Transcription of the non-coding RNA upperhand controls Hand2 expression and heart development

被引:282
作者
Anderson, Kelly M. [1 ,2 ]
Anderson, Douglas M. [1 ,2 ]
McAnally, John R. [1 ,2 ]
Shelton, John M. [3 ]
Bassel-Duby, Rhonda [1 ,2 ]
Olson, Eric N. [1 ,2 ]
机构
[1] Univ Texas Southwestern Med Ctr Dallas, Dept Mol Biol, Dallas, TX 75390 USA
[2] Univ Texas Southwestern Med Ctr Dallas, Hamon Ctr Regenerat Sci & Med, Dallas, TX 75390 USA
[3] Univ Texas Southwestern Med Ctr Dallas, Dept Internal Med, Dallas, TX 75390 USA
基金
美国国家卫生研究院;
关键词
RESPONSE ELEMENT; DHAND; ENHANCER; ACTIVATION; MORPHOGENESIS; PROMOTERS; LANDSCAPE; CHROMATIN; DISEASE; MUSCLE;
D O I
10.1038/nature20128
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
HAND2 is an ancestral regulator of heart development and one of four transcription factors that control the reprogramming of fibroblasts into cardiomyocytes(1-4). Deletion of Hand2 in mice results in right ventricle hypoplasia and embryonic lethality(1,5). Hand2 expression is tightly regulated by upstream enhancers(6,7) that reside within a super-enhancer delineated by histone 113 acetyl Lys27 (H3K27ac) modifications(8). Here we show that transcription of a Hand2-associated long non-coding RNA, which we named upperhand (Uph), is required to maintain the super-enhancer signature and elongation of RNA polymerase II through the Hand2 enhancer locus. Blockade of Uph transcription, but not knockdown of the mature transcript, abolished Hand2 expression, causing right ventricular hypoplasia and embryonic lethality in mice. Given the substantial number of uncharacterized promoter-associated long non-coding RNAs encoded by the mammalian genome(9), the Uph-Hand2 regulatory partnership offers a mechanism by which divergent non-coding transcription can establish a permissive chromatin environment.
引用
收藏
页码:433 / 436
页数:4
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