Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 5 de 5
Filter
Add more filters










Database
Language
Publication year range
1.
BMC Plant Biol ; 14: 343, 2014 Dec 10.
Article in English | MEDLINE | ID: mdl-25492565

ABSTRACT

BACKGROUND: Drought is by far the most important environmental factor contributing to yield losses in crops, including soybeans [Glycine max (L.) Merr.]. To address this problem, a gene that encodes an osmotin-like protein isolated from Solanum nigrum var. americanum (SnOLP) driven by the UBQ3 promoter from Arabidopsis thaliana was transferred into the soybean genome by particle bombardment. RESULTS: Two independently transformed soybean lines expressing SnOLP were produced. Segregation analyses indicated single-locus insertions for both lines. qPCR analysis suggested a single insertion of SnOLP in the genomes of both transgenic lines, but one copy of the hpt gene was inserted in the first line and two in the second line. Transgenic plants exhibited no remarkable phenotypic alterations in the seven analyzed generations. When subjected to water deficit, transgenic plants performed better than the control ones. Leaf physiological measurements revealed that transgenic soybean plants maintained higher leaf water potential at predawn, higher net CO2 assimilation rate, higher stomatal conductance and higher transpiration rate than non-transgenic plants. Grain production and 100-grain weight were affected by water supply. Decrease in grain productivity and 100-grain weight were observed for both transgenic and non-transgenic plants under water deficit; however, it was more pronounced for non-transgenic plants. Moreover, transgenic lines showed significantly higher 100-grain weight than non-transgenic plants under water shortage. CONCLUSIONS: This is the first report showing that expression of SnOLP in transgenic soybeans improved physiological responses and yield components of plants when subjected to water deficit, highlighting the potential of this gene for biotechnological applications.


Subject(s)
Gene Expression Regulation, Plant , Glycine max/genetics , Glycine max/metabolism , Plant Proteins/genetics , Solanum nigrum/genetics , Stress, Physiological/genetics , Water/metabolism , Droughts , Plant Leaves/metabolism , Plant Proteins/metabolism , Plants, Genetically Modified/genetics , Plants, Genetically Modified/metabolism
2.
Arch Virol ; 159(8): 1917-25, 2014 Aug.
Article in English | MEDLINE | ID: mdl-24562426

ABSTRACT

Hepatitis C virus (HCV) quasispecies constitute a dynamic population in a continuous process of variation and selection. To investigate effect of the immune system on the genetic variability of HCV, we compared the hypervariable region 1 (HVR1) of immunosuppressed patients with chronic renal failure (CRF group) to immunocompetent patients with HCV chronic infection (control group). The HVR1 from ten samples of each group was amplified, cloned and sequenced. The HCV quasispecies from the control group had a higher frequency of variable sites in HVR1 (83.9 % vs 59.3 %, p < 0.05), as well as a greater diversity within (intra-patient) and between samples, compared to the CRF group. The clustering of the majority of the quasispecies of the CRF group in the phylogenetic tree also showed the limited diversity of the quasispecies in immunosuppressed patients. Moreover, a higher variability of amino acids at positions 384, 386, 391, 394, 397, 398, 400, 405 and 410 was observed in the control group than in the CRF group, which showed a greater variability only at position 388 (p < 0.05). These data corroborates the hypothesis that the major selective pressure factor is the immune system, which promotes a high degree of diversity in the viral progeny and contributes to a constant evolution of HCV.


Subject(s)
Genetic Variation , Hepacivirus/genetics , Hepatitis C, Chronic/virology , Kidney Failure, Chronic/etiology , Adult , Aged , Brazil/epidemiology , Female , Hepacivirus/classification , Hepacivirus/isolation & purification , Hepacivirus/physiology , Hepatitis C, Chronic/complications , Humans , Kidney Failure, Chronic/virology , Male , Middle Aged , Molecular Sequence Data , Phylogeny , Young Adult
3.
BMC Genomics ; 14: 322, 2013 May 10.
Article in English | MEDLINE | ID: mdl-23663436

ABSTRACT

BACKGROUND: Root-knot nematodes (RKN- Meloidogyne genus) present extensive challenges to soybean crop. The soybean line (PI 595099) is known to be resistant against specific strains and races of nematode species, thus its differential gene expression analysis can lead to a comprehensive gene expression profiling in the incompatible soybean-RKN interaction. Even though many disease resistance genes have been studied, little has been reported about phytohormone crosstalk on modulation of ROS signaling during soybean-RKN interaction. RESULTS: Using 454 technology to explore the common aspects of resistance reaction during both parasitism and resistance phases it was verified that hormone, carbohydrate metabolism and stress related genes were consistently expressed at high levels in infected roots as compared to mock control. Most noteworthy genes include those encoding glycosyltransferases, peroxidases, auxin-responsive proteins and gibberellin-regulated genes. Our data analysis suggests the key role of glycosyltransferases, auxins and components of gibberellin signal transduction, biosynthesis and deactivation pathways in the resistance reaction and their participation in jasmonate signaling and redox homeostasis in mediating aspects of plant growth and responses to biotic stress. CONCLUSIONS: Based on this study we suggest a reasonable model regarding to the complex mechanisms of crosstalk between plant hormones, mainly gibberellins and auxins, which can be crucial to modulate the levels of ROS in the resistance reaction to nematode invasion. The model also includes recent findings concerning to the participation of DELLA-like proteins and ROS signaling controlling plant immune or stress responses. Furthermore, this study provides a dataset of potential candidate genes involved in both nematode parasitism and resistance, which can be tested further for their role in this biological process using functional genomics approaches.


Subject(s)
Disease Resistance/genetics , Gene Expression Profiling , Glycine max/parasitology , Host-Parasite Interactions , Plant Diseases/parasitology , Plant Growth Regulators/metabolism , Tylenchoidea/physiology , Animals , Gibberellins/metabolism , Indoleacetic Acids/metabolism , Plant Growth Regulators/genetics , Plant Proteins/genetics , Plant Proteins/metabolism , RNA, Messenger/genetics , RNA, Messenger/metabolism , Sequence Analysis , Glycine max/genetics , Glycine max/immunology , Glycine max/metabolism , Stress, Physiological/genetics , Transcription, Genetic
4.
Intervirology ; 54(3): 146-50, 2011.
Article in English | MEDLINE | ID: mdl-20948225

ABSTRACT

Early promoter activity of HPV-58 molecular variants isolated from high-grade cervical lesions in Brazil was compared. Luciferase reporter assays were conducted in C33 cells transfected with the complete long control region of 3 molecular variants of HPV-58 as well as HPV-58, -18 or -16 prototypes. The HPV-58 prototype and Bsb-329 and Bsb-367 variants showed a promoter activity similar to that of HPV-16, but lower than that of Bsb-295 and HPV-18. The introduction of the Bsb-295 7788 mutation into the HPV-58 prototype resulted in the enhancement of transcription closer to Bsb-295 and HPV-18. These results could impact the expression of E6 and E7 viral oncogenes.


Subject(s)
Molecular Typing , Papillomaviridae/classification , Papillomaviridae/genetics , Transcription, Genetic , Artificial Gene Fusion , Brazil , Cell Line , Cervix Uteri/pathology , Cervix Uteri/virology , Female , Genes, Reporter , Genotype , Humans , Luciferases/genetics , Luciferases/metabolism , Papillomaviridae/isolation & purification , Papillomavirus Infections/virology , Promoter Regions, Genetic
5.
J Med Virol ; 81(4): 685-92, 2009 Apr.
Article in English | MEDLINE | ID: mdl-19235839

ABSTRACT

More than 100 HPV types have been described, 13 of which are classified as high-risk due to their association with the development of cervical cancer. The intratype genomic diversity of HPV-16 and -18 has been studied extensively, while little data have been generated for other less common high-risk types. The present study explores the nucleotide variability and phylogeny of the high-risk HPV-31, -33, -35, -52, and -58, in samples from Central Brazil. For this purpose, the LCR and the E6 and L1 genes were sequenced. Several variants of these HPV types were detected, some of which have been detected in other parts of the world. Furthermore, new variants of all types examined were characterized in a total of 13 new variants. Based on the E6 and L1 sequences, variants were described comprising conservative and non-conservative amino acid changes. For phylogenetic tree construction, samples characterized in this study were compared to others described and submitted to GenBank previously. The phylogenetic analysis of HPV-31, -33, -35, and -58 isolates did not reveal ethnic or geographical clustering as observed previously for HPV-16 and -18. HPV-35 analysis showed a dichotomic branching characteristic of viral subtypes. Interestingly, four clusters relative to the analysis of HPV-52 isolates were identified, two of which could be classified as Asian and European branches. The genomic characterization of HPV variants is crucial for understanding the intrinsic geographical relatedness and biological differences of these viruses and contributes further to studies on their infectivity and pathogenicity.


Subject(s)
Genetic Variation , Papillomaviridae , Papillomavirus Infections/epidemiology , Phylogeny , Brazil/epidemiology , DNA, Viral/analysis , DNA, Viral/genetics , DNA, Viral/isolation & purification , Female , Humans , Molecular Sequence Data , Oncogene Proteins, Viral/genetics , Papillomaviridae/classification , Papillomaviridae/genetics , Papillomaviridae/isolation & purification , Papillomavirus Infections/virology , Risk , Sequence Analysis, DNA
SELECTION OF CITATIONS
SEARCH DETAIL
...