TY - JOUR
T1 - A functional regulatory variant of MYH3 influences muscle fiber-type composition and intramuscular fat content in pigs
AU - Cho, In-Cheol
AU - Park, Hee-Bok
AU - Ahn, Jin Seop
AU - Han, Sang-Hyun
AU - Lee, Jae-Bong
AU - Lim, Hyun-Tae
AU - Yoo, Chae-Kyoung
AU - Jung, Eun-Ji
AU - Kim, Dong-Hwan
AU - Sun, Wu-Sheng
AU - Ramayo-Caldas, Yuliaxis
AU - Kim, Sang-Geum
AU - Kang, Yong-Jun
AU - Kim, Yoo-Kyung
AU - Shin, Hyun-Sook
AU - Seong, Pil-Nam
AU - Hwang, In-Sul
AU - Park, Beom-Young
AU - Hwang, Seongsoo
AU - Lee, Sung-Soo
AU - Ryu, Youn-Chul
AU - Lee, Jun-Heon
AU - Ko, Moon-Suck
AU - Lee, Kichoon
AU - Andersson, Goran
AU - Perez-Enciso, Miguel
AU - Lee, Jeong-Woong
PY - 2019
Y1 - 2019
N2 - Muscle development and lipid accumulation in muscle critically affect meat quality of livestock. However, the genetic factors underlying myofiber-type specification and intramuscular fat (IMF) accumulation remain to be elucidated. Using two independent intercrosses between Western commercial breeds and Korean native pigs (KNPs) and a joint linkage-linkage disequilibrium analysis, we identified a 488.1-kb region on porcine chromosome 12 that affects both reddish meat color (a*) and IMF. In this critical region, only the MYH3 gene, encoding myosin heavy chain 3, was found to be preferentially overexpressed in the skeletal muscle of KNPs. Subsequently, MYH3-transgenic mice demonstrated that this gene controls both myofiber-type specification and adipogenesis in skeletal muscle. We discovered a structural variant in the promotor/regulatory region of MYH3 for which Q allele carriers exhibited significantly higher values of a* and IMF than q allele carriers. Furthermore, chromatin immunoprecipitation and cotransfection assays showed that the structural variant in the 5'-flanking region of MYH3 abrogated the binding of the myogenic regulatory factors (MYF5, MYOD, MYOG, and MRF4). The allele distribution of MYH3 among pig populations worldwide indicated that the MYH3 Q allele is of Asian origin and likely predates domestication. In conclusion, we identified a functional regulatory sequence variant in porcine MYH3 that provides novel insights into the genetic basis of the regulation of myofiber type ratios and associated changes in IMF in pigs. The MYH3 variant can play an important role in improving pork quality in current breeding programs.
AB - Muscle development and lipid accumulation in muscle critically affect meat quality of livestock. However, the genetic factors underlying myofiber-type specification and intramuscular fat (IMF) accumulation remain to be elucidated. Using two independent intercrosses between Western commercial breeds and Korean native pigs (KNPs) and a joint linkage-linkage disequilibrium analysis, we identified a 488.1-kb region on porcine chromosome 12 that affects both reddish meat color (a*) and IMF. In this critical region, only the MYH3 gene, encoding myosin heavy chain 3, was found to be preferentially overexpressed in the skeletal muscle of KNPs. Subsequently, MYH3-transgenic mice demonstrated that this gene controls both myofiber-type specification and adipogenesis in skeletal muscle. We discovered a structural variant in the promotor/regulatory region of MYH3 for which Q allele carriers exhibited significantly higher values of a* and IMF than q allele carriers. Furthermore, chromatin immunoprecipitation and cotransfection assays showed that the structural variant in the 5'-flanking region of MYH3 abrogated the binding of the myogenic regulatory factors (MYF5, MYOD, MYOG, and MRF4). The allele distribution of MYH3 among pig populations worldwide indicated that the MYH3 Q allele is of Asian origin and likely predates domestication. In conclusion, we identified a functional regulatory sequence variant in porcine MYH3 that provides novel insights into the genetic basis of the regulation of myofiber type ratios and associated changes in IMF in pigs. The MYH3 variant can play an important role in improving pork quality in current breeding programs.
UR - https://res.slu.se/id/publ/103684
U2 - 10.1371/journal.pgen.1008279
DO - 10.1371/journal.pgen.1008279
M3 - Journal article
SN - 1553-7390
VL - 15
JO - PLOS Genetics
JF - PLOS Genetics
IS - 10
M1 - e1008279
ER -