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AEBP2 as a transcriptional activator and its role in cell migration.

作者信息

Kim Hana, Ekram Muhammad B, Bakshi Arundhati, Kim Joomyeong

机构信息

Department of Biological Sciences, Louisiana State University, Baton Rouge, LA 70803, USA.

Department of Biological Sciences, Louisiana State University, Baton Rouge, LA 70803, USA.

出版信息

Genomics. 2015 Feb;105(2):108-15. doi: 10.1016/j.ygeno.2014.11.007. Epub 2014 Nov 28.

Abstract

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.

摘要

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