首页|基于RNA-Seq技术的毕赤酵母基因组重注释及新型强启动子的发现与序列分析

基于RNA-Seq技术的毕赤酵母基因组重注释及新型强启动子的发现与序列分析

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使用RNA-Seq技术,对毕赤酵母进行了转录组测序.基于测序结果,对现有毕赤酵母基因组进行了重注释,修正了基因组序列中的错误位点861处,发现了新转录本249个及可变剪切现象83个,并更正了553个转录本的错误注释.经过表达谱分析,在毕赤酵母中发现了2个新型强启动子,分别命名为P437和P1431,其驱动的转录本的最高转录水平分别为AOX1基因的1.78倍和3.40倍.序列分析显示,P437和P1431序列中存在着多个酵母转录因子的结合位点.
Genome Re-annotation,Novel Strong Promoter Discovery and Sequence Analysis of Pichia Pastoris Based on RNA-Seq
The transcriptome of Pichia pastoris was sequenced using RNA-Seq technique.Based on the sequencing data,the genome of Pichia pastoris was re-annotated,including 861 revised positions of the genome sequence,553 re-annotated transcripts,249 newly discovered transcripts and 83 alternative splices.In the analysis of gene expression profiling,2 novel strong promoters,named P437 and P1431 respectively,were discovered.The highest transcription levels of the transcripts directed by these promoters are,respectively,1.78 times and 3.40 times of that of AOX1 gene.Several binding sites of transcription factors were revealed in P437 and P1431 by sequence analysis.

Pichia pastorisRNA-Seqgenome re-annotationpromoter

亓飞、蔡孟浩、周祥山、张元兴

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华东理工大学生物反应器工程国家重点实验室,上海 200237

毕赤酵母 RNA-Seq 基因组重注释 启动子

上海市重点学科建设项目

B505

2014

华东理工大学学报(自然科学版)
华东理工大学

华东理工大学学报(自然科学版)

CSTPCDCSCDCHSSCD北大核心
影响因子:0.289
ISSN:1006-3080
年,卷(期):2014.40(2)
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