DNA Seq. 1998;9(2):89-100.

Sequencing of 42kb of the APO E-C2 gene cluster reveals a new gene: PEREC1.

Freitas EM, Zhang WJ, Lalonde JP, Tay GK, Gaudieri S, Ashworth LK, Van Bockxmeer FM, Dawkins RL.

Source

Centre for Molecular Immunology and Instrumentation, University of Westem Australia, Nedlands.

Abstract

Through the sequencing of a 42kb cosmid clone we describe a new gene, designated PEREC1, located approximately 1.5kb centromeric of the human apolipoprotein (APO) E-C2 cluster. The combination of dotplot analysis, predicted coding potential and interrogation of the Expressed Sequence Tag (EST) database determined the genomic organisation of PEREC1. Sequence alignment with multiple overlapping ESTs confirmed the predicted splice sites. The predicted cDNA and amino acid sequences of PEREC1 have extensive similarity to the Caenorhabditis elegans protein, C18E9.6. Conserved structural and functional motifs have been defined by combining nucleotide and amino acid analyses to identify third base degeneracy and therefore selection at the protein level. The Poliovirus Receptor Related Protein2 gene (PRR2), previously mapped to chromosome 19q13.2 by Fluorescent In-Situ Hybridisation, has also been located approximately 17kb centromeric of APO E.

PMID:: 10520737; [PubMed - indexed for MEDLINE]

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Research Support, Non-U.S. Gov't

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GENBANK/AB012576

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EBSCO

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NCI CPTC Antibody Characterization Program

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Sequencing of 42kb of the APO E-C2 gene cluster reveals a new gene: PEREC1.
Sequencing of 42kb of the APO E-C2 gene cluster reveals a new gene: PEREC1.
DNA Seq. 1998 ;9(2):89-100.

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