Filtering "genic" open reading frames from genomic DNA samples for advanced annotation

Journal Article · Wed Jun 15 00:00:00 EDT 2011 · BMC Genomics

DOI:https://doi.org/10.1186/1471-2164-12-s1-s5· OSTI ID:1626412

D'Angelo, Sara ^[1]; Velappan, Nileena ^[1]; Mignone, Flavio ^[2]; Santoro, Claudio ^[3]; Sblattero, Daniele ^[3]; Kiss, Csaba ^[1]; Bradbury, Andrew RM ^[1]

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1. Los Alamos National Lab. (LANL), Los Alamos, NM (United States). Bioscience Division
2. Univ. of Milan (Italy). School of Pharmacy. Dept. of Structural Chemistry and Inorganic Stereochemistry
3. Univ. of Eastern Piedmont, Novara (Italy). Dept. of Medical Sciences. IRCAD

Background: In order to carry out experimental gene annotation, DNA encoding open reading frames (ORFs) derived from real genes (termed “genic”) in the correct frame is required. When genes are correctly assigned, isolation of genic DNA for functional annotation can be carried out by PCR. However, not all genes are correctly assigned, and even when correctly assigned, gene products are often incorrectly folded when expressed in heterologous hosts. This is a problem that can sometimes be overcome by the expression of protein fragments encoding domains, rather than full-length proteins. One possible method to isolate DNA encoding such domains would to “filter” complex DNA (cDNA libraries, genomic and metagenomic DNA) for gene fragments that confer a selectable phenotype relying on correct folding, with all such domains present in a complex DNA sample, termed the “domainome”. Results: In this paper we discuss the preparation of diverse genic ORF libraries from randomly fragmented genomic DNA using ß-lactamase to filter out the open reading frames. By cloning DNA fragments between leader sequences and the mature ß-lactamase gene, colonies can be selected for resistance to ampicillin, conferred by correct folding of the lactamase gene. Our experiments demonstrate that the majority of surviving colonies contain genic open reading frames, suggesting that ß-lactamase is acting as a selectable folding reporter. Furthermore, different leaders (Sec, TAT and SRP), normally translocating different protein classes, filter different genic fragment subsets, indicating that their use increases the fraction of the “domainone” that is accessible. Conclusions: The availability of ORF libraries, obtained with the filtering method described here, combined with screening methods such as phage display and protein-protein interaction studies, or with protein structure determination projects, can lead to the identification and structural determination of functional genic ORFs. ORF libraries represent, moreover, a useful tool to proceed towards high-throughput functional annotation of newly sequenced genomes.

• Research Organization: Los Alamos National Laboratory (LANL), Los Alamos, NM (United States)
• Sponsoring Organization: USDOE Office of Science (SC), Biological and Environmental Research (BER). Biological Systems Science Division
• Grant/Contract Number: AC52-06NA25396
• OSTI ID: 1626412
• Journal Information: BMC Genomics, Vol. 12, Issue Suppl 1; ISSN 1471-2164
• Publisher: Springer
• Country of Publication: United States
• Language: English

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