Kim Hana, Ekram Muhammad B, Bakshi Arundhati, Kim Joomyeong
Department of Biological Sciences, Louisiana State University, Baton Rouge, LA 70803, USA.
Department of Biological Sciences, Louisiana State University, Baton Rouge, LA 70803, USA.
Genomics. 2015 Feb;105(2):108-15. doi: 10.1016/j.ygeno.2014.11.007. Epub 2014 Nov 28.
Aebp2 encodes an evolutionarily conserved zinc finger protein that has not been well studied so far, yet recent studies indicated that this gene is closely associated with the Polycomb Repressive Complex 2 (PRC2). Thus, the current study characterized the basic aspects of this gene, including alternative promoters and protein isoforms. According to the results, Aebp2 is controlled through three alternative promoters, deriving three different transcripts encoding the embryonic (32 kDa) and somatic (52 kDa) forms. Chromatin Immuno-Precipitation (ChIP) experiments revealed that AEBP2 binds to its own promoter as well as the promoters of Jarid2 and Snai2. While the embryonic form acts as a transcriptional repressor for Snai2, the somatic form functions as a transcriptional activator for Jarid2, Aebp2 and Snai2. Cell migration assays also demonstrated that the Aebp2 somatic form has an enhancing activity in cell migration. This is consistent with the functional association of Aebp2 with migratory neural crest cells. These results suggest that the two protein isoforms of AEBP2 may have opposite functions for the PcG target genes, and may play significant roles in cell migration during development.
Aebp2编码一种进化上保守的锌指蛋白,到目前为止尚未得到充分研究,但最近的研究表明该基因与多梳抑制复合体2(PRC2)密切相关。因此,本研究对该基因的基本方面进行了表征,包括可变启动子和蛋白质异构体。根据结果,Aebp2由三个可变启动子控制,产生三种不同的转录本,分别编码胚胎型(32 kDa)和体细胞型(52 kDa)形式。染色质免疫沉淀(ChIP)实验表明,AEBP2与其自身的启动子以及Jarid2和Snai2的启动子结合。虽然胚胎型作为Snai2的转录抑制因子起作用,但体细胞型作为Jarid2、Aebp2和Snai2的转录激活因子起作用。细胞迁移实验还表明,Aebp2体细胞型在细胞迁移中具有增强活性。这与Aebp2与迁移性神经嵴细胞的功能关联一致。这些结果表明,AEBP2的两种蛋白质异构体可能对PcG靶基因具有相反的功能,并且可能在发育过程中的细胞迁移中发挥重要作用。