22 research outputs found
Role of Mismatch Repair Enzymes in GAA•TTC Triplet-repeat Expansion in Friedreich Ataxia Induced Pluripotent Stem Cells
The genetic mutation in Friedreich ataxia (FRDA) is a hyperexpansion of the triplet-repeat sequence GAA•TTC within the first intron of the FXN gene. Although yeast and reporter construct models for GAA•TTC triplet-repeat expansion have been reported, studies on FRDA pathogenesis and therapeutic development are limited by the availability of an appropriate cell model in which to study the mechanism of instability of the GAA•TTC triplet repeats in the human genome. Herein, induced pluripotent stem cells (iPSCs) were generated from FRDA patient fibroblasts after transduction with the four transcription factors Oct4, Sox2, Klf4, and c-Myc. These cells were differentiated into neurospheres and neuronal precursors in vitro, providing a valuable cell model for FRDA. During propagation of the iPSCs, GAA•TTC triplet repeats expanded at a rate
of about two GAA•TTC triplet repeats/replication. However,
GAA•TTC triplet repeats were stable in FRDA fibroblasts and
neuronal stem cells. The mismatch repair enzymes MSH2,
MSH3, and MSH6, implicated in repeat instability in other triplet-repeat diseases, were highly expressed in pluripotent stem cells compared with fibroblasts and neuronal stem cells and occupied FXN intron 1. In addition, shRNA silencing of MSH2 and MSH6 impeded GAA•TTC triplet-repeat expansion. A specific pyrrole-imidazole polyamide targeting GAA•TTC triplet-repeat DNA partially blocked repeat expansion by displacing MSH2 from FXN intron 1 in FRDA iPSCs. These studies suggest that in FRDA, GAA•TTC triplet-repeat instability occurs in embryonic cells and involves the highly active mismatch repair system
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Sirt6 regulates TNFα secretion via hydrolysis of long chain fatty acyl lysine
The Sir2 family of enzymes or sirtuins are known as nicotinamide adenine dinucleotide (NAD)-dependent deacetylases1 and have been implicated in the regulation of transcription, genome stability, metabolism, and lifespan2, 3. However, four of the seven mammalian sirtuins have very weak deacetylase activity in vitro. Here we show that human Sirt6 efficiently removes long chain fatty acyl groups, such as myristoyl, from lysine residues. The crystal structure of Sirt6 reveals a large hydrophobic pocket that can accommodate long chain fatty acyl groups. We demonstrate further that Sirt6 promotes the secretion of tumor necrosis factor α (TNFα) by removing the fatty acyl modification on K19 and K20 of TNFα. Protein lysine fatty acylation has been known to occur in mammalian cells, but the function and regulatory mechanisms of this modification were unknown. Our data suggest that protein lysine fatty acylation is a novel mechanism that regulates protein secretion. The discovery of Sirt6 as an enzyme that controls protein lysine fatty acylation provides new opportunities to investigate the physiological function of the previously ignored protein posttranslational modification
Construção de um protótipo de Data Warehouse como suporte ao sistema de informação numa instituição de ensino superior
Uma das dificuldades que se verifica na extracção de informação numa organização é a falta de integração dos dados existentes dispersos em diversos formatos: ficheiros de processadores de texto, folhas de cálculo, bases de dados, entre outras fontes. A partir deste problema, este trabalho propõe a estruturação de um modelo de Data Warehouse com o objectivo de organizar, armazenar e integrar as informações provenientes de outros formatos e sistemas, numa única base de dados para uma futura utilização no suporte à tomada de decisão. Existem, neste momento, na comunidade de Data Warehousing duas principais abordagens, uma preconizada por William H. Inmon, mais centrada nos dados, e outra por Ralph Kimball, mais centrada no projecto.
Assim, com a metodologia proposta foi desenvolvido um caso de estudo com a finalidade de verificar e avaliar a aplicabilidade da metodologia no Instituto Politécnico de Tomar; ABSTRACT: One difficulty that exists in the extraction of information in organizations is the lack of integration of existing data scattered in various formats: word processing files, spreadsheets, databases, among other sources. From this problem, this paper proposes to structure a model of Data Warehouse in order to organize, store and integrate information from other systems and formats in a single database for future use in supporting decision making. There are at present in the community of Data Warehousing two main approaches, one advocated by William H. Inmon, more data-centric, and one by Ralph Kimball, more focused on the project.
So with the proposed methodology was developed a case study in order to verify and evaluate the applicability of the methodology at the Polytechnic Institute of Tomar
Thiosuccinyl Peptides as Sirt5-Specific Inhibitors
Sirtuins, a class of enzymes known as nicotinamide adenine
dinucleotide-dependent
deacetylases, have been shown to regulate a variety of biological
processes, including aging, transcription, and metabolism. Sirtuins
are considered promising targets for treating several human diseases.
There are seven sirtuins in humans (Sirt1–7). Small molecules
that can target a particular human sirtuin are important for drug
development and fundamental studies of sirtuin biology. Here we demonstrate
that thiosuccinyl peptides are potent and selective Sirt5 inhibitors.
The design of these inhibitors is based on our recent discovery that
Sirt5 prefers to catalyze the hydrolysis of malonyl and succinyl groups,
rather than an acetyl group, from lysine residues. Furthermore, among
the seven human sirtuins, Sirt5 is the only one that has this unique
acyl group preference. This study demonstrates that the different
acyl group preferences of different sirtuins can be conveniently utilized
to develop small molecules that selectively target different sirtuins
pH Responsive Polymer Micelles Enhances Inhibitory Efficacy on Metastasis of Murine Breast Cancer Cells
A pH sensitive micellar cargo was fabricated for pH triggered delivery of hydrophobic drug paclitaxel with pH controlled drug release profiles. The size, drug loading content, and encapsulation efficiency of PTX loaded micelles were 20–30 nm, 7.5%, 82.5%, respectively. PTX loaded PELA-PBAE micelles could enhance the intracellular uptake of a model drug significantly, with increased cytotoxicity and inhibition of tumor metastasis on 4T1 cells, as confirmed by wound healing assay and tumor cells invasion assay. The expression of metastasis and apoptosis correlated proteins on 4T1 cells decreased remarkably after intervention by PTX loaded polymer micelles, as demonstrated by western blotting and quantitative reverse transcriptional-polymerase chain reaction (qRT-PCR). Our results demonstrated the pH responsive polymer micelles might have the potential to be used in the treatment of metastatic breast tumors
Analysis and Discussion of Baoji “Shigu • Tian Xi Tai”, “Shigu • Sun City” Ground Source Heat Pump Energy Station System
Baoji “Shigu • Tian Xi Tai”, “Shigu • Sun City” ground source heat pump energy station system is an important energy supply project in Shigu. In this paper, we systematically introduce the design of green building and ground-source heat pump system, points of construction process, pre-cooling station technology, EMC economic model in detail. In addition, the ground source heat pump system of the project was tested in the field to analyze and evaluate the running performance of the system. We hope our research can provide some reference and help to the practitioners
Dph3 Is an Electron Donor for Dph1-Dph2 in the First Step of Eukaryotic Diphthamide Biosynthesis
Diphthamide, the
target of diphtheria toxin, is a unique posttranslational
modification on translation elongation factor 2 (EF2) in archaea and
eukaryotes. The biosynthesis of diphthamide was proposed to involve
three steps. The first step is the transfer of the 3-amino-3-carboxypropyl
group from <i>S</i>-adenosyl-l-methionine (SAM)
to the histidine residue of EF2, forming a C–C bond. Previous
genetic studies showed this step requires four proteins in eukaryotes,
Dph1–Dph4. However, the exact molecular functions for the four
proteins are unknown. Previous study showed that Pyrococcus
horikoshii Dph2 (PhDph2), a novel iron-sulfur cluster-containing
enzyme, forms a homodimer and is sufficient for the first step of
diphthamide biosynthesis <i>in vitro</i>. Here we demonstrate
by <i>in vitro</i> reconstitution that yeast Dph1 and Dph2
form a complex (Dph1-Dph2) that is equivalent to the homodimer of
PhDph2 and is sufficient to catalyze the first step <i>in vitro</i> in the presence of dithionite as the reductant. We further demonstrate
that yeast Dph3 (also known as KTI11), a CSL-type zinc finger protein,
can bind iron and in the reduced state can serve as an electron donor
to reduce the Fe-S cluster in Dph1-Dph2. Our study thus firmly establishes
the functions for three of the proteins involved in eukaryotic diphthamide
biosynthesis. For most radical SAM enzymes in bacteria, flavodoxins
and flavodoxin reductases are believed to serve as electron donors
for the Fe-S clusters. The finding that Dph3 is an electron donor
for the Fe-S clusters in Dph1-Dph2 is thus interesting and opens up
new avenues of research on electron transfer to Fe-S proteins in eukaryotic
cells
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An Immunosuppressive Antibody–Drug Conjugate
We have developed a novel antibody-drug conjugate (ADC) that can selectively deliver the Lck inhibitor dasatinib to human T lymphocytes. This ADC is based on a humanized antibody that selectively binds with high affinity to CXCR4, an antigen that is selectively expressed on hematopoietic cells. The resulting dasatinib-antibody conjugate suppresses T-cell-receptor (TCR)-mediated T-cell activation and cytokine expression with low nM EC50 and has minimal effects on cell viability. This ADC may lead to a new class of selective immunosuppressive drugs with improved safety and extend the ADC strategy to the targeted delivery of kinase inhibitors for indications beyond oncology
Table_2_pH Responsive Polymer Micelles Enhances Inhibitory Efficacy on Metastasis of Murine Breast Cancer Cells.DOCX
<p>A pH sensitive micellar cargo was fabricated for pH triggered delivery of hydrophobic drug paclitaxel with pH controlled drug release profiles. The size, drug loading content, and encapsulation efficiency of PTX loaded micelles were 20–30 nm, 7.5%, 82.5%, respectively. PTX loaded PELA-PBAE micelles could enhance the intracellular uptake of a model drug significantly, with increased cytotoxicity and inhibition of tumor metastasis on 4T1 cells, as confirmed by wound healing assay and tumor cells invasion assay. The expression of metastasis and apoptosis correlated proteins on 4T1 cells decreased remarkably after intervention by PTX loaded polymer micelles, as demonstrated by western blotting and quantitative reverse transcriptional-polymerase chain reaction (qRT-PCR). Our results demonstrated the pH responsive polymer micelles might have the potential to be used in the treatment of metastatic breast tumors.</p
Table_1_pH Responsive Polymer Micelles Enhances Inhibitory Efficacy on Metastasis of Murine Breast Cancer Cells.DOCX
<p>A pH sensitive micellar cargo was fabricated for pH triggered delivery of hydrophobic drug paclitaxel with pH controlled drug release profiles. The size, drug loading content, and encapsulation efficiency of PTX loaded micelles were 20–30 nm, 7.5%, 82.5%, respectively. PTX loaded PELA-PBAE micelles could enhance the intracellular uptake of a model drug significantly, with increased cytotoxicity and inhibition of tumor metastasis on 4T1 cells, as confirmed by wound healing assay and tumor cells invasion assay. The expression of metastasis and apoptosis correlated proteins on 4T1 cells decreased remarkably after intervention by PTX loaded polymer micelles, as demonstrated by western blotting and quantitative reverse transcriptional-polymerase chain reaction (qRT-PCR). Our results demonstrated the pH responsive polymer micelles might have the potential to be used in the treatment of metastatic breast tumors.</p