scholarly journals Identification of Cuts-specific Myogenic Marker Genes in Hanwoo by DNA Microarray

2010 ◽  
Vol 52 (4) ◽  
pp. 329-336 ◽  
Author(s):  
Eun-Ju Lee ◽  
Yu-Mi Shin ◽  
Hyun-Jeong Lee ◽  
Du-Hak Yoon ◽  
Tae-Hoon Chun ◽  
...  
Animals ◽  
2020 ◽  
Vol 11 (1) ◽  
pp. 34
Author(s):  
Anqi Li ◽  
Xiaotong Su ◽  
Yaning Wang ◽  
Gong Cheng ◽  
Linsen Zan ◽  
...  

In this study, we successfully established a co-culture system of bovine preadipocytes and myoblasts to explore the effect of exogenous addition of Neudesin neurotrophic factor (NENF) recombinant protein on the differentiation of adipocytes and myoblasts in co-culture. The optimal concentration of NENF recombinant protein was 100 pg/mL. NENF promoted the differentiation of bovine preadipocytes and inhibited the differentiation of bovine myoblasts when the cells were cultured separately. After adding NENF recombinant protein to the co-culture system, the accumulation of lipid droplets in bovine preadipocytes decreased, but the differentiation of bovine myoblasts did not change significantly. The results of real-time quantitative PCR (RT-qPCR) and Western blot showed that the expression levels of adipogenesis-related factors such as PPARγ, FABP4 and FASN were significantly down-regulated at the mRNA and protein levels in adipocytes, while myogenic marker genes such as MYOD1, MYOG and MYHC had no significant changes at the mRNA or protein levels in myoblasts. This differs from, and potentially conflicts with, the monoculture system, where NENF expression in each cell type changed with the cell microenvironment. Consequently, the molecular mechanism of marbling beef formation cannot be fully revealed using monocultures of adipocytes or myocytes.


2007 ◽  
Vol 55 (8) ◽  
pp. 3174-3179 ◽  
Author(s):  
Tomoyuki Fukasawa ◽  
Koichiro Murashima ◽  
Ichiro Matsumoto ◽  
Akira Hosono ◽  
Hiroki Ohara ◽  
...  

2013 ◽  
Vol 12 (4) ◽  
pp. 5348-5355 ◽  
Author(s):  
T. Ni ◽  
N. Wang ◽  
Z.G. Mao ◽  
M. Yao

2009 ◽  
Vol 6 (3) ◽  
pp. 254-262 ◽  
Author(s):  
Tomoyuki Fukasawa ◽  
Koichiro Murashima ◽  
Tomoko Nemoto ◽  
Ichiro Matsumoto ◽  
Jinichiro Koga ◽  
...  

2018 ◽  
Vol 53 (6) ◽  
pp. 1162-1168
Author(s):  
D.N. Efimov ◽  
◽  
Zh.V. Emanuylova ◽  
E.V. Zhuravleva ◽  
A.V. Egorova ◽  
...  
Keyword(s):  

2017 ◽  
Vol 68 (11) ◽  
pp. 2546-2550
Author(s):  
Monica Licker ◽  
Andrei Anghel ◽  
Roxana Moldovan ◽  
Elena Hogea ◽  
Delia Muntean ◽  
...  

Antimicrobial resistance (AMR) represents a real burden for the modern medicine. One of the most frecvently isolated hospital acquired (HA) pathogens wordlwide, is Methicillin resistant Staphylococcus aureus (MRSA). Recently not only HA, but also community-acquired MRSA (CA-MRSA) infections have been reported. A prospective study was performed between February 2009 and October 2010, with the aim to investigate bacterial resistance of CA-MRSA and HA-MRSA. DNA microarray technology has been used for the detection of 4 AMR genes for the studied MRSA strains. A number of 218 HA- S.aureus strains have been isolated, from which 89 (40. 82%) were MRSA. In the community, 1.553 S.aureus strains were isolated, out of which, 356 (22. 92%) were MRSA. From these, a number of 17 HA and 12 CA �MRSA strains have been analyzed by DNA microarray technology. From 100% phenotypically described HA- MRSA, we identified mecA gene in 10 strains (58. 83%). Other 6 strains (35. 29%) have been erm(A) positive and 4 (23. 53%) - tet(O) positive. 83. 33% (10 strains) from the CA strains had mecA gene, only one (8. 33%) was erm(A) positive and 4 (33. 33%) were erm(C) positive. DNA microarray is a method allowing the concomitant scan of multiple genes and can be done within a few hours. That type of rapid and reliable methods for antimicrobial sensitivity tests are important to start an appropriate therapy.


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