A single-cell atlas of transcribedcis-regulatory elements in the human genome

Author:

Moody JonathanORCID,Kouno Tsukasa,Kojima Miki,Koya Ikuko,Leon JulioORCID,Suzuki AkariORCID,Hasegawa Akira,Akiyama TaishinORCID,Akiyama NobukoORCID,Amagai MasayukiORCID,Chang Jen-ChienORCID,Fukushima-Nomura AyanoORCID,Handa Mika,Hino KazunoriORCID,Hino MizukiORCID,Hirata Tomoko,Imai YuukiORCID,Inoue Kazunori,Kawasaki HiroshiORCID,Kimura Toshihiro,Kinoshita TomofumiORCID,Kubo Ken-ichiroORCID,Kunii YasutoORCID,López-Redondo FernandoORCID,Manabe RiichiroORCID,Miyai TomohiroORCID,Morimoto SatoruORCID,Nagaoka Atsuko,Nakajima JunORCID,Noma ShoheiORCID,Okazaki YasushiORCID,Ozaki KokoroORCID,Saeki NoritakaORCID,Sakai HiroshiORCID,Seyama Kuniaki,Shibayama Youtaro,Sujino TomohisaORCID,Tagami MichihiraORCID,Takahashi HayatoORCID,Takao MasakiORCID,Takeshita MasaruORCID,Takiuchi Tsuyoshi,Terao ChikashiORCID,Yip Chi WaiORCID,Yoshinaga SatoshiORCID,Okano HideyukiORCID,Yahamoto KazuhikoORCID,Kasukawa TakeyaORCID,Ando YoshinariORCID,Carninci PieroORCID,Shin Jay W.ORCID,Hon Chung-ChauORCID

Abstract

SummaryTranscribed cis-regulatory elements (tCREs), such as promoters and enhancers, are fundamental to modulate gene expression and define cell identity. The detailed mapping of tCREs at single-cell resolution is essential for understanding the regulatory mechanisms that govern cellular functions. Prior tCRE catalogs, limited by bulk analysis, have often overlooked cellular heterogeneity. We have constructed a tCRE atlas using single-cell 5’-RNA-seq, capturing over 340,000 single-cells from 23 human tissues and annotating more than 175,000 tCREs, substantially enhancing the scope and granularity of existingcis-regulatory element annotations in the human genome. This atlas unveils patterns of gene regulation, revealing connections between broadly expressed promoters and cell type-specific distal tCREs. Assessing trait heritability at single-cell resolution with a novel tCRE module-based approach, we uncovered the nuanced trait-gene regulatory relationships across a continuum of cell populations, offering insights beyond traditional gene-level and bulk-sample analyses. Our study bridges the gap between gene regulation and trait heritability, underscoring the potential of single-cell analysis to elucidate the genetic foundations of complex traits. These insights set the stage for future research to investigate the impact of genetic variations on diseases at the individual level, advancing the understanding of cellular and molecular basis of trait heritability.

Publisher

Cold Spring Harbor Laboratory

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