# Large deletions in the DNA primase large subunit PRIM2 are associated with NADP‐malate dehydrogenase activity in a porcine F2 cross

**Authors:** Clemens Falker‐Gieske, Iulia Blaj, Ana‐Marija Krizanac, Isabel Kilic, Paula Reich, Jörn Bennewitz, Jens Tetens

PMC · DOI: 10.1002/age.70077 · Animal Genetics · 2026-02-02

## TL;DR

This study finds that large deletions in the PRIM2 gene are linked to NADP-malate dehydrogenase activity, which affects pig production traits.

## Contribution

The study identifies large intronic deletions in PRIM2 and other genes as potential causal variants for metabolic enzyme activity in pigs.

## Key findings

- Genetic and phenotypic correlations between production traits and enzyme activity were high.
- Large deletions in PRIM2 and other genes on SSC7 are associated with NADP-malate dehydrogenase content.
- Discovered structural variants were validated in independent pig populations.

## Abstract

Large porcine F2 crosses are a valuable resource for discovering QTL and genetic variants for relevant traits. Past studies have been largely limited to SNPs and short insertions and deletions. Structural variants (SVs) are becoming a major area of interest in this respect. Here we present results from a genome‐wide association study with SVs imputed from medium‐density SNP array to the whole genome sequence level that were used to investigate the genetic relationship between important production traits and metabolic enzyme activity in an F2 cross based on the breeds Meishan, Piétrain, and European wild boar. Genetic and phenotypic correlations between the two trait classes were high. We were able to pinpoint common genetic loci to a QTL on SSC7, encompassing numerous large intron deletions in the PRIM2 gene as well as in HMGCLL1, BMP5, TRERF1, COL21A1, LRRC1, and UBR2. The most pronounced genetic associations were observed for the content of NADP‐malate dehydrogenase in the tissue. Hence, we propose that the content and activity of malate dehydrogenase is directly connected to important pig production traits, and we present a comprehensive list of large intronic deletions as promising candidates for causality. The variants were validated in independent pig populations, where the majority of the discovered SVs were present, indicating that they are not only relevant to the breeds investigated here.

## Linked entities

- **Genes:** PRIM2 (DNA primase subunit 2) [NCBI Gene 5558], HMGCLL1 (3-hydroxy-3-methylglutaryl-CoA lyase like 1) [NCBI Gene 54511], BMP5 (bone morphogenetic protein 5) [NCBI Gene 653], TRERF1 (transcriptional regulating factor 1) [NCBI Gene 55809], COL21A1 (collagen type XXI alpha 1 chain) [NCBI Gene 81578], LRRC1 (leucine rich repeat containing 1) [NCBI Gene 55227], UBR2 (ubiquitin protein ligase E3 component n-recognin 2) [NCBI Gene 23304]
- **Species:** Sus scrofa (taxon 9823)

## Full-text entities

- **Genes:** RYR1 (ryanodine receptor 1) [NCBI Gene 396718] {aka CRC, RYR}, TRERF1 (transcriptional regulating factor 1) [NCBI Gene 100153071], SFTPC (surfactant protein C) [NCBI Gene 733580] {aka SFTP2, SP-C}, LRRC1 (leucine rich repeat containing 1) [NCBI Gene 100154780], MTOR (mechanistic target of rapamycin kinase) [NCBI Gene 100127359] {aka FRAP1}, G6PD (glucose-6-phosphate dehydrogenase) [NCBI Gene 100622986], HMGCLL1 (3-hydroxymethyl-3-methylglutaryl-CoA lyase like 1) [NCBI Gene 535508], IDH1 (isocitrate dehydrogenase (NADP(+)) 1) [NCBI Gene 102166364] {aka IDH, IDP}, PCSK1 (proprotein convertase subtilisin/kexin type 1) [NCBI Gene 281967] {aka PC1, PC3}, CYP11A1 (cytochrome P450 family 11 subfamily A member 1) [NCBI Gene 403329] {aka SSC}, HMGCL (3-hydroxy-3-methylglutaryl-CoA lyase) [NCBI Gene 317658], BFT (Average backfat thickness) [NCBI Gene 102657873], PRIM2 (DNA primase subunit 2) [NCBI Gene 100156829], COL21A1 (collagen type XXI alpha 1 chain) [NCBI Gene 100523618], MDH1 (malate dehydrogenase 1) [NCBI Gene 396894] {aka KAR, MDH}, PRIM2 (DNA primase subunit 2) [NCBI Gene 514682] {aka PRIM2A}, HMGCLL1 (3-hydroxy-3-methylglutaryl-CoA lyase like 1) [NCBI Gene 100627473], PCNA (proliferating cell nuclear antigen) [NCBI Gene 515499], BMP5 (bone morphogenetic protein 5) [NCBI Gene 100151964], UBR2 (ubiquitin protein ligase E3 component n-recognin 2) [NCBI Gene 100522688]
- **Diseases:** MDS (MESH:C538175), fat (MESH:D004620), PC (MESH:D015324), obesity (MESH:D009765)
- **Chemicals:** acetoacetate (MESH:C016635), carbon (MESH:D002244), malate (MESH:C030298), steroid hormones (MESH:D013256), oxaloacetate (MESH:D062907), cholesterol (MESH:D002784), acetyl-CoA (MESH:D000105), TCA (MESH:D014233), NADPH (MESH:D009249), lipid (MESH:D008055), pregnenolone (MESH:D011284), pyruvate (MESH:D019289), ADG (-), citric acid (MESH:D019343)
- **Species:** Equus caballus (domestic horse, species) [taxon 9796], Bos taurus (bovine, species) [taxon 9913], Sus scrofa (pig, species) [taxon 9823], Homo sapiens (human, species) [taxon 9606], Gallus gallus (bantam, species) [taxon 9031]
- **Mutations:** rs1112937671, C/T

## Full text

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## Figures

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## References

57 references — full list in the complete paper: https://tomesphere.com/paper/PMC12864183/full.md

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Source: https://tomesphere.com/paper/PMC12864183