The Release 5.1 Annotation of Drosophila melanogaster Heterochromatin

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The Release 5.1 Annotation of Drosophila melanogaster Heterochromatin by Christopher D. Smith, ShengQiang Shu, Christopher J. Mungall, and Gary H. Karpen Science Volume 316(5831):1586-1591 June 15, 2007 Published by AAAS

Fig. 1. Computational pipeline results used for the Release 5 Fig. 1. Computational pipeline results used for the Release 5.1 annotation. Computational pipeline results used for the Release 5.1 annotation. An Apollo (36) screenshot of the evidence (black region) and Release 5.1 annotations (light blue region) for scaffold CP000218, which was produced by merging, extending, and finishing the Release 3 WGS scaffolds (AABU01002750 and AABU010027230) (9). New cDNA evidence was used to merge the Release 3.2b annotations CG40067, CG17443, and CG40109 into one Release 5.1 gene (CG41520) and to identify an alternative exon for CG41250-RB (asterisk). ncRNA CG40375 is shown on the opposite strand to illustrate that it is nested within CG41520. CG40388 represents a Release 3.2b gene that is now annotated as a TE fragment. Complete annotation and evidence are shown in (11). Christopher D. Smith et al. Science 2007;316:1586-1591 Published by AAAS

Fig. 2. Evidence of D. melanogaster heterochromatin protein-coding gene annotations. Evidence of D. melanogaster heterochromatin protein-coding gene annotations. Venn diagrams show the percentage of protein-coding genes supported by gene prediction (pink), EST or cDNA (yellow), and/or BLASTX/TBLASTN comparative genomic evidence (blue). (A) Multi-exon genes are likely to be complete, whereas (B) single-exon genes are likely to represent genes that are fragmented across multiple scaffolds. The number of genes measured for each class are indicated, as well as the number and percent of genes with putative orthologs in melanogaster group species, nonmelanogaster group Drosophilids, or other insect species. Christopher D. Smith et al. Science 2007;316:1586-1591 Published by AAAS

Fig. 3. Comparative analysis summary for D Fig. 3. Comparative analysis summary for D. melanogaster heterochromatin genes. Comparative analysis summary for D. melanogaster heterochromatin genes. (A) Number of heterochromatin protein-coding genes with a predicted ortholog in a given species, ordered (left to right) by increasing evolutionary distance from D. melanogaster. (B) Frequency histograms showing the percentage of heterochromatin protein-coding genes with a predicted ortholog in the 16 insect species tested. (C) Scatter plots of intron lengths (bp) for euchromatin and heterochromatin protein-coding gene introns conserved in either D. erecta or D. virilis. Each data point refers to a single conserved intron. Correlation coefficients (r) for intron lengths are indicated. Christopher D. Smith et al. Science 2007;316:1586-1591 Published by AAAS

Fig. 4. Density of repeat and gene features across the heterochromatin. Density of repeat and gene features across the heterochromatin. The average percentages of indicated annotation types are shown for each chromosome region (total length in boxes below the x axis). Euchromatin is an average of the noncentric regions of arms 2, 3, and X only. 2Lh, 2Rh, 3Lh, 3Rh, and Xh describe heterochromatic regions that are contiguous with the chromosome arms, whereas the Het regions are mapped to arms and ordered, but not necessarily in the correct orientation (8, 9). The average percentages of sequences for LTR- and LINE-like retrotransposons (red), DNA transposons (green), other and unknown repeats (blue), and TRF tandem repeats and satellite sequences (gray) are indicated. The average number of genes per 100 kb is shown above each histogram. Christopher D. Smith et al. Science 2007;316:1586-1591 Published by AAAS

Fig. 5. Overrepresented GO terms in heterochromatin versus euchromatin genes. Overrepresented GO terms in heterochromatin versus euchromatin genes. The percentages of GO molecular-function domains for genes in heterochomatin (red) and euchromatin (blue) are shown. Numbers in parentheses indicate the actual number of domains in heterochromatin. P-value significance scores are shown to the right. Complete GO analyses are presented in the SOM text. Christopher D. Smith et al. Science 2007;316:1586-1591 Published by AAAS