Archive for the ‘researches 3’ Category

A Regulatory Role of the Rnq1 Non-Prion Domain for Prion Propagation and Polyglutamine Aggregates.

Sunday, March 16th, 2008

A Regulatory Role of the Rnq1 Non-Prion Domain for Prion Propagation and Polyglutamine Aggregates. Prions are infectious, self-propagating protein conformations. Rnq1 is required for the yeast prion [PIN(+)], which is necessary for the de novo induction of a second prion, [PSI(+)]. Here we isolate a [PSI(+)]-eliminating ...

Activator-to-repressor conversion of T-box transcription factors by the Ripply family of Groucho/TLE

Sunday, March 16th, 2008

Activator-to-repressor conversion of T-box transcription factors by the Ripply family of Groucho/TLE-associated mediators. The T-box family of transcription factors, defined by a conserved DNA binding domain called the T-box, regulates various aspects of embryogenesis by activating and/or repressing downstream genes. In spite of the biological significance ...

Multifactorial interplay controls the splicing profile of Alu derived exons.

Sunday, March 16th, 2008

Multifactorial interplay controls the splicing profile of Alu derived exons. Exonization of Alu elements creates primate-specific genomic diversity. Here we combine bioinformatic and experimental methodologies to reconstruct the molecular changes leading to exon selection. Our analyses revealed an intricate network involved in Alu exonization. A typical ...

SWI/SNF Mediates Polycomb Eviction and Epigenetic Reprogramming of the INK4b-ARF-INK4a Locus.

Sunday, March 16th, 2008

SWI/SNF Mediates Polycomb Eviction and Epigenetic Reprogramming of the INK4b-ARF-INK4a Locus. Stable silencing of the INK4b-ARF-INK4a tumor suppressor locus occurs in a variety of human cancers, including malignant rhabdoid tumors (MRTs). MRTs are extremely aggressive cancers, caused by the loss of the hSNF5 subunit of the ...

Interleukin-1 stimulates glutamate uptake in glial cells by accelerating membrane trafficking of Na+

Sunday, March 16th, 2008

Interleukin-1 stimulates glutamate uptake in glial cells by accelerating membrane trafficking of Na+/K+-ATPase via actin depolymerization. Interleukin-1 (IL-1) is a mediator of brain injury induced by ischemia, trauma, and chronic neurodegenerative disease. IL-1 also has a protective role by preventing neuronal cell death from glutamate neurotoxicity. ...

NELF and GAGA factor are linked to promoter proximal pausing at many genes in Drosophila.

Sunday, March 16th, 2008

NELF and GAGA factor are linked to promoter proximal pausing at many genes in Drosophila. Recent analyses of RNA polymerase II (Pol II) reveals that Pol II is concentrated at the promoters of many active and inactive genes. NELF causes Pol II to pause in the ...

Involvement of Actinin-4 in the Recruitment of JRAB/MICAL-L2 to Cell-Cell Junctions and the Formatio

Sunday, March 16th, 2008

Involvement of Actinin-4 in the Recruitment of JRAB/MICAL-L2 to Cell-Cell Junctions and the Formation of Functional Tight Junctions. Tight junctions (TJs) are cell-cell adhesive structures that undergo continuous remodeling. We previously demonstrated that Rab13 and a junctional Rab13-binding protein (JRAB)/molecule interacting with CasL-like 2 (MICAL-L2) localized ...

Rhythmic SAF-A binding underlies circadian transcription of the Bmal1 gene.

Sunday, March 16th, 2008

Rhythmic SAF-A binding underlies circadian transcription of the Bmal1 gene. Although Bmal1 is a key component of the mammalian clock system, little is understood about the actual mechanism of circadian Bmal1 gene transcription, particularly at the chromatin level. Here we discovered a unique chromatin structure within ...

Cdc1p is an ER-localized Putative Lipid Phosphatase that Affects Golgi Inheritance and Actin Polariz

Sunday, March 16th, 2008

Cdc1p is an ER-localized Putative Lipid Phosphatase that Affects Golgi Inheritance and Actin Polarization by Activating Ca2+ Signaling. In the budding yeast Saccharomyces cerevisiae, mutations in the essential gene CDC1 cause defects in Golgi inheritance and actin polarization. However, the biochemical function of Cdc1p is unknown. ...

Transcription regulation of rRNA gene by a multi-functional nucleolar protein, B23/nucleophosmin thr

Sunday, March 16th, 2008

Transcription regulation of rRNA gene by a multi-functional nucleolar protein, B23/nucleophosmin through its histone chaperone activity. It is well established that the transcription rate of the rRNA gene is closely associated with profound alterations in the cell growth rate. Regulation of the rRNA gene transcription is ...

ETO, but not leukemogenic fusion protein AML1/ETO, augments RBP-J{kappa}/SHARP-mediated repression o

Sunday, March 16th, 2008

ETO, but not leukemogenic fusion protein AML1/ETO, augments RBP-J{kappa}/SHARP-mediated repression of Notch target genes. Notch is a transmembrane receptor that determines cell fates and pattern formation in all animal species. After specific ligand binding, the intracellular part of Notch is cleaved off and translocates to the ...

HDAC inhibitor depsipeptide activates silenced genes through decreasing both CpG and H3K9 methylatio

Sunday, March 16th, 2008

HDAC inhibitor depsipeptide activates silenced genes through decreasing both CpG and H3K9 methylation on the promoter. Histone deacetylase inhibitor (HDACi) has been shown to demethylate mammalian genome, which further strengthens the concept that DNA methylation and histone modifications interact in regulation of gene expression. Here, we ...

Histone Deacetylase 4 Confers CaM Kinase II Responsiveness to Histone Deacetylase 5 by Oligomerizati

Sunday, March 16th, 2008

Histone Deacetylase 4 Confers CaM Kinase II Responsiveness to Histone Deacetylase 5 by Oligomerization. Calcium, calmodulin-dependent protein kinase II (CaMKII) phosphorylates histone deacetylase 4 (HDAC4), a class IIa HDAC, resulting in cytosolic accumulation of HDAC4 and de-repression of the MEF2 transcription factor. Phosphorylation by CaMKII requires ...

MURC, a muscle-restricted coiled-coil protein that modulates the Rho/ROCK pathway, induces cardiac d

Sunday, March 16th, 2008

MURC, a muscle-restricted coiled-coil protein that modulates the Rho/ROCK pathway, induces cardiac dysfunction and conduction disturbance. We identified a novel muscle-restricted putative coiled-coil protein, MURC, which is evolutionarily conserved from frog to human. MURC was localized to the cytoplasm with accumulation in the Z-line of the ...

FGFR2 phosphorylation on Serine 779 couples to 14-3-3 and regulates cell survival and proliferation.

Sunday, March 16th, 2008

FGFR2 phosphorylation on Serine 779 couples to 14-3-3 and regulates cell survival and proliferation. The fibroblast growth factors (FGFs) exert their diverse (or pleiotropic) biological responses through the binding and activation of specific cell surface receptors (FGFRs). While FGFRs are known to initiate intracellular signaling through ...

DEK is a poly(ADP-ribose)-acceptor in apoptosis and mediates resistance to genotoxic stress.

Sunday, March 16th, 2008

DEK is a poly(ADP-ribose)-acceptor in apoptosis and mediates resistance to genotoxic stress. DEK is a nuclear phosphoprotein implicated in oncogenesis and autoimmunity and a major component of metazoan chromatin. The intracellular cues that control DEK\'s binding to DNA and its pleiotropic functions in DNA- and RNA-dependent ...

Nischarin inhibits LIM Kinase to regulate Cofilin phosphorylation and Cell Invasion.

Sunday, March 16th, 2008

Nischarin inhibits LIM Kinase to regulate Cofilin phosphorylation and Cell Invasion. Nischarin is a novel protein that regulates cell migration by inhibiting p21 activated kinase (PAK). LIM kinase (LIMK) is a downstream effector of PAK, and it is known to play an important role in cell ...

Common variants in MODY genes and future risk of type 2 diabetes.

Sunday, March 16th, 2008

Common variants in MODY genes and future risk of type 2 diabetes. Objective: Mutations in the HNF-1alpha, HNF-4alpha, GCK and HNF-1beta genes cause Maturity Onset Diabetes of the Young (MODY), but it is not known whether common variants in these genes predict future type 2 diabetes ...

Identification of tyrosine posphatase 2(256-760) construct as a new, sensitive marker for the detect

Sunday, March 16th, 2008

Identification of tyrosine posphatase 2(256-760) construct as a new, sensitive marker for the detection of islet autoimmunity in type 2 diabetic patients (NIRAD Study 2). Objective: The presence of autoantibodies to islet antigens GAD and/or IA-2 in type 2 diabetic patients identifies those subjects (LADA) at ...

Beta-cell dysfunction in subjects with impaired glucose tolerance and early type 2 diabetes. Compari

Sunday, March 16th, 2008

Beta-cell dysfunction in subjects with impaired glucose tolerance and early type 2 diabetes. Comparison of surrogate markers with first phase insulin secretion from an intravenous glucose tolerance test. Objective: Methods to assess beta-cell function in clinical studies are limited. The aim of the current study was ...

Sequencing-based genotyping and association analysis of the MICA and MICB genes in type 1 diabetes.

Sunday, March 16th, 2008

Sequencing-based genotyping and association analysis of the MICA and MICB genes in type 1 diabetes. Objective: The non-classical major histocompatibility complex (MHC) class I chain related molecules (MIC), encoded within the MHC, function in immunity. The transmembrane polymorphism in MICA (MICA-STR) has been reported to be ...

Kinin B1 receptor deficiency leads to leptin hypersensitivity and resistance to obesity.

Sunday, March 16th, 2008

Kinin B1 receptor deficiency leads to leptin hypersensitivity and resistance to obesity. Objective: Kinins mediate pathophysiological processes related to hypertension, pain and inflammation through the activation of two G protein-coupled receptors, named B(1) and B(2). Although these peptides have been related to glucose homeostasis, their effects ...

Retinal and Cerebral Microvascular Signs and Diabetes: The Age, Gene/Environment Susceptibility-Reyk

Sunday, March 16th, 2008

Retinal and Cerebral Microvascular Signs and Diabetes: The Age, Gene/Environment Susceptibility-Reykjavik Study. Objective: Diabetes increases the risk for microvascular disease. The retina and the brain both have intricate microvascular systems that are developmentally similar. Here, we seek to examine whether microvascular lesions in the retina and ...

Central nervous system neuropeptide Y signaling modulates VLDL triglyceride secretion.

Sunday, March 16th, 2008

Central nervous system neuropeptide Y signaling modulates VLDL triglyceride secretion. Objective: Elevated triglyceride (TG) is the major plasma lipid abnormality in obese and diabetic patients and contributes to cardiovascular morbidity in these disorders. We sought to identify novel mechanisms leading to hypertriglyceridemia. Resistance to negative feedback ...

Haptoglobin genotype: a determinant of cardiovascular complication risk in type 1 diabetes.

Sunday, March 16th, 2008

Haptoglobin genotype: a determinant of cardiovascular complication risk in type 1 diabetes. Objective: Haptoglobin (Hp) is a plasma protein that binds free hemoglobin, thereby inhibiting hemoglobin-induced oxidative damage. We investigated the association between the Hp genotype and the incidence of coronary artery disease (CAD) in a ...

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