Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 3 de 3
Filter
Add more filters










Database
Language
Publication year range
1.
PLoS One ; 12(1): e0170618, 2017.
Article in English | MEDLINE | ID: mdl-28118403

ABSTRACT

Brachypodium distachyon (Brachypodium) is now intensively utilized as a model grass species in various biological studies. Its favorable cytological features create a unique foundation for a convenient system in mutagenesis, thereby potentially enabling the 'hot spots' and 'cold spots' of DNA damage in its genome to be analyzed. The aim of this study was to analyze the involvement of 5S rDNA, 25S rDNA, the Arabidopsis-type (TTTAGGG)n telomeric sequence and the Brachypodium-originated centromeric BAC clone CB33J12 in the micronuclei formation in Brachypodium root tip cells that were subjected to the chemical clastogenic agent maleic hydrazide (MH). To the best of our knowledge, this is the first use of a multicolor fluorescence in situ hybridization (mFISH) with four different DNA probes being used simultaneously to study plant mutagenesis. A quantitative analysis allowed ten types of micronuclei, which were characterized by the presence or absence of specific FISH signal(s), to be distinguished, thus enabling some specific rules governing the composition of the MH-induced micronuclei with the majority of them originating from the terminal regions of chromosomes, to be identified. The application of rDNA sequences as probes showed that 5S rDNA-bearing chromosomes are involved in micronuclei formation more frequently than the 25S rDNA-bearing chromosomes. These findings demonstrate the promising potential of Brachypodium to be a useful model organism to analyze the effects of various genotoxic agents on the plant nuclear genome stability, especially when the complex FISH-based and chromosome-specific approaches such as chromosome barcoding and chromosome painting will be applied in future studies.


Subject(s)
Brachypodium/genetics , Chromosome Painting/methods , Chromosomes, Plant/drug effects , Maleic Hydrazide/pharmacology , Micronuclei, Chromosome-Defective/chemically induced , Micronucleus Tests/methods , Mutagenesis , Mutagens/pharmacology , Brachypodium/drug effects , Centromere/drug effects , Centromere/ultrastructure , Chromosomes, Artificial, Bacterial/drug effects , Chromosomes, Plant/ultrastructure , DNA Probes , DNA, Ribosomal/genetics , Genome, Plant , Germination , Interphase , Mitosis , Plant Roots , RNA, Plant/biosynthesis , RNA, Plant/genetics , Seeds/drug effects , Telomere/drug effects , Telomere/ultrastructure
2.
Sci Rep ; 6: 21066, 2016 Feb 15.
Article in English | MEDLINE | ID: mdl-26875499

ABSTRACT

Disorazol, a macrocyclic polykitide produced by the myxobacterium Sorangium cellulosum So ce12 and it is reported to have potential cytotoxic activity towards several cancer cell lines, including multi-drug resistant cells. The disorazol biosynthetic gene cluster (dis) from Sorangium cellulosum (So ce12) was identified by transposon mutagenesis and cloned in a bacterial artificial chromosome (BAC) library. The 58-kb dis core gene cluster was reconstituted from BACs via Red/ET recombineering and expressed in Myxococcus xanthus DK1622. For the first time ever, a myxobacterial trans-AT polyketide synthase has been expressed heterologously in this study. Expression in M. xanthus allowed us to optimize the yield of several biosynthetic products using promoter engineering. The insertion of an artificial synthetic promoter upstream of the disD gene encoding a discrete acyl transferase (AT), together with an oxidoreductase (Or), resulted in 7-fold increase in disorazol production. The successful reconstitution and expression of the genetic sequences encoding for these promising cytotoxic compounds will allow combinatorial biosynthesis to generate novel disorazol derivatives for further bioactivity evaluation.


Subject(s)
Biosynthetic Pathways/genetics , Genetic Engineering , Recombination, Genetic , Cell Line, Tumor/drug effects , Chromosomes, Artificial, Bacterial/drug effects , Escherichia coli/genetics , Gene Expression Regulation, Bacterial , Humans , Multigene Family , Mutagenesis , Myxococcus xanthus/genetics , Myxococcus xanthus/metabolism , Oxazoles/metabolism
3.
Insect Mol Biol ; 22(5): 473-84, 2013 Oct.
Article in English | MEDLINE | ID: mdl-23841833

ABSTRACT

The western corn rootworm, Diabrotica virgifera virgifera, is a damaging pest of cultivated corn that was controlled by applications of cyclodiene insecticides from the late 1940s until resistance evolved ∼10 years later. Range expansion from the western plains into eastern USA coincides with resistance development. An alanine to serine amino acid substitution within the Rdl subunit of the gamma-aminobutyric acid (GABA) receptor confers resistance to cyclodiene insecticides in many species. We found that the non-synonymous single nucleotide polymorphism (SNP) G/T at the GABA receptor cDNA position 838 (G/T(838)) of D. v. virgifera resulted in the alanine to serine change, and the codominant SNP allele T(838) was genetically linked to survival of beetles in aldrin bioassays. A phenotypic gradient of decreasing susceptibility from west to east was correlated with higher frequencies of the resistance-conferring T(838) allele in the eastern-most populations. This pattern exists in opposition to perceived selective pressures since the more eastern and most resistant populations probably experienced reduced exposure. The reasons for the observed distribution are uncertain, but historical records of the range expansion combined with the distribution of susceptible and resistant phenotypes and genotypes provide an opportunity to better understand factors affecting the species' range expansion.


Subject(s)
Aldrin/toxicity , Coleoptera/genetics , Evolution, Molecular , Hydrocarbons, Chlorinated/toxicity , Insecticide Resistance/genetics , Insecticides/toxicity , Mutation , Receptors, GABA/genetics , Animals , Biological Assay/methods , Chromosomes, Artificial, Bacterial/drug effects , Chromosomes, Artificial, Bacterial/genetics , Coleoptera/metabolism , Insecticide Resistance/physiology , North America , Polymorphism, Single Nucleotide/drug effects , Receptors, GABA/physiology , Sequence Analysis, DNA
SELECTION OF CITATIONS
SEARCH DETAIL
...