scholarly journals Integrative analysis of methylomic and transcriptomic data in fetal sheep muscle tissues in response to maternal diet during pregnancy

BMC Genomics ◽  
2018 ◽  
Vol 19 (1) ◽  
Author(s):  
Hadjer Namous ◽  
Francisco Peñagaricano ◽  
Marcello Del Corvo ◽  
Emanuele Capra ◽  
David L. Thomas ◽  
...  
2020 ◽  
Vol 31 (9-12) ◽  
pp. 309-324
Author(s):  
Md Mahmodul Hasan Sohel ◽  
Bilal Akyuz ◽  
Yusuf Konca ◽  
Korhan Arslan ◽  
Kutlay Gurbulak ◽  
...  

2019 ◽  
Vol 20 (20) ◽  
pp. 5161
Author(s):  
Jianyu Ma ◽  
Caifang Ren ◽  
Hua Yang ◽  
Jie Zhao ◽  
Feng Wang ◽  
...  

The complement 1q binding protein C (C1QBP), also known as p32, is highly expressed in rapidly growing tissues and plays a crucial role in cell proliferation and apoptosis. However, there are no data interpreting its mechanisms in muscle development. To investigate the role of p32 in sheep muscle development, an 856 bp cDNA fragment of p32 containing an 837 bp coding sequence that encodes 278 amino acids was analyzed. We then revealed that the expression of p32 in the longissimus and quadricep muscles of fetal sheep was more significantly up-regulated than expression at other developmental stages. Furthermore, we found that the expression of p32 was increased during myoblasts differentiation in vitro. Additionally, the knockdown of p32 in sheep myoblasts effectively inhibited myoblast differentiation, proliferation, and promoted cell apoptosis in vitro. The interference of p32 also changed the energy metabolism from Oxidative Phosphorylation (OXPHOS) to glycolysis and activated AMP-activated protein kinase (AMPK) phosphorylation in sheep myoblasts in vitro. Taken together, our data suggest that p32 plays a vital role in the development of sheep muscle and provides a potential direction for future research on muscle development and some muscle diseases.


Author(s):  
Chinwe U Nwachukwu ◽  
Kathryn J Woad ◽  
Nicole Barnes ◽  
D S Gardner ◽  
Robert S Robinson

Maternal malnutrition has important developmental consequences for the fetus. Indeed, adverse fetal ovarian development could have lifelong impact, with potentially reduced ovarian reserve and fertility of the offspring. This study investigated the effect of maternal protein restriction on germ cell and blood vessel development in the fetal sheep ovary. Ewes were fed control (n=7) or low protein (n=8) diets (17.0g versus 8.7g crude protein.MJ-1 metabolizable energy) from conception to day 65 of gestation (gd65). On gd65, fetal ovaries were subjected to histological and immunohistochemical analysis to quantify germ cells (OCT4, VASA, DAZL), proliferation (Ki67), apoptosis (Caspase 3) and vascularisation (CD31). Protein restriction reduced fetal ovary weight (p<0.05), but had no effect on fetal weight (p>0.05). The density of germ cells was unaffected by maternal diet (p>0.05). In the ovarian cortex, OCT4+ve cells were more abundant than DAZL+ve (p<0.001) and VASA+ve cells (p<0.001). The numbers, density and estimated total weight of OCT4, DAZL, and VASA+ve cells within the ovigerous cords were similar in both dietary groups (p>0.05). Similarly, maternal protein restriction had no effect on germ cell proliferation or apoptotic indices (p>0.05) and the number, area and perimeter of medullary blood vessels and degree of microvascularisation in the cortex (p>0.05). In conclusion, maternal protein restriction decreased ovarian weight despite not affecting germ cell developmental progress, proliferation, apoptosis, or ovarian vascularity. This suggests that reduced maternal protein has potential to regulate ovarian development in the offspring.


2020 ◽  
Vol 16 (4) ◽  
pp. e1007771
Author(s):  
Hans-Ulrich Klein ◽  
Martin Schäfer ◽  
David A. Bennett ◽  
Holger Schwender ◽  
Philip L. De Jager

PROTEOMICS ◽  
2013 ◽  
Vol 13 (8) ◽  
pp. 1257-1275 ◽  
Author(s):  
Young-Eun Cho ◽  
Pyong-Gon Moon ◽  
Jeong-Eun Lee ◽  
Thoudam S. K. Singh ◽  
Wonku Kang ◽  
...  

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