TY - JOUR
T1 - Exon-intron split analysis reveals posttranscriptional regulatory signals induced by high and low n-6/n-3 polyunsaturated fatty acid ratio diets in piglets
AU - Manaig, Yron Joseph Yabut
AU - Mármol-Sánchez, Emilio
AU - Castelló, Anna
AU - Esteve-Codina, Anna
AU - Sandrini, Silvia
AU - Savoini, Giovanni
AU - Agazzi, Alessandro
AU - Sánchez, Armand
AU - Folch, Josep M.
N1 - Publisher Copyright:
© 2023 The Author(s). Published by Oxford University Press on behalf of the American Society of Animal Science.
PY - 2023/1/3
Y1 - 2023/1/3
N2 - Polyunsaturated fatty acids (PUFA), such as omega-6 (n-6) and omega-3 (n-3), play a vital role in nutrient metabolism, inflammatory response, and gene regulation. microRNAs (miRNA), which can potentially degrade targeted messenger RNAs (mRNA) and/or inhibit their translation, might play a relevant role in PUFA-related changes in gene expression. Although differential expression analyses can provide a comprehensive picture of gene expression variation, they are unable to disentangle when in the mRNA life cycle the regulation of expression is taking place, including any putative functional miRNA-driven repression. To capture this, we used an exon-intron split analysis (EISA) approach to account for posttranscriptional changes in response to extreme values of n-6/n-3 PUFA ratio. Longissimus dorsi muscle samples of male and female piglets from sows fed with n-6/n-3 PUFA ratio of 13:1 (SOY) or 4:1 (LIN), were analyzed in a bidirectional contrast (LIN vs. SOY, SOY vs. LIN). Our results allowed the identification of genes showing strong posttranscriptional downregulation signals putatively targeted by significantly upregulated miRNA. Moreover, we identified genes primarily involved in the regulation of lipid-related metabolism and immune response, which may be associated with the pro- and anti-inflammatory functions of the n-6 and n-3 PUFA, respectively. EISA allowed us to uncover regulatory networks complementing canonical differential expression analyses, thus providing a more comprehensive view of muscle metabolic changes in response to PUFA concentration.
AB - Polyunsaturated fatty acids (PUFA), such as omega-6 (n-6) and omega-3 (n-3), play a vital role in nutrient metabolism, inflammatory response, and gene regulation. microRNAs (miRNA), which can potentially degrade targeted messenger RNAs (mRNA) and/or inhibit their translation, might play a relevant role in PUFA-related changes in gene expression. Although differential expression analyses can provide a comprehensive picture of gene expression variation, they are unable to disentangle when in the mRNA life cycle the regulation of expression is taking place, including any putative functional miRNA-driven repression. To capture this, we used an exon-intron split analysis (EISA) approach to account for posttranscriptional changes in response to extreme values of n-6/n-3 PUFA ratio. Longissimus dorsi muscle samples of male and female piglets from sows fed with n-6/n-3 PUFA ratio of 13:1 (SOY) or 4:1 (LIN), were analyzed in a bidirectional contrast (LIN vs. SOY, SOY vs. LIN). Our results allowed the identification of genes showing strong posttranscriptional downregulation signals putatively targeted by significantly upregulated miRNA. Moreover, we identified genes primarily involved in the regulation of lipid-related metabolism and immune response, which may be associated with the pro- and anti-inflammatory functions of the n-6 and n-3 PUFA, respectively. EISA allowed us to uncover regulatory networks complementing canonical differential expression analyses, thus providing a more comprehensive view of muscle metabolic changes in response to PUFA concentration.
KW - Exon–intron split analysis
KW - messenger RNA
KW - microRNA
KW - piglets
KW - PUFA
KW - MicroRNAs/genetics
KW - Diet/veterinary
KW - Exons
KW - Introns
KW - Swine/genetics
KW - Male
KW - RNA, Messenger/genetics
KW - Fatty Acids, Unsaturated
KW - Animals
KW - Female
KW - Fatty Acids, Omega-3/pharmacology
UR - https://www.scopus.com/pages/publications/85171600781
U2 - 10.1093/jas/skad271
DO - 10.1093/jas/skad271
M3 - Article
C2 - 37561402
AN - SCOPUS:85171600781
SN - 0021-8812
VL - 101
JO - Journal of animal Science
JF - Journal of animal Science
M1 - skad271
ER -