An Expanded Registry of Candidate cis-Regulatory Elements for Studying Transcriptional Regulation [preprint]
Moore, Jill E ; Pratt, Henry E ; Fan, Kaili ; Phalke, Nishigandha ; Fisher, Jonathan ; Elhajjajy, Shaimae I ; Andrews, Gregory ; Gao, Mingshi ; Shedd, Nicole ; Fu, Yu ... show 10 more
Authors
Pratt, Henry E
Fan, Kaili
Phalke, Nishigandha
Fisher, Jonathan
Elhajjajy, Shaimae I
Andrews, Gregory
Gao, Mingshi
Shedd, Nicole
Fu, Yu
Lacadie, Matthew C
Meza, Jair
Ganna, Mohit
Choudhury, Eva
Swofford, Ross
Farrell, Nina P
Pampari, Anusri
Ramalingam, Vivekanandan
Reese, Fairlie
Borsari, Beatrice
Yu, Michelle
Wattenberg, Eve
Ruiz-Romero, Marina
Razavi-Mohseni, Milad
Xu, Jinrui
Galeev, Timur
Beer, Michael A
Guigó, Roderic
Gerstein, Mark
Engreitz, Jesse
Ljungman, Mats
Reddy, Timothy E
Snyder, Michael P
Epstein, Charles B
Gaskell, Elizabeth
Bernstein, Bradley E
Dickel, Diane E
Visel, Axel
Pennacchio, Len A
Mortazavi, Ali
Kundaje, Anshul
Weng, Zhiping
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Abstract
Mammalian genomes contain millions of regulatory elements that control the complex patterns of gene expression. Previously, The ENCODE consortium mapped biochemical signals across many cell types and tissues and integrated these data to develop a Registry of 0.9 million human and 300 thousand mouse candidate cis-Regulatory Elements (cCREs) annotated with potential functions. We have expanded the Registry to include 2.35 million human and 927 thousand 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 like STARR-seq, MPRA, CRISPR perturbation, and transgenic mouse assays now cover over 90% of human cCREs, revealing complex regulatory functions. We identified thousands of novel silencer cCREs and demonstrated their dual enhancer/silencer roles in different cellular contexts. Integrating the Registry with other ENCODE annotations facilitates genetic variation interpretation and trait-associated gene identification, exemplified by discovering 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.
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Moore JE, Pratt HE, Fan K, Phalke N, Fisher J, Elhajjajy SI, Andrews G, Gao M, Shedd N, Fu Y, Lacadie MC, Meza J, Ganna M, Choudhury E, Swofford R, Farrell NP, Pampari A, Ramalingam V, Reese F, Borsari B, Yu M, Wattenberg E, Ruiz-Romero M, Razavi-Mohseni M, Xu J, Galeev T, Beer MA, Guigó R, Gerstein M, Engreitz J, Ljungman M, Reddy TE, Snyder MP, Epstein CB, Gaskell E, Bernstein BE, Dickel DE, Visel A, Pennacchio LA, Mortazavi A, Kundaje A, Weng Z. An Expanded Registry of Candidate cis-Regulatory Elements for Studying Transcriptional Regulation. bioRxiv [Preprint]. 2024 Dec 26:2024.12.26.629296. doi: 10.1101/2024.12.26.629296. PMID: 39763870; PMCID: PMC11703161.
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This article is a preprint. Preprints are preliminary reports of work that have not been certified by peer review.