Nervous system-related gene regulatory networks and functional evolution of ETS proteins across species
Biosystems, ISSN: 0303-2647, Vol: 227, Page: 104891
2023
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Metrics Details
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Article Description
The ETS domain transcription factor family is one of the major transcription factor superfamilies that play regulatory roles in development, cell growth, and cancer progression. Although different functions of ETS member proteins in the nervous system have been demonstrated in various studies, their role in neuronal cell differentiation and the evolutionary conservation of its target genes have not yet been extensively studied. In this study, we focused on the regulatory role of ETS transcription factors in neuronal differentiation and their functional evolution by comparative transcriptomics. In order to investigate the regulatory role of ETS transcription factors in neuronal differentiation across species, transcriptional profiles of ETS members and their target genes were investigated by comparing differentially expressed genes and gene regulatory networks, which were analyzed using human, gorilla, mouse, fruit fly and worm transcriptomics datasets. Bioinformatics approaches to examine the evolutionary conservation of ETS transcription factors during neuronal differentiation have shown that ETS member proteins regulate genes associated with neuronal differentiation, nervous system development, axon, and synaptic regulation in different organisms. This study is a comparative transcriptomic study of ETS transcription factors in terms of neuronal differentiation using a gene regulatory network inference algorithm. Overall, a comparison of gene regulation networks revealed that ETS members are indeed evolutionarily conserved in the regulation of neuronal differentiation. Nonetheless, ETS, PEA3, and ELF subfamilies were found to be relatively more active transcription factors in the transcriptional regulation of neuronal differentiation.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S0303264723000667; http://dx.doi.org/10.1016/j.biosystems.2023.104891; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85152644232&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/37030605; https://linkinghub.elsevier.com/retrieve/pii/S0303264723000667; https://dx.doi.org/10.1016/j.biosystems.2023.104891
Elsevier BV
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