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.2003 Oct;13(10):2265-70.
doi: 10.1101/gr.1293003. Epub 2003 Sep 15.

The secreted protein discovery initiative (SPDI), a large-scale effort to identify novel human secreted and transmembrane proteins: a bioinformatics assessment

Hilary F Clark  1Austin L GurneyEvangeline AbayaKevin BakerDaryl BaldwinJennifer BrushJian ChenBernard ChowClarissa ChuiCraig CrowleyBridget CurrellBethanne DeuelPatrick DowdDan EatonJessica FosterChristopher GrimaldiQimin GuPhilip E HassSherry HeldensArthur HuangHok Seon KimLaura KlimowskiYisheng JinStephanie JohnsonJames LeeLhney LewisDongzhou LiaoMelanie MarkEdward RobbieCelina SanchezJill SchoenfeldSomasekar SeshagiriLaura SimmonsJennifer SinghVictoria SmithJeremy StinsonAlicia VagtsRichard VandlenColin WatanabeDavid WieandKathryn WoodsMing-Hong XieDaniel YansuraSothy YiGuoying YuJean YuanMin ZhangZemin ZhangAudrey GoddardWilliam I WoodPaul GodowskiAlane Gray
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The secreted protein discovery initiative (SPDI), a large-scale effort to identify novel human secreted and transmembrane proteins: a bioinformatics assessment

Hilary F Clark et al. Genome Res.2003 Oct.

Erratum in

  • Genome Res. 2003 Dec;13(12):2759

Abstract

A large-scale effort, termed the Secreted Protein Discovery Initiative (SPDI), was undertaken to identify novel secreted and transmembrane proteins. In the first of several approaches, a biological signal sequence trap in yeast cells was utilized to identify cDNA clones encoding putative secreted proteins. A second strategy utilized various algorithms that recognize features such as the hydrophobic properties of signal sequences to identify putative proteins encoded by expressed sequence tags (ESTs) from human cDNA libraries. A third approach surveyed ESTs for protein sequence similarity to a set of known receptors and their ligands with the BLAST algorithm. Finally, both signal-sequence prediction algorithms and BLAST were used to identify single exons of potential genes from within human genomic sequence. The isolation of full-length cDNA clones for each of these candidate genes resulted in the identification of >1000 novel proteins. A total of 256 of these cDNAs are still novel, including variants and novel genes, per the most recent GenBank release version. The success of this large-scale effort was assessed by a bioinformatics analysis of the proteins through predictions of protein domains, subcellular localizations, and possible functional roles. The SPDI collection should facilitate efforts to better understand intercellular communication, may lead to new understandings of human diseases, and provides potential opportunities for the development of therapeutics.

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Figures

Figure 1
Figure 1
SPDI flow diagram.
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References

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