Krox20 hindbrain regulation incorporates multiple modes of cooperation between cis-acting elements

被引:13
|
作者
Thierion, Elodie [1 ,2 ,4 ]
Le Men, Johan [1 ]
Collombet, Samuel [1 ]
Hernandez, Celine [1 ]
Coulpier, Fanny [1 ]
Torbey, Patrick [1 ]
Thomas-Chollier, Morgane [1 ]
Noordermeer, Daan [3 ]
Charnay, Patrick [1 ]
Gilardi-Hebenstreit, Pascale [1 ]
机构
[1] PSL Res Univ, IBENS, CNRS, Ecole Normale Super,INSERM, Paris, France
[2] UPMC Univ Paris 06, Sorbonne Univ, IFD, Paris, France
[3] Univ Paris Saclay, Univ Paris Sud, I2BC, CEA,CNRS, Gif Sur Yvette, France
[4] Univ Cambridge, Canc Res UK Cambridge Inst, Robinson Way, Cambridge, England
来源
PLOS GENETICS | 2017年 / 13卷 / 07期
关键词
TYROSINE KINASE; GENE-EXPRESSION; KROX-20; TRANSCRIPTION; ENHANCERS; PROTEINS; SPECIFICATION; SEGMENTATION; ARCHITECTURE; ACTIVATION;
D O I
10.1371/journal.pgen.1006903
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Developmental genes can harbour multiple transcriptional enhancers that act simultaneously or in succession to achieve robust and precise spatiotemporal expression. However, the mechanisms underlying cooperation between cis-acting elements are poorly documented, notably in vertebrates. The mouse gene Krox20 encodes a transcription factor required for the specification of two segments (rhombomeres) of the developing hindbrain. In rhombomere 3, Krox20 is subject to direct positive feedback governed by an autoregulatory enhancer, element A. In contrast, a second enhancer, element C, distant by 70 kb, is active from the initiation of transcription independent of the presence of the KROX20 protein. Here, using both enhancer knock-outs and investigations of chromatin organisation, we show that element C possesses a dual activity: besides its classical enhancer function, it is also permanently required in cis to potentiate the autoregulatory activity of element A, by increasing its chromatin accessibility. This work uncovers a novel, asymmetrical, long-range mode of cooperation between cis-acting elements that might be essential to avoid promiscuous activation of positive autoregulatory elements.
引用
收藏
页数:18
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