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Analysis of the p53/CEP-1 regulated non-coding transcriptome in C. elegans by an NSR-seq strategy
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作者 Derong Xu Guifeng Wei +4 位作者 Ping Lu Jianjun Luo Xiaomin Chen Geir Skogerbo Runsheng Chen 《Protein & Cell》 SCIE CAS CSCD 2014年第10期770-782,共13页
In recent years, large numbers of non-coding RNAs (ncR- NAs) have been identified in C. elegans but their functions are still not well studied. In C. elegans, CEP-1 is the sole homolog of the p53 family of genes. In... In recent years, large numbers of non-coding RNAs (ncR- NAs) have been identified in C. elegans but their functions are still not well studied. In C. elegans, CEP-1 is the sole homolog of the p53 family of genes. In order to obtain transcription profiles of ncRNAs regulated by CEP-1 under normal and UV stressed conditions, we applied the 'not-so- random' hexamers priming strategy to RNA sequencing in C. elegans, This NSR-seq strategy efficiently depleted rRNA transcripts from the samples and showed high technical replicability. We identified more than 1,000 ncR- NAs whose apparent expression was repressed by CEP-1, while around 200 were activated. Around 40% of the CEP-1 activated ncRNAs promoters contain a putative CEP-1- binding site. CEP-1 regulated ncRNAs were frequently clustered and concentrated on the X chromosome. These results indicate that numerous ncRNAs are involved in CEP-1 transcriptional network and that these are espe- cially enriched on the X chromosome in C. elegans. 展开更多
关键词 p53/CEP-1 C. elegans NCRNA removalrrna NSR-seq high technical replicability
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