# Detection of QTL controlling feed efficiency and excretion in chickens fed a wheat-based diet

**Authors:** Sandrine Mignon-Grasteau, Nicole Rideau, Irène Gabriel, Céline Chantry-Darmon, Marie-Yvonne Boscher, Nadine Sellier, Marie Chabault, Elisabeth Le Bihan-Duval, Agnès Narcy

PMC · DOI: 10.1186/s12711-015-0156-y · 2015-09-25

## TL;DR

This study identifies genetic regions in chickens linked to feed efficiency and excretion traits, which could help improve poultry production and reduce environmental impact.

## Contribution

The study detects multiple QTL regions in chickens related to feed efficiency and excretion traits using a large SNP dataset.

## Key findings

- Sixteen QTL for feed intake and thirteen for feed efficiency were identified across chicken chromosomes.
- Ninety QTL for anatomy-related traits were detected, with some showing genome-wide significance.
- QTL for excretion traits were found on chromosomes GGA16, 19, and 26, where multiple traits co-localized.

## Abstract

Improving feed efficiency is a major goal in poultry production in order to reduce production costs, increase the possibility of using alternative feedstuffs and decrease the volume of manure. However, in spite of their economic and environmental impact, very few quantitative trait loci (QTL) have been reported on these traits. Thus, we undertook the detection of QTL on 820 meat-type chickens from a F2 cross between D− and D+ lines that were divergently selected on low or high digestive efficiency at 3 weeks of age. Birds were measured for growth between 0 and 23 days, feed intake and feed conversion ratio between 9 and 23 days, breast and abdominal fat yields at 23 days, and the anatomy of their digestive tract (density, relative weight and length of the duodenum, jejunum, ileum, and ratio of proventriculus to gizzard weight) was examined. To evaluate excretion traits, fresh and dry weight, water content, pH, nitrogen to phosphorus ratio from 0 to 23 days, and pH of gizzard and jejunum contents at 23 days were measured. A set of 3379 single nucleotide polymorphisms distributed on 28 Gallus gallus (GGA) autosomes, the Z chromosome and one unassigned linkage group was used for QTL detection.

Using the QTLMap software developed for linkage analyses by interval mapping, we detected 16 QTL for feed intake, 13 for feed efficiency, 49 for anatomy-related traits, seven for growth, six for body composition and ten for excretion. Nine of these QTL were genome-wide significant (four for feed intake on GGA1, one for feed efficiency on GGA2, and four for anatomy on GGA1, 2, 3 and 4). GGA16, 19, and 26 carried many QTL for different types of traits that co-localize at the same position.

This study identified several QTL regions that are involved in the control of digestive efficiency in chicken. Further studies are needed to identify the genes that underlie these effects, and to validate these in other commercial populations and for different breeding environments.

The online version of this article (doi:10.1186/s12711-015-0156-y) contains supplementary material, which is available to authorized users.

## Linked entities

- **Species:** Gallus gallus (taxon 9031)

## Full-text entities

- **Genes:** SLC26A9 (solute carrier family 26 member 9) [NCBI Gene 428262], IL7R (interleukin 7 receptor) [NCBI Gene 426054] {aka CHIL-7Ralpha}, TAC1 (tachykinin precursor 1) [NCBI Gene 420573], GGA1 [NCBI Gene 418039], FGFR2 (fibroblast growth factor receptor 2) [NCBI Gene 396259] {aka BEK, bFGFR, cek3, chicken-bek}, Pnlip (pancreatic lipase) [NCBI Gene 69060] {aka 1810007A24Rik, PL, PTL}, PLA2G2A (phospholipase A2 group IIA) [NCBI Gene 426748] {aka IIE, PLA2}, GRP (gastrin releasing peptide) [NCBI Gene 425213], GGA2 (golgi associated, gamma adaptin ear containing, ARF binding protein 2) [NCBI Gene 416577], FGF1 (fibroblast growth factor 1) [NCBI Gene 396094] {aka ECGF, FGF-1}, GGA3 (golgi associated, gamma adaptin ear containing, ARF binding protein 3) [NCBI Gene 422121], CLDN3 (claudin 3) [NCBI Gene 374029] {aka claudin-3}, TAC3 (tachykinin 3) [NCBI Gene 107055422], GPR83 (G protein-coupled receptor 83) [NCBI Gene 428093], SREBF2 (sterol regulatory element binding transcription factor 2) [NCBI Gene 395304] {aka SREBP-2}, Slc22a4 (solute carrier family 22 (organic cation transporter), member 4) [NCBI Gene 30805] {aka Octn1}, Slc1a1 (solute carrier family 1 (neuronal/epithelial high affinity glutamate transporter, system Xag), member 1) [NCBI Gene 20510] {aka D130048G10Rik, EAAC1, EAAC2, EAAT3, MEAAC1}, EPCAM (epithelial cell adhesion molecule) [NCBI Gene 421292] {aka TACSTD1}, CRHR1 (corticotropin releasing hormone receptor 1) [NCBI Gene 374218], ELN (elastin) [NCBI Gene 396441], SLC1A1 (solute carrier family 1 member 1) [NCBI Gene 427352], Slc1a4 (solute carrier family 1 (glutamate/neutral amino acid transporter), member 4) [NCBI Gene 55963] {aka ASCT-1, ASCT1, SATT}, NGF (nerve growth factor) [NCBI Gene 396466] {aka NGFB, beta-NGF}, IL10 (interleukin 10) [NCBI Gene 428264] {aka IL-10, interleukin-10}, CLDN4 (claudin 4) [NCBI Gene 395144], FGF10 (fibroblast growth factor 10) [NCBI Gene 395432] {aka FGF}, NPTN (neuroplastin) [NCBI Gene 415316] {aka SDFR1}, COL3A1 (collagen type III alpha 1 chain) [NCBI Gene 396340] {aka collagen}, GGA1, 2, 3 and 4 [NCBI Gene 418039;416577;422121], MTOR (mechanistic target of rapamycin) [NCBI Gene 419455] {aka FRAP1}, Casp3 (caspase 3) [NCBI Gene 12367] {aka A830040C14Rik, AC-3, CASP-3, CC3, CPP-32, CPP32}, UGCG (UDP-glucose ceramide glucosyltransferase) [NCBI Gene 427335]
- **Diseases:** PHE (MESH:D010677), inflammatory (MESH:D007249), Meckel's diverticulum (MESH:D008467), ILD (MESH:D017563), BL (MESH:D002051), proventricular dilatation (MESH:D002311), weight gain (MESH:D015430), muscle contraction (MESH:C536214),  (MESH:D001835)
- **Chemicals:** bile acids (MESH:D001647), starch (MESH:D013213), glutamine (MESH:D005973), glucose (MESH:D005947), P (MESH:D010758), lipid (MESH:D008055), malic acid (MESH:C030298), pentobarbital (MESH:D010424), ergothionein (-), N (MESH:D009584)
- **Species:** Gallus gallus (bantam, species) [taxon 9031], Coturnix coturnix (Common quail, species) [taxon 9091], Homo sapiens (human, species) [taxon 9606], Mus musculus (house mouse, species) [taxon 10090]
- **Mutations:** rs14022155, rs29004800, rs15842421, rs13865892, rs15208685, rs15235010, rs15262904, rs13606082, rs16126655, rs15993613, rs14936549, rs14116110, rs16110590, rs16048502, rs14974160, rs15825400, rs15850796, rs13704690, rs14124099, rs15620835, rs14064923, rs13507599, rs14289024, rs14067631, rs13828473, rs14105389, rs14094799, rs13606421, rs16205037, rs15217571, rs16688631, rs15994240, rs15243050, rs16126120, rs16617921, rs16057130, rs15892308, rs14590462, rs14065910, rs13721291, rs14316939, rs13987585, rs14024860, rs14187077, rs14769351, rs16276740, rs14304396, rs13986943, rs15623939, rs14029626, rs13606162, rs14020873, rs15883120, rs16076471, rs15992576, rs15911337, rs14741743, rs15632811, rs14300646, rs14107424
- **Cell lines:** S2 — Drosophila melanogaster (Fruit fly), Spontaneously immortalized cell line (CVCL_Z232), DUL — Homo sapiens (Human), B-cell non-Hodgkin lymphoma, Transformed cell line (CVCL_XA38)

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC4582934/full.md

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Source: https://tomesphere.com/paper/PMC4582934