Differential expression analysis of lncRNA and mRNA in ovarian tissues of Pishan Red Sheep and Hu Sheep with distinct genotypes during estrus

Pishan Red Sheep and Hu Sheep are sheep breeds with exceptional reproductive characteristics. To investigate the similarities and differences in the expression of reproduction-related genes between these two breeds, this study utilized transcriptome sequencing to identify differentially expressed lncRNAs and mRNAs in ovarian tissues during estrus in Hu Sheep and Pishan Red Sheep carrying <i>FecB<sup>B+</sup></i> and <i>FecB<sup>++</sup></i> genotypes. Furthermore, we explored their potential impacts on fertility. Transcriptome sequencing of ovarian tissues generated 204.58 Gb of clean data. Bioinformatics analysis identified 34,651 lncRNAs, with differential expression analysis revealing 1,481 differentially expressed mRNAs and 698 differentially expressed lncRNAs. Differentially expressed RNAs associated with reproductive performance trends were screened through expression trend analysis. Functional enrichment analysis of target genes for these mRNAs and lncRNAs revealed significant enrichment in KEGG pathways such as "Cytokine-cytokine receptor interaction," "Hippo signaling pathway" and "MAPK signaling pathway" Key candidate mRNAs were identified, including <i>GDF9</i>, <i>GRIA4</i>, <i>HOXC9</i>, <i>HOXD3</i>, <i>MAPK8IP3</i>, <i>AMH</i>, <i>ANGPT2</i>, <i>FGF14</i>, <i>MAPK8IP1</i>, <i>MMP9</i>, and <i>BRINP3</i>. Additionally, critical regulatory relationships between lncRNAs and mRNAs were uncovered. For example, <i>MSTRG.61044.1</i> exhibited high expression in <i>FecB<sup>++</sup></i> genotype Pishan Red Sheep and may act as a hub regulator in follicular selection and hormonal responses by cis-regulating <i>MAPK8IP1</i> and trans-regulating <i>AMH</i>, <i>CCL25</i>, <i>MSTRG.23016.1</i> may regulate genes such as <i>MMP9</i> and <i>ANGPT2</i>, potentially participating in the modulation of the ovarian tissue remodeling microenvironment. In contrast, <i>MSTRG.15154.3</i> cis-regulates <i>ERBB4</i> to modulate the granulosa cell proliferation and differentiation process. The specifically highly expressed <i>MSTRG.2677.1</i> in Hu Sheep may be involved in maintaining ovarian stromal cell homeostasis through trans-regulation of <i>HGF</i> and <i>BRINP3</i>, <i>MSTRG.27015.1</i> and <i>MSTRG.60286.1</i> target <i>MAPK8IP3</i> and <i>PPP3CB</i> respectively, suggesting their potential roles in cell cycle regulation and oocyte maturation. These findings provide important molecular mechanisms and potential regulatory targets for improving reproductive performance in sheep.

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Journal
Frontiers in Veterinary Science
Published
2025-09-24
DOI
https://doi.org/10.3389/fvets.2025.1614599
Primary Topic
Cancer-related molecular mechanisms research
Type
article
Field-Weighted Citation Impact
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article

Differential expression analysis of lncRNA and mRNA in ovarian tissues of Pishan Red Sheep and Hu Sheep with distinct genotypes during estrus

Y Ye, Qifa Li, Gao Gong, Yiming Sulaiman et al.
Frontiers in Veterinary Science
Cancer-related molecular mechanisms research
article

Differential expression analysis of lncRNA and mRNA in ovarian tissues of Pishan Red Sheep and Hu Sheep with distinct genotypes during estrus

Y Ye, Qifa Li, Gao Gong, Yiming Sulaiman, Mengting Zhu, Xing Du, Aisima Muhetaer, Ayipare Kuxitaer
article en

Abstract

Pishan Red Sheep and Hu Sheep are sheep breeds with exceptional reproductive characteristics. To investigate the similarities and differences in the expression of reproduction-related genes between these two breeds, this study utilized transcriptome sequencing to identify differentially expressed lncRNAs and mRNAs in ovarian tissues during estrus in Hu Sheep and Pishan Red Sheep carrying <i>FecB<sup>B+</sup></i> and <i>FecB<sup>++</sup></i> genotypes. Furthermore, we explored their potential impacts on fertility. Transcriptome sequencing of ovarian tissues generated 204.58 Gb of clean data. Bioinformatics analysis identified 34,651 lncRNAs, with differential expression analysis revealing 1,481 differentially expressed mRNAs and 698 differentially expressed lncRNAs. Differentially expressed RNAs associated with reproductive performance trends were screened through expression trend analysis. Functional enrichment analysis of target genes for these mRNAs and lncRNAs revealed significant enrichment in KEGG pathways such as "Cytokine-cytokine receptor interaction," "Hippo signaling pathway" and "MAPK signaling pathway" Key candidate mRNAs were identified, including <i>GDF9</i>, <i>GRIA4</i>, <i>HOXC9</i>, <i>HOXD3</i>, <i>MAPK8IP3</i>, <i>AMH</i>, <i>ANGPT2</i>, <i>FGF14</i>, <i>MAPK8IP1</i>, <i>MMP9</i>, and <i>BRINP3</i>. Additionally, critical regulatory relationships between lncRNAs and mRNAs were uncovered. For example, <i>MSTRG.61044.1</i> exhibited high expression in <i>FecB<sup>++</sup></i> genotype Pishan Red Sheep and may act as a hub regulator in follicular selection and hormonal responses by cis-regulating <i>MAPK8IP1</i> and trans-regulating <i>AMH</i>, <i>CCL25</i>, <i>MSTRG.23016.1</i> may regulate genes such as <i>MMP9</i> and <i>ANGPT2</i>, potentially participating in the modulation of the ovarian tissue remodeling microenvironment. In contrast, <i>MSTRG.15154.3</i> cis-regulates <i>ERBB4</i> to modulate the granulosa cell proliferation and differentiation process. The specifically highly expressed <i>MSTRG.2677.1</i> in Hu Sheep may be involved in maintaining ovarian stromal cell homeostasis through trans-regulation of <i>HGF</i> and <i>BRINP3</i>, <i>MSTRG.27015.1</i> and <i>MSTRG.60286.1</i> target <i>MAPK8IP3</i> and <i>PPP3CB</i> respectively, suggesting their potential roles in cell cycle regulation and oocyte maturation. These findings provide important molecular mechanisms and potential regulatory targets for improving reproductive performance in sheep.

Frontiers in Veterinary ScienceVol. 12
Nanjing Agricultural University (CN), Xinjiang Agricultural University (CN)
Natural Science Foundation of Xinjiang
Openalex Percentile: Top 68%
Cancer-related molecular mechanisms research
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