<p>Mammalian genomes contain millions of regulatory elements that control the complex patterns of gene expression<sup><CitationRef CitationID="CR1">1</CitationRef></sup>. Previously, the&#xa0;ENCODE consortium mapped biochemical signals across hundreds of cell types and tissues and integrated these data to develop a registry containing 0.9 million human and 300,000 mouse candidate <i>cis</i>-regulatory elements (cCREs) annotated with potential functions<sup><CitationRef CitationID="CR2">2</CitationRef></sup>. Here we have expanded the registry to include 2.37 million human and 967,000 mouse cCREs, leveraging new ENCODE datasets and enhanced computational methods. This expanded registry covers hundreds of unique cell and tissue types, providing a comprehensive understanding of gene regulation. Functional characterization data from assays such as STARR-seq<sup><CitationRef CitationID="CR3">3</CitationRef></sup>, massively parallel reporter assay<sup><CitationRef CitationID="CR4">4</CitationRef></sup>, CRISPR perturbation<sup><CitationRef CitationID="CR5">5</CitationRef>,<CitationRef CitationID="CR6">6</CitationRef></sup> and transgenic mouse assays<sup><CitationRef CitationID="CR7">7</CitationRef></sup> have profiled more than 90% of human cCREs, revealing complex regulatory functions. We identified thousands of novel silencer cCREs and demonstrated their dual enhancer and silencer roles in different cellular contexts. Integrating the registry with other ENCODE annotations facilitates genetic variation interpretation and trait-associated gene identification, exemplified by the identification of <i>KLF1</i> as a novel causal gene for red blood cell traits. This expanded registry is a valuable resource for studying the regulatory genome and its impact on health and disease.</p>

错误:搜索内容不能为空,请输入英文关键词
错误:关键词超出字数限制,请精简
高级检索

An expanded registry of candidate cis-regulatory elements

  • Jill E. Moore,
  • Henry E. Pratt,
  • Kaili Fan,
  • Nishigandha Phalke,
  • Jonathan Fisher,
  • Shaimae I. Elhajjajy,
  • Gregory Andrews,
  • Mingshi Gao,
  • Nicole Shedd,
  • Yu Fu,
  • Matthew C. Lacadie,
  • Jair Meza,
  • Mansi Khandpekar,
  • Mohit Ganna,
  • Eva Choudhury,
  • Ross Swofford,
  • Huong Phan,
  • Christian C. Ramirez,
  • Maxwell Campbell,
  • Mary Likhite,
  • Nina P. Farrell,
  • Annika K. Weimer,
  • Anusri Pampari,
  • Vivekanandan Ramalingam,
  • Fairlie Reese,
  • Beatrice Borsari,
  • Xuezhu Yu,
  • Eve Wattenberg,
  • Marina Ruiz-Romero,
  • Milad Razavi-Mohseni,
  • Jinrui Xu,
  • Timur Galeev,
  • Andres Colubri,
  • Michael A. Beer,
  • Roderic Guigó,
  • Mark B. Gerstein,
  • Jesse M. Engreitz,
  • Mats Ljungman,
  • Timothy E. Reddy,
  • Michael P. Snyder,
  • Charles B. Epstein,
  • Elizabeth Gaskell,
  • Bradley E. Bernstein,
  • Diane E. Dickel,
  • Axel Visel,
  • Len A. Pennacchio,
  • Ali Mortazavi,
  • Anshul Kundaje,
  • Zhiping Weng

摘要

Mammalian genomes contain millions of regulatory elements that control the complex patterns of gene expression1. Previously, the ENCODE consortium mapped biochemical signals across hundreds of cell types and tissues and integrated these data to develop a registry containing 0.9 million human and 300,000 mouse candidate cis-regulatory elements (cCREs) annotated with potential functions2. Here we have expanded the registry to include 2.37 million human and 967,000 mouse cCREs, leveraging new ENCODE datasets and enhanced computational methods. This expanded registry covers hundreds of unique cell and tissue types, providing a comprehensive understanding of gene regulation. Functional characterization data from assays such as STARR-seq3, massively parallel reporter assay4, CRISPR perturbation5,6 and transgenic mouse assays7 have profiled more than 90% of human cCREs, revealing complex regulatory functions. We identified thousands of novel silencer cCREs and demonstrated their dual enhancer and silencer roles in different cellular contexts. Integrating the registry with other ENCODE annotations facilitates genetic variation interpretation and trait-associated gene identification, exemplified by the identification of KLF1 as a novel causal gene for red blood cell traits. This expanded registry is a valuable resource for studying the regulatory genome and its impact on health and disease.