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1.
Cell ; 174(2): 363-376.e16, 2018 07 12.
Artículo en Inglés | MEDLINE | ID: mdl-29887381

RESUMEN

Visualization of the transcriptome and the nuclear organization in situ has been challenging for single-cell analysis. Here, we demonstrate a multiplexed single-molecule in situ method, intron seqFISH, that allows imaging of 10,421 genes at their nascent transcription active sites in single cells, followed by mRNA and lncRNA seqFISH and immunofluorescence. This nascent transcriptome-profiling method can identify different cell types and states with mouse embryonic stem cells and fibroblasts. The nascent sites of RNA synthesis tend to be localized on the surfaces of chromosome territories, and their organization in individual cells is highly variable. Surprisingly, the global nascent transcription oscillated asynchronously in individual cells with a period of 2 hr in mouse embryonic stem cells, as well as in fibroblasts. Together, spatial genomics of the nascent transcriptome by intron seqFISH reveals nuclear organizational principles and fast dynamics in single cells that are otherwise obscured.


Asunto(s)
Hibridación Fluorescente in Situ/métodos , Transcriptoma , Animales , Dominio Catalítico , Línea Celular , Cromosomas/metabolismo , Fibroblastos/citología , Fibroblastos/metabolismo , Intrones , Ratones , Microscopía Fluorescente , Microscopía por Video , Células Madre Embrionarias de Ratones/citología , Células Madre Embrionarias de Ratones/metabolismo , ARN Polimerasa II/genética , ARN Polimerasa II/metabolismo , ARN Largo no Codificante/genética , ARN Mensajero/genética , Análisis de la Célula Individual
2.
Nature ; 568(7751): 235-239, 2019 04.
Artículo en Inglés | MEDLINE | ID: mdl-30911168

RESUMEN

Imaging the transcriptome in situ with high accuracy has been a major challenge in single-cell biology, which is particularly hindered by the limits of optical resolution and the density of transcripts in single cells1-5. Here we demonstrate an evolution of sequential fluorescence in situ hybridization (seqFISH+). We show that seqFISH+ can image mRNAs for 10,000 genes in single cells-with high accuracy and sub-diffraction-limit resolution-in the cortex, subventricular zone and olfactory bulb of mouse brain, using a standard confocal microscope. The transcriptome-level profiling of seqFISH+ allows unbiased identification of cell classes and their spatial organization in tissues. In addition, seqFISH+ reveals subcellular mRNA localization patterns in cells and ligand-receptor pairs across neighbouring cells. This technology demonstrates the ability to generate spatial cell atlases and to perform discovery-driven studies of biological processes in situ.


Asunto(s)
Encéfalo/anatomía & histología , Encéfalo/metabolismo , Hibridación Fluorescente in Situ/métodos , ARN Mensajero/análisis , ARN Mensajero/genética , Análisis de la Célula Individual/métodos , Transcriptoma/genética , Células 3T3 , Animales , Encéfalo/citología , Neuronas Dopaminérgicas/metabolismo , Células Endoteliales/metabolismo , Femenino , Perfilación de la Expresión Génica , Ligandos , Masculino , Ratones , Microglía/metabolismo , Especificidad de Órganos
3.
ChemSusChem ; 8(3): 544-51, 2015 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-25581231

RESUMEN

A fully integrated solar-driven water-splitting system comprised of WO3 /FTO/p(+) n Si as the photoanode, Pt/TiO2 /Ti/n(+) p Si as the photocathode, and Nafion as the membrane separator, was simulated, assembled, operated in 1.0 M HClO4 , and evaluated for performance and safety characteristics under dual side illumination. A multi-physics model that accounted for the performance of the photoabsorbers and electrocatalysts, ion transport in the solution electrolyte, and gaseous product crossover was first used to define the optimal geometric design space for the system. The photoelectrodes and the membrane separators were then interconnected in a louvered design system configuration, for which the light-absorbing area and the solution-transport pathways were simultaneously optimized. The performance of the photocathode and the photoanode were separately evaluated in a traditional three-electrode photoelectrochemical cell configuration. The photocathode and photoanode were then assembled back-to-back in a tandem configuration to provide sufficient photovoltage to sustain solar-driven unassisted water-splitting. The current-voltage characteristics of the photoelectrodes showed that the low photocurrent density of the photoanode limited the overall solar-to-hydrogen (STH) conversion efficiency due to the large band gap of WO3 . A hydrogen-production rate of 0.17 mL hr(-1) and a STH conversion efficiency of 0.24 % was observed in a full cell configuration for >20 h with minimal product crossover in the fully operational, intrinsically safe, solar-driven water-splitting system. The solar-to-hydrogen conversion efficiency, ηSTH , calculated using the multiphysics numerical simulation was in excellent agreement with the experimental behavior of the system. The value of ηSTH was entirely limited by the performance of the photoelectrochemical assemblies employed in this study. The louvered design provides a robust platform for implementation of various types of photoelectrochemical assemblies, and can provide an approach to significantly higher solar conversion efficiencies as new and improved materials become available.


Asunto(s)
Modelos Químicos , Procesos Fotoquímicos , Energía Solar , Agua/química , Electroquímica , Hidrógeno/química , Concentración de Iones de Hidrógeno , Reproducibilidad de los Resultados
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