cDNA cloning of a novel human gene NAKAP95, neighbor of A-kinase anchoring protein 95 (AKAP95) on chromosome 19p13.11–p13.12 region

被引:0
|
作者
N. Seki
N. Ueki
K. Yano
T. Saito
Y. Masuho
M. Muramatsu
机构
[1] Genome Research Group,
[2] National Institute Radiological Sciences,undefined
[3] Chiba,undefined
[4] Japan,undefined
[5] Laboratory of Gene Function II,undefined
[6] Kazusa DNA Research Institute,undefined
[7] Chiba,undefined
[8] Japan,undefined
[9] Helix Research Institute,undefined
[10] 1532-3 Yana,undefined
[11] Kisarazu,undefined
[12] Chiba 292-0812,undefined
[13] Japan Tel. +81-438-52-3966; Fax +81-438-52-3952 e-mail: mmasaaki@hri.co.jp,undefined
[14] Department of Biological Cybernetics,undefined
[15] Medical Research Institute,undefined
[16] Tokyo Medical Dental University,undefined
[17] Tokyo,undefined
[18] Japan,undefined
来源
Journal of Human Genetics | 2000年 / 45卷
关键词
Key words Cyclic AMP-dependent protein kinase (PKA); A-kinase anchoring proteins (AKAPs); AKAP95; Chromosome 19p13.11–p13.12; RH mapping; Genomic structure; Gene duplication;
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摘要
A-kinase anchoring protein 95 (AKAP95) is a nuclear protein which binds to the regulatory subunit (RII) of cyclic adenosine monophosphate (cAMP)-dependent protein kinase (PKA) and to DNA. A novel nuclear human gene which shares sequence homology with the human AKAP95 gene was identified by a nuclear transportation trap method. By polymerase chain reaction (PCR)-based analysis with both a human/rodent monochromosomal hybrid cell panel and a radiation hybrid panel, the gene was mapped to the chromosome 19p13.11–p13.12 region between markers WI-4669 and CHLC.GATA27C12. Furthermore, alignment with genomic sequences revealed that the gene and human AKAP95 resided tandemly only approximately 250 bp apart from each other. We designated this gene as neighbor of AKAP95 (NAKAP95). The exon-intron structure of NAKAP95 and AKAP95 was conserved, indicating that they may have evolved by gene duplication. The predicted protein product of the NAKAP95 gene consists of 646 amino acid residues, and NAKAP95 and AKAP95 had an overall 40% similarity, both having a potential nuclear localizing signal and two C2H2 type zinc finger motifs. The putative RII binding motif in AKAP95 was not conserved in NAKAP95. A reverse transcription coupled (RT)-PCR experiment revealed that the NAKAP95 gene was transcribed ubiquitously in various human tissues.
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页码:31 / 37
页数:6
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