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10.1093/nar/gkw1051

http://scihub22266oqcxt.onion/10.1093/nar/gkw1051
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C5388394!5388394!28180295
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suck abstract from ncbi


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pmid28180295      Nucleic+Acids+Res 2017 ; 45 (3): 1177-85
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  • A permissive chromatin state regulated by ZFP281-AFF3 in controlling the imprinted Meg3 polycistron #MMPMID28180295
  • Wang Y; Shen Y; Dai Q; Yang Q; Zhang Y; Wang X; Xie W; Luo Z; Lin C
  • Nucleic Acids Res 2017[Feb]; 45 (3): 1177-85 PMID28180295show ga
  • Genomic imprinting is an epigenetic regulation that leads to gene expression in a parent-of-origin specific manner. AFF3, the central component of the Super Elongation Complex-like 3 (SEC-L3), is enriched at both the intergenic-differentially methylated region (IG-DMR) and the Meg3 enhancer within the imprinted Dlk1-Dio3 locus to regulate the allele-specific gene expression in this locus. The localization of AFF3 to IG-DMR requires ZFP57. However, how AFF3 functions at the Meg3 enhancer in maintaining allele-specific gene expression remains unclear. Here, we demonstrate that AFF3 is associated with the Krüppel-like zinc finger protein ZFP281 in mouse embryonic stem (ES) cells. ZFP281 recruits AFF3 to the Meg3 enhancer within the imprinted Dlk1-Dio3 locus, thus regulating the allele-specific expression of the Meg3 polycistron. Our genome-wide analyses further identify ZFP281 as a critical factor generally associating with AFF3 at enhancers and functioning together with AFF3 in regulating the expression of a subset of genes. Our study suggests that different zinc finger proteins can recruit AFF3 to different regulatory elements and differentially regulate the function of AFF3 in a context-dependent manner.
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