- Open Access
A draft annotation and overview of the human genome
© Wright et al., licensee BioMed Central Ltd 2001
- Received: 12 February 2001
- Accepted: 1 June 2001
- Published: 4 July 2001
The recent draft assembly of the human genome provides a unified basis for describing genomic structure and function. The draft is sufficiently accurate to provide useful annotation, enabling direct observations of previously inferred biological phenomena.
We report here a functionally annotated human gene index placed directly on the genome. The index is based on the integration of public transcript, protein, and mapping information, supplemented with computational prediction. We describe numerous global features of the genome and examine the relationship of various genetic maps with the assembly. In addition, initial sequence analysis reveals highly ordered chromosomal landscapes associated with paralogous gene clusters and distinct functional compartments. Finally, these annotation data were synthesized to produce observations of gene density and number that accord well with historical estimates. Such a global approach had previously been described only for chromosomes 21 and 22, which together account for 2.2% of the genome.
We estimate that the genome contains 65,000-75,000 transcriptional units, with exon sequences comprising 4%. The creation of a comprehensive gene index requires the synthesis of all available computational and experimental evidence.
- Bacterial Artificial Chromosome
- Additional Data File
- Genomic Clone
- Radiation Hybrid
- Transcriptional Unit
The sequence of the human nuclear genome has been completed in draft form by an international public consortium consisting of 16 sequencing centers and associated computational facilities . A private commercial version of the genome has also been sequenced and assembled using a whole genome shotgun approach . Many lower organisms have been sequenced to date , but the 3.2 billion base pair (bp) human genome is approximately 25 times as large as the largest currently finished genomes - Drosophila melanogaster at 120 megabases (Mb)  and Arabidopsis thaliana at 115 Mb .
As of late 2000, the public human sequence was primarily based on approximately 24,000 accessioned bacterial artificial chromosome (BAC) clones covering 97% of the euchromatic portion of the genome . The sequence of these clones is approximately 93% complete to at least 4-fold coverage . Thirty percent of the genome is in finished form, including the entire sequence of chromosomes 21 and 22 . These clones represent the most complete sequence information available, with overlapping clones positioned on a framework map using restriction fingerprinting . However, reduction to a single consensus sequence permits placement of genes and other chromosomal structures in their proper positional context. Recently, the consortium has distributed a working draft assembly of the entire genome that removes redundancies, orients sequence fragments and clearly indicates gaps arising from sequencing and assembly. The total assembled length is 3.08 billion bp - about 4% smaller than estimates of genome size based on flow cytometry , presumably due to the exclusion of constitutive heterochromatic regions and centromeres. Major gaps (50-200 kilobases (kb)) comprise 16% of the assembly, whereas minor gaps (100 or fewer bp) and low-quality calls comprise 0.5%.
Large-scale sequencing will continue until at least 2003. The current coverage is, however, sufficient for the Human Genome Project to enter a new phase, in which the entire sequence can be analyzed to identify genes, regulatory regions and other genomic elements and structures. Linkage and genetic association studies can be immediately followed by investigation of candidate regions. The assembly provides simplified descriptions of the genome, as disparate data sources such as GenBank and numerous expressed sequence tag (EST) and protein databases are unified. Similarly, formerly independent maps, based on cytogenetic banding patterns, meiotic crossovers and radiation hybrids, may be placed within the single consensus sequence.
Combine and conquer
Public attention surrounding completion of the draft human sequence has fostered the impression that we are entering a 'post-genomic' era, and that description of genes and their functions is straightforward. However, the challenges in genome annotation remain daunting , and the research community can anticipate years of additional work and manual curation to produce a true gene map of high quality.
Functional annotation of the genome is primarily hampered by the lack of a unified transcript index. Current transcript information still largely consists of anonymous and highly redundant ESTs. The situation is further complicated by extensive splicing variation and elusive gene expression. To address these problems, the Ensembl consortium relies initially on computational prediction, followed by confirmation with EST/protein alignments . However, pure computational approaches can give differing results , and may miss 20% or more of transcript-supported exons . Other gene identification approaches rely on selecting and grouping ESTs into putative gene indices [14,15], or consensus sequences [16,17]. These approaches emphasize internal consistency and result in limited EST populations that only partially overlap. The genome sequence serves as a powerful arbiter of the quality of EST evidence, and will enable consolidation of additional exons into transcriptional units. Thus, we adopt a more inclusive approach.
Our approach is to combine the major public cDNA, EST and protein databases, resolve redundancies, and place the resulting exonic sequences uniquely on the genome using the program Blast. We refer to these genomic segments (technically high-scoring segment pairs ) as 'exons', although the alignment evidence awaits future biological confirmation. Splicing evidence was carefully maintained within genomic clones, and across clones using the fingerprint map. For a given transcript, only the best match to genomic sequence (using splicing evidence, length and high sequence identity) was preserved, resulting in a unique location for each exonic unit within each database. We have successfully applied this approach to integrate UniGene consensus sequences into the human genome draft .
To compile a truly unique exonic index, redundancies must also be resolved across transcript databases. We grouped the databases into ranked categories and ordered them within categories. Transcripts with known boundary information (using the untranslated region database (UTR-DB))  or full-length cDNAs in the human transcript database (HTDB)  were given precedence over other records. Consensus transcripts were given precedence over individual ESTs because they provide greatly improved specificity, splicing evidence and transcript integrity. We assembled UniGene-based human , mouse and rat consensus transcripts. Collectively, the databases represent almost all public information on known genes, transcripts and relevant homologous sequences. When aligned segments overlapped, only the segments from the highest-ranked categories were retained. After resolution of overlapping exons, a new exonic index of contiguous spliced components was formed. Each member of this new index inherited the rank of its highest-ranked exon, in order to facilitate subsequent identification of transcriptional units. Our approach also ensures that known genes are represented only once in the final gene map.
Identification of exons on the genome
Percent placed (%)
Total unique exons
Exons in complete ORFs
Exons in partial ORFs
Exon length (bp)
ORF length (bp)
Putative genes (non-splicing singletons)
Protein homology (Pfam hits)
When all of the databases are considered, 613,183 unique exons were placed, including 299,014 in complete open reading frames (ORFs) and 55,860 in partial ORFs. The total putative exonic lengths add to 106 Mb, or about 4% of the sequenced genome. About 50% of our described exonic sequences are in ORFs (Table 1). It is generally thought that the majority of exonic sequence is coding, suggesting that additional coding sequences remain to be discovered. This possible bias towards untranslated regions is to be expected, as current transcript information is largely derived from the 3' or 5' termini of cDNA libraries. At least 30-40% of the known genes or transcript indices contain one or more internal transcripts, suggesting alternative splicing, internal genes or occasional artifacts (misassembly or genomic contamination). The prevalence of alternative splicing remains unknown, but may occur frequently . 'Sandwiched' transcripts were merged with their flanking indices, unless both the internal and the flanking sequences were from distinct known genes (< 150 apparent internal genes). In addition, we observed a small number of apparently overlapping exons (about 530 on opposite strands) .
Genome-wide assessment of ab initio gene prediction methods
Our consolidated exonic index is of inherent biological interest, but it is desirable to further identify transcriptional boundaries to create a putative gene index. We used an approach designed to minimize fragmentation of exons and provide conservative gene counts (see Materials and methods). The following criteria were used to identify gene boundaries: known 5' or 3' UTR sequences in UTR-DB; full-length cDNAs in HTDB; exons in partial ORFs as possible boundaries of coding regions; exons without continuous ORFs as additional UTR sequences; CpG islands; and gene boundaries predicted by Genscan. Multiple in-frame exons in a continuous ORF were always considered part of a single gene, an approach that tends to consolidate exons rather than create spurious additional genes. Additional consolidation resulted from extension of boundaries for multiple exons not residing in ORFs until the occurrence of genomic landmarks described above. The success of this approach depends largely on the extension and consolidation of overlapping transcripts, and the integrity of ORFs and other genomic landmarks provided by the draft sequences.
Table 1 lists the number of genes added by each database to the cumulative sum. The total number of known genes in UTR-DB, HTDB and HINT is 16,673. This compares with 11,191 entries with at least partial functional annotation in UniGene (May 2000 build) and 11,863 entries in the HUGO Human Gene Nomenclature database . Approximately 48% of the transcriptional units were based on consensus transcripts and 28% based on individual ESTs. A total of 9,372 transcriptional units were based on singleton transcripts without splicing evidence. Single-exon (intronless) genes occur with appreciable frequency in the human genome . At least one third of the singletons in our gene index contain intact ORFs, and are predominantly histones, G-protein receptors, olfactory receptors, and cytokines or their homologs/paralogs. The remaining two-thirds of the singletons do not have intact ORFs, and possibly represent pseudogenes, genomic contamination or other artifacts. It is thought that most intronless genes originated from retrotranspositions of SINEs and LINEs . Thus, the total number of single-exon genes might be under-represented in this study, because of the repeat masking process necessary prior to our analysis. This also applies to the tRNA, rRNA and other snRNAs in the human genome, which have been similarly masked. A total of 1,437 units were supported only by rodent transcript consensus, predominantly derived from cDNA libraries of early embryogenesis or tissues of the central nervous system. An additional 3,154 units were identified on the basis of protein homology, with exons supported by at least one gene prediction program. Our approach yields an overall estimate of 75,982 transcriptional units, with 66,610 supported by multiple transcripts or individual transcripts with splicing evidence. Therefore, the consolidation and integration of mainly the transcript information into the genomic consensus assures that our putative gene index is largely based on experimental evidence, rather than ab initio gene prediction.
It is important to note that pseudogenes are common in the human genome, and are thought to largely originate from gene duplication or retrotransposition . The extent to which pseudogenes remain transcriptionally active is still largely unknown, however. It is also difficult to identify pseudogenes computationally. Although nonfunctional pseudogenes can have characteristic structural features, some functional genes can also exhibit such features .
We observed that 45% of the gene units were associated with CpG islands (defined as 10 kb upstream or within the gene). For the 6,500 known genes with known 5' boundaries, the value was 40%. The average genomic size of each of our transcriptional units from the first to last identified exon (including only transcript or protein-based exons) is approximately 12 kb. The overall average gene length is likely to be significantly longer, but full-length cDNA information is not yet available for most genes.
Comparison of gene counts
Ewing and Green  examined 680 assumed genes on chromosome 22 and found matches to 2% of a selected set of assembled EST contigs. The sampling approach assumes that the 680 genes represent 2% of all genes, resulting in an overall count of 34,000. An examination of evolutionarily conserved regions in known genes on chromosome 22 in humans compared to the fish Tetraodon nigroviridis  results in an estimate of around 30,000 genes, assuming a uniform rate of conserved regions per true gene. These approaches resulted in similar estimates when applied to larger sets of mRNAs or known genes, and are similar to the current 33,000 genes reported by Ensembl as having Genscan computational support and EST confirmation. All of these estimates are carefully constructed and remarkably concordant, and we propose possible explanations for the difference from our results. The differences do not result entirely from the reliance on transcriptional evidence, as has been proposed .
Our estimate of 854 genes on chromosome 22 is 25% greater than that of Ewing and Green , but represents only 1.4% (rather than 2%) of our gene total. It was noted  that high gene expression on chromosome 22 could result in low gene count estimates by biasing the reference sample. In addition, known genes may be more highly expressed than unknown genes, which presumably aided their initial identification and characterization. Our evaluation of EST evidence supports the existence of both forms of bias. We have found that 5% of Ewing and Green's original set of EST contigs (selected with less stringent criteria than those used to estimate gene counts) map to chromosome 22. An examination of UniGene transcripts (May 2000) reveals that the known genes contain a median of 41 entries, whereas anonymous transcripts contain a median of just two entries. This is not entirely explained by the greater length of the known gene-like transcripts (having been correctly assembled as a single unit). In dividing the number of ESTs in the consensus by its length, we obtain a median of 0.017 entries per base pair for known genes and 0.005 entries per base pair for anonymous transcripts. On chromosome 22, the median number of ESTs per anonymous transcript is three, which is significantly higher than that among other transcripts on the genome (geometric mean 3.76 versus 3.11 for other chromosomes, p < 0.0001, Wilcoxon rank-sum test). The estimate based on conserved regions  is calibrated using known genes. This approach also introduces bias, as such genes appear more likely to belong to the evolutionary core proteome. Known genes comprise 22% of all of our transcriptional units, but comprise 71% of our units which are conserved with rodents, Drosophila and Caenorhabditis elegans. A recent high gene estimate based on transcript evidence , again using chromosome 22, appears to result from less stringent alignment criteria, resulting in many putative genes.
As genomic annotation proceeds, the number of protein-coding genes will become clearer. Our approach seems to rule out artifactual or genomic contamination as the predominant explanation for transcriptional units with unknown function or protein homology. Ensembl has recently listed a count of 170,160 'confirmed' exons, whereas we report 299,014 in complete ORFs and many more in untranslated regions, suggesting that our approach identifies considerable additional transcription. We point out that only 58% of known genes exhibit protein homology (Table 1) and, for example, a large proportion of transcriptional units have not been functionally classified in Drosophila . We therefore propose that most of the unclassified transcriptional units are in fact coding - the lack of protein homology may reflect difficulty in studying these proteins, or rapid gene evolution, and some portion is likely to function at the RNA level .
The placement of transcriptional units is not without error, as most genomic clones are unfinished and the restriction fingerprint map can be subject to misassembly. To resolve placement errors, we used a relational database to integrate information from several independent maps, including Genemap'99, assembled genomic contigs, and fingerprint, radiation hybrid and cytogenetic maps (see Materials and methods). Placement required a minimum of three concordant criteria. Together, a total of 75,982 transcriptional units were placed on the genome, providing an initial glimpse of a complete gene map. The map and associated functional annotation are available as additional data files.
Ontological classification of 22,339 human gene products
Number of transcripts
Number of transcripts
Nucleotide and nucleic acid metabolism
Cell cycle regulator
Amino acid and derivative metabolism
Cytoskeleton structural protein
Proteolysis and peptidolysis
Monocarbon compound metabolism
Protein kinase inhibitor
Coenzyme and prosthetic group metabolism
Steroid compound metabolism
Protein phosphatase inhibitor
Small molecular transport
Organelle organization and biogenesis
Nuclear organization and biogenesis
Cytoplasm organization and biogenesis
G protein-linked receptor
Ligand binding or carrier
Neurogenesis and regeneration
The annotation also allows us to assess the protein composition of human versus other species. A BlastX result of E < 10-20 was required in cross-species DNA-protein alignments to be considered homologous. A total of 20,892 human transcriptional units (30% of all units) are homologous with at least one other species; 5,792 (10%) were conserved across mammals (mouse or rat), Drosophila, and C. elegans. A total of 1,759 (3%) were conserved across all of these species and yeast. These values are very consistent with a recent comparative genomic survey .
Global tissue expression profiles
During the assembly o UniGene , we retained the library source for each EST, via links provided by UniGene to the IMAGE consortium . Most of the 2,500 libraries comprising UniGene ESTs were derived from single tissues or embryonic stages, and we further standardized the library source annotation into 102 categories. Keywords and derived categories are available as additional data files. The most highly represented categories were various types of tumors (15.0% of all ESTs), fetal tissue (10.7%), embryo (6.2%), infant (5.1%), and testis (4.3%). We reasoned that some genes might exhibit highly tissue-specific expression, such that most of the ESTs comprising a transcript would be derived from the tissue. The identified genes are potential candidates for diseases of the involved tissues. Similar approaches have been used to identify candidate genes for pathologies of the prostate  and retina . We explore here the global nature of tissue/source specificity. The result was 7,459 HINT transcripts with highly significant tissue-specificity (11%). Many of these are known genes, and an examination of the most specific transcripts revealed clear relationships to the associated tissue. For example, a search for retina-specific genes revealed that the ten most significantly associated with retina include five known genes, all related to retina function. Four are implicated in retina pathology: GNAT1 and ARR (night blindness), RHO (retinitis pigmentosa), and GUCA1A (cone dystrophy). Similar results were observed in numerous other tissues, although not as obviously related to pathology. The results appear especially striking for tissues with substantial EST representation, including brain, lung, liver, kidney, and testis, suggesting that putative tissue involvement can be inferred for many anonymous ESTs. Where possible, the tissue expression profile has been incorporated into the annotation of our gene index. Approximately half (50.5%) of the tissue-specific clusters were from embryonic tissue libraries (while such tissue contributed 6.2% of all UniGene ESTs). This striking result is consistent with the highly regulated and specific nature of embryonic development . The embryo category is followed by brain (9.7% brain-specific versus 3.8% of ESTs) in number of tissue-specific clusters, kidney (5.5% versus 3.5%), and testis (6.1% versus 4.3%). We also examined the locations of the tissue-specific transcripts on the genome, and found no evidence of regional clustering (see description of regional functional clustering in Materials and methods).
A global view of the human genome
In keeping with the long-standing clinical importance of cytogenetics, it is important to align Giemsa-staining G (dark) cytobands versus R (pale) bands (ISCN 1995) to the assembly . Cytoband boundaries on genomic sequence have been depicted with apparent precision [13,42] but in fact are largely unknown. With only a few-fold genomic coverage, the gap sizes in unfinished sequence are difficult to estimate precisely. Thus, it is preferable to align the cytoband positions to the fixed assembly rather than the reverse. Such an 'assembly-corrected' alignment was performed using genes/ESTs that have been mapped cytogenetically and also placed on the assembly. This alignment is approximate, as the resolution of conventional staining techniques and fluorescence in situ hybridization (FISH) is limited to 1-3 Mb .
Density of genomic features
A total of 48,000 CpG islands were found on the assembly using standard criteria  (see Figure 1 legend), with a median length of 336 bp. As sequencing gaps are filled, this number may increase. Considering the varying definitions of CpG islands (especially the minimum length of CpG-rich region), this number is in close agreement with the estimate of 45,000 obtained by Antequera and Bird  using methylation-sensitive restriction enzymes. The CpG island density is also in agreement with a report of FISH karyotypes using CpG island probes  with contrasting fluorescent signal in late-replicating regions. Extended regions of high CpG island density, such as the terminus of 1p and 1q21-q22, are apparent in the FISH assay. Short spikes of CpG islands (for example, in 3p26 and 3p25 of Figure 1) do not obviously appear in the assay, perhaps because they are below the resolution of FISH or are part of transcriptionally active regions.
In contrast to exon and CpG island density, GC content shows limited variation - in the range 35-55% for most 1 Mb intervals. The overall GC content is 41.1%. This compares with estimates in the range of 40-41% based on density gradient centrifugation  and flow cytometry .
Consistent with previous reports  Alu repeats show an apparent positive correlation with exon, CpG and GC densities, while LINE1 densities do not show such correlation. Approximately 1.1 million Alu repeats were identified, as expected . However, a total of 758,000 LINE1 repeats were identified - 40% higher than estimates based on a sampling of sequenced regions . Minisatellites of the hypervariable family (20-50 bp repeat size) are dispersed throughout the genome but, as expected , show sharp spikes in subtelomeric regions of most chromosomes.
Comparison of cytogenetic bands
(a) Density of features per megabase in Giemsa-staining cytogenetic bands
(b) Correlation of features in 1Mb intervals
Comparisons to genetic and radiation hybrid maps
The radiation hybrid plots tend to be more linear, which is consistent with the model that radiation induces chromosomal breakpoints essentially uniformly . However, jumps in the Genebridge 4 (GB4) map occur at the centromere on most chromosomes. This may result from incomplete centromeric sequencing and assembly, so that a large centromeric gap might not appear as such. Alternatively, the jumps may reflect statistical difficulties in estimating break-point rates across the centromere. We note that no jump occurs in the G3 map, apparently because the higher radiation intensity produces insufficient marker pairs in the rescued hybrids that span the centromere. Thus, the jump cannot be accurately estimated and was simply suppressed in the published map . The GB4 jump is strikingly large on several chromosomes, and we propose that the jumps might reflect increased radiation sensitivity at the centromere. This hypothesis is worth additional investigation.
Clusters and compartments
As an example of functional duplication, we note that more than 60% of the entire zinc-finger (ZNF) families are mapped to chromosome 19, restricted to six large tandemly duplicated gene clusters spanning the chromosome. More than one type of ZNF is found within each cluster, presumably as a result of sequence divergence. A majority of these ZNFs densely populate the 22-27 Mb region (see Figure 5). The remaining ZNFs are mapped to 15q21 (bZIP), 7q11 (KRAB), 11q13 (C3HC4, 11q23 (C3HC4), 6p21 (C2H2), 1op11 (KRAB), 1oq11 (C2H2), 16p11 (C2H2) 9q22 (C2H2), and 3p21 (C2H2).
The largest functional group is related to phosphoryl transfer and protein kinases. Interestingly, many of the biological functions involving phosphoryl transfer form large gene clusters as well. For example, the mitogen-activated protein kinase family, phosphatidylinositol-4 phosphate 5-kinase family, protein kinase C family and at least 55 other diverse protein kinases are distributed in five gene clusters on chromosome 1, only about one third of which have been previously described. Similar gene clusters are also found on chromosomes 2, 3, 6,19, 22 and X. In addition, DNA repair genes form gene clusters on different chromosomes, with postmeiotic segregation proteins (PMS) on chromosome 7, glycosidases on chromosome 12, MutS homologs on chromosome 6, MutT homologs on chromosome X, MutL homologs on chromosome 2, Rad1/Rec1/Rad7 homologs on chromosome 10, excision repair on chromosome 11, and repair for single-strand nicks on chromosome 19. Additional regions of high and striking sequence similarity and the list of matching sequences with protein homology are provided in the additional data files.
Paralogous genes resulting from recent gene duplication might preserve the same functionality and regulatory apparatus as their progenitors. We used chromosome 19 as the model to test this hypothesis by comparing the cDNA library profiles of spatially adjacent paralogous genes. At least one of the ZNF clusters (22-27 Mb region, Figure 5) appears to be more recent than the remaining clusters on the same chromosome (> 80% sequence identity). Intriguingly, two distinct tissue library profiles were scored for a total of 38 mapped ZNF paralogs, with the telomeric portion of the cluster predominantly expressed in germ cells (589/622 ESTs). The remaining members of the cluster were primarily expressed in embryos 9-19 weeks of age (145/167 ESTs). The same phenomenon did not hold for the ZNF clusters, where sequence similarity is lower. We were motivated to find additional paralogous genes, with their regulation similarly preserved. We mapped gene indices on duplicated genomic sequences. Alcohol dehydrogenases (1, 2, 3, 4, 5 and 7) are tandemly duplicated on 4q21, with their transcripts consistently being over-represented in embryonic and fetal cDNA libraries. Similar observations were obtained for other gene clusters, including amylases on 1p21, annexins on 4q21, homeobox proteins on 7p15 and 17q21, metallothioneins on 16q13, crystalline proteins on 2q33, glutathione-S-transferases (m1, m2, m3, m4 and m5) on 1p13, histone families (H2A/H2B/H3/H4) on 6p21, killer cell lectin-like receptors on 12p13, proline-rich proteins on 12p13, protocadherins on 5p15, s100 calcium-binding proteins on 1q21, keratins on 17q12, ADP-ribosylation factors (3, 4 and 5) on 10q22, and the major histocompatibility complex on 6p21. Together, these observations strongly support the notion that much of the regional clustering of functionally related proteins originates from gene duplication.
Clustering of ontological groups
We also examined the locations of all transcriptional units that had been classified according to a gene ontology-derived schema (Table 3, and see Materials and methods) for evidence of regional clustering of functionally related proteins. We applied a test that corrected for regional gene density, and found substantial evidence for regional clustering among the transcripts belonging to the same category (see additional data files for location plots for the top 60 ontological categories). Such clustering is pervasive - much of it is likely to have arisen from duplication in which functional units have been preserved.
As an additional demonstration of the duplication phenomenon, we considered the occurrence of Pfam motifs within ORFs, with only the best Pfam match retained per ORF (around 1,930 of the 2,011 Pfam categories were represented). Matching successive runs of four or more (that occur at least three times on the genome) appear in the additional data files. Many of the runs occur on the near-diagonal. Most involve four identical Pfam categories in succession, or a double run of two categories, again pointing to local duplication.
We also examined the runs of six or more gene units in which the ontological classifications occur in the same order (or the reverse) in multiple locations on the genome. A dot-matrix plot across the genome appears in the additional data files. The plot shows clear evidence of local duplication, while the distant matches (even across chromosomes) are under investigation in the context of the complete sequence. We have noticed interesting associations among membrane proteins, ion channels, electron transporters, ATP-binding cassettes, and genes involving metabolism on chromosomes 2, 5 and 7. Proximity may be important for regulating functionally coupled genes, and intriguing observations of this phenomenon are well established in prokaryotic organisms  and recently reported in yeast . We are investigating the possibility that at least some of the positional-functional coupling may be due to regulated mechanisms other than gene duplication.
The human genome is a capacious resource that will support years of intensive investigation. The quality of the draft sequence has now reached the point that genetic maps can truly be integrated into the genome. Analysis at the sequence level shows pervasive local and distant duplication, much of which preserves function. We have found evidence for a large number of transcriptional units (65,000-75,000) and performed initial annotation and classification. The effective study of transcription and protein function requires the compilation of all available evidence of transcription and protein homology.
Since the initial submission of this manuscript, two reports have appeared [67,68] in which the human genome is analyzed and described. The raw genomic sequence used for the present study was generated by the Human Genome Consortium (HGC), and is principally the same as that used in their report . In our effort, we have benefited from early-release and open data policies adopted by the consortium. The three reports offer insights into varying aspects of the genome. In our report we have emphasized the compilation of all available transcriptional evidence, and have made observations of functional-positional clustering of genes and global tissue specificity that will provide the basis for in-depth investigation.
The other reports have arrived at estimates of approximately 30,000 genes in the genome, and the ensuing attention leaves the unfortunate impression that genomic analysis consists primarily of gene counting. While our estimate of 65,000-75,000 transcriptional units clearly differs from these estimates, it is useful to consider that there is much independent agreement in the reports. We have placed around 15,000 known genes in the genome, and described 33,000 that have substantial homology to the major protein databases. These figures are very comparable to the known and 'confirmed' genes, respectively, placed on the sequence by Celera Genomics and HGC. The Celera and HGC reports rely on a combination of computational gene prediction and transcriptional evidence to identify genes, in a manner that may be highly conservative. Our approach to identifying genes and exons is more heavily transcript-based, with the presumption that pure computational gene prediction may still have substantial false-negative rates. In applying this approach, we find experimental evidence for many novel exons with clear splicing evidence, on the order of twice as many as described in the other reports. This fact largely explains our greater number of transcriptional units, as our mean number of exons per transcriptional unit (613,183/759,822 = 8.07) is very comparable to the Celera and HGC reports.
We hold that the reliance on ab initio approaches presents difficulties, as known genes may be more highly expressed and may present a biased sample for calibration. Another difference in the approaches is that we have used pre-assembled consensus transcripts whenever possible in alignment to the genome. The use of such consensus sequences is likely to improve alignment, increase splicing evidence, and has been shown to improve the detection of protein homology . We propose that the remaining 32,000-42,000 units we have identified will represent a useful resource for additional investigation as genomic annotation proceeds. A comparison of all three approaches will surely yield new insights.
The 26 June 2000 version of the repeat-masked draft sequences was downloaded from the Ensembl Genome Server  and blasted against cDNA and protein sequences by using the Blast program compiled from the NCBI toolkit (6.1) on a 32-node SGI Linux/Intel Cluster, with four 550 MHz Pentium III Xeon processors and 2 GB of RAM on each node. The following databases were used: Human UTR-DB (EBI) (version 13) ; Human Transcript Database (Baylor University) (version 1) ; GenBank CDS (NCBI) (only PRI mRNA sequences were used, version 119) ; HINT (Ohio State University) ; EST Assembly Project (University of Washington) ; TIGR Human Gene Index (version 4.5) ; dbEST (NCBI) (version 119) ; MINT and RINT (Ohio State University) ; EMBL Rodent (EMBL) (version 63) ; SWISS-PROT (EMBL) (version 39) ; TrEMBL (EMBL) (version 14) ; PIR (MIPS-JIPID) (version 65) ; and Pfam (Sanger Centre) (version 5.4) . Gene prediction programs used are described in Table 2. The Mouse and Rat Indices of Non-redundant Transcripts (MINT and RINT) were derived from Mouse and Rat UniGene  using the same approach that we have applied to human UniGene . Briefly, chimeric sequences were removed, UniGene transcripts were assembled into sequence contigs, and links to progenitor records retained.
The genome-wide hit expectation value was set at E < 10-25 (BlastN) or E < 10-15 (BlastX) to filter out nonspecific high-scoring segment pairs (HSPs). Default parameters of Blast were used. The Blast report was parsed into field-specific tables using the program MSPcrunch Version 2.3 . The resulting table was processed using a set of Perl scripts by first retaining only the HSPs that were spliced from the same transcripts on the same genomic contig. The same process was then applied to the HSPs on the genomic sequences. Spliced HSPs from the same transcripts were retained, followed by the singleton HSPs that were both longer and higher in sequence identity over their overlapping counterparts, resulting in a unique placement for each cDNA segment on the genomic sequence.
Prediction of transcriptional units
A set of Perl scripts was used to implement the algorithm described below. Genomic clones were ordered and oriented using the fingerprint map and draft assembly. Within unfinished clones, sequence contigs were further ordered and oriented according to Ensembl's assembly . This mapping produced the positional context necessary for consolidating fragmented exon units. Where necessary, small sequencing gaps (100 bp or fewer) were ignored and genomic clones were considered contiguous except where a large gap was indicated in the draft assembly (> 50 kb). ORFs were determined using the program getorf . The exon index is an integrated table generated by a Sybase relational database, consisting of chromosome number, fingerprinted contig (FPC) ID, FPC contig order, BAC contig ID, BAC contig order, BAC contig orientation, starting position of exon on BAC contig, end position of exon on BAC contig, exon orientation, transcript orientation (available from GenBank, IMAGE, UniGene, HINT and dbEST), evidence (transcript, protein, gene prediction, ORF, Pfam), database name (Table 1), feature (poly(A) signal, CpG island, Genscan boundary), starting position on exon (or feature), end position on exon (or feature), score (BlastN, BlastX). The index was first ordered and oriented for the individual BAC contigs according to Ensembl or UCSC  maps. The resulting contigs were then ordered and oriented according to the FPC order and orientation information in the UCSC genome assembly, resulting in a numeric sorting order for all the individual contigs. In addition, large gap information (> 50 kb) available from the UCSC assembly was incorporated into the same index, where no overlapping information was available between presumably adjacent BACs.
The consolidation algorithm follows a hierarchy in which unit boundaries are respected for the highest-ranking feature. The features in descending ranking were: UTRs based on known UTR indices; exons containing no ORFs or incomplete ORFs; boundaries of known full-length cDNAs (HTDB-based indices); EST orientation information (5' or 3' origin from the original IMAGE, UniGene/HINT, and dbEST databases); and Genscan-predicted poly(A) signals. When clear boundary indicators were not available, information from the transcript indices HINT (assembled from UniGene)  and EG  were used directly as secondary evidence for potential gene boundaries. The rationale is that each UniGene cluster has at least one known gene, or two sets of ESTs representing both the 5' and 3' termini of a gene, or at least one EST containing a poly(A) signal . Similar stringent criteria were used in Ewing and Green's EST assemblies . Multiple exons not residing in intact ORFs were consolidated until the occurrence of exons in a partial or complete ORF. Multiple in-frame exons in a continuous ORF were always considered part of a single gene. To prevent any overconsolidation as a result of lack of transitional exons (in partial or complete ORFs) for adjacent genes, CpG islands, large gaps (> 50 kb) between exons and Genscan prediction were used as gene boundaries when higher-ranking boundary information was unavailable. In such instances, HINT and EG index identity was respected. Although a variety of criteria were used for determining transcriptional unit boundaries, the vast majority of the consolidation was achieved on the basis of terminal information from gene indices and transition and continuation of open reading frames.
A relational database was used to integrate multiple largely independent maps for the genomic clones, where transcripts had been placed. This integration thus results in a transcript map based on the order and position of genomic clones. Individual sequencing contigs within each unfinished clone were oriented using the Ensembl contig map . The fingerprint (see , version 15 June 2000), GoldenPath assembly (Versions 15 June and 5 September 2000), and radiation hybrid maps  were used to place genomic clones into their chromosomal context. As a substantial number of the clones in the working draft had not been physically typed with RH or genetic markers, the program e-PCR  and primers collected in the RHdb  and Genethon  were used under stringent criteria (mismatch = o, margin = 50, and word size = 7). Genetic mapping information was obtained from the Marshfield map . In addition, Genemap'99 for cDNA was integrated into the genomic clones harboring HINT consensus transcripts. For the HINT consensus with more than one mapped EST, an averaged RH position was used. Cytogenetic bands were inherited from the original UniGene database. Furthermore, we incorporated a weighted composite quality score for the following four maps: Genemap'99 (the number of consistently mapped ESTs and their associated genomic clones), e-PCR (the number of consistently mapped sequence-tagged sites (STSs) in a genomic clone), FPC (the supporting evidence in the original database), Blast (evidence of splicing). On the basis of such an integrated database schema, mapping information from sequence, clone, contigs, radiation hybrid and cytogenetic positions for a given transcript could be obtained through a SQL (Structured Query Language) join statement.
We noted the total number of ESTs contributed by each tissue to compute an expected proportion. For each HINT consensus transcript, we identified the tissue/source contributing the most ESTs to the consensus. The expected binomial distribution for the fixed number of ESTs in the consensus was used to compute a p-value, which was then Bonferroni-corrected for the 81 tissues × 67,000 HINT consensus transcripts.
G bands are known to be relatively AT-rich, but the precise relationship between sequence and cytoband position is too poorly understood to be used for alignment. Genes/ESTs with cytoband position appearing in UniGene were placed on the full genome assembly. Cytoband cutpoints were used to create a scatterplot with the center of the cytoband forming the x-coordinate, and assembly position as the y-coordinate. Outliers were identified as points lying more than 2.5 standard errors outside of prediction intervals from a third-degree polynomial regression fit. A Loess regression fit was used on the remaining points to estimate cytoband boundaries, with p and q arms fitted separately. Centromeres and heterochromatic regions were assumed not sequenced, on the basis of a review of current clone frameworks. Primary sources for assignments of genes to heterochromatic regions were examined and in most cases deemed inconclusive. An exception is chromosome 19, which has a considerable number of genes assigned to 19q12 and finished sequence in the region. Scatterplots and regression fits for the entire genome are in the additional data files.
Genomic feature correlations
All 1 Mb intervals were combined to produce Table 4, but statistical tests were performed by computing ratios and correlations within each chromosome separately, in order to account for correlation of features within each chromosome. These statistics were then compared across the chromosomes to an appropriate null value using single sample t-tests. Some of the features were skewed, and pairwise comparisons were performed using Spearman rank correlations. A Bonferroni multiple-comparison procedure was applied to the 15 unique correlations.
Regional functional clustering
Apparently significant clustering can arise from the fact that genes exhibit regional clustering. To correct for this, we considered the physical order of all mapped transcripts and calculated the distances (in ranked location) between transcripts belonging to the same ontological category. Under the null hypothesis, the transcripts in a category should be distributed uniformly among all mapped transcripts with ontological classification, and the successive distances are approximately truncated exponential. On this basis we compared the observed tenth percentile of successive distances to that under the null hypothesis to compute a p-value. All tests were highly significant, with p < 0.0001 for 59 of the 60 largest categories, and quantile-quantile plots with observed versus expected distributions showed striking evidence of clustering. These tests were confirmed with permutation tests with empirical generations under the null hypothesis. As a conservative correction for the possibility that separate transcriptional units might belong to the same gene, we considered successive distances for every other transcript. These tests were also significant, with p < 0.01 for the 60 categories.
Additional data files are available online as follows: transcriptional units; computational prediction; FPC, e-PCR, RH and assembly maps; functional annotation; tissue expression profiles; a global view of the human genome; density of genomic features; comparisons to genetic and RH maps; clusters and compartments; and clustering of ontological groups.
We thank the numerous investigators of the Human Genome Project for sequence availability and for open-data policies, Albert de la Chapelle for support and encouragement, Jian-Ping Guo, Solomon Gibbs, Dara Good-heart, Daolong Wang and Anthony Jakubisin for assistance, the Ohio Supercomputer Center (OSC) for invaluable assistance and computational resources, the Institute for Pure and Applied Mathematics at UCLA for provision of technical facilities, and LabBook.Com for database and user interface support. This work was supported in part by the Solove Research Foundation and NIH grant GM58934 (F.A.W.).
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