325: cis-pcQTL mapping reveals allelic proxitropy across neighboring human genes
Base by Base24 Mars

325: cis-pcQTL mapping reveals allelic proxitropy across neighboring human genes

Lawrence et al., The American Journal of Human Genetics - Using a cis-principal-component (pcQTL) approach in human GTEx tissues, the authors uncover novel multi-gene regulatory variants and 33% more GWAS colocalizations than single-gene eQTLs. Key terms: pcQTL, allelic proxitropy, GTEx, colocalization, HOXB.

Study Highlights:
The study analyzes 13 human GTEx tissues and identifies clusters of co-expressed neighboring genes, then applies PCA to cluster expression and maps cis-principal-component QTLs (pcQTLs). pcQTL discovery and fine-mapping used SuSiE and TensorQTL permutation-based FDR to identify an average of ~1,396 pcQTLs per tissue, ~27% of which were not found by single-gene eQTL mapping. pcQTLs tend to represent smaller effects distributed across multiple genes in a cluster and often colocalize with GWAS hits missed by single-gene methods. Functionally, pcQTLs increased GWAS colocalizations by 33%, highlighting multi-gene regulatory proxitropy as a source of complex-trait-associated variation.

Conclusion:
Cis-multi-gene pcQTL mapping uncovers novel regulatory loci and increases GWAS colocalizations compared with single-gene analyses, demonstrating that multi-gene approaches improve detection and interpretation of complex-trait-associated variants.

Music:
Enjoy the music based on this article at the end of the episode.

Article title:
Focus on single-gene effects limits discovery and interpretation of complex-trait-associated variants

First author:
Lawrence

Journal:
The American Journal of Human Genetics

DOI:
10.1016/j.ajhg.2026.02.022

Reference:
Lawrence, K.A., Gjorgjieva, T., Nachun, D., and Montgomery, S.B. (2026). Focus on single-gene effects limits discovery and interpretation of complex-trait-associated variants. The American Journal of Human Genetics 113, 1–10. https://doi.org/10.1016/j.ajhg.2026.02.022

License:
This episode is based on an open-access article published under the Creative Commons Attribution 4.0 International License (CC BY 4.0) - https://creativecommons.org/licenses/by/4.0/

Support:
Base by Base – Stripe donations: https://donate.stripe.com/7sY4gz71B2sN3RWac5gEg00

Official website https://basebybase.com

On PaperCast Base by Base you’ll discover the latest in genomics, functional genomics, structural genomics, and proteomics.

Episode link: https://basebybase.com/episodes/cis-pcqtl-allelic-proxitropy-gtex

QC:
This episode was checked against the original article PDF and publication metadata for the episode release published on 2026-03-24.

QC Scope:
- article metadata and core scientific claims from the narration
- excludes analogies, intro/outro, and music
- transcript coverage: Audited the transcript sections presenting the conceptual shift to neighborhood gene regulation (allelic proxytropy), the cis-pcQTL (pcQTL) methodology, GTEx tissue clustering, key quantitative results (novel pcQTLs, clusters, colocalizations), and concrete examples (HOXB cluster, IL-18 receptor genes), plus discussion
- transcript topics: Conceptual shift to gene neighborhoods and allelic proxytropy; cis-pcQTL (pcQTL) methodology and PCA-based signal extraction; GTEx tissue clusters and gene-neighborhood calling; pcQTL discovery statistics (clusters, pcQTLs per tissue, novel signals); pcQTLs and GWAS colocalizations; HOXB cluster example (HOXB3 vs HOXB4) and PC4

QC Summary:
- factual score: 10/10
- metadata score: 10/10
- supported core claims: 6
- claims flagged for review: 0
- metadata checks passed: 4
- metadata issues found: 0

Metadata Audited:
- article_doi
- article_title
- article_journal
- license

Factual Items Audited:
- pcQTLs reveal novel multi-gene regulatory variants missed by single-gene eQTLs
- average pcQTLs per tissue is 1,396
-...

Chapters
  • (00:00:00) - Deep Dive: The genome's interconnected networks
  • (00:05:27) - The Shared Signal of Genomic Science
  • (00:11:15) - Single gene mapping fails to explain complex traits
  • (00:18:13) - Understanding the genetics of human diseases
  • (00:20:39) - Beyond one gene

Det här avsnittet är hämtat från ett öppet RSS-flöde och publiceras inte av Podme. Det kan innehålla reklam.

Avsnitt(445)

444: Many-eyes or Sentinels? How Cost Curvature Shapes Collective Vigilance

444: Many-eyes or Sentinels? How Cost Curvature Shapes Collective Vigilance

Pilgrim C et al., PNAS - A minimal analytical model shows that whether animal groups adopt distributed low-level vigilance (many-eyes) or concentrated high-vigilance roles (sentinels) depends on how i...

19 Aug 24min

443: 5D‑ASO boosts exon 51 skipping and restores dystrophin in DMD models

443: 5D‑ASO boosts exon 51 skipping and restores dystrophin in DMD models

Feng P et al., PNAS - This paper describes a bipartite antisense oligonucleotide (5D‑ASO) design that appends a short 5′ splice site decoy tail to improve exon skipping, demonstrating robust efficacy ...

18 Aug 19min

442: When pumps go missing: Ca2+ control of PMCA2 in Tmc1 deafness mutants

442: When pumps go missing: Ca2+ control of PMCA2 in Tmc1 deafness mutants

Rolseth AB et al., Proceedings of the National Academy of Sciences (PNAS) - This study links reduced Ca2+ entry through mutant TMC1 mechanotransducer channels to decreased PMCA2 pump density in outer ...

17 Aug 22min

441: Evolutionary mapping of Cav1.3 functional sites

441: Evolutionary mapping of Cav1.3 functional sites

Tang X et al., PNAS - The authors apply an evolutionary sequence-covariation model to the Cav1.3 (CACNA1D) α1-subunit, map predicted pathogenicity onto structural models, and validate five predicted s...

14 Aug 24min

440: DENV-4: Suppressing DNA Repair and Causing Genome Damage

440: DENV-4: Suppressing DNA Repair and Causing Genome Damage

Lamkina EN et al., PNAS - This episode reviews a PNAS brief report showing that DENV-4 infection induces marked DNA damage in infected cells while broadly suppressing transcription of DNA repair pathw...

12 Aug 23min

439: Coembedding Sequence and Structure: CLSS Maps the Protein Universe

439: Coembedding Sequence and Structure: CLSS Maps the Protein Universe

Longo LM et al., PNAS - This episode summarizes a PNAS study introducing CLSS, a contrastive two-tower protein language model that coembeds domain sequences, structures, and subsequences into a shared...

11 Aug 23min

438: Mapping AIRE: a proactive atlas of 9,790 missense variants

438: Mapping AIRE: a proactive atlas of 9,790 missense variants

Axakova A et al., The American Journal of Human Genetics - Axakova et al. generated a variant effect map for AIRE using an insulin‑promoter GFP reporter in HEK293 cells to measure the functional impac...

10 Aug 24min

437: Cell villages and Dirichlet modeling map human cell fitness genetics

437: Cell villages and Dirichlet modeling map human cell fitness genetics

Hanson C et al., The American Journal of Human Genetics - Hanson et al. combine pooled multi-donor human neural progenitor cell "villages" with Townlet, a hierarchical Dirichlet regression model, to e...

9 Aug 28min

Populärt inom Vetenskap

dumma-manniskor
p3-dystopia
allt-du-velat-veta
hacka-livet
bildningspodden
rss-vetenskapsradion
medicinvetarna
halsorevolutionen
svd-nyhetsartiklar
ufo-sverige
rss-vetenskapsradion-2
rss-ufobortom-rimligt-tvivel
sexet
paranormalt-med-caroline-giertz
vetenskapsradion
det-morka-psyket
rss-spraket
rss-kriminologerna
barnpsykologerna
psykologisk-forskning