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BTB/POZ转录调节因子Kaiso的核输入

Nuclear import of the BTB/POZ transcriptional regulator Kaiso.

作者信息

Kelly Kevin F, Otchere Abena A, Graham Monica, Daniel Juliet M

机构信息

Department of Biology, McMaster University, 1280 Main Street West, Hamilton, ON, L8S 4K1, Canada.

出版信息

J Cell Sci. 2004 Dec 1;117(Pt 25):6143-52. doi: 10.1242/jcs.01541.

Abstract

Kaiso is a BTB/POZ transcription factor that functions in vitro as a transcriptional repressor of the matrix metalloproteinase gene matrilysin and the non-canonical Wnt signaling gene Wnt-11, and as an activator of the acetylcholine-receptor-clustering gene rapsyn. Similar to other BTB/POZ proteins (e.g. Bcl-6, PLZF, HIC-1), endogenous Kaiso localizes predominantly to the nuclei of mammalian cells. To date, however, the mechanism of nuclear import for most POZ transcription factors, including Kaiso, remain unknown. Here, we report the identification and characterization of a highly basic nuclear localization signal (NLS) in Kaiso. The functionality of this NLS was verified by its ability to target a heterologous beta-galactosidase/green-fluorescent-protein fusion protein to nuclei. The mutation of one positively charged lysine to alanine in the NLS of full-length Kaiso significantly inhibited its nuclear localization in various cell types. In addition, wild-type Kaiso, but not NLS-defective Kaiso, interacted directly with the nuclear import receptor Importin-alpha2 both in vitro and in vivo. Finally, minimal promoter assays using a sequence-specific Kaiso-binding-site fusion with luciferase as reporter demonstrated that the identified NLS was crucial for Kaiso-mediated transcriptional repression. The identification of a Kaiso NLS thus clarifies the mechanism by which Kaiso translocates to the nucleus to regulate transcription of genes with diverse roles in cell growth and development.

摘要

Kaiso是一种BTB/POZ转录因子,在体外作为基质金属蛋白酶基因基质溶解素和非经典Wnt信号基因Wnt-11的转录抑制因子,以及乙酰胆碱受体聚集基因rapsyn的激活因子发挥作用。与其他BTB/POZ蛋白(如Bcl-6、PLZF、HIC-1)类似,内源性Kaiso主要定位于哺乳动物细胞的细胞核。然而,迄今为止,包括Kaiso在内的大多数POZ转录因子的核输入机制仍不清楚。在此,我们报告了Kaiso中一个高度碱性的核定位信号(NLS)的鉴定和特征。该NLS的功能通过其将异源β-半乳糖苷酶/绿色荧光蛋白融合蛋白靶向细胞核的能力得到验证。全长Kaiso的NLS中一个带正电荷的赖氨酸突变为丙氨酸显著抑制了其在各种细胞类型中的核定位。此外,野生型Kaiso而非NLS缺陷型Kaiso在体外和体内均直接与核输入受体Importin-α2相互作用。最后,使用与荧光素酶融合的序列特异性Kaiso结合位点作为报告基因的最小启动子分析表明,鉴定出的NLS对Kaiso介导的转录抑制至关重要。因此,Kaiso NLS的鉴定阐明了Kaiso转运至细胞核以调节在细胞生长和发育中具有不同作用的基因转录的机制。

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