Dipartimento di Biochimica e Biotecnologie Mediche, Università di Napoli Federico II, Via S. Pansini 5, 80131 Napoli, Italy.
Int J Biochem Cell Biol. 2011 Apr;43(4):470-3. doi: 10.1016/j.biocel.2010.12.020. Epub 2010 Dec 25.
The Kruppel-like zinc finger protein ZNF224 was originally identified as the transcriptional repressor of the human aldolase A gene. ZNF224 transcriptional repression depends on interaction with the corepressor KAP-1 and the recruitment of enzyme activities modifying chromatin, in accordance with repression mechanism of KRAB-ZFP family. Recently, the arginine methyltransferase PRMT5 was demonstrated to play a crucial role in the transcriptional ZNF224 repressor complex. An alternatively spliced isoform, ZNF255, arises from the ZNF224 gene. ZNF224 and ZNF255 have a distinct pattern of distribution within the cell and display a specific pattern of interaction with different molecular partners. These isoform-specific interactions seem to control different cellular pathways. These findings suggest that ZNF224 is a multifunctional protein and that alternative splicing, sub-cellular compartmentalization and isoform-specific interactions may modulate its activity.
锌指蛋白 224(Kruppel-like zinc finger protein ZNF224)最初被鉴定为人类醛缩酶 A 基因的转录抑制剂。ZNF224 的转录抑制依赖于与核心抑制因子 KAP-1 的相互作用以及募集修饰染色质的酶活性,符合 KRAB-ZFP 家族的抑制机制。最近,精氨酸甲基转移酶 PRMT5 被证明在 ZNF224 转录抑制剂复合物中发挥关键作用。锌指蛋白 224 基因还会产生一个选择性剪接的异构体 ZNF255。ZNF224 和 ZNF255 在细胞内的分布模式不同,并与不同的分子伴侣显示出特定的相互作用模式。这些异构体特异性相互作用似乎控制着不同的细胞通路。这些发现表明 ZNF224 是一种多功能蛋白,选择性剪接、亚细胞区室化和异构体特异性相互作用可能调节其活性。