Literature DB >> 29106906

Transcriptional regulation of Nfix by NFIB drives astrocytic maturation within the developing spinal cord.

Elise Matuzelski1, Jens Bunt2, Danyon Harkins1, Jonathan W C Lim2, Richard M Gronostajski3, Linda J Richards4, Lachlan Harris1, Michael Piper5.   

Abstract

During mouse spinal cord development, ventricular zone progenitor cells transition from producing neurons to producing glia at approximately embryonic day 11.5, a process known as the gliogenic switch. The transcription factors Nuclear Factor I (NFI) A and B initiate this developmental transition, but the contribution of a third NFI member, NFIX, remains unknown. Here, we reveal that ventricular zone progenitor cells within the spinal cord express NFIX after the onset of NFIA and NFIB expression, and after the gliogenic switch has occurred. Mice lacking NFIX exhibit normal neurogenesis within the spinal cord, and, while early astrocytic differentiation proceeds normally, aspects of terminal astrocytic differentiation are impaired. Finally, we report that, in the absence of Nfia or Nfib, there is a marked reduction in the spinal cord expression of NFIX, and that NFIB can transcriptionally activate Nfix expression in vitro. These data demonstrate that NFIX is part of the downstream transcriptional program through which NFIA and NFIB coordinate gliogenesis within the spinal cord. This hierarchical organisation of NFI protein expression and function during spinal cord gliogenesis reveals a previously unrecognised auto-regulatory mechanism within this gene family.
Copyright © 2017 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Astrocyte; GFAP; Gliogenesis; NFIA; NFIB; NFIX; Nuclear Factor I; Spinal cord

Mesh:

Substances:

Year:  2017        PMID: 29106906     DOI: 10.1016/j.ydbio.2017.10.019

Source DB:  PubMed          Journal:  Dev Biol        ISSN: 0012-1606            Impact factor:   3.582


  19 in total

1.  Single-Cell RNA-Seq Analysis of Retinal Development Identifies NFI Factors as Regulating Mitotic Exit and Late-Born Cell Specification.

Authors:  Brian S Clark; Genevieve L Stein-O'Brien; Fion Shiau; Gabrielle H Cannon; Emily Davis-Marcisak; Thomas Sherman; Clayton P Santiago; Thanh V Hoang; Fatemeh Rajaii; Rebecca E James-Esposito; Richard M Gronostajski; Elana J Fertig; Loyal A Goff; Seth Blackshaw
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Journal:  Mol Cell       Date:  2019-07-30       Impact factor: 17.970

3.  Common Regulatory Targets of NFIA, NFIX and NFIB during Postnatal Cerebellar Development.

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Review 4.  Regulation of GFAP Expression.

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6.  STAU2 binds a complex RNA cargo that changes temporally with production of diverse intermediate progenitor cells during mouse corticogenesis.

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7.  Deletion of NFIX results in defective progression through meiosis within the mouse testis†.

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9.  Transcriptional regulation of ependymal cell maturation within the postnatal brain.

Authors:  Diana Vidovic; Raul Ayala Davila; Richard M Gronostajski; Tracey J Harvey; Michael Piper
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10.  Control of neurogenic competence in mammalian hypothalamic tanycytes.

Authors:  Sooyeon Yoo; Juhyun Kim; Pin Lyu; Thanh V Hoang; Alex Ma; Vickie Trinh; Weina Dai; Lizhi Jiang; Patrick Leavey; Leighton Duncan; Jae-Kyung Won; Sung-Hye Park; Jiang Qian; Solange P Brown; Seth Blackshaw
Journal:  Sci Adv       Date:  2021-05-28       Impact factor: 14.136

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