The analyses of human inherited disease and tissue-specific proteins in the interaction network.
Аннотация
OBJECTIVES
With the announcement of human proteome and interaction data, it becomes possible to comprehensively investigate the tissue-expression and network properties of inherited disease proteins. In this study, our goal was to develop methods to map the disease and expression data and analyze the disorder-tissue associations.
METHODS
In this paper, we manually classified the human disease proteins into 22 disorder classes and systematically analyzed the properties of disease proteins in different disorder classes. Then, we investigated the similarity of different disorder classes by computing the overlap of different disorder proteins and networks. We proposed two novel measures, Enrichment Ratio and P-value for comparative analysis of disease proteins across tissues and revealed the associations between disorder classes and tissues/cells.
RESULTS
Compared with non-disease proteins, disease proteins tend to express in more tissues, have higher expression levels and interact with more other proteins in the network. The overlap percentages of networks are much higher than those of proteins, implying that different disorder classes usually influence each other by means of their interacting neighbors. The metabolic, muscular and hematologic proteins are related with most tissues/cells, and cancer proteins are closely associated with the disorders in immune cells.
CONCLUSION
This paper provided novel methods to investigate proteome-wide disease proteins and their interacting networks in order to understand different disease's associations.
Предметные рубрики MeSH
Подготовка и перевод публикации
Обработка статьи · этапы, ошибки и управление
Ошибки и ограничения
История · было → стало
Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.
Тип публикации указан по данным источника. Уровень доказательности автоматически не присваивается.