Antibody-free profiling of transcription factor occupancy during early embryogenesis by FitCUT&RUN
Author(s) -
Xiangxiu Wang,
Wen Wang,
Yiman Wang,
Jia Chen,
Guifen Liu,
Yong Zhang
Publication year - 2021
Publication title -
genome research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 9.556
H-Index - 297
eISSN - 1549-5469
pISSN - 1088-9051
DOI - 10.1101/gr.275837.121
Subject(s) - biology , maternal to zygotic transition , homeobox protein nanog , zebrafish , transcription factor , microbiology and biotechnology , embryogenesis , embryonic stem cell , genetics , gene , embryo , induced pluripotent stem cell , zygote
Key transcription factors (TFs) play critical roles in zygotic genome activation (ZGA) during early embryogenesis, whereas genome-wide occupancies of only a few factors have been profiled during ZGA due to the limitation of cell numbers or the lack of high-quality antibodies. Here, we present FitCUT&RUN, a modified CUT&RUN method, in which an Fc fragment of immunoglobulin G is used for tagging, to profile TF occupancy in an antibody-free manner and demonstrate its reliability and robustness using as few as 5000 K562 cells. We applied FitCUT&RUN to zebrafish undergoing embryogenesis to generate reliable occupancy profiles of three known activators of zebrafish ZGA: Nanog, Pou5f3, and Sox19b. By profiling the time-series occupancy of Nanog during zebrafish ZGA, we observed a clear trend toward a gradual increase in Nanog occupancy and found that Nanog occupancy prior to the major phase of ZGA is important for the activation of some early transcribed genes.
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