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| Status |
Public on Feb 09, 2023 |
| Title |
Regulatory dissection of the severe COVID-19 risk locus introgressed by Neanderthals. |
| Organisms |
Homo sapiens; synthetic construct |
| Experiment type |
Other
|
| Summary |
Individuals infected with the SARS-CoV-2 virus present with a wide variety of phenotypes ranging from asymptomatic to severe and even lethal outcomes. Past research has revealed a genetic haplotype on chromosome 3 that entered the human population via introgression from Neanderthals as the strongest genetic risk factor for the severe COVID-19 phenotype. However, the specific variants along this introgressed haplotype that contribute to this risk and the biological mechanisms that are involved remain unclear. Here, we assess the variants present on the risk haplotype for their likelihood of driving the severe COVID-19 phenotype. We do this by first exploring their impact on the regulation of genes involved in COVID-19 infection using a variety of population genetics and functional genomics tools. We then perform an locus-specific massively parallel reporter assay to individually assess the regulatory potential of each allele on the haplotype in a multipotent immune-related cell line. We ultimately reduce the set of over 600 linked genetic variants to identify 4 introgressed alleles that are strong functional candidates for driving the association between this locus and the severe COVID-19. These variants likely drive the locus’ impact on severity by putatively modulating the regulation of two critical chemokine receptor genes: CCR1 and CCR5. These alleles are ideal targets for future functional investigations into the interaction between host genomics and COVID-19 outcomes.
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| Overall design |
MPRA testing the regulatory potential of 613 variants along the introgressed risk haplotype for severe COVID-19 on chromosome 3 in K562 cells. 22 postive and 22 negative controls were also included constituting the most and least acvtive sequences in a past K562 MPRA (GEO: GSE169200). MPRA design closely followed Tewhey et al. 2016. 4 Replicates were performed.
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| Web link |
https://elifesciences.org/articles/71235/figures
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| Contributor(s) |
Jagoda E, Marnetto D, Montinaro F, Richard D, Pagani L, Capellini TD, Senevirathne G, Gonzalez V, Baid K, Falzarano D, LeBlanc EV, Colpitts CC, Banerjee A |
| Citation(s) |
36763080 |
| |
| Submission date |
Jun 06, 2021 |
| Last update date |
May 17, 2023 |
| Contact name |
Terence D Capellini |
| E-mail(s) |
[email protected], [email protected]
|
| Phone |
6173010673
|
| Organization name |
Harvard Univserity
|
| Department |
Human Evolutionary Biology
|
| Lab |
Capellini
|
| Street address |
11 Divinity Avenue
|
| City |
Cambridge |
| State/province |
MA |
| ZIP/Postal code |
02138 |
| Country |
USA |
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| Platforms (2) |
| GPL15520 |
Illumina MiSeq (Homo sapiens) |
| GPL17769 |
Illumina MiSeq (synthetic construct) |
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| Samples (8)
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| Relations |
| BioProject |
PRJNA735528 |
| SRA |
SRP322920 |
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