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逆转座子衍生的PEG11/RTL1的异位表达导致臀肌肥大。

Ectopic Expression of Retrotransposon-Derived PEG11/RTL1 Contributes to the Callipyge Muscular Hypertrophy.

作者信息

Xu Xuewen, Ectors Fabien, Davis Erica E, Pirottin Dimitri, Cheng Huijun, Farnir Frédéric, Hadfield Tracy, Cockett Noelle, Charlier Carole, Georges Michel, Takeda Haruko

机构信息

Unit of Animal Genomics, GIGA Research Center and Faculty of Veterinary Medicine, University of Liège, 1 Avenue de l'Hôpital, Liège, Belgium.

Transgenic platform, FARAH and GIGA Research Center, University of Liège, 1 Avenue de l'Hôpital, Liège, Belgium.

出版信息

PLoS One. 2015 Oct 16;10(10):e0140594. doi: 10.1371/journal.pone.0140594. eCollection 2015.

Abstract

The callipyge phenotype is an ovine muscular hypertrophy characterized by polar overdominance: only heterozygous +Mat/CLPGPat animals receiving the CLPG mutation from their father express the phenotype. +Mat/CLPGPat animals are characterized by postnatal, ectopic expression of Delta-like 1 homologue (DLK1) and Paternally expressed gene 11/Retrotransposon-like 1 (PEG11/RTL1) proteins in skeletal muscle. We showed previously in transgenic mice that ectopic expression of DLK1 alone induces a muscular hypertrophy, hence demonstrating a role for DLK1 in determining the callipyge hypertrophy. We herein describe newly generated transgenic mice that ectopically express PEG11 in skeletal muscle, and show that they also exhibit a muscular hypertrophy phenotype. Our data suggest that both DLK1 and PEG11 act together in causing the muscular hypertrophy of callipyge sheep.

摘要

臀肌肥大表型是一种绵羊肌肉肥大,其特征为极性超显性:只有从父亲那里遗传到CLPG突变的杂合子+Mat/CLPGPat动物才表现出该表型。+Mat/CLPGPat动物的特征是出生后骨骼肌中Delta样1同源物(DLK1)和父源表达基因11/反转录转座子样1(PEG11/RTL1)蛋白的异位表达。我们之前在转基因小鼠中发现,单独异位表达DLK1会诱导肌肉肥大,从而证明DLK1在决定臀肌肥大方面发挥作用。我们在此描述了新产生的在骨骼肌中异位表达PEG11的转基因小鼠,并表明它们也表现出肌肉肥大表型。我们的数据表明,DLK1和PEG11共同作用导致了臀肌肥大绵羊的肌肉肥大。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e9e/4608697/496c0374685e/pone.0140594.g001.jpg

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