| Literature DB >> 28522536 |
Peng Yang1, Yixuan Wang1,2, Don Hoang1, Matthew Tinkham1, Anamika Patel3, Ming-An Sun1, Gernot Wolf1, Mairead Baker1, Huan-Chieh Chien4,5, Kuan-Yu Nick Lai4,5, Xiaodong Cheng3, Che-Kun James Shen6,5, Todd S Macfarlan7.
Abstract
Insulin-like growth factor 2 (IGF2) is the major fetal growth hormone in mammals. We identify zinc finger protein 568 (ZFP568), a member of the rapidly evolving Kruppel-associated box-zinc finger protein (KRAB-ZFP) family linked primarily to silencing of endogenous retroelements, as a direct repressor of a placental-specific Igf2 transcript (designated Igf2-P0) in mice. Loss of Zfp568, which causes gastrulation failure, or mutation of the ZFP568-binding site at the Igf2-P0 promoter causes inappropriate Igf2-P0 activation. Deletion of Igf2 can completely rescue Zfp568 gastrulation phenotypes through late gestation. Our data highlight the exquisite selectivity with which members of the KRAB-ZFP family repress their targets and identify an additional layer of transcriptional control of a key growth factor regulating fetal and placental development.Entities:
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Year: 2017 PMID: 28522536 PMCID: PMC6309218 DOI: 10.1126/science.aah6895
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 47.728