL,Moseley ZP,Nowell CL,Patel RK,Rodgers MC,Patel RK,Shihab YA,Walker AP,Glover SR,Foster SD,

    更新日期:2018-12-01 00:00:00

  • Axial distortion as a sensor of supercoil changes: a molecular model for the homeostatic regulation of DNA gyrase.

    abstract::Negative supercoiling stimulates transcription of many genes. In contrast, transcription of the genes coding for DNA gyrase is subject to a novel mechanism of autoregulation, wherein relaxation of the template DNA stimulates their transcription. Since DNA gyrase is the sole supercoiling activity in the eubacterial cel...

    journal_title:Journal of genetics

    pub_type: 杂志文章

    doi:10.1007/BF02717907

    authors: Unniraman S,Nagaraja V

    更新日期:2001-12-01 00:00:00

  • Ellis-van Creveld syndrome and profound deafness resulted by sequence variants in the EVC/EVC2 and TMC1 genes.

    abstract::Ellis-van Creveld syndrome is an autosomal recessive skeletal dysplasia primarily characterized by the features such as disproportionate dwarfism, short ribs, short limbs, dysplastic nails, cardiovascular malformations, post-axial polydactyly (PAP) (bilateral) of hands and feet. EVC/EVC2 located in head-to-head arrang...

    journal_title:Journal of genetics

    pub_type: 杂志文章

    doi:10.1007/s12041-017-0868-6

    authors: Umair M,Seidel H,Ahmed I,Ullah A,Haack TB,Alhaddad B,Jan A,Rafique A,Strom TM,Ahmad F,Meitinger T,Ahmad W

    更新日期:2017-12-01 00:00:00

  • Multidimensional analysis of Drosophila wing variation in Evolution Canyon.

    abstract::Environmental stress has been suggested to be a major evolutionary force, both through inducing strong selection and because of its direct impact on developmental buffering processes that alter the evolvability of organisms. In particular, temperature has attracted much attention because of its importance as an ecolog...

    journal_title:Journal of genetics

    pub_type: 杂志文章

    doi:10.1007/s12041-008-0063-x

    authors: Debat V,Cornette R,Korol AB,Nevo E,Soulet D,David JR

    更新日期:2008-12-01 00:00:00

  • Advances in the discovery of genetic risk factors for complex forms of neurodegenerative disorders: contemporary approaches, success, challenges and prospects.

    abstract::Neurodegenerative diseases constitute a large proportion of disorders in elderly, majority being sporadic in occurrence with ∼5-10% familial. A strong genetic component underlies the Mendelian forms but nongenetic factors together with genetic vulnerability contributes to the complex sporadic forms. Several gene disco...

    journal_title:Journal of genetics

    pub_type: 杂志文章,评审

    doi:

    authors: Kumar S,Yadav N,Pandey S,Thelma BK

    更新日期:2018-07-01 00:00:00

  • Correlation analysis of mandarin fish (Siniperca chuatsi) growth hormone gene polymorphisms and growth traits.

    abstract::Screening of trait-associated molecular markers can be used to enhance the efficiency of selective breeding. Previously, we produced the first high-density genetic linkage map for the mandarin fish (Siniperca chuatsi) and identified 11 quantitative-trait loci significantly associated with growth, of which one is locat...

    journal_title:Journal of genetics

    pub_type: 杂志文章

    doi:

    authors: Sun CF,Sun HL,Dong JJ,Tian YY,Hu J,Ye X

    更新日期:2019-06-01 00:00:00

  • Genetics of ulcerative colitis: putting into perspective the incremental gains from Indian studies.

    abstract::Ulcerative colitis (UC), one of the two clinical subtypes of inflammatory bowel disease is perceived as a potential 'sleeping giant' in the Indian subcontinent. Clinical manifestation is overall believed to be the same across ethnic groups but overwhelming genetics from large European and fewer non-European studies ha...

    journal_title:Journal of genetics

    pub_type: 杂志文章,评审

    doi:

    authors: Juyal G,Sood A,Midha V,Thelma BK

    更新日期:2018-12-01 00:00:00

  • MiR-27b promotes sheep skeletal muscle satellite cell proliferation by targeting myostatin gene.

    abstract::To investigate the role of miR-27b in sheep skeletal muscle development, here we first cloned the sequence of sheep pre-miR-27b, then further investigated its expression pattern in sheep skeletal muscle in vivo, the relationship of miR-27b expression and sheep skeletal muscle satellite cell proliferation and different...

    journal_title:Journal of genetics

    pub_type: 杂志文章

    doi:

    authors: Zhang W,Wang SY,Deng SY,Gao L,Yang LW,Liu XN,Shi GQ

    更新日期:2018-12-01 00:00:00

  • J. B. S. Haldane and the origin of life.

    abstract::In 1929 the British biologist John Burdon Sanderson Haldane published a hypothesis on the origin of life on earth, which was one of the most emblematic of the interwar period. It was a scenario describing the progressive evolution of matter on the primitive earth and the emergence of life. Firstly, this paper presents...

    journal_title:Journal of genetics

    pub_type: 传,历史文章,杂志文章

    doi:10.1007/s12041-017-0831-6

    authors: Tirard S

    更新日期:2017-11-01 00:00:00

  • The birth and development of the DNA theory of inheritance: sixty years since the discovery of the structure of DNA.

    abstract::The development of the DNA theory of inheritance culminated in the publication of the molecular structure of DNA 60 years ago. This paper describes this development, beginning with the discovery of DNA as a chemical substance by Friedrich Miescher in 1869, followed by its basic chemical analysis and demonstration of i...

    journal_title:Journal of genetics

    pub_type: 历史文章,杂志文章,评审

    doi:10.1007/s12041-014-0337-4

    authors: Portin P

    更新日期:2014-04-01 00:00:00

  • Fitness differences due to allelic variation at Esterase-4 locus in Drosophila ananassae.

    abstract::Esterases are known to play essential role inmetabolism, reproductive physiology and behaviour of Drosophila. Esterases are highly polymorphic enzymes in Drosophila, but the polymorphism of these enzymes is not well studied in Drosophila ananassae. Recent studies on esterase polymorphism in D. ananassae revealed that ...

    journal_title:Journal of genetics

    pub_type: 杂志文章

    doi:10.1007/s12041-017-0814-7

    authors: Krishnamoorti K,Singh AK

    更新日期:2017-09-01 00:00:00

  • Intraspecific chromosomal and genetic polymorphism in Brassica napus L. detected by cytogenetic and molecular markers.

    abstract::The application of DNA intercalator 9-aminoacridine allowed us to increase the resolution of chromosome C-banding and DAPI-banding patterns and to investigate chromosomal polymorphism in karyotypes of seven spring and six winter rape varieties. It was shown that the pericentromeric and intercalary C-bands of most of t...

    journal_title:Journal of genetics

    pub_type: 杂志文章

    doi:10.1007/s12041-014-0351-6

    authors: Amosova AV,Zemtsova LV,Grushetskaya ZE,Samatadze TE,Mozgova GV,Pilyuk YE,Volovik VT,Melnikova NV,Zelenin AV,Lemesh VA,Muravenko OV

    更新日期:2014-04-01 00:00:00

  • Meiotic behaviour of tetraploid wheats (Triticum turgidum L.) and their synthetic hexaploid wheat derivates influenced by meiotic restitution and heat stress.

    abstract::Meiotic restitution is considered to be a common mechanism of polyploidization in plants and hence is one of the most important processes in plant speciation. Meiotic behaviour of plant chromosomes is influenced by both genetic and environmental factors. In this study, the meiotic behaviour of cereal crops was investi...

    journal_title:Journal of genetics

    pub_type: 杂志文章

    doi:10.1007/s12041-010-0058-2

    authors: Rezaei M,Arzani A,Sayed-Tabatabaei BE

    更新日期:2010-12-01 00:00:00

  • Mutation analysis of codons 345 and 347 of rhodopsin gene in Indian retinitis pigmentosa patients.

    abstract::More than 100 mutations have been reported till date in the rhodopsin gene in patients with retinitis pigmentosa. The present study was undertaken to detect the reported rhodopsin gene point mutations in Indian retinitis pigmentosa patients. We looked for presence or absence of codon 345 and 347 mutations in exon 5 of...

    journal_title:Journal of genetics

    pub_type: 杂志文章

    doi:10.1007/BF02728336

    authors: Dikshit M,Agarwal R

    更新日期:2001-08-01 00:00:00

  • Genetics of sex determination in the haplodiploid wasp Nasonia vitripennis (Hymenoptera: Chalcidoidea).

    abstract::The parasitoid wasp Nasonia vitripennis reproduces by haplodiploidy; males are haploid and females are diploid. Sex determination in Nasonia is not governed by complementary alleles at one or more sex loci. As in most other insects, the sex-determining pathway consists of the basal switch doublesex that is sex-specifi...

    journal_title:Journal of genetics

    pub_type: 杂志文章

    doi:10.1007/s12041-010-0045-7

    authors: Beukeboom LW,van de Zande L

    更新日期:2010-09-01 00:00:00

  • Case report of newborn with de novo partial trisomy 2q31.2-37.3 and monosomy 9p24.3.

    abstract::We describe a newborn female with a de novo duplication of chromosomes 2q31.2 and 2q37.3, and a de novo monosomy 9p24.3. The clinical findings of this patient include congenital heart defects, dysmorphic facial features, hypotonia, feeding difficulties and microcephaly. Ultrasonographic prenatal findings were negative...

    journal_title:Journal of genetics

    pub_type: 杂志文章

    doi:

    authors: Colangelo M,Alfonsi M,Palka C,Zio EZ,Renzo SD,Guanciali-Franchi P,Palka G

    更新日期:2018-03-01 00:00:00

  • Psychiatric features and variable neurodevelopment outcome in four females with IQSEC2 spectrum disorder.

    abstract::IQSEC2 is an X-linked gene highly expressed at the excitatory synapses where it plays a crucial role in α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptor trafficking and synaptic plasticity. To date, several males and females with severe to profound intellectual disability have been reported harbouring fra...

    journal_title:Journal of genetics

    pub_type: 杂志文章

    doi:

    authors: Accogli A,Eric Jarvis G,Schiavetto A,Lai L,Amirali EL,Jimenez Cruz DA,Rivière JB,Trakadis Y

    更新日期:2020-01-01 00:00:00

  • Molecular genetic analysis of consanguineous families with primary microcephaly identified pathogenic variants in the ASPM gene.

    abstract::Autosomal recessive primary microcephaly is a rare genetic disorder that is characterized by reduced head circumference and a varying degree of intellectual disability. Genetic studies on consanguineous families with primary microcephaly have identified 15 (MCPH) causative genes that include MCPH1, WDR62, CDK5RAP2, CA...

    journal_title:Journal of genetics

    pub_type: 杂志文章

    doi:10.1007/s12041-017-0759-x

    authors: Khan MA,Windpassinger C,Ali MZ,Zubair M,Gul H,Abbas S,Khan S,Badar M,Mohammad RM,Nawaz Z

    更新日期:2017-06-01 00:00:00

  • Time for the zebrafish ENCODE.

    abstract::Genomics research in recent years, especially the human ENCODE project, have made great strides in understanding the genomic and epigenomic structure and organization of humans. These advances promise a new era of precision medicine, through a better understanding of the genomic correlates of human physiology and prom...

    journal_title:Journal of genetics

    pub_type: 杂志文章

    doi:10.1007/s12041-013-0313-4

    authors: Sivasubbu S,Sachidanandan C,Scaria V

    更新日期:2013-12-01 00:00:00

  • Drosophila simulans Lethal hybrid rescue mutation (Lhr) rescues inviable hybrids by restoring X chromosomal dosage compensation and causes fluctuating asymmetry of development.

    abstract::The Drosophila simulans Lhr rescues lethal hybrids from the cross of D. melanogaster and D. simulans. We describe here, the phenotypes of Lhr dependent rescue hybrids and demonstrate the effects of Lhr on functional morphology of the salivary chromosomes in the hybrids. Our results reveal that the phenotypes of the 'L...

    journal_title:Journal of genetics

    pub_type: 杂志文章

    doi:10.1007/s12041-007-0028-5

    authors: Chatterjee RN,Chatterjee P,Pal A,Pal-Bhadra M

    更新日期:2007-12-01 00:00:00

  • Novel alternatively spliced isoforms of MEF2A and their mRNA expression patterns in pigs.

    abstract::The present study aimed to identify the alternatively spliced isoforms of pig MEF2A gene and to determine theirmRNA expression patterns. Four alternatively spliced isoforms of pig MEF2A gene (i.e. MEF2A1, MEF2A2, MEF2A3 and MEF2A4) were cloned according to the results of transcriptome sequencing. The fifth to eighth e...

    journal_title:Journal of genetics

    pub_type: 杂志文章

    doi:

    authors: Guo XH,Zhang Q,Li M,Gao PF,Cao GQ,Cheng ZM,Zhang NF,Yu Le B,Liu JF,Liu XJ,Li BG

    更新日期:2018-09-01 00:00:00

  • Cloning, characterization and promoter analysis of common carp hairy/Enhancer-of-split-related gene, her6.

    abstract::Some members of hairy/Enhancer-of-split-related gene (HES) family have important effects on axial mesoderm segmentation and the establishment and maintenance of the somite fringe. In fishes, the her6 gene, a member of the HES family, is the homologue of hes1 in mammals and chicken. In this study, the her6 gene and its...

    journal_title:Journal of genetics

    pub_type: 杂志文章

    doi:10.1007/BF02935327

    authors: Liu J,Sun YH,Wang N,Wang YP,Zhu ZY

    更新日期:2006-12-01 00:00:00

  • Chromosomal structural changes and microsatellite variations in newly synthesized hexaploid wheat mediated by unreduced gametes.

    abstract::Allohexaploid wheat was derived from interspecific hybridization, followed by spontaneous chromosome doubling. Newly synthesized hexaploid wheat by crossing Triticum turgidum and Aegilops tauschii provides a classical model to understand the mechanisms of allohexaploidization in wheat. However, immediate chromosome le...

    journal_title:Journal of genetics

    pub_type: 杂志文章

    doi:10.1007/s12041-016-0704-4

    authors: Li H,Wang Y,Guo X,Du Y,Wang C,Ji W

    更新日期:2016-12-01 00:00:00