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Severe COVID-19 associated variants linked to chemokine receptor gene control in monocytes and macrophages.

ABSTRACT: Genome-wide association studies have identified 3p21.31 as the main risk locus for severe disease in COVID-19 patients, although underlying biological mechanisms remain elusive. We performed a comprehensive epigenomic dissection of the 3p21.31 locus, identifying a CTCF-dependent tissue-specific 3D regulatory chromatin hub that controls the activity of several tissue-homing chemokine receptor (CCR) genes in monocytes and macrophages. Risk SNPs colocalized with regulatory elements and were linked to increased expression of CCR1, CCR2 and CCR5 in monocytes and macrophages. As excessive organ infiltration of inflammatory monocytes and macrophages is a hallmark of severe COVID-19, our findings provide a rationale for the genetic association of 3p21.31 variants with elevated risk of hospitalization upon SARS-CoV-2 infection.

SUBMITTER: Stikker B

PROVIDER: S-EPMC7836105 | biostudies-literature | 2021 Jun

REPOSITORIES: biostudies-literature

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Severe COVID-19 associated variants linked to chemokine receptor gene control in monocytes and macrophages.

Stikker Bernard B Stik Grégoire G Hendriks Rudi W RW Stadhouders Ralph R

bioRxiv : the preprint server for biology 20210611

Genome-wide association studies have identified 3p21.31 as the main risk locus for severe disease in COVID-19 patients, although underlying biological mechanisms remain elusive. We performed a comprehensive epigenomic dissection of the 3p21.31 locus, identifying a CTCF-dependent tissue-specific 3D regulatory chromatin hub that controls the activity of several tissue-homing chemokine receptor (CCR) genes in monocytes and macrophages. Risk SNPs colocalized with regulatory elements and were linked ...[more]

PMID: 33501435

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