Volume 45, Issue 5 pp. 475-483
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Molecular Cloning and Characterization of a Superoxide Dismutase (sod) Gene in Pneumocystis carinii

Cecile-Marie Denis

Corresponding Author

Cecile-Marie Denis

INSERM U42, 369, rue Jules Guesde, B. P. 39. 59651 Villeneuve d'Ascq Ceclex, France

Faculty of Science. 13. rue de Tout. 59000 Lille, France

Molecular Infectious Diseases Group. Institute of Molecular Medicine, University of Oxford, John Radcliffe Hospital, Headington. Oxford OX3 9DU England.

To whom correspondence should be addressed. Telephone: 1-865-22-23-44; Fax: 1-865-22-26-26, Email: [email protected]Search for more papers by this author
Karine Guyot

Karine Guyot

INSERM U42, 369, rue Jules Guesde, B. P. 39. 59651 Villeneuve d'Ascq Ceclex, France

Department of Ecosystem Microbiology, Pasteur Institute of Lille. 59019 Lille. France

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Ann E. Wakefield

Ann E. Wakefield

Molecular Infectious Diseases Group. Institute of Molecular Medicine, Oxford, UK

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Daniel Dive

Daniel Dive

INSERM U42, 369, rue Jules Guesde, B. P. 39. 59651 Villeneuve d'Ascq Ceclex, France

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Eduardo Dei-Cas

Eduardo Dei-Cas

Faculty of Medicine, Regional Hospital Center, I. place de Verdun. 59X50 Lille, France

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Daniel Camus

Daniel Camus

INSERM U42, 369, rue Jules Guesde, B. P. 39. 59651 Villeneuve d'Ascq Ceclex, France

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Carmen Odberg-Ferragut

Carmen Odberg-Ferragut

INSERM U42, 369, rue Jules Guesde, B. P. 39. 59651 Villeneuve d'Ascq Ceclex, France

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First published: 02 May 2007
Citations: 13

Abstract

This work reports the isolation and characterization of a gene encoding a superoxide dismutase (SOD. EC.1.15.1.1.) from Pneumocystis carinii derived from rat. Sense and antisense oligonucleotides, deduced from SOD amino acid sequences from a wide variety of organisms, allowed amplification of a 669 bp genomic DNA fragment specific to this P. carinii. RACE-PCR was used to obtain the major pan of the complementary DNA; the 5- and 3′-genomic regions were obtained respectively from a Mbo I subgenomic library and from an amplified fragment using oligonucleotides designed from the cDNA sequence. Comparison of genomic and cDNA sequences showed an open reading frame of 660 bp interrupted by seven small introns. The deduced amino acid sequence contained 220 residues. Protein sequence alignment demonstrated the highest homology (50.5% identity. 70.3% similarity) with Saccharomyces cerevisiae manganese-SOD (MnSOD) suggesting that P. carinii SOD belongs to the mitochondrial MnSOD group. A putative targeting peptide found at the 5′-end of the P. carinii SOD sequence also suggested its mitochondrial localization.

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