van Roy Frans M, McCrea Pierre D
Molecular Cell Biology Unit, Department for Molecular Biomedical Research, VIB-Ghent University, Technologiepark 927, B-9052 Ghent, Belgium.
Nat Rev Cancer. 2005 Dec;5(12):956-64. doi: 10.1038/nrc1752.
Kaiso belongs to the zinc finger and broad-complex, tramtrack and bric-a-brac/poxvirus and zinc finger (BTB/POZ) protein family that has been implicated in tumorigenesis. Kaiso was first discovered in a complex with the armadillo-domain protein p120ctn and later shown to function as a transcriptional repressor. As p120ctn seems to relieve Kaiso-mediated repression, its altered intracellular localization in some cancer cells might result in aberrant Kaiso nuclear activity. Intriguingly, Kaiso's target genes include both methylated and sequence-specific recognition sites. The latter include genes that are modulated by the canonical Wnt (beta-catenin-T-cell factor) signalling pathway. Further interest in Kaiso stems from findings that its cytoplasmic versus nuclear localization is modulated by complex cues from the microenvironment.
Kaiso属于锌指与泛素连接酶、Tramtrack和bric-a-brac/痘病毒与锌指(BTB/POZ)蛋白家族,该家族与肿瘤发生有关。Kaiso最初是在与犰狳结构域蛋白p120ctn的复合物中被发现的,后来被证明具有转录抑制因子的功能。由于p120ctn似乎能解除Kaiso介导的抑制作用,其在某些癌细胞中细胞内定位的改变可能导致Kaiso核活性异常。有趣的是,Kaiso的靶基因包括甲基化和序列特异性识别位点。后者包括受经典Wnt(β-连环蛋白-T细胞因子)信号通路调控的基因。对Kaiso的进一步关注源于以下发现,即其在细胞质与细胞核中的定位受微环境复杂信号的调节。