TY - JOUR
T1 - Effect of strontium on transcription factors identified by transcriptome analyses of bovine ruminal epithelial cells
AU - Tan, Panpan
AU - Wang, Yazhou
AU - Mei, Linshan
AU - Loor, Juan J.
AU - Zhao, Chenxu
AU - Kong, Yezi
AU - Zeng, Fangyuan
AU - Zhao, Baoyu
AU - Wang, Jianguo
N1 - The authors would like to thank the support of the China National Natural Science Foundation and Department of Science and Technology of Shaanxi Province, and thank the editors and reviewers for their critical reading and constructive suggestions.
This work was supported by the National Natural Science Foundation of China (grant numbers 32273085, 32102742), the National Key R&D Program of China (grant numbers 2023YFD1801100), and the Key Research and Development Program of Shaanxi (grant numbers 2021NY-022).
PY - 2024/12
Y1 - 2024/12
N2 - Background: Strontium (Sr) has similar physicochemical properties as calcium (Ca) and is often used to evaluate the absorption of this mineral. Because the major route of Ca absorption in the bovine occurs in the rumen, it is essential to understand whether Sr impacts the ruminal epithelial cells and to what extent. Results: In the present study, RNA sequencing and assembled transcriptome assembly were used to identify transcription factors (TFs), screening and bioinformatics analysis in bovine ruminal epithelial cells treated with Sr. A total of 1405 TFs were identified and classified into 64 families based on an alignment of conserved domains. A total of 174 differently expressed TFs (DE-TFs) were increased and 52 DE-TFs were decreased; the biological process-epithelial cell differentiation was inhibited according to the GSEA-GO analysis of TFs; The GO analysis of DE-TFs was enriched in the DNA binding. Protein-protein interaction network (PPI) found 12 hubs, including SMAD4, SMAD2, SMAD3, SP1, GATA2, NR3C1, PPARG, FOXO1, MEF2A, NCOA2, LEF1, and ETS1, which verified genes expression levels by real-time PCR. Conclusions: In this study, SMAD2, PPARG, LEF1, ETS1, GATA2, MEF2A, and NCOA2 are potential candidates that could be targeted by Sr to mediate cell proliferation and differentiation, as well as lipid metabolism. Hence, these results enhance the comprehension of Sr in the regulation of transcription factors and provide new insight into the study of Sr biological function in ruminant animals.
AB - Background: Strontium (Sr) has similar physicochemical properties as calcium (Ca) and is often used to evaluate the absorption of this mineral. Because the major route of Ca absorption in the bovine occurs in the rumen, it is essential to understand whether Sr impacts the ruminal epithelial cells and to what extent. Results: In the present study, RNA sequencing and assembled transcriptome assembly were used to identify transcription factors (TFs), screening and bioinformatics analysis in bovine ruminal epithelial cells treated with Sr. A total of 1405 TFs were identified and classified into 64 families based on an alignment of conserved domains. A total of 174 differently expressed TFs (DE-TFs) were increased and 52 DE-TFs were decreased; the biological process-epithelial cell differentiation was inhibited according to the GSEA-GO analysis of TFs; The GO analysis of DE-TFs was enriched in the DNA binding. Protein-protein interaction network (PPI) found 12 hubs, including SMAD4, SMAD2, SMAD3, SP1, GATA2, NR3C1, PPARG, FOXO1, MEF2A, NCOA2, LEF1, and ETS1, which verified genes expression levels by real-time PCR. Conclusions: In this study, SMAD2, PPARG, LEF1, ETS1, GATA2, MEF2A, and NCOA2 are potential candidates that could be targeted by Sr to mediate cell proliferation and differentiation, as well as lipid metabolism. Hence, these results enhance the comprehension of Sr in the regulation of transcription factors and provide new insight into the study of Sr biological function in ruminant animals.
KW - Cell differentiation
KW - Lipid metabolism
KW - Strontium
KW - Transcription factors
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U2 - 10.1186/s12917-024-03929-9
DO - 10.1186/s12917-024-03929-9
M3 - Article
C2 - 38459489
AN - SCOPUS:85187132720
SN - 1746-6148
VL - 20
JO - BMC Veterinary Research
JF - BMC Veterinary Research
IS - 1
M1 - 88
ER -