Genetic architecture of gene regulation in Indonesian populations identifies QTLs associated with global and local ancestries

Journal article


Natri, Heini M., Hudjashov, Georgi, Jacobs, Guy, Kusuma, Pradiptajati, Saag, Lauri, Darusallam, Chelzie Crenna, Metspalu, Mait, Sudoyo, Herawati, Cox, Murray P., Gallego Romero, Irene and Banovich, Nicholas E.. (2022). Genetic architecture of gene regulation in Indonesian populations identifies QTLs associated with global and local ancestries. American Journal of Human Genetics. 109(1), pp. 50-65. https://doi.org/10.1016/j.ajhg.2021.11.017
AuthorsNatri, Heini M., Hudjashov, Georgi, Jacobs, Guy, Kusuma, Pradiptajati, Saag, Lauri, Darusallam, Chelzie Crenna, Metspalu, Mait, Sudoyo, Herawati, Cox, Murray P., Gallego Romero, Irene and Banovich, Nicholas E.
Abstract

Lack of diversity in human genomics limits our understanding of the genetic underpinnings of complex traits, hinders precision medicine, and contributes to health disparities. To map genetic effects on gene regulation in the underrepresented Indonesian population, we have integrated genotype, gene expression, and CpG methylation data from 115 participants across three island populations that capture the major sources of genomic diversity in the region. In a comparison with European datasets, we identify eQTLs shared between Indonesia and Europe as well as population-specific eQTLs that exhibit differences in allele frequencies and/or overall expression levels between populations. By combining local ancestry and archaic introgression inference with eQTLs and methylQTLs, we identify regulatory loci driven by modern Papuan ancestry as well as introgressed Denisovan and Neanderthal variation. GWAS colocalization connects QTLs detected here to hematological traits, and further comparison with European datasets reflects the poor overall transferability of GWAS statistics across diverse populations. Our findings illustrate how population-specific genetic architecture, local ancestry, and archaic introgression drive variation in gene regulation across genetically distinct and in admixed populations and highlight the need for performing association studies on non-European populations.

Year2022
JournalAmerican Journal of Human Genetics
Journal citation109 (1), pp. 50-65
PublisherCell Press
ISSN0002-9297
Digital Object Identifier (DOI)https://doi.org/10.1016/j.ajhg.2021.11.017
PubMed ID34919805
Scopus EID2-s2.0-85181896076
Open accessPublished as ‘gold’ (paid) open access
Page range50-65
FunderRoyal Society of New Zealand
Center for Evolution and Medicine, Arizona State University (ASU)
Marcia and Frank Carlucci Charitable Foundation
The Prevent Cancer Foundation
European Union Horizon 2020
European Regional Development Fund (FEDER)
Estonian Research Council
Publisher's version
License
File Access Level
Open
Output statusPublished
Publication dates
Online06 Jan 2022
Publication process dates
Accepted16 Nov 2021
Deposited23 Apr 2025
Supplemental file
License
File Access Level
Open
Grant ID17-MAU-040 810645
2014-2020.4.01.16-0030
2014-2020.4.01.15-0012
PRG243
Additional information

© 2021 The Author(s). This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).

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