The GATA transcription factor GtaC regulates early developmental gene expression dynamics in Dictyostelium

In many systems, including the social amoeba Dictyostelium discoideum , development is often marked by dynamic morphological and transcriptional changes orchestrated by key transcription factors. However, efforts to examine sequential genome-wide changes of gene regulation in developmental processes...

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Veröffentlicht in:Nature communications 2015-07, Vol.6 (1), p.7551-7551, Article 7551
Hauptverfasser: Santhanam, Balaji, Cai, Huaqing, Devreotes, Peter N., Shaulsky, Gad, Katoh-Kurasawa, Mariko
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Sprache:eng
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Zusammenfassung:In many systems, including the social amoeba Dictyostelium discoideum , development is often marked by dynamic morphological and transcriptional changes orchestrated by key transcription factors. However, efforts to examine sequential genome-wide changes of gene regulation in developmental processes have been fairly limited. Here we report the developmental regulatory dynamics of GtaC, a GATA-type zinc-finger transcription factor, through the analyses of serial ChIP- and RNA-sequencing data. GtaC is essential for developmental progression, decoding extracellular cAMP pulses during early development and may play a role in mediating cell-type differentiation at later stages. We find that GtaC exhibits temporally distinctive DNA-binding patterns concordant with each developmental stage. We identify direct GtaC targets and observe cotemporaneous GtaC-binding and developmental expression regulation. Our results suggest that GtaC regulates multiple physiological processes as Dictyostelium transitions from a group of unicellular amoebae to an integrated multicellular organism. Development involves dynamic transcriptional changes. By serial ChIP- and RNA-sequencing, here, the authors show that GtaC, a GATA type transcription factor, exhibits temporally distinctive DNA binding and regulation of gene expression concordant with the development in the social amoeba Dictyostelium discoideum .
ISSN:2041-1723
2041-1723
DOI:10.1038/ncomms8551