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Cited 14 time in webofscience Cited 16 time in scopus
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DNA methylation patterns and gene expression associated with litter size in Berkshire pig placentaopen access

Authors
Hwang, Jung HyeAn, Sang MiKwon, SeulgiPark, Da HyeKim, Tae WanKang, Deok GyeongYu, Go EunKim, Il-SukPark, Hwa ChunHa, JeongimKim, Chul Wook
Issue Date
7-Sep-2017
Publisher
PUBLIC LIBRARY SCIENCE
Citation
PLOS ONE, v.12, no.9
Indexed
SCIE
SCOPUS
Journal Title
PLOS ONE
Volume
12
Number
9
URI
https://scholarworks.bwise.kr/gnu/handle/sw.gnu/13484
DOI
10.1371/journal.pone.0184539
ISSN
1932-6203
Abstract
Increasing litter size is of great interest to the pig industry. DNA methylation is an important epigenetic modification that regulates gene expression, resulting in livestock phenotypes such as disease resistance, milk production, and reproduction. We classified Berkshire pigs into two groups according to litter size and estimated breeding value: smaller (SLG) and larger (LLG) litter size groups. Genome-wide DNA methylation and gene expression were analyzed using placenta genomic DNA and RNA to identify differentially methylated regions (DMRs) and differentially expressed genes (DEGs) associated with litter size. The methylation levels of CpG dinucleotides in different genomic regions were noticeably different between the groups, while global methylation pattern was similar, and excluding intergenic regions they were found the most frequently in gene body regions. Next, we analyzed RNA-Seq data to identify DEGs between the SLG and LLG groups. A total of 1591 DEGs were identified: 567 were downregulated and 1024 were upregulated in LLG compared to SLG. To identify genes that simultaneously exhibited changes in DNA methylation and mRNA expression, we integrated and analyzed the data from bisulfite-Seq and RNA-Seq. Nine DEGs positioned in DMRs were found. The expression of only three of these genes (PRKG2, CLCA4, and PCK1) was verified by RT-qPCR. Furthermore, we observed the same methylation patterns in blood samples as in the placental tissues by PCR-based methylation analysis. Together, these results provide useful data regarding potential epigenetic markers for selecting hyperprolific sows.
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