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Transient genome-wide interactions of the master transcription factor NLP7 initiate a rapid nitrogen-response cascade.


ABSTRACT: Dynamic reprogramming of gene regulatory networks (GRNs) enables organisms to rapidly respond to environmental perturbation. However, the underlying transient interactions between transcription factors (TFs) and genome-wide targets typically elude biochemical detection. Here, we capture both stable and transient TF-target interactions genome-wide within minutes after controlled TF nuclear import using time-series chromatin immunoprecipitation (ChIP-seq) and/or DNA adenine methyltransferase identification (DamID-seq). The transient TF-target interactions captured uncover the early mode-of-action of NIN-LIKE PROTEIN 7 (NLP7), a master regulator of the nitrogen signaling pathway in plants. These transient NLP7 targets captured in root cells using temporal TF perturbation account for 50% of NLP7-regulated genes not detectably bound by NLP7 in planta. Rapid and transient NLP7 binding activates early nitrogen response TFs, which we validate to amplify the NLP7-initiated transcriptional cascade. Our approaches to capture transient TF-target interactions genome-wide can be applied to validate dynamic GRN models for any pathway or organism of interest.

SUBMITTER: Alvarez JM 

PROVIDER: S-EPMC7052136 | biostudies-literature | 2020 Mar

REPOSITORIES: biostudies-literature

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Transient genome-wide interactions of the master transcription factor NLP7 initiate a rapid nitrogen-response cascade.

Alvarez José M JM   Schinke Anna-Lena AL   Brooks Matthew D MD   Pasquino Angelo A   Leonelli Lauriebeth L   Varala Kranthi K   Safi Alaeddine A   Krouk Gabriel G   Krapp Anne A   Coruzzi Gloria M GM  

Nature communications 20200302 1


Dynamic reprogramming of gene regulatory networks (GRNs) enables organisms to rapidly respond to environmental perturbation. However, the underlying transient interactions between transcription factors (TFs) and genome-wide targets typically elude biochemical detection. Here, we capture both stable and transient TF-target interactions genome-wide within minutes after controlled TF nuclear import using time-series chromatin immunoprecipitation (ChIP-seq) and/or DNA adenine methyltransferase ident  ...[more]

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