Koch P, Bohlmann I, Schäfer M, Hansen-Hagge T E, Kiyoi H, Wilda M, Hameister H, Bartram C R, Janssen J W
Institute of Human Genetics, University of Heidelberg, Im Neuenheimer Feld 328, D-69120 Heidelberg, Germany.
Biochem Biophys Res Commun. 2000 Nov 11;278(1):241-9. doi: 10.1006/bbrc.2000.3788.
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).
在克隆t(5;14)(q34;q11)(急性淋巴细胞白血病中一种反复出现的易位)断点处基因的过程中,我们分离并鉴定了位于5q34的一个新基因,以及位于8p11 - 12的一个与之密切相关的人类同源基因(氨基酸同一性为66%)。它们的N端存在一个输入蛋白β N端结构域,大小约为110 kD,具有核定位,且该同源基因与最近提交的一种RanGTP结合蛋白(RanBP16)的基因相同,这表明其蛋白质是核转运受体输入蛋白β超家族的一个新成员,因此称为RanBP17。对人类组织的Northern印迹分析显示,RanBP16基因具有普遍的表达模式,而RanBP17基因的表达模式非常局限,在睾丸和胰腺中高表达。这两个基因在进化上是保守的,与它们的小鼠对应物具有高度(99%和94%)的氨基酸保守性,并且与秀丽隐杆线虫的一种蛋白质产物(C35A5.8)具有显著的相似性(40%)。