ConservedCis-Acting Range Extender Element Mediates Extreme Long-Range Enhancer Activity in Mammals

Author:

Bower GraceORCID,Hollingsworth Ethan W.ORCID,Jacinto Sandra,Clock BenjaminORCID,Cao Kaitlyn,Liu Mandy,Dziulko Adam,Alcaina-Caro AnaORCID,Xu Qianlan,Skowronska-Krawczyk DorotaORCID,Lopez-Rios Javier,Dickel Diane E.,Bardet Anaïs F.,Pennacchio Len A.,Visel Axel,Kvon Evgeny Z.ORCID

Abstract

AbstractWhile most mammalian enhancers regulate their cognate promoters over moderate distances of tens of kilobases (kb), some enhancers act over distances in the megabase range. The sequence features enabling such extreme-distance enhancer-promoter interactions remain elusive. Here, we usedin vivoenhancer replacement experiments in mice to show that short– and medium-range enhancers cannot initiate gene expression at extreme-distance range. We uncover a novel conservedcis-acting element,RangeEXtender (REX), that confers extreme-distance regulatory activity and is located next to a long-range enhancer ofSall1. The REX element itself has no endogenous enhancer activity. However, addition of the REX to other short– and mid-range enhancers substantially increases their genomic interaction range. In the most extreme example observed, addition of the REX increased the range of an enhancer by an order of magnitude, from its native 71kb to 840kb. The REX element contains highly conserved [C/T]AATTA homeodomain motifs. These motifs are enriched around long-range limb enhancers genome-wide, including the ZRS, a benchmark long-range limb enhancer ofShh. Mutating the [C/T]AATTA motifs within the ZRS does not affect its limb-specific enhancer activity at short range, but selectively abolishes its long-range activity, resulting in severe limb reduction in knock-in mice. In summary, we identify a sequence signature globally associated with long-range enhancer-promoter interactions and describe a prototypical REX element that is necessary and sufficient to confer extreme-distance gene activation by remote enhancers.

Publisher

Cold Spring Harbor Laboratory

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3