Search results for "cell fate"

showing 10 items of 75 documents

Asymmetric cell division requires specific mechanisms for adjusting global transcription

2017

Most cells divide symmetrically into two approximately identical cells. There are many examples, however, of asymmetric cell division that can generate sibling cell size differences. Whereas physical asymmetric division mechanisms and cell fate consequences have been investigated, the specific problem caused by asymmetric division at the transcription level has not yet been addressed. In symmetrically dividing cells the nascent transcription rate increases in parallel to cell volume to compensate it by keeping the actualmRNA synthesis rate constant. This cannot apply to the yeast Saccharomyces cerevisiae, where this mechanism would provoke a neverending increasing mRNA synthesis rate in sma…

0301 basic medicineSaccharomyces cerevisiae ProteinsTranscription GeneticCell divisionRNA StabilitySaccharomyces cerevisiaeSaccharomyces cerevisiaeCell fate determinationBiotecnologia03 medical and health sciences0302 clinical medicineRNA Polymerase ITranscription (biology)GeneticsAsymmetric cell divisionRNA MessengerCèl·lules DivisióMolecular BiologyCell SizeMessenger RNAbiologyCell CycleRNADNA-Directed RNA Polymerasesbiology.organism_classificationYeastCell biology030104 developmental biologyCell Division030217 neurology & neurosurgeryNucleic Acids Research
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ceRNA Network Regulation of TGF-β, WNT, FOXO, Hedgehog Pathways in the Pharynx of Ciona robusta

2021

The transforming growth factor-β (TGF-β) family of cytokines performs a multifunctional signaling, which is integrated and coordinated in a signaling network that involves other pathways, such as Wintless, Forkhead box-O (FOXO) and Hedgehog and regulates pivotal functions related to cell fate in all tissues. In the hematopoietic system, TGF-β signaling controls a wide spectrum of biological processes, from immune system homeostasis to the quiescence and self-renewal of hematopoietic stem cells (HSCs). Recently an important role in post-transcription regulation has been attributed to two type of ncRNAs: microRNAs and pseudogenes. Ciona robusta, due to its philogenetic position close to verte…

0301 basic medicineascidianpseudogenepseudogeneslcsh:ChemistryTransforming Growth Factor betaProtein Interaction MappingHomeostasisRNA-Seqlcsh:QH301-705.53' Untranslated RegionsSpectroscopyTissue homeostasisForkhead Box Protein O1Wnt signaling pathwayHigh-Throughput Nucleotide Sequencingvirus diseasesGeneral Medicinefemale genital diseases and pregnancy complicationsComputer Science ApplicationsCell biologyNGSStem cellTGF-βCell fate determinationBiologyCatalysisArticleInorganic ChemistryWNT03 medical and health sciencesmicroRNAAnimalsCell LineageHedgehog ProteinsTGF-Physical and Theoretical ChemistryMolecular BiologyHedgehogneoplasmsmiRNA030102 biochemistry & molecular biologyCompeting endogenous RNAOrganic ChemistryfungiComputational BiologyHematopoiesisWnt ProteinsMicroRNAs030104 developmental biologylcsh:Biology (General)lcsh:QD1-999Gene Expression RegulationImmune SystemPharynxFOXOCionaTransforming growth factorInternational Journal of Molecular Sciences
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Molecular Insights Into Therapeutic Potential of Autophagy Modulation by Natural Products for Cancer Stem Cells

2020

Autophagy, a cellular self-digestion process that is activated in response to stress, has a functional role in tumor formation and progression. Cancer stem cells (CSCs) accounting for a minor proportion of total cancer cells-have distinct self-renewal and differentiation abilities and promote metastasis. Researchers have shown that a numeral number of natural products using traditional experimental methods have been revealed to target CSCs. However, the specific role of autophagy with respect to CSCs and tumorigenesis using natural products are still unknown. Currently, CSCs are considered to be one of the causative reasons underlying the failure of anticancer treatment as a result of tumor…

0301 basic medicineautophagycancer stem cellnatural productsReviewCell fate determinationBiologymedicine.disease_causeMetastasisCell and Developmental Biologystemness03 medical and health sciences0302 clinical medicineCancer stem cellmedicinelcsh:QH301-705.5Transcription factorAutophagychemoresistanceCancerCell Biologymedicine.diseaseTumor formation030104 developmental biologylcsh:Biology (General)030220 oncology & carcinogenesisCancer researchCarcinogenesisDevelopmental BiologyFrontiers in Cell and Developmental Biology
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2018

During gastrulation, embryonic cells become specified into distinct germ layers. In mouse, this continues throughout somitogenesis from a population of bipotent stem cells called neuromesodermal progenitors (NMps). However, the degree of self-renewal associated with NMps in the fast-developing zebrafish embryo is unclear. With a genetic clone tracing method, we labelled early embryonic progenitors and find a strong clonal similarity between spinal cord and mesoderm tissues. We followed individual cell lineages by light-sheet imaging, revealing a common neuromesodermal lineage contribution to a subset of spinal cord tissue across the anterior-posterior body axis. An initial population subdiv…

0301 basic medicineeducation.field_of_studyMesodermPopulationGerm layerBiologyCell fate determinationEmbryonic stem cellCell biologyGastrulation03 medical and health sciences030104 developmental biologymedicine.anatomical_structureSomitogenesismedicineCompartment (development)educationMolecular BiologyDevelopmental BiologyDevelopment
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Advanced mechanotherapy: Biotensegrity  for governing metastatic tumor cell fate via modulating the extracellular matrix.

2021

Mechano-transduction is the procedure of mechanical stimulus translation via cells, among substrate shear flow, topography, and stiffness into a biochemical answer. TAZ and YAP are transcriptional coactivators which are recognized as relay proteins that promote mechano-transduction within the Hippo pathway. With regard to healthy cells in homeostasis, mechano-transduction regularly restricts proliferation, and TAZ and YAP are totally inactive. During cancer development a YAP/TAZ - stimulating positive response loop is formed between the growing tumor and the stiffening ECM. As tumor developments, local stromal and cancerous cells take advantage of mechanotransduction to enhance proliferatio…

0303 health sciencesHippo signaling pathwayStromal cellChemistryPharmaceutical ScienceCell Differentiation02 engineering and technologyCell fate determination021001 nanoscience & nanotechnologyPhosphoproteinsMechanotransduction CellularCell biologyExtracellular MatrixExtracellular matrix03 medical and health sciencesMechanobiologyTumor progressionNeoplasmsHumansMechanotransduction0210 nano-technologyMechanotherapy030304 developmental biologyAdaptor Proteins Signal TransducingJournal of controlled release : official journal of the Controlled Release Society
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Criss‐crossing autism spectrum disorder and adult neurogenesis

2021

Autism spectrum disorder (ASD) comprises a group of multifactorial neurodevelopmental disorders primarily characterized by deficits in social interaction and repetitive behavior. Although the onset is typically in early childhood, ASD poses a lifelong challenge for both patients and caretakers. Adult neurogenesis (AN) is the process by which new functional neurons are created from neural stem cells existing in the post-natal brain. The entire event is based on a sequence of cellular processes, such as proliferation, specification of cell fate, maturation, and ultimately, synaptic integration into the existing neural circuits. Hence, AN is implicated in structural and functional brain plasti…

AdultAutism Spectrum DisorderNeurogenesisNeurogenesisCell fate determinationBiologymedicine.diseaseAffect (psychology)BiochemistryFMR1Neural stem cellCellular and Molecular NeuroscienceNeural Stem CellsNeurodevelopmental DisordersAutism spectrum disorderChild Preschoolmental disordersmedicineBiological neural networkAnimalsHumansEarly childhoodNeuroscienceJournal of Neurochemistry
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p62: Friend or Foe? Evidences for OncoJanus and NeuroJanus Roles

2020

p62 is a versatile protein involved in the delicate balance between cell death and survival, which is fundamental for cell fate decision in the context of both cancer and neurodegenerative diseases. As an autophagy adaptor, p62 recognizes polyubiquitin chains and interacts with LC3, thereby targeting the selected cargo to the autophagosome with consequent autophagic degradation. Beside this function, p62 behaves as an interactive hub in multiple signalling including those mediated by Nrf2, NF-κB, caspase-8, and mTORC1. The protein is thus crucial for the control of oxidative stress, inflammation and cell survival, apoptosis, and metabolic reprogramming, respectively. As a multifunctional pr…

AutophagosomeProgrammed cell deathP62ApoptosisContext (language use)mTORC1Cell fate determinationBiologyCatalysislcsh:ChemistryInorganic ChemistryStress granuleAutophagymedicinePhysical and Theoretical Chemistrylcsh:QH301-705.5Molecular BiologySpectroscopyCancerNeurodegenerative diseasesOrganic ChemistryNeurodegenerationAutophagyGeneral Medicinemedicine.diseaseComputer Science ApplicationsCell biologylcsh:Biology (General)lcsh:QD1-999International Journal of Molecular Sciences
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Detection of condition-specific marker genes from RNA-seq data with MGFR

2019

The identification of condition-specific genes is key to advancing our understanding of cell fate decisions and disease development. Differential gene expression analysis (DGEA) has been the standard tool for this task. However, the amount of samples that modern transcriptomic technologies allow us to study, makes DGEA a daunting task. On the other hand, experiments with low numbers of replicates lack the statistical power to detect differentially expressed genes. We have previously developed MGFM, a tool for marker gene detection from microarrays, that is particularly useful in the latter case. Here, we have adapted the algorithm behind MGFM to detect markers in RNA-seq data. MGFR groups s…

Bioinformaticslcsh:MedicineRNA-SeqComputational biologyMarker genesCell fate determinationBiologyMarker geneGeneral Biochemistry Genetics and Molecular BiologyTranscriptomeBioconductor03 medical and health sciences0302 clinical medicineGene expressionSingle cellRNA-SeqTranscriptomicsGene030304 developmental biology0303 health sciencesGeneral Neurosciencelcsh:RCell-type specificityGenomicsGeneral MedicineTissue specificity030220 oncology & carcinogenesisGene expressionR-packageDNA microarrayGeneral Agricultural and Biological SciencesPeerJ
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The Muscleblind family of proteins: an emerging class of regulators of developmentally programmed alternative splicing.

2006

Alternative splicing is widely used to generate protein diversity and to control gene expression in many biological processes, including cell fate determination and apoptosis. In this review, we focus on the Muscleblind family of tissue-specific alternative splicing regulators. Muscleblind proteins bind pre-mRNA through an evolutionarily conserved tandem CCCH zinc finger domain. Human Muscleblind homologs MBNL1, MBNL2 and MBNL3 promote inclusion or exclusion of specific exons on different pre-mRNAs by antagonizing the activity of CUG-BP and ETR-3-like factors (CELF proteins) bound to distinct intronic sites. The relative activities of Muscleblind and CELF proteins control a key developmenta…

Cancer ResearchCellular differentiationMolecular Sequence DataRNA-binding proteinCell fate determinationBiologychemistry.chemical_compoundExonMiceMBNL1AnimalsHumansMyotonic DystrophyAmino Acid SequenceMolecular BiologyGeneticsZinc fingerAlternative splicingGene Expression Regulation DevelopmentalRNA-Binding ProteinsCell DifferentiationZinc FingersCell BiologyAlternative SplicingchemistryRNA splicingDevelopmental BiologyDifferentiation; research in biological diversity
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The Embryonic Central Nervous System Lineages ofDrosophila melanogaster

1996

In Drosophila, central nervous system (CNS) formation starts with the delamination from the neuroectoderm of about 30 neuroblasts (NBs) per hemisegment. They give rise to approximately 350 neurons and 30 glial cells during embryonic development. Understanding the mechanisms leading to cell fate specification and differentiation in the CNS requires the identification of the NB lineages. The embryonic lineages derived from 17 NBs of the ventral part of the neuroectoderm have previously been described (Bossing et al., 1996). Here we present 13 lineages derived from the dorsal part of the neuroectoderm and we assign 12 of them to identified NBs. Together, the 13 lineages comprise approximately …

Cell divisionNeuroectodermLineage (evolution)food and beveragesAnatomyCell BiologyBiologyCell fate determinationEmbryonic stem cellCell biologynervous systemNeuroblastVentral nerve cordembryonic structuresGanglion mother cellMolecular BiologyDevelopmental BiologyDevelopmental Biology
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