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  2. Animal Science A4
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Please use this identifier to cite or link to this item: http://krishi.icar.gov.in/jspui/handle/123456789/49215
Title: Transcriptome profiling of different developmental stages of corpus luteum during the estrous cycle in pigs
Other Titles: Not Available
Authors: Jaya Bharati, NH Mohan, Satish Kumar, Jayashree Gogoi, Sai Kumar, Bosco Jose, Meeti Punetha, Sanjib Borah, Amit Kumar, Mihir Sarkar
ICAR Data Use Licennce: http://krishi.icar.gov.in/PDF/ICAR_Data_Use_Licence.pdf
Author's Affiliated institute: ICAR::National Research Centre on Pig
Published/ Complete Date: 2021-01-01
Project Code: IXX15063
Keywords: Corpus luteum, Transcriptome, Angiogenesis, Steroidogenesis, Proliferation, Luteolysis
Publisher: Elsevier
Citation: Bharati, Jaya, N. H. Mohan, Satish Kumar, Jayashree Gogoi, Sai Kumar, Bosco Jose, Meeti Punetha, Sanjib Borah, Amit Kumar, and Mihir Sarkar. "Transcriptome profiling of different developmental stages of corpus luteum during the estrous cycle in pigs." Genomics 113, no. 1 (2021): 366-379.
Series/Report no.: Not Available;
Abstract/Description: 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.
Description: Not Available
Type(s) of content: Research Paper
Sponsors: Not Available
Language: English
Name of Journal: Genomics
Journal Type: Peer Reviewed
NAAS Rating: 12.21
Impact Factor: 6.21
Volume No.: 113(1)
Page Number: 366-379
Name of the Division/Regional Station: Not Available
Source, DOI or any other URL: https://doi.org/10.1016/j.ygeno.2020.12.008
URI: http://krishi.icar.gov.in/jspui/handle/123456789/49215
Appears in Collections:AS-NRCP-Publication

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