TY - JOUR
T1 - Identification of genes regulating growth and fatness traits in pig through hypothalamic transcriptome analysis
AU - Pérez-Montarelo, Dafne
AU - Madsen, Ole
AU - Alves, Estefânia
AU - Rodríguez, M. Carmen
AU - Folch, Josep María
AU - Noguera, José Luis
AU - Groenen, Martien A.M.
AU - Fernández, Ana I.
PY - 2014/3/15
Y1 - 2014/3/15
N2 - Previous studies on Iberian × Landrace (IBMAP) pig intercrosses have enabled the identification of several quantitative trait locus (QTL) regions related to growth and fatness traits; however, the genetic variation underlying those QTLs are still unknown. These traits are not only relevant because of their impact on economically important production traits, but also because pig constitutes a widely studied animal model for human obesity and obesity-related diseases. The hypothalamus is the main gland regulating growth, food intake, and fat accumulation. Therefore, the aim of this work was to identify genes and/or gene transcripts involved in the determination of growth and fatness in pig by a comparison of the whole hypothalamic transcrip-tome (RNA-Seq) in two groups of phenotypically divergent IBMAP pigs. Around 16,000 of the ~25.010 annotated genes were expressed in these hypothalamic samples, with most of them showing intermediate expression levels. Functional analyses supported the key role of the hypothalamus in the regulation of growth, fat accumulation, and energy expenditure. Moreover, 58,927 potentially new isoforms were detected. More than 250 differentially expressed genes and novel transcript isoforms were identified between the two groups of pigs. Twenty-one DE genes/transcripts that colocalized in previously identified QTL regions and/or whose biological functions are related to the traits of interest were explored in more detail. Additionally, the transcription factors potentially regulating these genes and the subjacent networks and pathways were also analyzed. This study allows us to propose strong candidate genes for growth and fatness based on expression patterns, genomic location, and network interactions. © 2014 the American Physiological Society.
AB - Previous studies on Iberian × Landrace (IBMAP) pig intercrosses have enabled the identification of several quantitative trait locus (QTL) regions related to growth and fatness traits; however, the genetic variation underlying those QTLs are still unknown. These traits are not only relevant because of their impact on economically important production traits, but also because pig constitutes a widely studied animal model for human obesity and obesity-related diseases. The hypothalamus is the main gland regulating growth, food intake, and fat accumulation. Therefore, the aim of this work was to identify genes and/or gene transcripts involved in the determination of growth and fatness in pig by a comparison of the whole hypothalamic transcrip-tome (RNA-Seq) in two groups of phenotypically divergent IBMAP pigs. Around 16,000 of the ~25.010 annotated genes were expressed in these hypothalamic samples, with most of them showing intermediate expression levels. Functional analyses supported the key role of the hypothalamus in the regulation of growth, fat accumulation, and energy expenditure. Moreover, 58,927 potentially new isoforms were detected. More than 250 differentially expressed genes and novel transcript isoforms were identified between the two groups of pigs. Twenty-one DE genes/transcripts that colocalized in previously identified QTL regions and/or whose biological functions are related to the traits of interest were explored in more detail. Additionally, the transcription factors potentially regulating these genes and the subjacent networks and pathways were also analyzed. This study allows us to propose strong candidate genes for growth and fatness based on expression patterns, genomic location, and network interactions. © 2014 the American Physiological Society.
KW - Fatness
KW - Growth
KW - Hypothalamus
KW - Porcine
KW - RNA-seq
U2 - 10.1152/physiolgenomics.00151.2013
DO - 10.1152/physiolgenomics.00151.2013
M3 - Article
SN - 1094-8341
VL - 46
SP - 195
EP - 206
JO - Physiological Genomics
JF - Physiological Genomics
IS - 6
ER -