Transcriptome profiling of different developmental stages of corpus luteum during the estrous cycle in pigs

被引:11
作者
Bharati, Jaya [1 ]
Mohan, N. H. [1 ]
Kumar, Satish [2 ]
Gogoi, Jayashree [3 ]
Kumar, Sai [4 ]
Jose, Bosco [4 ]
Punetha, Meeti [4 ]
Borah, Sanjib [3 ]
Kumar, Amit [5 ]
Sarkar, Mihir [4 ]
机构
[1] ICAR Natl Res Ctr Pig, Anim Physiol, Gauhati 781131, Assam, India
[2] ICAR Natl Res Ctr Pig, Anim Genet & Breeding, Gauhati 781131, Assam, India
[3] Assam Agr Univ, Lakhimpur Coll Vet Sci, North Lakhimpur, Assam, India
[4] ICAR Indian Vet Res Inst, Div Physiol & Climatol, Bareilly, Uttar Pradesh, India
[5] ICAR Indian Vet Res Inst, Div Anim Genet & Breeding, Bareilly, Uttar Pradesh, India
关键词
Corpus luteum; Transcriptome; Angiogenesis; Steroidogenesis; Proliferation; Luteolysis; ENDOTHELIAL GROWTH-FACTOR; PORCINE CORPORA-LUTEA; EARLY-PREGNANCY; FACTOR-I; RNA-SEQ; PROMOTES ANGIOGENESIS; OVARIAN-FUNCTION; GENE-EXPRESSION; GRANULOSA-CELLS; MODULATORY ROLE;
D O I
10.1016/j.ygeno.2020.12.008
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
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 log(2)(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.
引用
收藏
页码:366 / 379
页数:14
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