TY - JOUR
T1 - CEBPβ binding directly to the promoter region drives CEBPɑ transcription and improves FABP4 transcriptional activity in adipose tissue of yak (Bos grunniens)
AU - Gui, Linsheng
AU - Raza, Sayed Haidar Abbas
AU - Ma, Boyan
AU - Easa, Ahmed A.
AU - Althobaiti, Fayez
AU - Shukry, Mustafa
AU - Alotaibi, Mashael Alhumaidi
AU - Al Hazani, Tahani Mohamed Ibrahim
AU - Dawood, Mahmoud A.O.
AU - Khan, Rajwali
AU - Jahejo, Ali Raza
AU - Shater, Abdullah F.
AU - Abd El-Aziz, Ayman H.
AU - Quan, Guobo
AU - Alanbari, Khawla Hassan
AU - Wang, Lei
N1 - Publisher Copyright:
© 2021 Elsevier Ltd
PY - 2021/12
Y1 - 2021/12
N2 - Fatty acid binding protein 4 (FABP4) was crucial to fatty acid uptake and intracellular transport. However, the mechanisms regulating yak (Bos grunniens) FABP4 transcription were not determined. In the current study, predominant expression levels of yak FABP4 were identified in subcutaneous fat and longissimus dorsi muscles by quantitative real-time polymerase chain reactions (qPCR). The CCAAT/enhancer binding protein alpha (CEBPα) and myocyte enhancer factor 2A (MEF2A), as transcriptional activator or repressor in the promoter region of FABP4, were confirmed by both site-directed mutagenesis experiment and chromatin immunoprecipitation assay. Additionally, molecular mechanisms of CEBPɑ regulation were analyzed to explore the transcriptional regulatory property of FABP4, which indicated that transcriptional activity of CEBPɑ depended on CCAAT/ enhancer binding protein beta (CEBPβ) transcription factor. Our results demonstrated that CEBPβ binding directly to the promoter region drove CEBPɑ transcription, improving yak FABP4 transcriptional activity in adipocytes. This mechanism expanded the information on the transcriptional regulatory network of adipogenesis.
AB - Fatty acid binding protein 4 (FABP4) was crucial to fatty acid uptake and intracellular transport. However, the mechanisms regulating yak (Bos grunniens) FABP4 transcription were not determined. In the current study, predominant expression levels of yak FABP4 were identified in subcutaneous fat and longissimus dorsi muscles by quantitative real-time polymerase chain reactions (qPCR). The CCAAT/enhancer binding protein alpha (CEBPα) and myocyte enhancer factor 2A (MEF2A), as transcriptional activator or repressor in the promoter region of FABP4, were confirmed by both site-directed mutagenesis experiment and chromatin immunoprecipitation assay. Additionally, molecular mechanisms of CEBPɑ regulation were analyzed to explore the transcriptional regulatory property of FABP4, which indicated that transcriptional activity of CEBPɑ depended on CCAAT/ enhancer binding protein beta (CEBPβ) transcription factor. Our results demonstrated that CEBPβ binding directly to the promoter region drove CEBPɑ transcription, improving yak FABP4 transcriptional activity in adipocytes. This mechanism expanded the information on the transcriptional regulatory network of adipogenesis.
KW - Expression
KW - FABP4
KW - Transcriptional activity
KW - Yak adipocyte
UR - https://www.scopus.com/pages/publications/85118565889
U2 - 10.1016/j.rvsc.2021.10.018
DO - 10.1016/j.rvsc.2021.10.018
M3 - Article
C2 - 34749102
AN - SCOPUS:85118565889
SN - 0034-5288
VL - 141
SP - 174
EP - 179
JO - Research in Veterinary Science
JF - Research in Veterinary Science
ER -