Identification of a novel putative Ran-binding protein and its close homologue

被引:30
作者
Koch, P
Bohlmann, I
Schäfer, M
Hansen-Hagge, TE
Kiyoi, H
Wilda, M
Hameister, H
Bartram, CR
Janssen, JWG
机构
[1] Univ Heidelberg, Inst Human Genet, D-69120 Heidelberg, Germany
[2] Humboldt Univ, Charite, Fak Med, Dept Dermatol, D-10117 Berlin, Germany
[3] Nagoya Univ, Sch Med, Dept Infect Dis, Higashi Ku, Nagoya, Aichi 461, Japan
[4] Univ Ulm, Dept Clin Genet, D-89069 Ulm, Germany
关键词
chromosomal breakpoint; leukemia; importin-beta; RanGTP binding protein; t(5; 14) (q34; q11); RNA expression; nuclear transport receptor; KIAA0745; RanBP16; RanBP17;
D O I
10.1006/bbrc.2000.3788
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In the process of cloning genes at the breakpoint of t(5;14) (q34;q11), a recurring translocation in acute lymphoblastic leukemia, we isolated and characterized a novel gene at 5q34, and a close human homologue (66% amino acid identity) located at 8p11-12. The presence of an importin-beta N-terminal domain at their N-terminus, their size of approximately 110 kD, their nuclear localization and the identity of the homologue to a gene of a recently submitted RanGTP binding protein (RanBP16), suggest that its protein is a novel member of the importin-beta superfamily of nuclear transport receptors, therefore called RanBP17. Northern blot analysis of human tissues revealed a ubiquitous expression pattern of the RanBP16 gene and a very restricted expression pattern of the RanBP17 gene, showing high expression in testis and pancreas. Both genes are evolutionary conserved and show a high (99 and 94%) amino acid conservation with their murine counterparts and a striking similarity (40%) to a protein product of Caenorhabditis elegans (C35A5.8). (C) 2000 Academic Press.
引用
收藏
页码:241 / 249
页数:9
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