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Targeted DamID to understand transcription factor genomic occupancy in human foetal lung progenitor cells. Targeted DamID to understand transcription factor genomic occupancy in human foetal lung progenitor cells

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NIAID Data Ecosystem2026-03-13 收录
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https://www.ncbi.nlm.nih.gov/bioproject/PRJNA784520
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In order to study the genomic occupancy of transcription factors, including SOX9, ETV4 and ETV5, in human foetal lung tip progenitor cells, we have introduced Targeted DamID system via lentivirus in a human foetal lung tissue derived organoid culture (Nikolic et al., 2017). We were able to identify the corresponding TF motif enrichment and discovered a potential co-regulation function of SOX9 and ETV factors in human feotal lung progenitor cells. This study has pioneered the use of targeted DamID approach in tissue derived organoid system. Overall design: We used 4 different independent organoid lines treated as replicates, all of which are around 8 pcw. We introduced the SOX9 targeted DamID into organoids via lentiviral transduction and compared with the results from organoids with Dam only controls. In a following-up experimental setting, we introduced ETV4 and ETV5 targeted DamID into organoids via lentiviral transduction and compared with the results from organoids with Dam only controls.
创建时间:
2021-11-29
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