Sequencing of 42kb of the APO E-C2 gene cluster reveals a new gene: PEREC1
被引:4
作者:
Freitas, EM
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机构:Univ Western Australia, Ctr Mol Immunol & Instrumentat, Nedlands, WA 6009, Australia
Freitas, EM
Zhang, WJ
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机构:Univ Western Australia, Ctr Mol Immunol & Instrumentat, Nedlands, WA 6009, Australia
Zhang, WJ
Lalonde, JP
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机构:Univ Western Australia, Ctr Mol Immunol & Instrumentat, Nedlands, WA 6009, Australia
Lalonde, JP
Tay, GK
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机构:Univ Western Australia, Ctr Mol Immunol & Instrumentat, Nedlands, WA 6009, Australia
Tay, GK
Gaudieri, S
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机构:Univ Western Australia, Ctr Mol Immunol & Instrumentat, Nedlands, WA 6009, Australia
Gaudieri, S
Ashworth, LK
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机构:Univ Western Australia, Ctr Mol Immunol & Instrumentat, Nedlands, WA 6009, Australia
Ashworth, LK
Van Bockxmeer, FM
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机构:Univ Western Australia, Ctr Mol Immunol & Instrumentat, Nedlands, WA 6009, Australia
Van Bockxmeer, FM
Dawkins, RL
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机构:Univ Western Australia, Ctr Mol Immunol & Instrumentat, Nedlands, WA 6009, Australia
Dawkins, RL
机构:
[1] Univ Western Australia, Ctr Mol Immunol & Instrumentat, Nedlands, WA 6009, Australia
[2] Univ Calif Lawrence Livermore Natl Lab, Ctr Human Genome, Livermore, CA USA
来源:
DNA SEQUENCE
|
1998年
/
9卷
/
02期
基金:
英国医学研究理事会;
关键词:
D O I:
10.3109/10425179809086433
中图分类号:
Q81 [生物工程学(生物技术)];
Q93 [微生物学];
学科分类号:
071005 ;
0836 ;
090102 ;
100705 ;
摘要:
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.