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1.
PLoS One ; 8(11): e79385, 2013.
Article in English | MEDLINE | ID: mdl-24244492

ABSTRACT

The transposons of the Bari family are mobile genetic elements widespread in the Drosophila genus. However, despite a broad diffusion, virtually no information is available on the mechanisms underlying their mobility. In this paper we report the functional characterization of the Bari elements transposition system. Using the Bari1 element as a model, we investigated the subcellular localization of the transposase, its physical interaction with the transposon, and its catalytic activity. The Bari1 transposase localized in the nucleus and interacted with the terminal sequences of the transposon both in vitro and in vivo, however, no transposition activity was detected in transposition assays. Profiling of mRNAs expressed by the transposase gene revealed the expression of abnormal, internally processed transposase transcripts encoding truncated, catalytically inactive transposase polypeptides. We hypothesize that a post-transcriptional control mechanism produces transposase-derived polypeptides that effectively repress transposition. Our findings suggest further clues towards understanding the mechanisms that control transposition of an important class of mobile elements, which are both an endogenous source of genomic variability and widely used as transformation vectors/biotechnological tools.


Subject(s)
DNA Transposable Elements , Drosophila/genetics , Drosophila/metabolism , Transposases/metabolism , Amino Acid Sequence , Animals , Cell Line , Drosophila Proteins/genetics , Heat-Shock Proteins/genetics , Humans , Intracellular Space/metabolism , Inverted Repeat Sequences , Male , Molecular Sequence Data , Mutation , Nucleic Acid Conformation , Protein Binding , Protein Transport , RNA Splicing , Sequence Alignment , Transcription, Genetic , Transposases/chemistry , Transposases/genetics
2.
Biol Trace Elem Res ; 143(1): 518-29, 2011 Oct.
Article in English | MEDLINE | ID: mdl-20882365

ABSTRACT

The present study investigated the effects of using arsenic (As) contaminated irrigation water in Lactuca sativa L. cropping. Two different arsenic concentrations, i.e., 25 and 85 µg L(-1) and two different soils, i.e., sandy and clay loam, were taken into account. We determined the arsenic mobility in the different soil fractions, its amount in groundwater, and the phytotoxicity and genotoxicity. Nuclear magnetic resonance (NMR) and inductively coupled plasma (ICP) were used to assess the lettuce metabolic profile changes and the arsenic uptake by the plant, respectively, as a function of the various conditions studied, i.e., As content and type of soil. Data indicated that at both concentrations in sandy soil, arsenic is in part quickly leached and thus present in groundwater and in part absorbed by the vegetable, being therefore readily available for assimilation by consumption. NMR results reported a large modification of the metabolic pattern, which was depending on the pollutant amount. In clay loam soil, the groundwater had a low As content with respect to sandy soil, and NMR and ICP performed on the lettuce did not reveal severe changes related to As, most likely because the metalloid is bound to the colloidal fraction.


Subject(s)
Arsenic/toxicity , Groundwater/analysis , Lactuca/drug effects , Soil/analysis , Water Pollutants, Chemical/toxicity , Agricultural Irrigation , Magnetic Resonance Spectroscopy
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