| Literature DB >> 33309770 |
Jaya Bharati1, N H Mohan1, Satish Kumar2, Jayashree Gogoi3, Sai Kumar4, Bosco Jose4, Meeti Punetha4, Sanjib Borah3, Amit Kumar5, Mihir Sarkar6.
Abstract
To better understand the molecular basis of corpus luteum (CL) development and function RNA-Seq was utilized to identify differentially expressed genes (DEGs) in porcine CL during different physiological stages of the estrous cycle viz. early (EL), mid (ML), late (LL) and regressed (R) luteal. Stage wise comparisons obtained 717 (EL vs. ML), 568 (EL vs. LL), 527 (EL vs. R), 786 (ML vs. LL), 474 (ML vs. R) and 534 (LL vs. R) DEGs with log2(FC) ≥1 and p < 0.05. The process of angiogenesis, steroidogenesis, signal transduction, translation, cell proliferation and tissue remodelling were significantly (p < 0.05) enriched in EL, ML and LL stages, where as apoptosis was most active in regressed stage. Pathway analysis revealed that most annotated genes were associated with lipid metabolism, translation, immune and endocrine system pathways depicting intra-luteal control of diverse CL function. The network analysis identified genes AR, FOS, CDKN1A, which were likely the novel hub genes regulating CL physiology.Entities:
Keywords: Angiogenesis; Corpus luteum; Luteolysis; Proliferation; Steroidogenesis; Transcriptome
Mesh:
Year: 2020 PMID: 33309770 DOI: 10.1016/j.ygeno.2020.12.008
Source DB: PubMed Journal: Genomics ISSN: 0888-7543 Impact factor: 5.736