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1.
Nat Methods ; 14(8): 775-781, 2017 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-28775673

RESUMEN

Access to primary research data is vital for the advancement of science. To extend the data types supported by community repositories, we built a prototype Image Data Resource (IDR) that collects and integrates imaging data acquired across many different imaging modalities. IDR links data from several imaging modalities, including high-content screening, super-resolution and time-lapse microscopy, digital pathology, public genetic or chemical databases, and cell and tissue phenotypes expressed using controlled ontologies. Using this integration, IDR facilitates the analysis of gene networks and reveals functional interactions that are inaccessible to individual studies. To enable re-analysis, we also established a computational resource based on Jupyter notebooks that allows remote access to the entire IDR. IDR is also an open source platform that others can use to publish their own image data. Thus IDR provides both a novel on-line resource and a software infrastructure that promotes and extends publication and re-analysis of scientific image data.


Asunto(s)
Sistemas de Administración de Bases de Datos , Bases de Datos Factuales , Interpretación de Imagen Asistida por Computador/métodos , Difusión de la Información/métodos , Programas Informáticos , Interfaz Usuario-Computador , Algoritmos , Edición , Integración de Sistemas
2.
Nat Commun ; 6: 8400, 2015 Oct 12.
Artículo en Inglés | MEDLINE | ID: mdl-26455310

RESUMEN

The amazing structural variety of cells is matched only by their functional diversity, and reflects the complex interplay between biochemical and mechanical regulation. How both regulatory layers generate specifically shaped cellular domains is not fully understood. Here, we report how cell growth domains are shaped in fission yeast. Based on quantitative analysis of cell wall expansion and elasticity, we develop a model for how mechanics and cell wall assembly interact and use it to look for factors underpinning growth domain morphogenesis. Surprisingly, we find that neither the global cell shape regulators Cdc42-Scd1-Scd2 nor the major cell wall synthesis regulators Bgs1-Bgs4-Rgf1 are reliable predictors of growth domain geometry. Instead, their geometry can be defined by cell wall mechanics and the cortical localization pattern of the exocytic factors Sec6-Syb1-Exo70. Forceful re-directioning of exocytic vesicle fusion to broader cortical areas induces proportional shape changes to growth domains, demonstrating that both features are causally linked.


Asunto(s)
Exocitosis , Modelos Biológicos , Schizosaccharomyces/crecimiento & desarrollo , Fenómenos Biomecánicos , Ciclo Celular , Pared Celular/metabolismo , Schizosaccharomyces/metabolismo , Proteína de Unión al GTP cdc42/metabolismo
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