The Drosophila melanogaster transcriptome by paired-end RNA sequencing

被引:102
作者
Daines, Bryce [1 ,2 ]
Wang, Hui [2 ]
Wang, Liguo [3 ]
Li, Yumei [1 ,2 ]
Han, Yi [2 ]
Emmert, David [4 ]
Gelbart, William [4 ]
Wang, Xia [1 ,2 ]
Li, Wei [3 ,5 ]
Gibbs, Richard [1 ,2 ]
Chen, Rui [1 ,2 ]
机构
[1] Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA
[2] Baylor Coll Med, Human Genome Sequencing Ctr, Houston, TX 77030 USA
[3] Baylor Coll Med, Dan L Duncan Canc Ctr, Houston, TX 77030 USA
[4] Harvard Univ, Dept Mol & Cellular Biol, Cambridge, MA 02138 USA
[5] Baylor Coll Med, Dept Mol & Cellular Biol, Houston, TX 77030 USA
关键词
GENE-EXPRESSION; Y-CHROMOSOME; IDENTIFICATION; GENOME; SEQ;
D O I
10.1101/gr.107854.110
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
RNA-seq was used to generate an extensive map of the Drosophila melanogaster transcriptome by broad sampling of 10 developmental stages. In total, 142.2 million uniquely mapped 64-100-bp paired-end reads were generated on the Illumina GA II yielding 3563 sequencing coverage. More than 95% of FlyBase genes and 90% of splicing junctions were observed. Modifications to 30% of FlyBase gene models were made by extension of untranslated regions, inclusion of novel exons, and identification of novel splicing events. A total of 319 novel transcripts were identified, representing a 2% increase over the current annotation. Alternate splicing was observed in 31% of D. melanogaster genes, a 38% increase over previous estimations, but significantly less than that observed in higher organisms. Much of this splicing is subtle such as tandem alternate splice sites.
引用
收藏
页码:315 / 324
页数:10
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