# Strand-Specific RNA Sequencing Reveals Gene Expression Patterns in F1 Chick Breast Muscle and Liver after Hatching

**Authors:** Jianfei Zhao, Meiying Chen, Zhengwei Luo, Pengxin Cui, Peng Ren, Ye Wang

PMC · DOI: 10.3390/ani14091335 · 2024-04-29

## TL;DR

This study uses RNA sequencing to explore gene expression in F1 chicken breast muscle and liver, finding that additivity is the main pattern and identifying genes linked to growth and development.

## Contribution

The study reveals additivity as the dominant gene expression pattern in post-hatch F1 chickens and identifies growth-related genes and pathways.

## Key findings

- Additivity is the predominant gene expression pattern in F1 chicken breast muscle and liver.
- GO analysis identified 11 growth and development-related biological processes with key genes like STAT5A and TGFB2.
- KEGG analysis uncovered six growth-related pathways involving genes such as SLC27A4 and GLUL.

## Abstract

Understanding post-hatch gene expression patterns is crucial for exploring the genetic basis underlying economically important traits in the crossbreeding of chickens, which has been rarely studied. Therefore, we conducted gene expression analysis on F1 chicken breast muscle and liver tissues using ssRNA-seq at 28 days. The study revealed additivity as the predominant gene expression pattern in post-hatch muscle and liver. GO analysis identified 11 biological process terms associated with growth and development in differentially expressed gene sets and non-additive gene sets, including key genes like STAT5A and TGFB2. KEGG analysis uncovered six growth-related pathways with genes such as SLC27A4 and GLUL. These findings provide valuable insights for domestic animal crossbreeding.

Heterosis refers to the phenomenon where hybrids exhibit superior performance compared to the parental phenotypes and has been widely utilized in crossbreeding programs for animals and crops, yet the molecular mechanisms underlying this phenomenon remain enigmatic. A better understanding of the gene expression patterns in post-hatch chickens is very important for exploring the genetic basis underlying economically important traits in the crossbreeding of chickens. In this study, breast muscle and liver tissues (n = 36) from full-sib F1 birds and their parental pure lines were selected to identify gene expression patterns and differentially expressed genes (DEGs) at 28 days of age by strand-specific RNA sequencing (ssRNA-seq). This study indicates that additivity is the predominant gene expression pattern in the F1 chicken post-hatch breast muscle (80.6% genes with additivity) and liver (94.2% genes with additivity). In breast muscle, Gene Ontology (GO) enrichment analysis revealed that a total of 11 biological process (BP) terms closely associated with growth and development were annotated in the identified DEG sets and non-additive gene sets, including STAT5A, TGFB2, FGF1, IGF2, DMA, FGF16, FGF12, STAC3, GSK3A, and GRB2. Kyoto Encyclopedia of Genes and Genomes (KEGG) annotation presented that a total of six growth- and development-related pathways were identified, involving key genes such as SLC27A4, GLUL, TGFB2, COX17, and GSK3A, including the PPAR signaling pathway, TGF-beta signaling pathway, and mTOR signaling pathway. Our results may provide a theoretical basis for crossbreeding in domestic animals.

## Linked entities

- **Genes:** STAT5A (signal transducer and activator of transcription 5A) [NCBI Gene 6776], TGFB2 (transforming growth factor beta 2) [NCBI Gene 7042], SLC27A4 (solute carrier family 27 member 4) [NCBI Gene 10999], GLUL (glutamate-ammonia ligase) [NCBI Gene 2752], FGF1 (fibroblast growth factor 1) [NCBI Gene 2246], IGF2 (insulin like growth factor 2) [NCBI Gene 3481], HLA-DMA (major histocompatibility complex, class II, DM alpha) [NCBI Gene 3108], FGF16 (fibroblast growth factor 16) [NCBI Gene 8823], FGF12 (fibroblast growth factor 12) [NCBI Gene 2257], STAC3 (SH3 and cysteine rich domain 3) [NCBI Gene 246329], GSK3A (glycogen synthase kinase 3 alpha) [NCBI Gene 2931], GRB2 (growth factor receptor bound protein 2) [NCBI Gene 2885], COX17 (cytochrome c oxidase copper chaperone COX17) [NCBI Gene 10063]
- **Species:** Gallus gallus (taxon 9031)

## Full-text entities

- **Genes:** DMA (major histocompatibility complex B, class II alpha chain DMA) [NCBI Gene 417050] {aka B-DMA, B-MA1, BMA1, DMA1, HLA-DMA, MHC-DMA}, PPARA (peroxisome proliferator activated receptor alpha) [NCBI Gene 374120] {aka PPAR}, TGFB2 (transforming growth factor beta 2) [NCBI Gene 421352] {aka TGF-beta-2}, COX17 (COX17, cytochrome c oxidase copper chaperone) [NCBI Gene 770190], FGF12 (fibroblast growth factor 12) [NCBI Gene 395704] {aka FHF-1, FHF1}, SLC27A4 (solute carrier family 27 member 4) [NCBI Gene 417220] {aka FATP4}, IGF2 (insulin like growth factor 2) [NCBI Gene 395097] {aka IGF-II}, GRB2 (growth factor receptor bound protein 2) [NCBI Gene 386572], FGF1 (fibroblast growth factor 1) [NCBI Gene 396094] {aka ECGF, FGF-1}, GLUL (glutamate-ammonia ligase) [NCBI Gene 396489] {aka p42}, MTOR (mechanistic target of rapamycin) [NCBI Gene 419455] {aka FRAP1}, FGF16 (fibroblast growth factor 16) [NCBI Gene 422330]
- **Species:** Gallus gallus (bantam, species) [taxon 9031]

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11083249/full.md

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Source: https://tomesphere.com/paper/PMC11083249