Genomic structure and chromosomal localization of the gene encoding TRAX, a Translin-associated factor X

被引:0
作者
G. Meng
K. Aoki
K. Tokura
K. Nakahara
J. Inazawa
M. Kasai
机构
[1] Department of Immunology,
[2] National Institute of Infectious Diseases,undefined
[3] 1-23-1 Toyama,undefined
[4] Shinjuku-ku,undefined
[5] Tokyo 162-8640,undefined
[6] Japan Tel. +81-3-5285-1111,undefined
[7] ext. 2130; Fax +81-3-5285-1150 e-mail: masataka@nih.go.jp,undefined
[8] Department of Hematology (Internal Medicine),undefined
[9] The University of Tokyo,undefined
[10] Tokyo,undefined
[11] Japan,undefined
[12] Department of Laboratory Medicine,undefined
[13] The University of Tokyo,undefined
[14] Tokyo,undefined
[15] Japan,undefined
[16] Department of Molecular Cytogenetics,undefined
[17] Division of Genetics,undefined
[18] Medical Research Institute,undefined
[19] Tokyo Medical and Dental University,undefined
[20] Tokyo,undefined
[21] Japan,undefined
来源
Journal of Human Genetics | 2000年 / 45卷
关键词
Key wordsTRAX; Chromosome 1q41; Nuclear targeting motif; Translin; Leucine zipper; Heteropolymer;
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摘要
The TRAX gene encodes a Translin-associated 33-kDa protein partner, TRAX. The TRAX protein has extensive amino acid homology with Translin, and contains bipartite nuclear targeting sequences, suggesting a possible role in the selective nuclear transport of Translin lacking any nuclear targeting motifs. In the present study, genomic clones of the human TRAX gene were isolated to determine the complete genomic organization. The genomic structure of the human TRAX gene was similar to that of the human Translin gene, consisting of six exons and five introns, encompassing approximately 27 kb in genomic DNA. Northern blot analysis revealed a predominant transcript of approximately 2.7 kb, and its distribution in various tissues was like that of Translin. Chromosomal mapping by fluorescence in situ hybridization (FISH) analysis allowed localization of the TRAX gene to human chromosome 1q41.
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页码:305 / 308
页数:3
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