Whole Transcriptome Profiling Reveals the ceRNA Network
in Chicken T Cells with Stable CD8A Overexpression
Yanli Du1,
Wei Huang1,
Kun Wang2, Xiannian Zi2, Dalia
Fouad3, Farid Shokry Ataya4,
Changrong Ge2, Muhammad Sarfaraz Iqbal5
and Jinshan Ran1*
1College
of Agronomy and Life Sciences, Kunming University,
Kunming 650200, Yunnan Province, China;
2Yunnan Provincial Key Laboratory of Animal
Nutrition and Feed, Yunnan Agricultural University,
Kunming 650201, Yunnan Province, China; 3Department
of Zoology, College of Science, King Saud University, PO
Box 22452, Riyadh 11495, Saudi Arabia; 4Department
of Biochemistry, College of Science, King Saud
University, PO Box 2455, Riyadh 11451, Saudi Arabia;
5State Key Laboratory of Microbial
Metabolism, School of Life Sciences and Biotechnology,
Shanghai Jiao Tong University, 800 Dongchuan Road,
Minhang District, Shanghai 200240, China.
The CD8ɑ (CD8A) gene plays an important role in immune
function, particularly in T cells. Our previous study
demonstrated that CD8A overexpression promotes T-cell
activation. Coding and non-coding RNAs are presumed to
participate in CD8A‑related molecular events in chicken
T cells; however, their expression patterns and
underlying molecular links remain largely unclear. To
address this knowledge gap, we performed whole-transcriptome
RNA-seq to analyze mRNA, lncRNA, miRNA and circRNA
expression profiles in chicken T cells with CD8A
overexpression. The results
revealed
1502 significantly differentially expressed (DE) genes,
290 DE-lncRNAs, 23 DE-circRNAs, alongside 27 DE-miRNAs.
From our computationally predicted ceRNA interaction
dataset, CD8A overexpression correlates with the
enrichment of multiple functional pathways, including
“positive regulation of cytokine production involved in
inflammatory response”, “positive regulation of
chemokine-mediated signaling pathway,” and “positive
regulation of hormone biosynthetic process”, which may
potentially contribute to chicken T-cell activation.
Additionally, 7 genes were significantly enriched in the
GO terms and KEGG pathways, like HIF1A, KPNA6, AKT3,
INPP5K, TASOR, IL20 and AQR. They were immune genes
regulated by miR-212-5p, miR-153-5p_L+1,
miR-11987L_1+1_1ss8TA, miR-30a-3p, miR-130-3p and
PC-3p-865_3810. The above-mentioned miRNAs showed
competitive combinations with additional lncRNAs, such
as MSTRG.3834.4, MSTRG.7401.2, MSTRG.2136.8,
MSTRG.8713.1, MSTRG.2549.18, MSTRG.7401.2, MSTRG.7401.3
and MSTRG.7882.7 etc., through circRNAs such as
cirRNA3035 and cirRNA3926. Consequently, CD8A is
associated with T-cell activation and immune responses
in chickens, which may be linked to the computationally
predicted ceRNA interactions and related pathways.
To Cite This Article:
Du Y, Huang W, Wang K, Zi X, Fouad D, Ataya FS, Ge C,
IqbalMS and Ran J, 2026.
Whole transcriptome profiling reveals the ceRNA network
in chicken T cells with stable CD8A overexpression.
Pak Vet J, 46(9): 2270-2281.
http://dx.doi.org/10.29261/pakvetj/2026.221