Hessabi B, Schmidt I, Walther R
Department of Biochemistry, Medical School, Ernst-Moritz-Arndt-University, Greifswald, Germany.
Biochem Biophys Res Commun. 2000 Apr 21;270(3):695-700. doi: 10.1006/bbrc.2000.2491.
NK-2 family members of homeodomain proteins have been identified as important regulators of growth and development in the ventral forebrain, heart, lung, and thyroid. In addition, Nk2.2 expression has been detected in the pancreas, where it is vital for the final differentiation of beta-cells. In our present paper, we have analyzed the domains necessary for nuclear transport of Nkx2.2. With the help of deletion mutants we identified two separate nuclear localization signals (NLS). Interestingly, both NLSs are situated in the homeodomain. They belong to the monopartite class of NLS; the proximal NLS has the sequence KKRKRR and lies at the very N-terminus of the homeodomain, while the more distal NLS RYKMKRAR is at the homeodomain C-terminus. Each NLS per se is sufficient for nuclear transport of Nkx2.2 into the nucleus, although inefficiently. Both identified NLSs act cooperatively in mediating complete nuclear transport of Nkx2.2.
同源异型域蛋白的NK-2家族成员已被确定为腹侧前脑、心脏、肺和甲状腺生长发育的重要调节因子。此外,已在胰腺中检测到Nk2.2的表达,它对β细胞的最终分化至关重要。在我们目前的论文中,我们分析了Nkx2.2核转运所需的结构域。借助缺失突变体,我们确定了两个独立的核定位信号(NLS)。有趣的是,两个NLS都位于同源异型域中。它们属于单分型NLS;近端NLS的序列为KKRKRR,位于同源异型域的最N端,而更远端的NLS RYKMKRAR位于同源异型域的C端。每个NLS本身足以将Nkx2.2转运到细胞核中,尽管效率不高。所确定的两个NLS在介导Nkx2.2的完全核转运中协同作用。