The TALE Factors and Nuclear Factor Y Cooperate to Drive Transcription at Zygotic Genome Activation

The TALE factors, comprising the pbx and prep/meis gene families, are transcription factors (TFs) vital to the proper formation of anterior anatomical structures during embryonic development. Although best understood as essential cofactors for tissue-specific TFs such as the hox genes during segment...

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Main Author: Stanney, William J., III
Format: Others
Published: eScholarship@UMMS 2019
Subjects:
NFY
Online Access:https://escholarship.umassmed.edu/gsbs_diss/1045
https://escholarship.umassmed.edu/cgi/viewcontent.cgi?article=2054&context=gsbs_diss
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spelling ndltd-umassmed.edu-oai-escholarship.umassmed.edu-gsbs_diss-20542021-08-23T17:15:10Z The TALE Factors and Nuclear Factor Y Cooperate to Drive Transcription at Zygotic Genome Activation Stanney, William J., III The TALE factors, comprising the pbx and prep/meis gene families, are transcription factors (TFs) vital to the proper formation of anterior anatomical structures during embryonic development. Although best understood as essential cofactors for tissue-specific TFs such as the hox genes during segmentation, the TALE factors also form complexes with nuclear factor Y (NFY) in the early zygote. In zebrafish, Pbx4, Prep1, and NFY are maternally deposited and can access their DNA binding sites in compact chromatin. Our results suggest that TALE/NFY complexes have a unique role in early embryonic development which is distinct from each factor’s independent functions at later stages. To characterize these TALE/NFY complexes, we employed high-throughput transcriptomic and genomic techniques in zebrafish embryos. Using dominant negatives to disrupt the function of each factor, we find that they display similar, but not identical, loss-of-function phenotypes and co-regulate genes involved in transcription regulation and embryonic development. Independently, the TALE factors regulate homeobox genes and NFY governs cilia-related genes. ChIP-seq analysis at zygotic genome activation reveals that the TALE factors occupy DECA sites adjacent to CCAAT boxes near genes expressed early in development and involved with transcription regulation. Finally, DNA elements containing TALE and NFY binding sites drive reporter gene expression in transgenic zebrafish, and disruption of TALE/NFY binding via mutation or dominant negatives eliminates this expression. Taken together, this data suggests that the TALE factors and NFY cooperate to regulate a set of development and transcription control genes in early zygotic development but also have independent roles after gastrulation. 2019-08-06T07:00:00Z text application/pdf https://escholarship.umassmed.edu/gsbs_diss/1045 https://escholarship.umassmed.edu/cgi/viewcontent.cgi?article=2054&context=gsbs_diss Licensed under a Creative Commons license http://creativecommons.org/licenses/by-nc/4.0/ GSBS Dissertations and Theses eScholarship@UMMS transcription embryogenesis maternal zygotic enhancer nucleosome pioneer factor epigenetics TALE NFY Biochemistry Developmental Biology Molecular Biology
collection NDLTD
format Others
sources NDLTD
topic transcription
embryogenesis
maternal
zygotic
enhancer
nucleosome
pioneer factor
epigenetics
TALE
NFY
Biochemistry
Developmental Biology
Molecular Biology
spellingShingle transcription
embryogenesis
maternal
zygotic
enhancer
nucleosome
pioneer factor
epigenetics
TALE
NFY
Biochemistry
Developmental Biology
Molecular Biology
Stanney, William J., III
The TALE Factors and Nuclear Factor Y Cooperate to Drive Transcription at Zygotic Genome Activation
description The TALE factors, comprising the pbx and prep/meis gene families, are transcription factors (TFs) vital to the proper formation of anterior anatomical structures during embryonic development. Although best understood as essential cofactors for tissue-specific TFs such as the hox genes during segmentation, the TALE factors also form complexes with nuclear factor Y (NFY) in the early zygote. In zebrafish, Pbx4, Prep1, and NFY are maternally deposited and can access their DNA binding sites in compact chromatin. Our results suggest that TALE/NFY complexes have a unique role in early embryonic development which is distinct from each factor’s independent functions at later stages. To characterize these TALE/NFY complexes, we employed high-throughput transcriptomic and genomic techniques in zebrafish embryos. Using dominant negatives to disrupt the function of each factor, we find that they display similar, but not identical, loss-of-function phenotypes and co-regulate genes involved in transcription regulation and embryonic development. Independently, the TALE factors regulate homeobox genes and NFY governs cilia-related genes. ChIP-seq analysis at zygotic genome activation reveals that the TALE factors occupy DECA sites adjacent to CCAAT boxes near genes expressed early in development and involved with transcription regulation. Finally, DNA elements containing TALE and NFY binding sites drive reporter gene expression in transgenic zebrafish, and disruption of TALE/NFY binding via mutation or dominant negatives eliminates this expression. Taken together, this data suggests that the TALE factors and NFY cooperate to regulate a set of development and transcription control genes in early zygotic development but also have independent roles after gastrulation.
author Stanney, William J., III
author_facet Stanney, William J., III
author_sort Stanney, William J., III
title The TALE Factors and Nuclear Factor Y Cooperate to Drive Transcription at Zygotic Genome Activation
title_short The TALE Factors and Nuclear Factor Y Cooperate to Drive Transcription at Zygotic Genome Activation
title_full The TALE Factors and Nuclear Factor Y Cooperate to Drive Transcription at Zygotic Genome Activation
title_fullStr The TALE Factors and Nuclear Factor Y Cooperate to Drive Transcription at Zygotic Genome Activation
title_full_unstemmed The TALE Factors and Nuclear Factor Y Cooperate to Drive Transcription at Zygotic Genome Activation
title_sort tale factors and nuclear factor y cooperate to drive transcription at zygotic genome activation
publisher eScholarship@UMMS
publishDate 2019
url https://escholarship.umassmed.edu/gsbs_diss/1045
https://escholarship.umassmed.edu/cgi/viewcontent.cgi?article=2054&context=gsbs_diss
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